Mingrong Lv

No. 81 Meishan Road
Hefei, 230032, China

Last Updated: 09/26/2026

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Found 64 publications

PRRC2A deficiency disrupts m6A-dependent RNA processing and meiosis in human spermatogenesis.

PRRC2A deficiency disrupts m6A-dependent RNA processing and meiosis in human spermatogenesis.

Journal: Molecular human reproduction

Published: February 26, 2026

Mapping the Non-Canonical Splicing Variants: Decrypting the Hidden Genetic Architecture of Idiopathic Male Infertility.

Mapping the Non-Canonical Splicing Variants: Decrypting the Hidden Genetic Architecture of Idiopathic Male Infertility.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: August 12, 2025

Cognition of the association between sexual dysfunction and fertility.

Cognition of the association between sexual dysfunction and fertility.

Journal: Sexual medicine

Published: February 13, 2025

Broadening the ARMC2 mutational phenotype: linking multiple morphological abnormalities of the Flagella to Pulmonary Manifestations in Primary Ciliary Dyskinesia.

Broadening the ARMC2 mutational phenotype: linking multiple morphological abnormalities of the Flagella to Pulmonary Manifestations in Primary Ciliary Dyskinesia.

Journal: Reproductive biology and endocrinology : RB&E

Published: August 07, 2024

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility.

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility.

Journal: Human genomics

Published: June 21, 2024

Association of FOXL2 and ERCC6 variants with premature ovarian insufficiency and their potential use in clinical IVF guidance.

Association of FOXL2 and ERCC6 variants with premature ovarian insufficiency and their potential use in clinical IVF guidance.

Journal: Gene

Published: June 14, 2024

Aberrant acetylation caused by a CDYL splicing mutation contributes to thin mid-piece related asthenoteratozoospermia and male infertility.

Aberrant acetylation caused by a CDYL splicing mutation contributes to thin mid-piece related asthenoteratozoospermia and male infertility.

Journal: Andrology

Published: May 30, 2024

Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and mice.

Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and mice.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: April 18, 2024

Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants.

Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants.

Journal: iScience

Published: March 03, 2024

Differential methylation patterns in paternally imprinted gene promoter regions in sperm from hepatitis B virus infected individuals.

Differential methylation patterns in paternally imprinted gene promoter regions in sperm from hepatitis B virus infected individuals.

Journal: BMC molecular and cell biology

Published: December 19, 2023

Identification of deleterious variants in nine polycystic kidney disease affected families.

Identification of deleterious variants in nine polycystic kidney disease affected families.

Journal: Gene

Published: December 08, 2023

Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.

Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.

Journal: Science China. Life sciences

Published: November 21, 2023

Showing 1-12 of 64

Last Updated: 09/26/2026