Search

everythinglearnresearchcommunity

for

Search:↓

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Type I interferons play a key role in the development of various skin diseases.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

ΔNp63α stops TAp73β from working in skin cancer by blocking its access to specific genes, not by directly interacting with it.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

The skin and thymus develop similarly to protect and support immunity.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Mutations in certain receptors can cause diseases and offer new treatment options.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

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

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

Finasteride can cause sexual problems and depression in young men.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

A new gene mutation linked to a skin condition was found in a Spanish family.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Whale genes show changes that help them live in water, like less hair and better flippers.