Citations (29)
Keep up to date with the latest research on this topic with citation updates for this article.
Articles from other publishers (29)
Bashar Alkhatib, Cunren Liu & Rosa Serra. (2018) Tgfbr2 is required in Acan‐expressing cells for maintenance of the intervertebral and sternocostal joints. JOR SPINE 1:2, pages e1025.
Crossref
Crossref
Emily K. Mis, Karel F. LiemJr.Jr., Yong Kong, Nancy B. Schwartz, Miriam Domowicz & Scott D. Weatherbee. (2014) Forward genetics defines Xylt1 as a key, conserved regulator of early chondrocyte maturation and skeletal length. Developmental Biology 385:1, pages 67-82.
Crossref
Crossref
Cong Tian, Heping Yu, Bin Yang, Fengchan Han, Ye Zheng, Cynthia F. Bartels, Deborah Schelling, James E. Arnold, Peter C. Scacheri & Qing Yin Zheng. (2012) Otitis Media in a New Mouse Model for CHARGE Syndrome with a Deletion in the Chd7 Gene. PLoS ONE 7:4, pages e34944.
Crossref
Crossref
Sara Temiyasathit, W. Joyce Tang, Philipp Leucht, Charles T. Anderson, Stefanie D. Monica, Alesha B. Castillo, Jill A. Helms, Tim Stearns & Christopher R. Jacobs. (2012) Mechanosensing by the Primary Cilium: Deletion of Kif3A Reduces Bone Formation Due to Loading. PLoS ONE 7:3, pages e33368.
Crossref
Crossref
Kathleen A. Silva & John P. Sundberg. 2012. The Laboratory Mouse. The Laboratory Mouse
781
808
.
Andras Nagy, Marina Gertsenstein, Kristina Vintersten & Richard Behringer. (2009) Alizarin Red Staining of Post-natal Bone in Mouse. Cold Spring Harbor Protocols 2009:3, pages pdb.prot5171.
Crossref
Crossref
Buer Song, Courtney J. Haycraft, Hwa-seon Seo, Bradley K. Yoder & Rosa Serra. (2007) Development of the post-natal growth plate requires intraflagellar transport proteins. Developmental Biology 305:1, pages 202-216.
Crossref
Crossref
Courtney J. HaycraftQihong ZhangBuer SongWalker S. JacksonPeter J. DetloffRosa SerraBradley K. Yoder. (2007) Intraflagellar transport is essential for endochondral bone formation. Development 134:2, pages 307-316.
Crossref
Crossref
Erika A. Bosman, Andrew C. Penn, John C. Ambrose, Ross Kettleborough, Derek L. Stemple & Karen P. Steel. (2005) Multiple mutations in mouse Chd7 provide models for CHARGE syndrome. Human Molecular Genetics 14:22, pages 3463-3476.
Crossref
Crossref
Yu-Wen Zhang, Yanli Su, Nathan Lanning, Pamela J. Swiatek, Roderick T. Bronson, Robert Sigler, Richard W. Martin & George F. Vande Woude. (2005)
Targeted disruption of
Mig-6
in the mouse genome leads to early onset degenerative joint disease
. Proceedings of the National Academy of Sciences 102:33, pages 11740-11745.
Crossref
Crossref
Riikka Ylönen, Tuomo Kyrönlahti, Malin Sund, Mika Ilves, Petri Lehenkari, Juha Tuukkanen & Taina Pihlajaniemi. (2005) Type XIII Collagen Strongly Affects Bone Formation in Transgenic Mice. Journal of Bone and Mineral Research 20:8, pages 1381-1393.
Crossref
Crossref
Hsiao-Man Ivy Yu, Boris Jerchow, Tzong-Jen Sheu, Bo Liu, Frank Costantini, J. Edward Puzas, Walter Birchmeier & Wei Hsu. (2005) The role of Axin2 in calvarial morphogenesis and craniosynostosis. Development 132:8, pages 1995-2005.
Crossref
Crossref
Maureen K. Bunger, Jacqueline A. Walisser, Ruth Sullivan, Paul A. Manley, Susan M. Moran, Vicki L. Kalscheur, Ricki J. Colman & Christopher A. Bradfield. (2005) Progressive arthropathy in mice with a targeted disruption of theMop3/Bmal-1 locus. genesis 41:3, pages 122-132.
