Lv41
660 积分 2022-03-06 加入
Skipping of exon 12 as a consequence of a point mutation (1898 + 5G → T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family
2个月前
已关闭
Defective piRNA Processing and Azoospermia
6个月前
已完结
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype
7个月前
已完结
Novel substituted 1,8‐naphthyridines: Design, synthesis, radiolabeling, and evaluation of apoptosis and topoisomerase II inhibition
1年前
已完结
Neuroimmune transcriptome changes in patient brains of psychiatric and neurological disorders
1年前
已完结
A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism
1年前
已完结
Analyses of the autism-associated neuroligin-3 R451C mutation in human neurons reveal a gain-of-function synaptic mechanism
1年前
已完结
Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK–IDH2 pathway
1年前
已完结
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