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Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

FTase and GGTase-I are essential for skin keratinocyte health.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

Chronic T. gondii infection may harm male fertility.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

A new gene, JMJD1C, may affect testosterone levels in men.

Mutations in specific genes cause different types of ectodermal dysplasias.

TGF-β2 plays a key role in human hair growth and development.

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

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

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

MAD2B slows down the growth of skin cells that are important for hair development by interacting with TCF4.

Thymosin beta 4 may help hair growth and could be a treatment for hair issues.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

TCDD reduces EGF receptors in the liver, affecting growth and development.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

BIK1 gene helps plants resist some pathogens but makes them more vulnerable to others.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

BST2 is a key marker for hair loss disease alopecia areata.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.