Tanveer Abbas

443 Huangshan Road
Hefei, 230027, China

Last Updated: 09/26/2026

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Found 19 publications

Corrigendum to "Novel bi-allelic variants in DNAH10 lead to multiple morphological abnormalities of sperm flagella and male infertility".

Corrigendum to "Novel bi-allelic variants in DNAH10 lead to multiple morphological abnormalities of sperm flagella and male infertility".

Journal: Asian journal of andrology

Published: August 12, 2025

Novel PNLDC1 mutations underlie nonobstructive azoospermia in humans and mice.

Novel PNLDC1 mutations underlie nonobstructive azoospermia in humans and mice.

Journal: Human molecular genetics

Published: April 22, 2025

Telomerase as a therapeutic Bullseye: advances in cancer treatment and clinical trials : A comprehensive review of small molecule inhibitors, antisense oligonucleotides, and immunotherapeutic strategies targeting the telomerase catalytic subunit (hTERT).

Telomerase as a therapeutic Bullseye: advances in cancer treatment and clinical trials : A comprehensive review of small molecule inhibitors, antisense oligonucleotides, and immunotherapeutic strategies targeting the telomerase catalytic subunit (hTERT).

Journal: Biological research

Published: March 25, 2025

A novel mutation in CFAP58 leads to MMAF in humans and mice by disrupting CP assembly.

A novel mutation in CFAP58 leads to MMAF in humans and mice by disrupting CP assembly.

Journal: Human molecular genetics

Published: January 30, 2025

Novel mutations in FSIP2 cause male infertility through multiple morphological abnormalities of the sperm flagella.

Novel mutations in FSIP2 cause male infertility through multiple morphological abnormalities of the sperm flagella.

Journal: Asian journal of andrology

Published: January 30, 2025

A novel frameshift variant in AXDND1 may cause multiple morphological abnormalities of the sperm flagella in a consanguineous Pakistani family.

A novel frameshift variant in AXDND1 may cause multiple morphological abnormalities of the sperm flagella in a consanguineous Pakistani family.

Journal: Asian journal of andrology

Published: December 30, 2024

Homozygous CCDC146 mutation causes oligoasthenoteratozoospermia in humans and mice.

Homozygous CCDC146 mutation causes oligoasthenoteratozoospermia in humans and mice.

Journal: Zoological research

Published: September 08, 2024

Novel bi-allelic variants in DNAH10 lead to multiple morphological abnormalities of sperm flagella and male infertility.

Novel bi-allelic variants in DNAH10 lead to multiple morphological abnormalities of sperm flagella and male infertility.

Journal: Asian journal of andrology

Published: June 07, 2024

Novel biallelic ADCY10 variants cause asthenozoospermia with excessive residual cytoplasm and hydronephrosis in humans.

Novel biallelic ADCY10 variants cause asthenozoospermia with excessive residual cytoplasm and hydronephrosis in humans.

Journal: Reproductive biomedicine online

Published: May 17, 2024

A homozygous nonsense variant in HENMT1 causes male infertility in humans and mice.

A homozygous nonsense variant in HENMT1 causes male infertility in humans and mice.

Journal: Andrology

Published: April 26, 2024

A novel homozygous splicing mutation in AK7 causes multiple morphological abnormalities of sperm flagella in patients from consanguineous Pakistani families.

A novel homozygous splicing mutation in AK7 causes multiple morphological abnormalities of sperm flagella in patients from consanguineous Pakistani families.

Journal: Asian journal of andrology

Published: April 07, 2024

A homozygous ARMC3 splicing variant causes asthenozoospermia and flagellar disorganization in a consanguineous family.

A homozygous ARMC3 splicing variant causes asthenozoospermia and flagellar disorganization in a consanguineous family.

Journal: Clinical genetics

Published: March 07, 2024

Showing 1-12 of 19

Last Updated: 09/26/2026