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	4881.	Age-dependent increase of discoidin domain receptor 2 and matrix metalloproteinase 13 expression in temporomandibular joint cartilage of type IX and type XI collagen-deficient mice. [electronic resource] by Lam, N P Li, Y Waldman, A B Brussiau, J Lee, P L Olsen, B R Xu, L Producer: 20080102 In: Archives of oral biology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4882.	BMP2, but not BMP4, is crucial for chondrocyte proliferation and maturation during endochondral bone development. [electronic resource] by Shu, Bing Zhang, Ming Xie, Rong Wang, Meina Jin, Hongting Hou, Wei Tang, Dezhi Harris, Stephen E Mishina, Yuji O'Keefe, Regis J Hilton, Matthew J Wang, Yongjun Chen, Di Producer: 20120222 In: Journal of cell science vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4883.	The immunoreceptor adapter protein DAP12 suppresses B lymphocyte-driven adaptive immune responses. [electronic resource] by Nakano-Yokomizo, Takako Tahara-Hanaoka, Satoko Nakahashi-Oda, Chigusa Nabekura, Tsukasa Tchao, Nadia K Kadosaki, Momoko Totsuka, Naoya Kurita, Naoki Nakamagoe, Kiyotaka Tamaoka, Akira Takai, Toshiyuki Yasui, Teruhito Kikutani, Hitoshi Honda, Shin-ichiro Shibuya, Kazuko Lanier, Lewis L Shibuya, Akira Producer: 20111017 In: The Journal of experimental medicine vol. 208 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4884.	Patient-derived skeletal dysplasia induced pluripotent stem cells display abnormal chondrogenic marker expression and regulation by BMP2 and TGFβ1. [electronic resource] by Saitta, Biagio Passarini, Jenna Sareen, Dhruv Ornelas, Loren Sahabian, Anais Argade, Shilpa Krakow, Deborah Cohn, Daniel H Svendsen, Clive N Rimoin, David L Producer: 20150205 In: Stem cells and development vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4885.	Ophthalmic findings in Frank-ter Haar syndrome: report of a sibling pair. [electronic resource] by Chang, Ta C Bauer, Mislen Puerta, Herminia S Greenberg, Matthew B Cavuoto, Kara M Producer: 20180615 In: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4886.	PERK leads a hub dictating pancreatic β cell homoeostasis. [electronic resource] by Kefalas, George Larose, Louise Producer: 20180806 In: Biology of the cell vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4887.	BMPs regulate multiple aspects of growth-plate chondrogenesis through opposing actions on FGF pathways. [electronic resource] by Yoon, Byeong S Pogue, Robert Ovchinnikov, Dmitri A Yoshii, Isaac Mishina, Yuji Behringer, Richard R Lyons, Karen M Producer: 20070209 In: Development (Cambridge, England) vol. 133 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4888.	CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta. [electronic resource] by Morello, Roy Bertin, Terry K Chen, Yuqing Hicks, John Tonachini, Laura Monticone, Massimiliano Castagnola, Patrizio Rauch, Frank Glorieux, Francis H Vranka, Janice Bächinger, Hans Peter Pace, James M Schwarze, Ulrike Byers, Peter H Weis, MaryAnn Fernandes, Russell J Eyre, David R Yao, Zhenqiang Boyce, Brendan F Lee, Brendan Producer: 20061204 In: Cell vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4889.	Pseudoachondroplasia and multiple epiphyseal dysplasia: a 7-year comprehensive analysis of the known disease genes identify novel and recurrent mutations and provides an accurate assessment of their relative contribution. [electronic resource] by Jackson, Gail C Mittaz-Crettol, Laureane Taylor, Jacqueline A Mortier, Geert R Spranger, Juergen Zabel, Bernhard Le Merrer, Martine Cormier-Daire, Valerie Hall, Christine M Offiah, Amaka Wright, Michael J Savarirayan, Ravi Nishimura, Gen Ramsden, Simon C Elles, Rob Bonafe, Luisa Superti-Furga, Andrea Unger, Sheila Zankl, Andreas Briggs, Michael D Producer: 20120423 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4890.	