Access the full text.
Sign up today, get DeepDyve free for 14 days.
Loading next page...
/lp/wiley/the-role-of-wnt1-mutant-variant-wnt1c-677c-t-in-osteogenesis-ayj04ttyAW
References (86)
-
Clara Barbirato, Maíra Trancozo, M. Almeida, Almeida Ls, Santos To, Duarte Jc, M. Rebouças, Sipolatti, V. Nunes, Flávia Paula (2015)
Mutational characterization of the P3H1/CRTAP/CypB complex in recessive osteogenesis imperfecta.Genetics and molecular research : GMR, 14 4
-
R. Morello, P. Esposito
Osteogenesis Imperfecta.Proceedings of the Royal Society of Medicine, 21 12
-
(2018)
Monoallelic and biallelic -
( Ozer, F. F. , Dagdelen, S. , & Erbas, T. (2018). Relation of RANKL and OPG levels with bone resorption in patients with acromegaly and prolactinoma. Hormone and Metabolic Research, 50(7), 562–567. 10.1055/a-0630-1529 29895074)
Ozer, F. F. , Dagdelen, S. , & Erbas, T. (2018). Relation of RANKL and OPG levels with bone resorption in patients with acromegaly and prolactinoma. Hormone and Metabolic Research, 50(7), 562–567. 10.1055/a-0630-1529 29895074Ozer, F. F. , Dagdelen, S. , & Erbas, T. (2018). Relation of RANKL and OPG levels with bone resorption in patients with acromegaly and prolactinoma. Hormone and Metabolic Research, 50(7), 562–567. 10.1055/a-0630-1529 29895074, Ozer, F. F. , Dagdelen, S. , & Erbas, T. (2018). Relation of RANKL and OPG levels with bone resorption in patients with acromegaly and prolactinoma. Hormone and Metabolic Research, 50(7), 562–567. 10.1055/a-0630-1529 29895074
-
( Fiscaletti, M. , Biggin, A. , Bennetts, B. , Wong, K. , Briody, J. , Pacey, V. , … Munns, C. F. (2018). Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment. Bone, 110, 66–75. 10.1016/j.bone.2018.01.031 29382611)
Fiscaletti, M. , Biggin, A. , Bennetts, B. , Wong, K. , Briody, J. , Pacey, V. , … Munns, C. F. (2018). Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment. Bone, 110, 66–75. 10.1016/j.bone.2018.01.031 29382611Fiscaletti, M. , Biggin, A. , Bennetts, B. , Wong, K. , Briody, J. , Pacey, V. , … Munns, C. F. (2018). Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment. Bone, 110, 66–75. 10.1016/j.bone.2018.01.031 29382611, Fiscaletti, M. , Biggin, A. , Bennetts, B. , Wong, K. , Briody, J. , Pacey, V. , … Munns, C. F. (2018). Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment. Bone, 110, 66–75. 10.1016/j.bone.2018.01.031 29382611
-
S. Fahiminiya, J. Majewski, J. Mort, P. Moffatt, F. Glorieux, F. Rauch (2013)
Mutations in WNT1 are a cause of osteogenesis imperfectaJournal of Medical Genetics, 50
-
S. Holmen, C. Zylstra, A. Mukherjee, R. Sigler, M. Faugere, M. Bouxsein, L. Deng, T. Clemens, B. Williams (2005)
Essential Role of β-Catenin in Postnatal Bone Acquisition*Journal of Biological Chemistry, 280
-
H. Blair, Q. Larrouture, Yanan Li, Hang Lin, Donna Beer-Stoltz, Li Liu, R. Tuan, L. Robinson, P. Schlesinger, D. Nelson (2016)
Osteoblast Differentiation and Bone Matrix Formation In Vivo and In Vitro.Tissue engineering. Part B, Reviews, 23 3
-
M. Fiscaletti, A. Biggin, B. Bennetts, Karen Wong, J. Briody, V. Pacey, C. Birman, C. Munns (2018)
Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment.Bone, 110
-
R. Mäkitie, A. Kämpe, F. Taylan, O. Mäkitie (2017)
Recent Discoveries in Monogenic Disorders of Childhood Bone FragilityCurrent Osteoporosis Reports, 15
-
( Janda, C. Y. , Waghray, D. , Levin, A. M. , Thomas, C. , & Garcia, K. C. (2012). Structural basis of Wnt recognition by Frizzled. Science, 337(6090), 59–64. 10.1126/science.1222879 22653731)
Janda, C. Y. , Waghray, D. , Levin, A. M. , Thomas, C. , & Garcia, K. C. (2012). Structural basis of Wnt recognition by Frizzled. Science, 337(6090), 59–64. 10.1126/science.1222879 22653731Janda, C. Y. , Waghray, D. , Levin, A. M. , Thomas, C. , & Garcia, K. C. (2012). Structural basis of Wnt recognition by Frizzled. Science, 337(6090), 59–64. 10.1126/science.1222879 22653731, Janda, C. Y. , Waghray, D. , Levin, A. M. , Thomas, C. , & Garcia, K. C. (2012). Structural basis of Wnt recognition by Frizzled. Science, 337(6090), 59–64. 10.1126/science.1222879 22653731
-
( Yasuda, H. , Shima, N. , Nakagawa, N. , Yamaguchi, K. , Kinosaki, M. , Mochizuki, S. , … Suda, T. (1998). Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis‐inhibitory factor and is identical to TRANCE/RANKL. PNAS, 95(7), 3597–3602. 10.1073/pnas.95.7.3597 9520411)
Yasuda, H. , Shima, N. , Nakagawa, N. , Yamaguchi, K. , Kinosaki, M. , Mochizuki, S. , … Suda, T. (1998). Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis‐inhibitory factor and is identical to TRANCE/RANKL. PNAS, 95(7), 3597–3602. 10.1073/pnas.95.7.3597 9520411Yasuda, H. , Shima, N. , Nakagawa, N. , Yamaguchi, K. , Kinosaki, M. , Mochizuki, S. , … Suda, T. (1998). Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis‐inhibitory factor and is identical to TRANCE/RANKL. PNAS, 95(7), 3597–3602. 10.1073/pnas.95.7.3597 9520411, Yasuda, H. , Shima, N. , Nakagawa, N. , Yamaguchi, K. , Kinosaki, M. , Mochizuki, S. , … Suda, T. (1998). Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis‐inhibitory factor and is identical to TRANCE/RANKL. PNAS, 95(7), 3597–3602. 10.1073/pnas.95.7.3597 9520411
