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Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

Myrtus communis Linn is a versatile medicinal plant used for treating many health issues and as a food additive.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Managing multiple autoimmune diseases in one patient is very challenging.

Vitiligo often starts young, is linked to family history and stress, and requires comprehensive care including psychological support.

U.S. dermatology residents need more education and experience with LGBT patients to improve their cultural competency.

Hair loss, known as androgenic alopecia, can start in teenage years and may not always be hormone-related. It's important to do extra tests in young cases and remember it can greatly affect a teenager's mental health.

A gene mutation causes woolly hair in a Syrian patient.

The article described symptoms and treatments for four common hair problems but didn't give detailed information.

Canadian porcupines in a Japanese zoo passed a skin fungus to each other.

Most vitiligo patients in Makkah are young women, often with family history and thyroid issues.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Minoxidil helps hair growth in people with monilethrix without side effects.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Hair loss during breast cancer treatment affects each woman differently, influenced by her environment and family.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

AGA increased yearly, type I most common, and family history and seborrheic dermatitis often linked.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

The document listed medical job ads and guidelines for breast cancer screening.

No treatment alters the natural progression of alopecia areata, and effectiveness varies, with some possibly working better in children.

Activin helps skin growth and healing mainly through stromal cells and affects keratinocytes based on its amount.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

An 18-year-old girl was diagnosed with a rare hereditary hair loss condition, despite no family history.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

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.

FGF13 gene changes cause excessive hair growth in a rare condition.