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A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

Two main types of fibroblasts with unique functions and additional subtypes were identified in human skin.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

Unique genes in hair follicle cells help tissue regeneration.

HFMs can help study hair growth and test potential hair growth drugs.

Epidermal growth factor disrupts hair and gland formation in bandicoots.

ADF8 and ADF11 help root hairs grow by responding to hormones and environmental signals.

OR2AT4 helps reduce aging and cell damage in human skin cells.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Dermal EZH2 controls skin cell development and hair growth in mice.

EZH2 is essential for hair growth and skin cell development.

The Fas/FasL pathway may play a role in alopecia areata.

Normal skin results from interactions between EGF and the Tabby mutation.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Ginsenoside F2 from ginseng may increase hair growth better than standard treatments by affecting cell growth signals.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

FLRG and follistatin have different roles in wound healing.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Fibroblast growth factors are crucial for hair follicle development and regeneration.

VEGFR-2 is active in hair follicles, sebaceous glands, sweat glands, and skin on the human scalp.

Fadrozole and Finasteride change frog sex ratios and cause intersex animals with altered gene expressions.