Search

everythinglearnresearchcommunity

for

Search:↓

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

The same gene mutation can cause different symptoms in family members.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

A medication may help with hair growth in psoriasis, and a skin condition might be linked to a specific bacteria.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

p2y5, now called LPA6, is a receptor important for human hair growth.

Dimethylarsinic acid speeds up skin tumor growth in certain mice.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

A 9-year-old boy had a rare scalp condition usually seen in young men.

Gabapentin helps with scalp itch, dutasteride works for frontal fibrosing alopecia, and more research is needed for better PCA treatments.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

CAG repeat numbers in the AR gene likely don't affect male pattern baldness in Korean men.

The medicine Cyclosporin A might cause excessive hair growth by reducing a protein that controls hair growth.

New genes linked to male pattern baldness were found on chromosome 20p11.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

Different PADI isoforms help cells develop diverse functions.

CAP1 helps Arabidopsis plants grow better under ammonium stress.

Amyloid deposits linked to a type of protein may cause a unique pattern of hair loss by disrupting hair growth cycles.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

A blood test level of 3.2 ng/mL of Antimüllerian hormone is good for identifying polycystic ovarian morphology in European women aged 25–45.

Lower MC2R expression may contribute to alopecia areata.

Combining diphenylcyclopropenone with anthralin is more effective for hair regrowth in alopecia areata than using diphenylcyclopropenone alone, but may cause more side effects.

Men with Addison disease should be screened for X-linked adrenoleukodystrophy if they have hair loss.