Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.
第一作者:
Darryl Y,Nishimura
第一单位:
Department of Pediatrics, Division of Medical Genetics, University of Iowa, Iowa City, IA 52242, USA.
作者:
医学主题词
动物(Animals);细胞凋亡(Apoptosis);巴德特-别德尔综合征(Bardet-Biedl Syndrome);纤毛(Cilia);疾病模型, 动物(Disease Models, Animal);基因打靶(Gene Targeting);人类(Humans);肾疾病, 囊性(Kidney Diseases, Cystic);男(雄)性(Male);小鼠(Mice);小鼠, 基因敲除(Mice, Knockout);肥胖症(Obesity);表型(Phenotype);光感受器细胞, 脊椎动物(Photoreceptor Cells, Vertebrate);色素性视网膜炎(Retinitis Pigmentosa);视紫质(Rhodopsin);感觉障碍(Sensation Disorders);社会优势(Social Dominance);精子发生(Spermatogenesis)
DOI
10.1073/pnas.0405496101
PMID
15539463
发布时间
2022-03-16
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