Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

BLH308, with persimmon leaf, green tea, and sophora fruit extracts, safely increased hair density and thickness.

The S1PR 1&4 modulator may effectively treat alopecia areata by reducing hair loss and immune cell activity.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Researchers found 15 new genetic links to skin traits in Japanese women.

No significant link was found between the rs1998076 gene variant and hair loss in Indonesians.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

A specific gene mutation causes different hair defects in Indian monilethrix families.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

DHHB from Platycladus orientalis L. promotes hair growth and could be a natural alternative to current treatments.

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

Longer CAG repeats in gene linked to more severe hair loss in females.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

Certain genetic variations are linked to hair loss in Mexican men.

A single recessive gene causes sparse hair in certain Japanese White rabbits.

RORA may help regulate hair growth by affecting hair follicle stem cells.

CD117 and platelet-derived growth factor receptor α may play a role in alopecia areata.