Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

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

The targeted nanohybrids effectively reduced psoriasis symptoms and improved skin health.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

BBS7 is crucial for healthy gums and teeth by supporting cell and blood vessel function.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Accurate protein modeling can help develop new treatments for prostate cancer and other diseases.

BBS7 is crucial for maintaining healthy gums by regulating important signaling pathways.

Two new gene mutations cause a rare hair disorder.

Different combinations of human hair keratins affect how hair fibers form.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Aromoline and DRD4 are potential targets for osteoarthritis treatment.

BBS7 is essential for healthy gums by supporting cell function and blood flow.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

PolyQ repeats in neural proteins evolve together, affecting brain function and disease.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Desmoglein 3 organization in cell connections changes without calcium, affecting cell adhesion.

Testosterone affects androgen receptors and lipid storage in cells, while DHEA does not convert to testosterone or affect these receptors in the same way.

DHA derivatives, especially didocosahexaenoin, effectively kill prostate cancer cells and may offer a safer cancer treatment option.

BBS7 is crucial for maintaining periodontal health by supporting Shh signaling.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The study created a model to help design new inhibitors for steroidal 5α-reductase enzymes.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

A protein called desmoglein 3 is important for keeping hair follicle stem cells inactive and helps in their regeneration.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.