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A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

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

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

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.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

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

Women with hair loss have more androgen receptors in certain hair follicles.

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

The rs6152 allele is not a good marker for baldness in the Indonesian population, but family history, age, gender, high blood pressure, and body weight are linked to the risk.

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

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

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

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

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

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

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

A woman lost all her body hair after hepatitis C treatment, but it started to grow back a year after stopping the treatment.

Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

Lichen planus is a skin condition that can resolve on its own, is linked to hepatitis C, and increases the risk of skin cancer.

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.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

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.

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

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

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

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

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