-
(2005)
Essential role -
( Barbirato, C. , Trancozo, M. , Almeida, M. G. , Almeida, L. S. , Santos, T. O. , Duarte, J. C. , … Paula, F. (2015). Mutational characterization of the P3H1/CRTAP/CypB complex in recessive osteogenesis imperfecta. Genetics and Molecular Research [Electronic Resource], 14(4), 15848–15858. 10.4238/2015.December.1.36 )
Barbirato, C. , Trancozo, M. , Almeida, M. G. , Almeida, L. S. , Santos, T. O. , Duarte, J. C. , … Paula, F. (2015). Mutational characterization of the P3H1/CRTAP/CypB complex in recessive osteogenesis imperfecta. Genetics and Molecular Research [Electronic Resource], 14(4), 15848–15858. 10.4238/2015.December.1.36Barbirato, C. , Trancozo, M. , Almeida, M. G. , Almeida, L. S. , Santos, T. O. , Duarte, J. C. , … Paula, F. (2015). Mutational characterization of the P3H1/CRTAP/CypB complex in recessive osteogenesis imperfecta. Genetics and Molecular Research [Electronic Resource], 14(4), 15848–15858. 10.4238/2015.December.1.36 , Barbirato, C. , Trancozo, M. , Almeida, M. G. , Almeida, L. S. , Santos, T. O. , Duarte, J. C. , … Paula, F. (2015). Mutational characterization of the P3H1/CRTAP/CypB complex in recessive osteogenesis imperfecta. Genetics and Molecular Research [Electronic Resource], 14(4), 15848–15858. 10.4238/2015.December.1.36
-
(2018)
Novel familial mutation -
Fei Liu, S. Kohlmeier, Cun-Yu Wang (2008)
Wnt signaling and skeletal development.Cellular signalling, 20 6
-
D. Glass, P. Bialek, J. Ahn, M. Starbuck, M. Patel, H. Clevers, M. Taketo, Fanxin Long, A. McMahon, R. Lang, G. Karsenty (2005)
Canonical Wnt signaling in differentiated osteoblasts controls osteoclast differentiation.Developmental cell, 8 5
-
(2002)
Bone morphogenetic protein receptor -
(2016)
Variable brain -
(2000)
Direct stimulation of osteoclas - tic -
Li‐an Wu, Feng Wang, K. Donly, Andrew Baker, Chunyan Wan, Daoshu Luo, M. MacDougall, Shuo Chen (2015)
Establishment of Immortalized BMP2/4 Double Knock‐Out Osteoblastic Cells Is Essential for Study of Osteoblast Growth, Differentiation, and OsteogenesisJournal of Cellular Physiology, 231
-
S. Holmen, C. Zylstra, A. Mukherjee, R. Sigler, M. Faugere, M. Bouxsein, L. Deng, T. Clemens, B. Williams (2005)
Essential role of beta-catenin in postnatal bone acquisition.The Journal of biological chemistry, 280 22
-
( Rauch, F. , & Glorieux, F. H. (2004). Osteogenesis imperfecta. Lancet, 363(9418), 1377–1385. 10.1016/s0140-6736(04)16051-0 15110498)
Rauch, F. , & Glorieux, F. H. (2004). Osteogenesis imperfecta. Lancet, 363(9418), 1377–1385. 10.1016/s0140-6736(04)16051-0 15110498Rauch, F. , & Glorieux, F. H. (2004). Osteogenesis imperfecta. Lancet, 363(9418), 1377–1385. 10.1016/s0140-6736(04)16051-0 15110498, Rauch, F. , & Glorieux, F. H. (2004). Osteogenesis imperfecta. Lancet, 363(9418), 1377–1385. 10.1016/s0140-6736(04)16051-0 15110498
-
( Zhong, Z. , Ethen, N. J. , & Williams, B. O. (2014). WNT signaling in bone development and homeostasis. Wiley Interdisciplinary Reviews‐Developmental Biology, 3(6), 489–500. 10.1002/wdev.159 25270716)
Zhong, Z. , Ethen, N. J. , & Williams, B. O. (2014). WNT signaling in bone development and homeostasis. Wiley Interdisciplinary Reviews‐Developmental Biology, 3(6), 489–500. 10.1002/wdev.159 25270716Zhong, Z. , Ethen, N. J. , & Williams, B. O. (2014). WNT signaling in bone development and homeostasis. Wiley Interdisciplinary Reviews‐Developmental Biology, 3(6), 489–500. 10.1002/wdev.159 25270716, Zhong, Z. , Ethen, N. J. , & Williams, B. O. (2014). WNT signaling in bone development and homeostasis. Wiley Interdisciplinary Reviews‐Developmental Biology, 3(6), 489–500. 10.1002/wdev.159 25270716
-
I. Kramer, C. Halleux, Hansjoerg Keller, Marco Pegurri, Jonathan Gooi, P. Weber, Jian Feng, L. Bonewald, M. Kneissel (2010)
Osteocyte Wnt/β-Catenin Signaling Is Required for Normal Bone HomeostasisMolecular and Cellular Biology, 30
-
( Forlino, A. , Cabral, W. A. , Barnes, A. M. , & Marini, J. C. (2011). New perspectives on osteogenesis imperfecta. Nature Reviews Endocrinology, 7(9), 540–557. 10.1038/nrendo.2011.81 )
Forlino, A. , Cabral, W. A. , Barnes, A. M. , & Marini, J. C. (2011). New perspectives on osteogenesis imperfecta. Nature Reviews Endocrinology, 7(9), 540–557. 10.1038/nrendo.2011.81Forlino, A. , Cabral, W. A. , Barnes, A. M. , & Marini, J. C. (2011). New perspectives on osteogenesis imperfecta. Nature Reviews Endocrinology, 7(9), 540–557. 10.1038/nrendo.2011.81 , Forlino, A. , Cabral, W. A. , Barnes, A. M. , & Marini, J. C. (2011). New perspectives on osteogenesis imperfecta. Nature Reviews Endocrinology, 7(9), 540–557. 10.1038/nrendo.2011.81
