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Research 991–1000 of 1000+
- Restricted effects of androgens on glucocorticoid signaling in the mouse prefrontal cortex and midbrain
- Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Differential transcriptome study on the damage of testicular tissues caused by chronic infection of T. gondii in mice
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Autophagy critically controls skin inflammation and apoptosis-induced stem cell activation
- TRPV3 Ion Channel: From Gene to Pharmacology
- Exome analysis for Cronkhite-Canada syndrome: A case report
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Identification of llama KRTAP7-1 and KRTAP8-1 fiber genes and polymorphism screening