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The Indus River dolphin has low genetic diversity due to a past bottleneck and human impact.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

New genetic variants linked to inherited ichthyoses were identified, offering insights for potential gene therapy.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

SLC24A5 shows a clear selective sweep, but no link to UV radiation intensity.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

The study found key long non-coding RNAs involved in yak hair growth cycles.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

ceRNA networks offer potential treatments for skin aging and wound healing.

Forensic DNA phenotyping faces challenges due to inconsistent terminology, limited genetic understanding, and debates over technology and models.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

The study identified key genes and pathways that influence goat wool quality and growth.

Gap junctions help control feather pattern formation by enabling cell communication.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

FGFR2 signaling controls Merkel cell formation in different skin regions.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

The scraggly mutation causes hair loss and skin defects in mice.

Genes linked to coat color and fiber length in Chinese goats were identified.

Recent selection on immune response genes was identified across seven ethnicities.

AR polyglycine repeat doesn't cause baldness.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

Spt4 and Spt6 are essential for fat cell development.

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