Search

everythinglearnresearchcommunity

for

Search:↓

A patient with a scalp condition and benign skin tumor experienced hair loss and did not improve with treatment, choosing not to have surgery despite a small cancer risk.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

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

SCUBE3 is a potential target for cancer and alopecia treatment but is challenging to target due to its varied roles.

Early recognition and multidisciplinary management of Whitaker syndrome can improve patient outcomes.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

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 AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

The hr gene is linked to hair loss in Valle del Belice sheep.

Olfactory receptors found outside the nose may offer new treatments for diseases like cancer and help in wound healing and hair growth.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

Modern lifestyles harm beneficial microbes, affecting health.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Brassinosteroids may be useful in treating cancer, infections, and other diseases.

Zebrafish need MYC and FGF to regenerate inner ear hair cells.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Evaluate and manage androgen excess in women with a systematic approach, considering both physical and psychological impacts.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

LHX2 is crucial for development, tissue repair, and preventing diseases.

Targeting the p63 gene could help treat skin diseases.

Long-term skin biopsy cultures can produce many fibroblasts that remain functional and can be reprogrammed.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

ICP5249 helps hair grow by activating a specific cell pathway.

Hair growth and development are controlled by specific signaling pathways.

Alopecia areata is caused by immune system attacks on hair follicles, often triggered by viral infections.

Keratin is crucial for skin barrier formation and affects mitochondrial function.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

A new 3D culture system helps grow and study mouse skin stem cells for a long time.