Search

everythinglearnresearchcommunity

for

Search:↓

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Vitamin D receptor FokI gene variation is not linked to alopecia areata.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

Researchers found 15 new genetic links to skin traits in Japanese women.

Certain genes may be linked to autoimmune conditions in people with alopecia areata.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Higher levels of IL-1R1 and hsa-miR-19b-3p may help diagnose and predict alopecia areata severity.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Mutations in the DSG4 gene cause specific hair and scalp issues.

New genetic mutations causing hair loss were found in a Chinese family.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Genetic marker rs12558842 strongly linked to male hair loss.

The Fas/FasL pathway may play a role in alopecia areata.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Malondialdehyde-modified DNA may trigger an immune response in alopecia areata patients.

Scientists discovered two versions of a new human hair keratin gene.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Higher PD-1 levels mean fewer CD8+ T cells in alopecia areata hair follicles.

Somatic BHD mutations are rare in Japanese renal tumors.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.