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A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

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

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Sex neurosteroids cause different effects on hippocampal synaptic plasticity in males and females.

MED1 is essential for normal hair growth and maintaining hair follicle stem cells.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

The Androgen Receptor could be a target for treating diseases like cancer, but more research is needed to confirm the effectiveness of potential treatments.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Identified genes linked to male-pattern baldness may help develop new treatments.

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

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

Generalized vitiligo in Chinese patients is linked to other autoimmune diseases, especially in familial cases.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

Trichoscopy helps tell apart Frontal Fibrosing Alopecia and Lichen planopilaris by showing different hair and scalp features.

Too much prolactin can cause menstrual problems, infertility, and sexual issues in women.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

More research is needed to understand sex and racial differences in long COVID.

Future treatments for androgenic alopecia may focus on reactivating hair follicle stem cells and improving drug delivery.