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Wen-Jun Long Selected Research

DAX-1 Orphan Nuclear Receptor

2/2020A Novel NR0B1 Gene Mutation Causes Different Phenotypes in Two Male Patients with Congenital Adrenal Hypoplasia.

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Wen-Jun Long Research Topics

Disease

1Alzheimer Disease (Alzheimer's Disease)
12/2021
1Hypogonadism (Hypergonadotropic Hypogonadism)
02/2020
1Familial Hypoadrenocorticism
02/2020
1Addison Disease (Addison's Disease)
02/2020
1Insulin Resistance
10/2018
1Obesity
10/2018

Drug/Important Bio-Agent (IBA)

1Complement C3b (C3bi)IBA
12/2021
1DAX-1 Orphan Nuclear ReceptorIBA
02/2020
1Interleukin-18 (Interleukin 18)IBA
10/2018
1Therapeutic UsesIBA
10/2018
1Insulin (Novolin)FDA Link
10/2018