-
Rongrong Zhang, B. Oyajobi, S. Harris, Di Chen, Christopher Tsao, H. Deng, Ming Zhao (2013)
Wnt/β-catenin signaling activates bone morphogenetic protein 2 expression in osteoblasts.Bone, 52 1
-
(2013)
Wnt/beta-catenin signaling activates bone -
Shahida Moosa, G. Yamamoto, L. Garbes, Katharina Keupp, A. Beleza‐Meireles, C. Moreno, E. Valadares, Sérgio Sousa, S. Maia, J. Saraiva, R. Honjo, C. Kim, Hamilton Menezes, E. Lausch, Pablo Lorini, A. Lamounier, Tulio Carniero, C. Giunta, M. Rohrbach, M. Janner, O. Semler, Filippo Beleggia, Yun Li, G. Yigit, N. Reintjes, J. Altmüller, P. Nürnberg, D. Cavalcanti, B. Zabel, M. Warman, D. Bertola, B. Wollnik, C. Netzer (2019)
Autosomal Recessive Mutations in MESD Cause Osteogenesis Imperfecta.American journal of human genetics
-
(2008)
Wnt signaling and skele -
( Aldinger, K. A. , Mendelsohn, N. J. , Chung, B. H. , Zhang, W. , Cohn, D. H. , Fernandez, B. , … Curry, C. J. (2016). Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations. Journal of Medical Genetics, 53(6), 427–430. 10.1136/jmedgenet-2015-103476 26671912)
Aldinger, K. A. , Mendelsohn, N. J. , Chung, B. H. , Zhang, W. , Cohn, D. H. , Fernandez, B. , … Curry, C. J. (2016). Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations. Journal of Medical Genetics, 53(6), 427–430. 10.1136/jmedgenet-2015-103476 26671912Aldinger, K. A. , Mendelsohn, N. J. , Chung, B. H. , Zhang, W. , Cohn, D. H. , Fernandez, B. , … Curry, C. J. (2016). Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations. Journal of Medical Genetics, 53(6), 427–430. 10.1136/jmedgenet-2015-103476 26671912, Aldinger, K. A. , Mendelsohn, N. J. , Chung, B. H. , Zhang, W. , Cohn, D. H. , Fernandez, B. , … Curry, C. J. (2016). Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations. Journal of Medical Genetics, 53(6), 427–430. 10.1136/jmedgenet-2015-103476 26671912
-
( Li, L. , Mao, B. , Li, S. , Xiao, J. , Wang, H. , Zhang, J. , … Zhang, X. (2019). Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta. Human Mutation, 40(5), 588–600. 10.1002/humu.23718 30715774)
Li, L. , Mao, B. , Li, S. , Xiao, J. , Wang, H. , Zhang, J. , … Zhang, X. (2019). Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta. Human Mutation, 40(5), 588–600. 10.1002/humu.23718 30715774Li, L. , Mao, B. , Li, S. , Xiao, J. , Wang, H. , Zhang, J. , … Zhang, X. (2019). Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta. Human Mutation, 40(5), 588–600. 10.1002/humu.23718 30715774, Li, L. , Mao, B. , Li, S. , Xiao, J. , Wang, H. , Zhang, J. , … Zhang, X. (2019). Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta. Human Mutation, 40(5), 588–600. 10.1002/humu.23718 30715774
-
R. Baron, M. Kneissel (2013)
WNT signaling in bone homeostasis and disease: from human mutations to treatmentsNature Medicine, 19
-
(2018)
Novel familial mutation of LRP 5 causing high -
( Roetzer, K. M. , Uyanik, G. , Brehm, A. , Zwerina, J. , Zandieh, S. , Czech, T. , … Klaushofer, K. (2018). Novel familial mutation of LRP5 causing high bone mass: Genetic analysis, clinical presentation, and characterization of bone matrix mineralization. Bone, 107, 154–160. 10.1016/j.bone.2017.12.002 29208525)
Roetzer, K. M. , Uyanik, G. , Brehm, A. , Zwerina, J. , Zandieh, S. , Czech, T. , … Klaushofer, K. (2018). Novel familial mutation of LRP5 causing high bone mass: Genetic analysis, clinical presentation, and characterization of bone matrix mineralization. Bone, 107, 154–160. 10.1016/j.bone.2017.12.002 29208525Roetzer, K. M. , Uyanik, G. , Brehm, A. , Zwerina, J. , Zandieh, S. , Czech, T. , … Klaushofer, K. (2018). Novel familial mutation of LRP5 causing high bone mass: Genetic analysis, clinical presentation, and characterization of bone matrix mineralization. Bone, 107, 154–160. 10.1016/j.bone.2017.12.002 29208525, Roetzer, K. M. , Uyanik, G. , Brehm, A. , Zwerina, J. , Zandieh, S. , Czech, T. , … Klaushofer, K. (2018). Novel familial mutation of LRP5 causing high bone mass: Genetic analysis, clinical presentation, and characterization of bone matrix mineralization. Bone, 107, 154–160. 10.1016/j.bone.2017.12.002 29208525
-
Lulu Li, Bin Mao, Shan Li, Ji-fang Xiao, Han Wang, Jing Zhang, X. Ren, Yanzhou Wang, Yiyang Wu, Yixuan Cao, Chao-xia Lu, Jinsong Gao, Yi You, F. Zhao, Xingzhu Geng, Ya Xiao, Chendan Jiang, Yuqian Ye, Tao Yang, Xiuli Zhao, Xue Zhang (2019)
Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfectaHuman Mutation, 40
-
( Martinez‐Glez, V. , Valencia, M. , Caparros‐Martin, J. A. , Aglan, M. , Temtamy, S. , Tenorio, J. , … Ruiz‐Perez, V. L. (2012). Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta. Human Mutation, 33(2), 343–350. 10.1002/humu.21647 22052668)
