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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Glycine is a key transmitter in rat spinal cord synapses, often alongside GABA.

Most people have similar hair protein patterns, but a rare variant was found in two women.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

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

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

A gene variation is linked to hair thickness in Asians.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

A new gene mutation is linked to monilethrix in the studied family.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Lower PPARγ levels and specific gene variations are linked to more severe Frontal Fibrosing Alopecia.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A new DSG4 gene mutation causes hair defects in a young girl.

The MTR gene affects wool quality and production in Chinese Merino sheep.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.