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

GRK2 is essential for healthy hair follicle function, and its absence can lead to hair loss and cysts.

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

Using special RNA to target a mutant gene fixed hair problems in mice.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

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.

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

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

Aromatase gene variation may increase female hair loss risk.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

The treatment with valproate, acetylcarnitine, folic acid, and vitamin B12 may improve muscle strength in children with SMA without significant side effects.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Genetic variations affecting skin structure play a key role in severe acne.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

A new mouse mutation causes skin and hair defects due to a gene change.

Both HLA-B and MICA are independently linked to alopecia areata.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

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.

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.

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.

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.