Martinez‐Glez, V. , Valencia, M. , Caparros‐Martin, J. A. , Aglan, M. , Temtamy, S. , Tenorio, J. , … Ruiz‐Perez, V. L. (2012). Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta. Human Mutation, 33(2), 343–350. 10.1002/humu.21647 22052668Martinez‐Glez, V. , Valencia, M. , Caparros‐Martin, J. A. , Aglan, M. , Temtamy, S. , Tenorio, J. , … Ruiz‐Perez, V. L. (2012). Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta. Human Mutation, 33(2), 343–350. 10.1002/humu.21647 22052668, Martinez‐Glez, V. , Valencia, M. , Caparros‐Martin, J. A. , Aglan, M. , Temtamy, S. , Tenorio, J. , … Ruiz‐Perez, V. L. (2012). Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta. Human Mutation, 33(2), 343–350. 10.1002/humu.21647 22052668
-
Rachel Keller, T. Tran, Shawna Pyott, M. Pepin, R. Savarirayan, G. McGillivray, D. Nickerson, M. Bamshad, P. Byers (2017)
Monoallelic and Biallelic CREB3L1 Variant Causes Mild and Severe Osteogenesis Imperfecta, RespectivelyGenetics in medicine : official journal of the American College of Medical Genetics, 20
-
C. Laine, K. Joeng, Philippe Campeau, R. Kiviranta, Kati Tarkkonen, M. Grover, James Lu, M. Pekkinen, M. Wessman, T. Heino, Vappu Nieminen-Pihala, Mira Aronen, T. Laine, H. Kröger, W. Cole, A. Lehesjoki, Lisette Nevarez, D. Krakow, C. Curry, D. Cohn, R. Gibbs, Brendan Lee, O. Mäkitie (2013)
WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta.The New England journal of medicine, 368 19
-
A. Forlino, W. Cabral, Aileen Barnes, J. Marini (2011)
New perspectives on osteogenesis imperfectaNature Reviews Endocrinology, 7
-
( Moosa, S. , Yamamoto, G. L. , Garbes, L. , Keupp, K. , Beleza‐Meireles, A. , Moreno, C. A. , … Netzer, C. (2019). Autosomal‐recessive mutations in MESD cause osteogenesis imperfecta. American Journal of Human Genetics, 105(4), 836–843. 10.1016/j.ajhg.2019.08.008 31564437)
Moosa, S. , Yamamoto, G. L. , Garbes, L. , Keupp, K. , Beleza‐Meireles, A. , Moreno, C. A. , … Netzer, C. (2019). Autosomal‐recessive mutations in MESD cause osteogenesis imperfecta. American Journal of Human Genetics, 105(4), 836–843. 10.1016/j.ajhg.2019.08.008 31564437Moosa, S. , Yamamoto, G. L. , Garbes, L. , Keupp, K. , Beleza‐Meireles, A. , Moreno, C. A. , … Netzer, C. (2019). Autosomal‐recessive mutations in MESD cause osteogenesis imperfecta. American Journal of Human Genetics, 105(4), 836–843. 10.1016/j.ajhg.2019.08.008 31564437, Moosa, S. , Yamamoto, G. L. , Garbes, L. , Keupp, K. , Beleza‐Meireles, A. , Moreno, C. A. , … Netzer, C. (2019). Autosomal‐recessive mutations in MESD cause osteogenesis imperfecta. American Journal of Human Genetics, 105(4), 836–843. 10.1016/j.ajhg.2019.08.008 31564437
-
( Laine, C. M. , Joeng, K. S. , Campeau, P. M. , Kiviranta, R. , Tarkkonen, K. , Grover, M. , … Makitie, O. (2013). WNT1 mutations in early‐onset osteoporosis and osteogenesis imperfecta. New England Journal of Medicine, 368(19), 1809–1816. 10.1056/NEJMoa1215458 23656646)
Laine, C. M. , Joeng, K. S. , Campeau, P. M. , Kiviranta, R. , Tarkkonen, K. , Grover, M. , … Makitie, O. (2013). WNT1 mutations in early‐onset osteoporosis and osteogenesis imperfecta. New England Journal of Medicine, 368(19), 1809–1816. 10.1056/NEJMoa1215458 23656646Laine, C. M. , Joeng, K. S. , Campeau, P. M. , Kiviranta, R. , Tarkkonen, K. , Grover, M. , … Makitie, O. (2013). WNT1 mutations in early‐onset osteoporosis and osteogenesis imperfecta. New England Journal of Medicine, 368(19), 1809–1816. 10.1056/NEJMoa1215458 23656646, Laine, C. M. , Joeng, K. S. , Campeau, P. M. , Kiviranta, R. , Tarkkonen, K. , Grover, M. , … Makitie, O. (2013). WNT1 mutations in early‐onset osteoporosis and osteogenesis imperfecta. New England Journal of Medicine, 368(19), 1809–1816. 10.1056/NEJMoa1215458 23656646
-
( Glass, D. A. , 2nd , Bialek , P. , Ahn , J. D., Starbuck, M. , Patel, M. S. , Clevers, H. , … Karsenty, G. (2005). Canonical Wnt signaling in differentiated osteoblasts controls osteoclast differentiation. Developmental Cell, 8(5), 751–764. 10.1016/j.devcel.2005.02.017 15866165)
Glass, D. A. , 2nd , Bialek , P. , Ahn , J. D., Starbuck, M. , Patel, M. S. , Clevers, H. , … Karsenty, G. (2005). Canonical Wnt signaling in differentiated osteoblasts controls osteoclast differentiation. Developmental Cell, 8(5), 751–764. 10.1016/j.devcel.2005.02.017 15866165Glass, D. A. , 2nd , Bialek , P. , Ahn , J. D., Starbuck, M. , Patel, M. S. , Clevers, H. , … Karsenty, G. (2005). Canonical Wnt signaling in differentiated osteoblasts controls osteoclast differentiation. Developmental Cell, 8(5), 751–764. 10.1016/j.devcel.2005.02.017 15866165, Glass, D. A. , 2nd , Bialek , P. , Ahn , J. D., Starbuck, M. , Patel, M. S. , Clevers, H. , … Karsenty, G. (2005). Canonical Wnt signaling in differentiated osteoblasts controls osteoclast differentiation. Developmental Cell, 8(5), 751–764. 10.1016/j.devcel.2005.02.017 15866165
