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research Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat

16 citations , December 2020 in “PloS one”

Researchers found WNT10A to be a key gene in developing goat hair follicles.

The Activin Binding Proteins Follistatin and Follistatin-Related Protein Are Differentially Regulated In Vitro and During Cutaneous Wound Repair

research The activin binding proteins follistatin and follistatin-related protein are differentially regulated in vitro and during cutaneous wound repair

46 citations , December 2001 in “Journal of Endocrinology/Journal of endocrinology”

FLRG and follistatin have different roles in wound healing.

research Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome

3 citations , May 2022 in “The journal of investigative dermatology/Journal of investigative dermatology”

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

research 131 Mutational landscape of extramammary Paget disease

April 2018 in “Journal of Investigative Dermatology”

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

research Transgenic HPV11-E2 protein modulates URR activity in vivo

2 citations , February 2023 in “Transgenic Research”

The E2 protein affects gene activity in hair follicles of mice.

research The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation

68 citations , December 2010 in “The journal of investigative dermatology/Journal of investigative dermatology”

HOXC13 is essential for hair and nail development by regulating Foxn1.

research JAK-centric explainable few-shot gene-expression diagnosis framework for alopecia via MultiPLIER priors and relation-style set-to-set comparison

January 2026 in “Frontiers in Molecular Biosciences”

A new method helps diagnose alopecia areata using specific gene markers and could guide targeted treatments.

research Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families

11 citations , February 2011 in “The Journal of Dermatology”

Mutations in the hairless gene cause a rare form of permanent hair loss.

research A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females

103 citations , March 2015 in “Nature Communications”

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

research 087 Basal-to-inflammatory transition and tumor resistance via crosstalk with a pro-inflammatory stromal niche

July 2024 in “Journal of Investigative Dermatology”

research Nε-(carboxymethyl) lysine (CML) inhibits hair follicle formation by suppressing hair bulb condensation

November 2016 in “The Molecular Biology Society of Japan”

research Controlled Delivery of T-box21 Small Interfering RNA Ameliorates Autoimmune Alopecia (Alopecia Areata) in a C3H/HeJ Mouse Model

69 citations , February 2008 in “The American journal of pathology”

Controlled delivery of specific RNA and IL-4 restored hair growth in mice with autoimmune alopecia.

research scRNA+TCR-seq Reveals the Proportion and Characteristics of Dual TCR Treg Cells in Mouse Lymphoid and Non-lymphoid Tissues

July 2025

Dual TCR Treg cells are common in mouse tissues and vary by location.

research Selection signatures in goats reveal a novel deletion mutant underlying cashmere yield and diameter

November 2022 in “Gigascience”

A specific genetic deletion in goats affects cashmere yield and thickness.

Association Between Genetically Predicted Leukocyte Telomere Length and Non-Scarring Alopecia: A Two-Sample Mendelian Randomization Study

research Association between genetically predicted leukocyte telomere length and non-scarring alopecia: A two-sample Mendelian randomization study

4 citations , January 2023 in “Frontiers in Immunology”

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

research Increased Expression of TSPEAR in Colorectal Cancer Predicts Poor Prognosis

January 2022 in “Research Square (Research Square)”

High TSPEAR levels in colorectal cancer predict worse outcomes.

Immune Deficiency-Related Enteropathy-Lymphocytopenia-Alopecia Syndrome Results from Tetratricopeptide Repeat Domain 7A Deficiency

research Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency

64 citations , August 2014 in “The journal of allergy and clinical immunology/Journal of allergy and clinical immunology/The journal of allergy and clinical immunology”

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Study of Human Leukocyte Antigen in 13 Cases of Familial Frontal Fibrosing Alopecia: CYP21A2 Gene p.V281L Mutation from Congenital Adrenal Hyperplasia Linked to HLA Class I Haplotype HLA-A*33:01; B*14:02; C*08:02 as a Genetic Marker

research Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A33:01 ; B14:02; C*08:02 as a genetic marker

7 citations , January 2019 in “Australasian Journal of Dermatology”

A genetic marker linked to a type of hair loss was found in most patients studied.

research Epidermal growth factor and transferrin receptor expression in human embryonic and fetal epidermal cells

10 citations , December 1990 in “Archives of Dermatological Research”

research Integrative analysis of Iso-Seq and RNA-seq data reveals transcriptome complexity and differential isoform in skin tissues of different hair length Yak

5 citations , May 2024 in “BMC Genomics”

Different genes affect hair length in yaks.

research 415 IL-17C: Checkpoint in innate skin immunology

April 2018 in “Journal of Investigative Dermatology”

IL-17C is important in inflammatory skin diseases and could be a target for treatment.

A Variant of the Glucocorticoid Receptor Gene Is Not Associated with Adrenal Androgen Excess in Women with Polycystic Ovary Syndrome

research A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome

20 citations , December 2000 in “Fertility and Sterility”

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

research Differential expression of keratin 19 in normal human epithelial tissues revealed by monospecific monoclonal antibodies

159 citations , October 1986 in “The Histochemical Journal”

research Identification of llama KRTAP7-1 and KRTAP8-1 fiber genes and polymorphism screening

2 citations , May 2019 in “Small ruminant research”

Mutations in specific llama genes may affect fiber quality for textiles.

research 085 Post-translational regulation of hair keratins in transfected COS-1 cells

July 1995 in “Journal of Dermatological Science”

research Chaperones as thermodynamic sensors

August 2013 in “Nature Reviews Drug Discovery”

New cancer treatments show promise in reducing tumor growth and improving skin regeneration in mice.

RORA Regulates Autophagy in Hair Follicle Stem Cells by Upregulating the Expression Level of the Sqstm1 Gene

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