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

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

A mouse gene mutation increases the risk of skin cancer.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

The authors maintain that shorter androgen receptor alleles may lead to milder COVID-19 by positively affecting the immune response, not due to changes in testosterone levels or activity.

DNMT3A is crucial for healthy skin and hair growth.

Activating Wnt in skin cells controls the number of hair follicles by directing cell movement and fate.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

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

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

A gene mutation in mice causes permanent hair loss and skin issues.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Redheaded people may have evolved to efficiently make vitamin D in areas with less sunlight.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

The enzyme 5α-reductase is important for proper blood vessel development during the fertility-related transformation of the uterus lining.