-
( Kaneko, H. , Arakawa, T. , Mano, H. , Kaneda, T. , Ogasawara, A. , Nakagawa, M. , … Hakeda, Y. (2000). Direct stimulation of osteoclastic bone resorption by bone morphogenetic protein (BMP)‐2 and expression of BMP receptors in mature osteoclasts. Bone, 27(4), 479–486.11033442)
Kaneko, H. , Arakawa, T. , Mano, H. , Kaneda, T. , Ogasawara, A. , Nakagawa, M. , … Hakeda, Y. (2000). Direct stimulation of osteoclastic bone resorption by bone morphogenetic protein (BMP)‐2 and expression of BMP receptors in mature osteoclasts. Bone, 27(4), 479–486.11033442Kaneko, H. , Arakawa, T. , Mano, H. , Kaneda, T. , Ogasawara, A. , Nakagawa, M. , … Hakeda, Y. (2000). Direct stimulation of osteoclastic bone resorption by bone morphogenetic protein (BMP)‐2 and expression of BMP receptors in mature osteoclasts. Bone, 27(4), 479–486.11033442, Kaneko, H. , Arakawa, T. , Mano, H. , Kaneda, T. , Ogasawara, A. , Nakagawa, M. , … Hakeda, Y. (2000). Direct stimulation of osteoclastic bone resorption by bone morphogenetic protein (BMP)‐2 and expression of BMP receptors in mature osteoclasts. Bone, 27(4), 479–486.11033442
-
( Zhang, R. , Oyajobi, B. O. , Harris, S. E. , Chen, D. , Tsao, C. , Deng, H. W. , & Zhao, M. (2013). Wnt/beta‐catenin signaling activates bone morphogenetic protein 2 expression in osteoblasts. Bone, 52(1), 145–156. 10.1016/j.bone.2012.09.029 23032104)
Zhang, R. , Oyajobi, B. O. , Harris, S. E. , Chen, D. , Tsao, C. , Deng, H. W. , & Zhao, M. (2013). Wnt/beta‐catenin signaling activates bone morphogenetic protein 2 expression in osteoblasts. Bone, 52(1), 145–156. 10.1016/j.bone.2012.09.029 23032104Zhang, R. , Oyajobi, B. O. , Harris, S. E. , Chen, D. , Tsao, C. , Deng, H. W. , & Zhao, M. (2013). Wnt/beta‐catenin signaling activates bone morphogenetic protein 2 expression in osteoblasts. Bone, 52(1), 145–156. 10.1016/j.bone.2012.09.029 23032104, Zhang, R. , Oyajobi, B. O. , Harris, S. E. , Chen, D. , Tsao, C. , Deng, H. W. , & Zhao, M. (2013). Wnt/beta‐catenin signaling activates bone morphogenetic protein 2 expression in osteoblasts. Bone, 52(1), 145–156. 10.1016/j.bone.2012.09.029 23032104
-
H. Kaneko, H. Kaneko, T. Arakawa, H. Mano, T. Kaneda, A. Ogasawara, M. Nakagawa, Y. Toyama, Y. Yabe, M. Kumegawa, Y. Hakeda (2000)
Direct stimulation of osteoclastic bone resorption by bone morphogenetic protein (BMP)-2 and expression of BMP receptors in mature osteoclasts.Bone, 27 4
-
( Fahiminiya, S. , Majewski, J. , Mort, J. , Moffatt, P. , Glorieux, F. H. , & Rauch, F. (2013). Mutations in WNT1 are a cause of osteogenesis imperfecta. Journal of Medical Genetics, 50(5), 345–348. 10.1136/jmedgenet-2013-101567 23434763)
Fahiminiya, S. , Majewski, J. , Mort, J. , Moffatt, P. , Glorieux, F. H. , & Rauch, F. (2013). Mutations in WNT1 are a cause of osteogenesis imperfecta. Journal of Medical Genetics, 50(5), 345–348. 10.1136/jmedgenet-2013-101567 23434763Fahiminiya, S. , Majewski, J. , Mort, J. , Moffatt, P. , Glorieux, F. H. , & Rauch, F. (2013). Mutations in WNT1 are a cause of osteogenesis imperfecta. Journal of Medical Genetics, 50(5), 345–348. 10.1136/jmedgenet-2013-101567 23434763, Fahiminiya, S. , Majewski, J. , Mort, J. , Moffatt, P. , Glorieux, F. H. , & Rauch, F. (2013). Mutations in WNT1 are a cause of osteogenesis imperfecta. Journal of Medical Genetics, 50(5), 345–348. 10.1136/jmedgenet-2013-101567 23434763
-
R. Levasseur, D. Lacombe, M. Vernejoul (2005)
LRP5 mutations in osteoporosis-pseudoglioma syndrome and high-bone-mass disorders.Joint, bone, spine : revue du rhumatisme, 72 3
-
Ming Zhao, S. Harris, D. Horn, Z. Geng, R. Nishimura, G. Mundy, Di Chen (2002)
Bone morphogenetic protein receptor signaling is necessary for normal murine postnatal bone formationThe Journal of Cell Biology, 157
-
F. Ozer, S. Dagdelen, T. Erbas (2018)
Relation of RANKL and OPG Levels with Bone Resorption in Patients with Acromegaly and ProlactinomaHormone and Metabolic Research, 50
-
( Takahashi, N. , Maeda, K. , Ishihara, A. , Uehara, S. , & Kobayashi, Y. (2011). Regulatory mechanism of osteoclastogenesis by RANKL and Wnt signals. Frontiers in Bioscience (Landmark Ed), 16, 21–30.)
Takahashi, N. , Maeda, K. , Ishihara, A. , Uehara, S. , & Kobayashi, Y. (2011). Regulatory mechanism of osteoclastogenesis by RANKL and Wnt signals. Frontiers in Bioscience (Landmark Ed), 16, 21–30.Takahashi, N. , Maeda, K. , Ishihara, A. , Uehara, S. , & Kobayashi, Y. (2011). Regulatory mechanism of osteoclastogenesis by RANKL and Wnt signals. Frontiers in Bioscience (Landmark Ed), 16, 21–30., Takahashi, N. , Maeda, K. , Ishihara, A. , Uehara, S. , & Kobayashi, Y. (2011). Regulatory mechanism of osteoclastogenesis by RANKL and Wnt signals. Frontiers in Bioscience (Landmark Ed), 16, 21–30.