Crossref
Crossref
Michael O. Baffi, Erin Slattery, Philip Sohn, Harold L. Moses, Anna Chytil & Rosa Serra. (2004) Conditional deletion of the TGF-β type II receptor in Col2a expressing cells results in defects in the axial skeleton without alterations in chondrocyte differentiation or embryonic development of long bones. Developmental Biology 276:1, pages 124-142.
Crossref
Crossref
Rosemarie Seymour, Tsutomu Ichiki, Igor Mikaelian, Dawnalyn Boggess, Kathleen A. Silva & John P. Sundberg. 2004. The Laboratory Mouse. The Laboratory Mouse
495
516
.
Qihong Zhang, Noel S. Murcia, Laura R. Chittenden, William G. Richards, Edward J. Michaud, Richard P. Woychik & Bradley K. Yoder. (2003) Loss of theTg737 protein results in skeletal patterning defects. Developmental Dynamics 227:1, pages 78-90.
Crossref
Crossref
Kyriakos D Economides, Lori Zeltser & Mario R Capecchi. (2003) Hoxb13 mutations cause overgrowth of caudal spinal cordand tail vertebrae. Developmental Biology 256:2, pages 317-330.
Crossref
Crossref
Mylvaganam Jeyakumar, David Smith, Elena Eliott-Smith, Mario Cortina-Borja, Gabriele Reinkensmeier, Terry D. Butters, Thorsten Lemm, Konrad Sandhoff, V.Hugh Perry, Raymond A. Dwek & Frances M. Platt. (2002) An Inducible Mouse Model of Late Onset Tay–Sachs Disease. Neurobiology of Disease 10:3, pages 201-210.
Crossref
Crossref
Yuanxiang Zhao & S.Steven Potter. (2002) Functional Comparison of the Hoxa 4, Hoxa 10, and Hoxa 11 Homeoboxes. Developmental Biology 244:1, pages 21-36.
Crossref
Crossref
Richard Smith, Norman Hawes, James Miller, John Sundberg & Simon John. 2001. Systematic Evaluation of the Mouse Eye. Systematic Evaluation of the Mouse Eye.
Yuanxiang Zhao & S. Steven Potter. (2001)
Functional specificity of the
Hoxa13
homeobox
. Development 128:16, pages 3197-3207.
Crossref
Crossref
Peter Bialek, Chi-Tsung J. Chan & Siu-Pok Yee. (2000) Characterization of a Novel Insertional Mouse Mutation, kkt: A Closely Linked Modifier of Pax1. Developmental Biology 218:2, pages 354-366.
Crossref
Crossref
Willi Jahnen-Dechent, Thorsten Schinke, Andreas Trindl, Werner Müller-Esterl, Fred Sablitzky, Sibylle Kaiser & Manfred Blessing. (1997) Cloning and Targeted Deletion of the Mouse Fetuin Gene. Journal of Biological Chemistry 272:50, pages 31496-31503.
Crossref
Crossref
Rosa Serra, Mahlon Johnson, Ellen H. Filvaroff, James LaBorde, Daniel M. Sheehan, Rik Derynck & Harold L. Moses. (1997) Expression of a Truncated, Kinase-Defective TGF-β Type II Receptor in Mouse Skeletal Tissue Promotes Terminal Chondrocyte Differentiation and Osteoarthritis. The Journal of Cell Biology 139:2, pages 541-552.
Crossref
Crossref
C.L. PeichelB. PrabhakaranT.F. Vogt. (1997) The mouse Ulnaless mutation deregulates posterior HoxD gene expression and alters appendicular patterning. Development 124:18, pages 3481-3492.
Crossref
Crossref
N.Ray Dunn, Glenn E. Winnier, Linda K. Hargett, Jeffrey J. Schrick, Agnes B. Fogo & Brigid L.M. Hogan. (1997) Haploinsufficient Phenotypes inBmp4Heterozygous Null Mice and Modification by Mutations inGli3andAlx4. Developmental Biology 188:2, pages 235-247.
Crossref
Crossref
Thomas F. Vogt & Philip Leder. (1996) Polydactyly in theStrong's luxoid mouse is suppressed bylimb deformity alleles. Developmental Genetics 19:1, pages 33-42.
Crossref
Crossref
Jeffrey L. Crosby, Don S. Varnum, Linda L. Washburn & Joseph H. Nadeau. (1992) Disorganization is a completely dominant gain-of-function mouse mutation causing sporadic developmental defects. Mechanisms of Development 37:3, pages 121-126.
Crossref
Crossref
Paul B. Selby. 1990. Issues and Reviews in Teratology. Issues and Reviews in Teratology
181
253
.