Suchergebnisse - "Wen, Pengqiang"

PubPharm (17)

1

Ubiquitination and deubiquitination of 4E-T regulate neural progenitor cell maintenance and neurogenesis by controlling P-body formation

enthalten in: Cell reports | 2022

von Kedia, S. | Aghanoori, M. | Burns, K. | +11

2

Case Report : Long-term follow-up of desert hedgehog variant caused 46, XY gonadal dysgenesis with multiple complications in a Chinese child

enthalten in: Frontiers in genetics | 2022

von Pan, L. | Li, Z. | Su, Z. | +7

3

Gender difference in clinical manifestations of KBG syndrome due to variants of ANKRD11 gene

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2021

von Yang, Y. | Wen, P. | Su, Z. | +2

4

Nucleocytoplasmic transport of the RNA-binding protein CELF2 regulates neural stem cell fates

enthalten in: Cell reports | 2021

von MacPherson, M. | Erickson, S. | Kopp, D. | +23

5

Nucleocytoplasmic Transport of RNA-Binding Proteins Regulates Neural Stem Cell Fates

enthalten in: ResearchSquare.com | 2021

von MacPherson, M. | Erickson, S. | Kopp, D. | +15

6

Correlation between variants of CYP21A2 gene promoter region and nonclassical 21-hydroxylase deficiency

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020

von Huang, S. | Su, Z. | Zhang, L. | +2

7

Long-term follow-up in a Chinese child with congenital lipoid adrenal hyperplasia due to a StAR gene mutation

enthalten in: BMC endocrine disorders | 2018

von Zhao, X. | Su, Z. | Liu, X. | +6

8

Long-term follow-up in a Chinese child with congenital lipoid adrenal hyperplasia due to a StAR gene mutation

enthalten in: BMC endocrine disorders | 2018

von Zhao, X. | Su, Z. | Liu, X. | +6

9

Long-term follow-up in a Chinese child with congenital lipoid adrenal hyperplasia due to a StAR gene mutation

enthalten in: BMC endocrine disorders | 2018

von Zhao, X. | Su, Z. | Liu, X. | +6

10

Clinical features and genetic analysis of a case with carnitine palmitoyltransferase 1A deficiency

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017

von Cui, D. | Hu, Y. | Shen, D. | +7