-
( Wright, H. L. , McCarthy, H. S. , Middleton, J. , & Marshall, M. J. (2009). RANK, RANKL and osteoprotegerin in bone biology and disease. Current Reviews in Musculoskeletal Medicine, 2(1), 56–64. 10.1007/s12178-009-9046-7 19468919)
Wright, H. L. , McCarthy, H. S. , Middleton, J. , & Marshall, M. J. (2009). RANK, RANKL and osteoprotegerin in bone biology and disease. Current Reviews in Musculoskeletal Medicine, 2(1), 56–64. 10.1007/s12178-009-9046-7 19468919Wright, H. L. , McCarthy, H. S. , Middleton, J. , & Marshall, M. J. (2009). RANK, RANKL and osteoprotegerin in bone biology and disease. Current Reviews in Musculoskeletal Medicine, 2(1), 56–64. 10.1007/s12178-009-9046-7 19468919, Wright, H. L. , McCarthy, H. S. , Middleton, J. , & Marshall, M. J. (2009). RANK, RANKL and osteoprotegerin in bone biology and disease. Current Reviews in Musculoskeletal Medicine, 2(1), 56–64. 10.1007/s12178-009-9046-7 19468919
-
( Keller, R. B. , Tran, T. T. , Pyott, S. M. , Pepin, M. G. , Savarirayan, R. , McGillivray, G. , … Byers, P. H. (2018). Monoallelic and biallelic CREB3L1 variant causes mild and severe osteogenesis imperfecta, respectively. Genetics in Medicine, 20(4), 411–419. 10.1038/gim.2017.115 28817112)
Keller, R. B. , Tran, T. T. , Pyott, S. M. , Pepin, M. G. , Savarirayan, R. , McGillivray, G. , … Byers, P. H. (2018). Monoallelic and biallelic CREB3L1 variant causes mild and severe osteogenesis imperfecta, respectively. Genetics in Medicine, 20(4), 411–419. 10.1038/gim.2017.115 28817112Keller, R. B. , Tran, T. T. , Pyott, S. M. , Pepin, M. G. , Savarirayan, R. , McGillivray, G. , … Byers, P. H. (2018). Monoallelic and biallelic CREB3L1 variant causes mild and severe osteogenesis imperfecta, respectively. Genetics in Medicine, 20(4), 411–419. 10.1038/gim.2017.115 28817112, Keller, R. B. , Tran, T. T. , Pyott, S. M. , Pepin, M. G. , Savarirayan, R. , McGillivray, G. , … Byers, P. H. (2018). Monoallelic and biallelic CREB3L1 variant causes mild and severe osteogenesis imperfecta, respectively. Genetics in Medicine, 20(4), 411–419. 10.1038/gim.2017.115 28817112
-
( Kramer, I. , Halleux, C. , Keller, H. , Pegurri, M. , Gooi, J. H. , Weber, P. B. , … Kneissel, M. (2010). Osteocyte Wnt/beta‐catenin signaling is required for normal bone homeostasis. Molecular and Cellular Biology, 30(12), 3071–3085. 10.1128/MCB.01428-09 20404086)
Kramer, I. , Halleux, C. , Keller, H. , Pegurri, M. , Gooi, J. H. , Weber, P. B. , … Kneissel, M. (2010). Osteocyte Wnt/beta‐catenin signaling is required for normal bone homeostasis. Molecular and Cellular Biology, 30(12), 3071–3085. 10.1128/MCB.01428-09 20404086Kramer, I. , Halleux, C. , Keller, H. , Pegurri, M. , Gooi, J. H. , Weber, P. B. , … Kneissel, M. (2010). Osteocyte Wnt/beta‐catenin signaling is required for normal bone homeostasis. Molecular and Cellular Biology, 30(12), 3071–3085. 10.1128/MCB.01428-09 20404086, Kramer, I. , Halleux, C. , Keller, H. , Pegurri, M. , Gooi, J. H. , Weber, P. B. , … Kneissel, M. (2010). Osteocyte Wnt/beta‐catenin signaling is required for normal bone homeostasis. Molecular and Cellular Biology, 30(12), 3071–3085. 10.1128/MCB.01428-09 20404086
-
H. Yasuda, N. Shima, N. Nakagawa, K. Yamaguchi, M. Kinosaki, S. Mochizuki, Akihiro Tomoyasu, K. Yano, M. Goto, A. Murakami, E. Tsuda, T. Morinaga, K. Higashio, N. Udagawa, N. Takahashi, T. Suda (1998)
Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/RANKL.Proceedings of the National Academy of Sciences of the United States of America, 95 7
-
(2000)
Direct stimulation of osteoclas -
J. Marini, A. Reich, S. Smith (2014)
Osteogenesis imperfecta due to mutations in non-collagenous genes: lessons in the biology of bone formationCurrent Opinion in Pediatrics, 26
-
( Zhao, M. , Harris, S. E. , Horn, D. , Geng, Z. , Nishimura, R. , Mundy, G. R. , & Chen, D. (2002). Bone morphogenetic protein receptor signaling is necessary for normal murine postnatal bone formation. Journal of Cell Biology, 157(6), 1049–1060. 10.1083/jcb.200109012 12058020)
Zhao, M. , Harris, S. E. , Horn, D. , Geng, Z. , Nishimura, R. , Mundy, G. R. , & Chen, D. (2002). Bone morphogenetic protein receptor signaling is necessary for normal murine postnatal bone formation. Journal of Cell Biology, 157(6), 1049–1060. 10.1083/jcb.200109012 12058020Zhao, M. , Harris, S. E. , Horn, D. , Geng, Z. , Nishimura, R. , Mundy, G. R. , & Chen, D. (2002). Bone morphogenetic protein receptor signaling is necessary for normal murine postnatal bone formation. Journal of Cell Biology, 157(6), 1049–1060. 10.1083/jcb.200109012 12058020, Zhao, M. , Harris, S. E. , Horn, D. , Geng, Z. , Nishimura, R. , Mundy, G. R. , & Chen, D. (2002). Bone morphogenetic protein receptor signaling is necessary for normal murine postnatal bone formation. Journal of Cell Biology, 157(6), 1049–1060. 10.1083/jcb.200109012 12058020
-
(2013)
WNT1 mutations -
( Blair, H. C. , Larrouture, Q. C. , Li, Y. , Lin, H. , Beer‐Stoltz, D. , Liu, L. , … Nelson, D. J. (2017). Osteoblast differentiation and bone matrix formation in vivo and in vitro. Tissue Engineering Part B: Reviews, 23(3), 268–280. 10.1089/ten.TEB.2016.0454 27846781)
