Fengsong Wang

No. 81, Mei Shan Road
Hefei, 230032, China

Last Updated: 09/26/2026

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Found 36 publications

Correction: Supervillin promotes epithelialmesenchymal transition and metastasis of hepatocellular carcinoma in hypoxia via activation of the RhoA/ROCK-ERK/p38pathway.

Correction: Supervillin promotes epithelialmesenchymal transition and metastasis of hepatocellular carcinoma in hypoxia via activation of the RhoA/ROCK-ERK/p38pathway.

Journal: Journal of experimental & clinical cancer research : CR

Published: September 05, 2026

RPL27 Promotes Gastric Cancer Progression by Enhancing Oxidative Phosphorylation Via FMC1.

RPL27 Promotes Gastric Cancer Progression by Enhancing Oxidative Phosphorylation Via FMC1.

Journal: Cell biology international

Published: May 05, 2026

Biallelic mutations in ANAPC13 cause female infertility characterized by oocyte maturation arrest both in humans and mice.

Biallelic mutations in ANAPC13 cause female infertility characterized by oocyte maturation arrest both in humans and mice.

Journal: American journal of obstetrics and gynecology

Published: December 04, 2025

Novel Variants in MDC1 are Associated With Severe Oligoasthenoteratozoospermia.

Novel Variants in MDC1 are Associated With Severe Oligoasthenoteratozoospermia.

Journal: Clinical genetics

Published: June 06, 2025

Novel CYLC1 variants are associated with male infertility due to sperm head deformity.

Novel CYLC1 variants are associated with male infertility due to sperm head deformity.

Journal: Journal of assisted reproduction and genetics

Published: March 22, 2025

Novel and recurrent hemizygous variants in BCORL1 cause oligoasthenoteratozoospermia by interfering transcription.

Novel and recurrent hemizygous variants in BCORL1 cause oligoasthenoteratozoospermia by interfering transcription.

Journal: Andrology

Published: April 19, 2024

A homozygous loss-of-function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans.

A homozygous loss-of-function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans.

Journal: Andrology

Published: April 18, 2024

The absence of the ribosomal protein Rpl2702 elicits the MAPK-mTOR signaling to modulate mitochondrial morphology and functions.

The absence of the ribosomal protein Rpl2702 elicits the MAPK-mTOR signaling to modulate mitochondrial morphology and functions.

Journal: Redox biology

Published: April 05, 2024

GSE1 promotes the proliferation and migration of lung adenocarcinoma cells by downregulating KLF6 expression.

GSE1 promotes the proliferation and migration of lung adenocarcinoma cells by downregulating KLF6 expression.

Journal: Cell biology international

Published: March 19, 2024

Biallelic variants in MAD2L1BP (p31comet) cause female infertility characterized by oocyte maturation arrest.

Biallelic variants in MAD2L1BP (p31comet) cause female infertility characterized by oocyte maturation arrest.

Journal: eLife

Published: December 18, 2022

An apparatus for qualitative assessment of the shading ratio of oblique illumination and real-time high-contrast imaging.

An apparatus for qualitative assessment of the shading ratio of oblique illumination and real-time high-contrast imaging.

Journal: Journal of biophotonics

Published: April 21, 2022

A homozygous missense mutation in TBPL2 is associated with oocyte maturation arrest and degeneration.

A homozygous missense mutation in TBPL2 is associated with oocyte maturation arrest and degeneration.

Journal: Clinical genetics

Published: February 19, 2021

Showing 1-12 of 36

Last Updated: 09/26/2026