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The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Certain circular RNAs help cashmere goats grow more hair.

The SOSTDC1 gene is crucial for determining sheep wool type.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

Protein ubiquitylation is crucial for controlling stem cell functions and could be targeted for cancer treatment.

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

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

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

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

CRISPR-based tools improve understanding and treatment of skin development and conditions.

SLICK cattle have better heat tolerance due to specific gene expression and pathway differences.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

UTX is important for skin health and its loss can lead to skin issues, especially in females.

New mutations in the DSG4 gene cause a rare hair condition.

A specific gene mutation causes long hair in Angora rabbits.

Certain genes in European Merino sheep help them adapt to different climates.

The conclusion is that exogen is a unique hair cycle phase and the new sampling method specifically targets this stage, which may help in future hair loss research.

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

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

The conclusion is that a new method could improve the identification of autoimmune targets in alopecia areata, despite some limitations.

m6A-circHECA may affect cashmere goat hair growth and is possibly controlled by gene promoter methylation.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The DNA of ancient Koreans from the Three Kingdoms period shows a mix of northern Chinese and Japanese-Jomon ancestry, revealing two distinct genetic groups.