Search

everythinglearnresearchcommunity

for

Search:↓

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A specific gene mutation causes congenital hair loss.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

There's no significant genetic link between male pattern baldness and COVID-19.

The document concludes that understanding health requires considering evolutionary perspectives on reproductive fitness, and recognizing the complexity of factors like diet, testosterone, and sexual orientation.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.

The meeting presented new findings on hair stem cells, pigmentation, genetics, and modern hair treatment techniques.

Hair samples can be used to create stem cells easily and non-invasively.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

EDA2R gene linked to hair loss.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Mutations in the KRT85 gene cause hair and nail problems.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

5-alpha reductase deficiency leads to male sexual development issues and treatments like finasteride help with prostate enlargement and hair loss.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

An 81-year-old man's white hair began to regain its original color while he was treated with lenalidomide, suggesting that graying hair might be reversible.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

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

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.