Search

everythinglearnresearchcommunity

for

Search:↓

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

Hairless gene not strongly linked to baldness.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Linoleic acid is important for healthy skin, and while most people get enough from their diet, not having enough can cause skin and hair problems.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Linoleic acid is essential for healthy skin, and while deficiency is rare in Western societies, it can cause dry, scaly skin and hair loss.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The research suggests that p63 and TGF-β1 may help determine tumor type and malignancy in hair follicle and sebaceous tumors.

Eating vegetarian, having allergies, and family history might be linked to getting gray hair early.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Excessive hair loss can be an early sign of celiac disease.

The COVID-19 pandemic did not significantly change stress levels in preschoolers, but higher-income families' children showed higher stress.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.

Many young women have Polycystic Ovarian Syndrome (PCOS), which is often linked with irregular periods, depression, low self-esteem, and insomnia. Lifestyle and diet changes, along with regular counseling, can help manage these symptoms.

Certain types of alopecia areata are linked to allergies, autoimmune diseases, and family history.

The Polish medical societies have redefined metabolic syndrome and recommend lifestyle changes, certain medications, and possibly bariatric surgery for treatment. They also discuss managing related health conditions.

Chinese men have lower AGA rates than Caucasians, with type III vertex most common; family history is important.

Children with alopecia areata should only have thyroid screening if they have Down syndrome, a history of atopy, family history of thyroid disease, or signs of thyroid problems.

Premature hair graying in young Turkish adults is more likely if they have stress, a family history of graying, drink alcohol, have chronic diseases, are older, or are taller.