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A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

A girl inherited excessive body hair from her mother and grandmother.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Fatty acid transport protein 4 is essential for skin and hair development.

Certain proteins can either protect against or increase the risk of hypertrophic scars.

Hormone-replacement therapy improved a woman's skin condition known as lymphomatoid papulosis.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

Mutations in the androgen receptor gene cause various disorders.

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

Hirsutism is excessive male-pattern hair growth mainly caused by ovarian hormones, and severe cases may require costly treatment with side effects.

Overexpression of the HE4 gene in mice causes eye inflammation and cloudiness.

The exact cause of increased 5α-reductase activity leading to hirsutism in women is still unknown.

Certain gene variations might be linked to severe acne in women but not in men.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

The study concluded that genetic mutations affect human hair diseases and identified key genes and pathways involved in hair growth and cycling.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.