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L-cysteine slows down the breaking of bonds in hair due to electrostatic interactions.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

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

Certain gene changes and hormone levels are linked to female hair loss.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

HLD10 can include increased body hair and Mongolian spots.

A new therapy for a skin blistering condition has not been developed yet.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Schizophrenia risk genes may affect early brain development, contributing to the disease.

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

Two peptides, RMYYY and VMYMI, may be effective anti-inflammatory drugs.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Nociplastic pain is a complex, heritable trait with genetic links to chronic and neuropathic pain.

Apoptosis may play a role in feather and hair development, SF-36 is better for mental health in skin patients, a psoriasis gene is found in Caucasians, eosinophils might not be crucial for some skin allergies, and changes in atopic dermatitis could increase skin sensitivity.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Mutations in specific genes cause different types of ectodermal dysplasias.

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

Removing certain hair follicle stem cells worsens skin reactions to allergens.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.