Search

everythinglearnresearchcommunity

for

Search:↓

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Certain genetic variants may increase the risk of developing PCOS.

New mutations in the hairless gene may cause hair loss and affect bone development.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

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

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

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Radiographers in private hospitals face many health issues due to heavy workloads and long hours.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

A specific gene variant may increase the risk of developing Alopecia Areata.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A KRT32 gene variant causes loose anagen hair syndrome.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

CT60 polymorphism might increase the risk of Alopecia Areata.

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

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.