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research Association between angiotensin‐converting enzyme gene insertion deletion polymorphism and androgenetic alopecia susceptibility among Egyptian patients: A preliminary case‐controlled study

1 citations , September 2021 in “Journal of Cosmetic Dermatology”

Certain gene variations may increase the risk of hair loss in Egyptians.

research Hair-specific expression of chloramphenicol acetyltransferase in transgenic mice under the control of an ultra-high-sulfur keratin promoter.

33 citations , September 1990 in “Proceedings of the National Academy of Sciences”

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

research The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep

January 2002 in “Agritrop (Cirad)”

The hr gene is linked to hair loss in Valle del Belice sheep.

research Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions

23 citations , July 2003 in “Journal of Investigative Dermatology”

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

research Faculty Opinions recommendation of Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis.

October 2011 in “Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature”

Certain gene variations are significantly linked to hair loss, especially in white people.

research The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures

64 citations , March 2004 in “The journal of investigative dermatology/Journal of investigative dermatology”

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

research Detection of Type IIHair Keratin Gene in a Family with Monilethrix

January 2010 in “Chinese Journal of Dermatovenereology of Integrated Traditional and Western Medicine”

A unique gene mutation was found in a family with monilethrix.

research Analysis Polymorphism of Androgen Receptor in Cases of Androgenetic Alopecia

January 2011 in “The Chinese Journal of Dermatovenereology”

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

research Study on genetic polymorphisms of androgen receptor gene and 5α-reductase genes of Han men with androgenetic alopecia in the Eastern China

January 2006 in “Chinese Journal of Dermatology”

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

research Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome

1 citations , September 2019 in “Steroids”

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

research 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation

April 2017 in “Journal of Investigative Dermatology”

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

research The Region Coding for the Helix Termination Motif and the Adjacent Intron 6 of the Human Type I Hair Keratin Gene hHa2 Contains Three Natural, Closely Spaced Polymorphic Sites

6 citations , March 1996 in “Journal of Investigative Dermatology”

research Amphiregulin in Fibrotic Diseases and Cancer

4 citations , July 2025 in “International Journal of Molecular Sciences”

Targeting amphiregulin may improve treatment for fibrosis and cancer.

research Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review

3 citations , January 2013 in “Dermatology”

New genetic mutations causing hair loss were found in a Chinese family.

research A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)

28 citations , June 1998 in “Clinical Genetics”

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

research The IRE gene encodes a protein kinase homologue and modulates root hair growth in Arabidopsis

66 citations , May 2002 in “The Plant Journal”

The IRE gene is important for normal root hair growth in Arabidopsis plants.

research Two Hydroxyproline Galactosyltransferases, GALT5 and GALT2, Function in Arabinogalactan-Protein Glycosylation, Growth and Development in Arabidopsis

63 citations , May 2015 in “PloS one”

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

research Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene

94 citations , April 2002 in “The Journal of clinical endocrinology and metabolism/Journal of clinical endocrinology & metabolism”

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

research Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?

46 citations , February 2016 in “Experimental Dermatology”

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

research Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene

139 citations , September 2001 in “The journal of investigative dermatology/Journal of investigative dermatology”

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

research FGFR2 is associated with hair thickness in Asian populations

45 citations , July 2009 in “Journal of human genetics”

A gene variation is linked to hair thickness in Asians.

Bioinformatic Analysis of Gene Expression Data Reveals Src Family Protein Tyrosine Kinases as Key Players in Androgenetic Alopecia

research Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia

June 2023 in “Frontiers in Medicine”

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Lack of Concordance and Linkage Disequilibrium Among Brothers for Androgenetic Alopecia and CAG/GGC Haplotypes of the Androgen Receptor Gene in Mexican Families

research Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and CAG/GGC haplotypes of the androgen receptor gene in Mexican families

2 citations , July 2015 in “Journal of Cosmetic Dermatology”

No clear link between specific gene and hair loss in Mexican brothers.

research The Peach RGF/GLV Signaling Peptide pCTG134 Is Involved in a Regulatory Circuit That Sustains Auxin and Ethylene Actions

9 citations , October 2017 in “Frontiers in plant science”

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

research Conditional expression of the ErbB2 oncogene elicits reversible hyperplasia in stratified epithelia and up-regulation of TGFα expression in transgenic mice

150 citations , June 1999 in “Oncogene”

research The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach

15 citations , April 2002 in “British Journal of Dermatology”

Hairless gene not strongly linked to baldness.

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