Showing results (6081-6090 of 7,441) with videos related to
Sort By:
Pageof 745
Nature Genetics|March 15, 2022
Systematic reconstruction of cellular trajectories across mouse embryogenesisChengxiang Qiu, Junyue Cao, Beth K Martin, et al.Nature Genetics|March 25, 2022
HLA autoimmune risk alleles restrict the hypervariable region of T cell receptorsKazuyoshi Ishigaki, Kaitlyn A Lagattuta, Yang Luo, et al.Nature Genetics|November 5, 1999
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly geneL C Papadopoulou, C M Sue, M M Davidson, et al.Nature Genetics|November 5, 1999
Perlecan is essential for cartilage and cephalic developmentE Arikawa-Hirasawa, H Watanabe, H Takami, et al.Nature Genetics|August 4, 1999
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiencyA Brooks-Wilson, M Marcil, S M Clee, et al.Nature Genetics|August 4, 1999
Klf4 is a transcription factor required for establishing the barrier function of the skinJ A Segre, C Bauer, E FuchsNature Genetics|September 2, 1999
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBATL Feliubadaló, M Font, J Purroy, et al.Nature Genetics|September 2, 1999
Pancreas dorsal lobe agenesis and abnormal islets of Langerhans in Hlxb9-deficient miceK A Harrison, J Thaler, S L Pfaff, et al.Nature Genetics|September 2, 1999
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasiaJ R Hurvitz, W M Suwairi, W Van Hul, et al.Nature Genetics|September 2, 1999
Ocular albinism: evidence for a defect in an intracellular signal transduction systemM V Schiaffino, M d'Addio, A Alloni, et al.Pageof 745