Search

everythinglearnresearchcommunity

for

Search:↓

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

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

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Specific keratin gene mutations can cause monilethrix.

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

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Farudodstat may effectively treat alopecia areata without harmful side effects.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

Certain blood markers, especially MLR, can help diagnose alopecia areata.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Injecting certain cells into mice caused hair loss, which was preventable with a specific inhibitor.

Daclizumab may cause psoriasis-like skin problems in multiple sclerosis patients.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Alopecia affects patients' quality of life, with younger patients and longer-lasting hair loss experiencing greater impact.

Vitiligo is not linked to coeliac disease, but a small number of alopecia areata patients may have it, suggesting they should be tested for coeliac disease.

Researchers found a gene mutation responsible for a rare hair loss condition.

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

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

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

CD2 might be a new treatment target for patchy alopecia areata.