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Function (Oxford, England)|January 15, 2024
POMC Neuron BBSome Regulation of Body Weight is Independent of its Ciliary FunctionDeng-Fu Guo, Paul A Williams, Connor Laule, et al.Nature Genetics|March 1, 1993
Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS geneB E Nichols, V C Sheffield, K Vandenburgh, et al.Ophthalmology|December 1, 1991
Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin geneE M Stone, A E Kimura, B E Nichols, et al.Brain Research. Molecular Brain Research|May 13, 1999
Expression pattern and in situ localization of the mouse homologue of the human MYOC (GLC1A) gene in adult brainR E Swiderski, L Ying, M D Cassell, et al.Human Molecular Genetics|August 13, 1998
Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutationC Heaney, H Shalev, K Elbedour, et al.Bone|May 13, 2016
Bardet-Biedl syndrome 3 regulates the development of cranial base midline structuresMakiri Kawasaki, Yayoi Izu, Tadayoshi Hayata, et al.American Journal of Medical Genetics|December 23, 1999
Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21N M Ghiasvand, A B Kanis, C Helms, et al.Surgery|August 1, 1993
Composite kidney-islet transplantation prevents recurrent autoimmune beta-cell destructionS T Bartlett, G A Hadley, B Dirden, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1992
Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosaG A Fishman, K Vandenburgh, E M Stone, et al.NAR Genomics and Bioinformatics|December 3, 2021
PEPATAC: an optimized pipeline for ATAC-seq data analysis with serial alignmentsJason P Smith, M Ryan Corces, Jin Xu, et al.Pageof 41