Search

everythinglearnresearchcommunity

for

Search:↓

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Scalp melanoma, a deadly skin cancer, is often found late due to its hard-to-see location, especially in older men. Early detection, possible treatments, and the role of hairdressers in spotting it early are discussed. More research is needed to improve detection and treatment.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Hair shaft disorders are diagnosed through examination and history, with general care and some treatments offering improvement.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

iPSCs can help treat genetic skin disorders by creating healthy skin cells from a small biopsy.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Human hair loss may have evolved to help increase brain size.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

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

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

Edar signaling is crucial for proper hair follicle development and function.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Hair follicle studies suggest that maintaining telomere length could help treat hair loss and graying, but it's uncertain if mouse results apply to humans.

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

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

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