Identification of two novel critical mutations in PCNT gene resulting in microcephalic osteodysplastic primordial dwarfism type II associated with multiple intracranial aneurysms. [electronic resource] by Li, Fei-Feng Wang, Xu-Dong Zhu, Min-Wei Lou, Zhi-Hong Zhang, Qiong Zhu, Chun-Yu Feng, Hong-Lin Lin, Zhi-Guo Liu, Shu-Lin Producer: 20160823 In: Metabolic brain disease vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4891.	TREM2 sustains microglial expansion during aging and response to demyelination. [electronic resource] by Poliani, Pietro Luigi Wang, Yaming Fontana, Elena Robinette, Michelle L Yamanishi, Yoshinori Gilfillan, Susan Colonna, Marco Producer: 20150817 In: The Journal of clinical investigation vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4892.	Small RNAs derived from lncRNA RNase MRP have gene-silencing activity relevant to human cartilage-hair hypoplasia. [electronic resource] by Rogler, Leslie E Kosmyna, Brian Moskowitz, David Bebawee, Remon Rahimzadeh, Joseph Kutchko, Katrina Laederach, Alain Notarangelo, Luigi D Giliani, Silvia Bouhassira, Eric Frenette, Paul Roy-Chowdhury, Jayanta Rogler, Charles E Producer: 20140805 In: Human molecular genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4893.	Phenotypic variations of cartilage hair hypoplasia: granulomatous skin inflammation and severe T cell immunodeficiency as initial clinical presentation in otherwise well child with short stature. [electronic resource] by McCann, Liza J McPartland, Jo Barge, Dawn Strain, Lisa Bourn, David Calonje, Eduardo Verbov, Julian Riordan, Andrew Kokai, George Bacon, Chris M Wright, Michael Abinun, Mario Producer: 20141017 In: Journal of clinical immunology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4894.	Neuron subset-specific Pten deletion induces abnormal skeletal activity in mice. [electronic resource] by Lugo, Joaquin N Thompson, Marjorie H Huber, Philippe Smith, Gregory Kwon, Ronald Y Producer: 20170516 In: Experimental neurology vol. 291 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4895.	Skeletal Dysplasias: What Every Bone Health Clinician Needs to Know. [electronic resource] by Nikkel, Sarah M Producer: 20180727 In: Current osteoporosis reports vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4896.	Sixteen years and counting: the current understanding of fibroblast growth factor receptor 3 (FGFR3) signaling in skeletal dysplasias. [electronic resource] by Foldynova-Trantirkova, Silvie Wilcox, William R Krejci, Pavel Producer: 20120423 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4897.	Exome sequencing identifies PDE4D mutations as another cause of acrodysostosis. [electronic resource] by Michot, Caroline Le Goff, Carine Goldenberg, Alice Abhyankar, Avinash Klein, Céline Kinning, Esther Guerrot, Anne-Marie Flahaut, Philippe Duncombe, Alice Baujat, Genevieve Lyonnet, Stanislas Thalassinos, Caroline Nitschke, Patrick Casanova, Jean-Laurent Le Merrer, Martine Munnich, Arnold Cormier-Daire, Valérie Producer: 20120531 In: American journal of human genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4898.	Fatal adult-onset antibody deficiency syndrome in a patient with cartilage hair hypoplasia. [electronic resource] by Horn, Julia Schlesier, Michael Warnatz, Klaus Prasse, Antje Superti-Furga, Andrea Peter, Hans-Hartmut Salzer, Ulrich Producer: 20110131 In: Human immunology vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4899.	Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+). [electronic resource] by Wyandt, H E Hecht, F Lovrien, E W Stewart, R E Producer: 19720627 In: Cytogenetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4900.	Vertebrate Sprouty genes are induced by FGF signaling and can cause chondrodysplasia when overexpressed. [electronic resource] by Minowada, G Jarvis, L A Chi, C L Neubüser, A Sun, X Hacohen, N Krasnow, M A Martin, G R Producer: 19991119 In: Development (Cambridge, England) vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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