Blair, H. C. , Larrouture, Q. C. , Li, Y. , Lin, H. , Beer‐Stoltz, D. , Liu, L. , … Nelson, D. J. (2017). Osteoblast differentiation and bone matrix formation in vivo and in vitro. Tissue Engineering Part B: Reviews, 23(3), 268–280. 10.1089/ten.TEB.2016.0454 27846781Blair, H. C. , Larrouture, Q. C. , Li, Y. , Lin, H. , Beer‐Stoltz, D. , Liu, L. , … Nelson, D. J. (2017). Osteoblast differentiation and bone matrix formation in vivo and in vitro. Tissue Engineering Part B: Reviews, 23(3), 268–280. 10.1089/ten.TEB.2016.0454 27846781, Blair, H. C. , Larrouture, Q. C. , Li, Y. , Lin, H. , Beer‐Stoltz, D. , Liu, L. , … Nelson, D. J. (2017). Osteoblast differentiation and bone matrix formation in vivo and in vitro. Tissue Engineering Part B: Reviews, 23(3), 268–280. 10.1089/ten.TEB.2016.0454 27846781
-
C. Janda, D. Waghray, A. Levin, Christoph Thomas, K. Garcia (2012)
Structural Basis of Wnt Recognition by FrizzledScience, 337
-
Yang-Jia Cao, Hao Zhang, Zhenlin Zhang (2019)
NOVEL MUTATIONS IN THE WNT1, TMEM38B, P4HB, AND PLS3 GENES IN FOUR UNRELATED CHINESE FAMILIES WITH OSTEOGENESIS IMPERFECTA.Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists, 25 3
-
V. Martínez-Glez, María Valencia, J. Caparros-Martin, M. Aglan, S. Temtamy, J. Tenorio, Verónica Pulido, Uschi Lindert, M. Rohrbach, D. Eyre, C. Giunta, P. Lapunzina, V. Ruiz-Perez (2012)
Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfectaHuman Mutation, 33
-
N. Takahashi, Kazuhiro Maeda, Akihiro Ishihara, Shunsuke Uehara, Yasuhiro Kobayashi (2011)
Regulatory mechanism of osteoclastogenesis by RANKL and Wnt signals.Frontiers in bioscience, 16
-
(2020)
The role of WNT1 mutant variant (WNT1) in osteogenesis imperfecta -
K. Roetzer, G. Uyanik, A. Brehm, J. Zwerina, S. Zandieh, T. Czech, P. Roschger, B. Misof, K. Klaushofer (2018)
Novel familial mutation of LRP5 causing high bone mass: Genetic analysis, clinical presentation, and characterization of bone matrix mineralization.Bone, 107
-
J. Marini, A. Forlino, H. Bächinger, N. Bishop, P. Byers, A. Paepe, F. Fassier, N. Fratzl-Zelman, K. Kozloff, D. Krakow, K. Montpetit, O. Semler (2012)
Osteogenesis imperfectaNature Reviews Disease Primers, 3
-
(2017)
Osteoblast differentiation and bone matrix -
(2018)
Relation of RANKL -
( Cao, Y. J. , Zhang, H. , & Zhang, Z. L. (2019). Novel mutations in the Wnt1, Tmem38b, P4hb, and Pls3 genes in four unrelated Chinese families with osteogenesis imperfecta. Endocrine Practice, 25(3), 230–241. 10.4158/EP-2018-0443 30913006)
Cao, Y. J. , Zhang, H. , & Zhang, Z. L. (2019). Novel mutations in the Wnt1, Tmem38b, P4hb, and Pls3 genes in four unrelated Chinese families with osteogenesis imperfecta. Endocrine Practice, 25(3), 230–241. 10.4158/EP-2018-0443 30913006Cao, Y. J. , Zhang, H. , & Zhang, Z. L. (2019). Novel mutations in the Wnt1, Tmem38b, P4hb, and Pls3 genes in four unrelated Chinese families with osteogenesis imperfecta. Endocrine Practice, 25(3), 230–241. 10.4158/EP-2018-0443 30913006, Cao, Y. J. , Zhang, H. , & Zhang, Z. L. (2019). Novel mutations in the Wnt1, Tmem38b, P4hb, and Pls3 genes in four unrelated Chinese families with osteogenesis imperfecta. Endocrine Practice, 25(3), 230–241. 10.4158/EP-2018-0443 30913006
-
( Makitie, R. E. , Kampe, A. J. , Taylan, F. , & Makitie, O. (2017). Recent discoveries in monogenic disorders of childhood bone fragility. Current Osteoporosis Reports, 15(4), 303–310. 10.1007/s11914-017-0388-6 28646443)
Makitie, R. E. , Kampe, A. J. , Taylan, F. , & Makitie, O. (2017). Recent discoveries in monogenic disorders of childhood bone fragility. Current Osteoporosis Reports, 15(4), 303–310. 10.1007/s11914-017-0388-6 28646443Makitie, R. E. , Kampe, A. J. , Taylan, F. , & Makitie, O. (2017). Recent discoveries in monogenic disorders of childhood bone fragility. Current Osteoporosis Reports, 15(4), 303–310. 10.1007/s11914-017-0388-6 28646443, Makitie, R. E. , Kampe, A. J. , Taylan, F. , & Makitie, O. (2017). Recent discoveries in monogenic disorders of childhood bone fragility. Current Osteoporosis Reports, 15(4), 303–310. 10.1007/s11914-017-0388-6 28646443
-
H. Wright, H. McCarthy, J. Middleton, M. Marshall (2009)
RANK, RANKL and osteoprotegerin in bone biology and diseaseCurrent Reviews in Musculoskeletal Medicine, 2
-
(2007)
Wnt signaling and the regulation -
(2005)
Canonical Wnt signaling -
(2018)
Novel variant in Sp 7 / Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment -
( Holmen, S. L. , Zylstra, C. R. , Mukherjee, A. , Sigler, R. E. , Faugere, M. C. , Bouxsein, M. L. , … Williams, B. O. (2005). Essential role of beta‐catenin in postnatal bone acquisition. Journal of Biological Chemistry, 280(22), 21162–21168. 10.1074/jbc.M501900200 15802266)
Holmen, S. L. , Zylstra, C. R. , Mukherjee, A. , Sigler, R. E. , Faugere, M. C. , Bouxsein, M. L. , … Williams, B. O. (2005). Essential role of beta‐catenin in postnatal bone acquisition. Journal of Biological Chemistry, 280(22), 21162–21168. 10.1074/jbc.M501900200 15802266Holmen, S. L. , Zylstra, C. R. , Mukherjee, A. , Sigler, R. E. , Faugere, M. C. , Bouxsein, M. L. , … Williams, B. O. (2005). Essential role of beta‐catenin in postnatal bone acquisition. Journal of Biological Chemistry, 280(22), 21162–21168. 10.1074/jbc.M501900200 15802266, Holmen, S. L. , Zylstra, C. R. , Mukherjee, A. , Sigler, R. E. , Faugere, M. C. , Bouxsein, M. L. , … Williams, B. O. (2005). Essential role of beta‐catenin in postnatal bone acquisition. Journal of Biological Chemistry, 280(22), 21162–21168. 10.1074/jbc.M501900200 15802266
