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Bone|August 8, 2012
Deterioration of fracture healing in the mouse model of NF1 long bone dysplasiaT El Khassawna, D Toben, M Kolanczyk, et al.Cytogenetic and Genome Research|July 9, 2004
RNAi knock-down mice: an emerging technology for post-genomic functional geneticsD Prawitt, L Brixel, C Spangenberg, et al.Genomics|July 25, 2000
Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene familyT Enklaar, M Esswein, M Oswald, et al.Molecular and Cellular Biology|February 18, 1999
The Wilms' tumor suppressor gene (wt1) product regulates Dax-1 gene expression during gonadal differentiationJ Kim, D Prawitt, N Bardeesy, et al.Aging Cell|September 5, 2024
Targeting TGF-β signaling, oxidative stress, and cellular senescence rescues osteoporosis in gerodermia osteodysplasticaW L Chan, C H Bucher, J Goldes, et al.Human Genetics|August 14, 2001
Improved definition of chromosomal breakpoints using high-resolution multicolour bandingJ Lemke, I Chudoba, G Senger, et al.Genes & Development|November 1, 1994
A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament proteinY Chan, I Anton-Lamprecht, Q C Yu, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 28, 1998
Cloning, characterization, and chromosomal assignment of the human ortholog of murine Zfp-37, a candidate gene for Nager syndromeS D Dreyer, L Zhou, M A Machado, et al.Journal of Medical Genetics|April 5, 2005
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)K W Kjaer, L Hansen, G C Schwabe, et al.Nature Genetics|May 20, 1998
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndromeS D Dreyer, G Zhou, A Baldini, et al.Pageof 18