Lv1
60 积分 2024-10-11 加入
First large-scale screening of Notch biallelic variants implicates novel candidate genes in congenital hypothyroidism
19天前
已完结
Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway
1个月前
已完结
Clinical, biochemical characteristics and genotype-phenotype analysis of congenital hypothyroidism diagnosed by newborn screening in China
2个月前
已完结
Clinical, biochemical characteristics and genotype-phenotype analysis of congenital hypothyroidism diagnosed by newborn screening in China
2个月前
已完结
Identification and Functional Analysis of Novel Dual Oxidase 2 (DUOX2) Mutations in Children with Congenital or Subclinical Hypothyroidism
2个月前
已完结
Identification and Functional Analysis of Novel Dual Oxidase 2 (DUOX2) Mutations in Children with Congenital or Subclinical Hypothyroidism
2个月前
已完结
Genetic recording and in situ readout of single-cell signaling memory
2个月前
已完结
Regulating the immune system via IL-15 transpresentation
2个月前
已完结
Macrophages support pancreatic development
3个月前
已完结
Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway
3个月前
已完结
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