-
( Marini, J. C. , Reich, A. , & Smith, S. M. (2014). Osteogenesis imperfecta due to mutations in non‐collagenous genes: Lessons in the biology of bone formation. Current Opinion in Pediatrics, 26(4), 500–507. 10.1097/MOP.0000000000000117 25007323)
Marini, J. C. , Reich, A. , & Smith, S. M. (2014). Osteogenesis imperfecta due to mutations in non‐collagenous genes: Lessons in the biology of bone formation. Current Opinion in Pediatrics, 26(4), 500–507. 10.1097/MOP.0000000000000117 25007323Marini, J. C. , Reich, A. , & Smith, S. M. (2014). Osteogenesis imperfecta due to mutations in non‐collagenous genes: Lessons in the biology of bone formation. Current Opinion in Pediatrics, 26(4), 500–507. 10.1097/MOP.0000000000000117 25007323, Marini, J. C. , Reich, A. , & Smith, S. M. (2014). Osteogenesis imperfecta due to mutations in non‐collagenous genes: Lessons in the biology of bone formation. Current Opinion in Pediatrics, 26(4), 500–507. 10.1097/MOP.0000000000000117 25007323
-
Z. Zhong, Nicole Ethen, B. Williams (2014)
WNT signaling in bone development and homeostasisWiley Interdisciplinary Reviews: Developmental Biology, 3
-
R. Baron, G. Rawadi (2007)
Wnt signaling and the regulation of bone massCurrent Osteoporosis Reports, 5
-
( Liu, F. , Kohlmeier, S. , & Wang, C. Y. (2008). Wnt signaling and skeletal development. Cellular Signalling, 20(6), 999–1009. 10.1016/j.cellsig.2007.11.011 18164181)
Liu, F. , Kohlmeier, S. , & Wang, C. Y. (2008). Wnt signaling and skeletal development. Cellular Signalling, 20(6), 999–1009. 10.1016/j.cellsig.2007.11.011 18164181Liu, F. , Kohlmeier, S. , & Wang, C. Y. (2008). Wnt signaling and skeletal development. Cellular Signalling, 20(6), 999–1009. 10.1016/j.cellsig.2007.11.011 18164181, Liu, F. , Kohlmeier, S. , & Wang, C. Y. (2008). Wnt signaling and skeletal development. Cellular Signalling, 20(6), 999–1009. 10.1016/j.cellsig.2007.11.011 18164181
-
K. Aldinger, N. Mendelsohn, B. Chung, Wenjuan Zhang, D. Cohn, B. Fernandez, F. Alkuraya, W. Dobyns, C. Curry (2015)
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutationsJournal of Medical Genetics, 53
-
( Baron, R. , & Rawadi, G. (2007). Wnt signaling and the regulation of bone mass. Current Osteoporosis Reports, 5(2), 73–80.17521509)
Baron, R. , & Rawadi, G. (2007). Wnt signaling and the regulation of bone mass. Current Osteoporosis Reports, 5(2), 73–80.17521509Baron, R. , & Rawadi, G. (2007). Wnt signaling and the regulation of bone mass. Current Osteoporosis Reports, 5(2), 73–80.17521509, Baron, R. , & Rawadi, G. (2007). Wnt signaling and the regulation of bone mass. Current Osteoporosis Reports, 5(2), 73–80.17521509
-
(1998)
Osteoclast differentiation factor -
(2010)
Osteocyte Wnt/beta-catenin signaling -
( Levasseur, R. , Lacombe, D. , & de Vernejoul, M. C. (2005). LRP5 mutations in osteoporosis‐pseudoglioma syndrome and high‐bone‐mass disorders. Joint, Bone, Spine, 72(3), 207–214. 10.1016/j.jbspin.2004.10.008 15850991)
Levasseur, R. , Lacombe, D. , & de Vernejoul, M. C. (2005). LRP5 mutations in osteoporosis‐pseudoglioma syndrome and high‐bone‐mass disorders. Joint, Bone, Spine, 72(3), 207–214. 10.1016/j.jbspin.2004.10.008 15850991Levasseur, R. , Lacombe, D. , & de Vernejoul, M. C. (2005). LRP5 mutations in osteoporosis‐pseudoglioma syndrome and high‐bone‐mass disorders. Joint, Bone, Spine, 72(3), 207–214. 10.1016/j.jbspin.2004.10.008 15850991, Levasseur, R. , Lacombe, D. , & de Vernejoul, M. C. (2005). LRP5 mutations in osteoporosis‐pseudoglioma syndrome and high‐bone‐mass disorders. Joint, Bone, Spine, 72(3), 207–214. 10.1016/j.jbspin.2004.10.008 15850991
-
( Wu, L. A. , Wang, F. , Donly, K. J. , Baker, A. , Wan, C. , Luo, D. , … Chen, S. (2016). Establishment of immortalized BMP2/4 double knock‐out osteoblastic cells is essential for study of osteoblast growth, differentiation, and osteogenesis. Journal of Cellular Physiology, 231(6), 1189–1198. 10.1002/jcp.25266 26595646)
Wu, L. A. , Wang, F. , Donly, K. J. , Baker, A. , Wan, C. , Luo, D. , … Chen, S. (2016). Establishment of immortalized BMP2/4 double knock‐out osteoblastic cells is essential for study of osteoblast growth, differentiation, and osteogenesis. Journal of Cellular Physiology, 231(6), 1189–1198. 10.1002/jcp.25266 26595646Wu, L. A. , Wang, F. , Donly, K. J. , Baker, A. , Wan, C. , Luo, D. , … Chen, S. (2016). Establishment of immortalized BMP2/4 double knock‐out osteoblastic cells is essential for study of osteoblast growth, differentiation, and osteogenesis. Journal of Cellular Physiology, 231(6), 1189–1198. 10.1002/jcp.25266 26595646, Wu, L. A. , Wang, F. , Donly, K. J. , Baker, A. , Wan, C. , Luo, D. , … Chen, S. (2016). Establishment of immortalized BMP2/4 double knock‐out osteoblastic cells is essential for study of osteoblast growth, differentiation, and osteogenesis. Journal of Cellular Physiology, 231(6), 1189–1198. 10.1002/jcp.25266 26595646
- Publisher
- Wiley
- Copyright
- © 2020 John Wiley & Sons Ltd/University College London
- ISSN
- 0003-4800
- eISSN
- 1469-1809
- DOI
- 10.1111/ahg.12399
- Publisher site
- See Article on Publisher Site
Abstract
Journal
Annals of Human Genetics – Wiley
Published: Nov 1, 2020
Keywords: ; ;