Lv11
40 积分 2022-03-22 加入
Germline-derived GNAS-Gsα variants associated with both gain-of-function and loss-of-function phenotypes
3小时前
已关闭
Mechanistic and therapeutic relationships of traumatic brain injury and γ-amino-butyric acid (GABA)
8天前
已完结
IGF-1 ameliorates streptozotocin-induced pancreatic β cell dysfunction and apoptosis via activating IRS1/PI3K/Akt/FOXO1 pathway
19天前
已完结
Activation of the MAPK pathway (RASopathies) and partial growth hormone insensitivity
19天前
已完结
Spectrum of Insulin-Like Growth Factor Deficiency
19天前
已完结
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature
1个月前
已完结
Pediatric Continuous Reference Intervals of Serum Insulin-like Growth Factor 1 Levels in a Healthy Chinese Children Population – Based on PRINCE Study
1个月前
已完结
Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene
3个月前
已完结
Natural history and genetic spectrum of the Turkish metaphyseal dysplasia cohort, including rare types caused by biallelic COL10A1, COL2A1, and LBR variants
3个月前
已完结
Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic COL10A1 variant
3个月前
已完结
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