Search

everythinglearnresearchcommunity

for

Search:↓

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Genetic factors could lead to personalized treatments for hair loss.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Certain gene variations are linked to the thickness of cashmere goat hair.

Different rheumatological diseases can cause specific skin problems.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

The MTR gene affects wool quality and production in Chinese Merino sheep.

Mercury allergy linked to specific genes may contribute to burning mouth syndrome, and silicon might play a role in maintaining healthy hair.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

The Rotterdam Study investigates diseases in older adults and has produced many research findings.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Keratinocytes help heal skin wounds by interacting with immune cells and producing substances that kill pathogens.

The document concludes that specific itchy skin diseases during pregnancy have varying fetal risks and treatments, including corticosteroids and other medications.

EDA2R gene linked to hair loss.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

Celiac disease can cause skin problems that may get better with a gluten-free diet.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Alopecia Areata is a complex, unpredictable autoimmune hair loss condition with limited treatment options and a significant psychological impact.

Pregnancy can change skin disease severity, with some conditions improving and others worsening, and treatment should balance benefits and fetal safety.

Pregnancy can cause specific skin conditions that need correct diagnosis and treatment to protect both mother and baby.

Finasteride can cause sexual problems and depression in young men.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Early-onset baldness is linked to a higher risk of aggressive prostate cancer in African-American men, especially before age 60.

Some diseases can improve the outcomes of other diseases, leading to new treatment possibilities.

Finasteride side effects in young men may be linked to specific gene variations.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.