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Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

New findings suggest potential treatments for melanoma, hyperpigmentation, hair defects, and multiple sclerosis, and show skin microbiome changes don't cause atopic dermatitis.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

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

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

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

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Hair loss gene linked to prostate issues.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

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

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

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

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Certain gene variations may increase the risk of hair loss in Egyptians.

Certain gene variations may increase the risk and severity of alopecia areata.

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

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.