Suchergebnisse - "Ma, Xixiang"

PubPharm (16)

1

hnRNPU is required for spermatogonial stem cell pool establishment in mice

enthalten in: Cell reports | 2024

von Wen, Y. | Zhou, S. | Gui, Y. | +11

2

Transcriptome analysis of meiotic and post-meiotic spermatogenic cells reveals the potential hub genes of aging on the decline of male fertility

enthalten in: Gene | 2024

von Gui, Y. | Ma, X. | Xiong, M. | +10

3

ADAD2 interacts with RNF17 in P-bodies to repress the Ping-pong cycle in pachytene piRNA biogenesis

enthalten in: The Journal of cell biology | 2023

von Xiong, M. | Yin, L. | Gui, Y. | +13

4

hnRNPH1 establishes Sertoli-germ cell crosstalk through cooperation with PTBP1 and AR, and is essential for male fertility in mice

enthalten in: Development (Cambridge, England) | 2023

von Feng, S. | Wen, H. | Liu, K. | +8

CommentIn: J Urol. 2023 Nov;210(5):814-816. - PMID 37615283

5

METTL21A, a Non-Histone Methyltransferase, Is Dispensable for Spermatogenesis and Male Fertility in Mice

enthalten in: International journal of molecular sciences | 2022

von Li, J. | Feng, S. | Ma, X. | +2

6

Pathological and molecular examination findings in postmortem testis biopsies reveal spermatogenesis damages in COVID-19 patients

enthalten in: ResearchSquare.com | 2021

von Ma, X. | Guan, C. | Chen, R. | +12

7

Pathological and molecular examinations of postmortem testis biopsies reveal SARS-CoV-2 infection in the testis and spermatogenesis damage in COVID-19 patients

enthalten in: Cellular & molecular immunology | 2021

von Ma, X. | Guan, C. | Chen, R. | +11

CommentIn: Fertil Steril. 2021 Apr;115(4):811-812. - PMID 33832740

8

hnRNPU in Sertoli cells cooperates with WT1 and is essential for testicular development by modulating transcriptional factors Sox8/9

enthalten in: Theranostics | 2021

von Wen, Y. | Ma, X. | Wang, X. | +8

9

An Immunological Perspective : What Happened to Pregnant Women After Recovering From COVID-19?

enthalten in: Frontiers in immunology | 2021

von Zhao, S. | Xie, T. | Shen, L. | +7

10

A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B

enthalten in: Epilepsia | 2018

von Ma, H. | Feng, S. | Deng, X. | +14