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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Longer CAG repeats in gene linked to more severe hair loss in females.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

A specific gene mutation causes long hair in Angora rabbits.

The same gene mutation can cause different symptoms in family members.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

A mutation in the Sgkl gene causes defective hair growth in mice.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

Your genes, especially IL-1a, can predict how well a hair growth treatment with platelet rich plasma will work for you.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

TRPS1 is crucial for bone, kidney, and hair follicle development.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

Targeting mitophagy may help treat alopecia areata by reducing inflammasome activation.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

MCHR2 gene duplications may be linked to alopecia areata.