Search

everythinglearnresearchcommunity

for

Search:↓

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

A specific gene change is linked to severe hair loss.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

UC.145 may be a new biomarker for predicting gastric cancer.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

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

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

Mechanical stress causes ligament thickening through WISP-1 and Hedgehog signaling.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

OsUEV1B protein is essential for controlling phosphate levels in rice.

MPA increases cancer spread by boosting Eph A2 activity.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Agomelatine may help reduce benign prostatic hyperplasia by blocking certain inflammatory pathways.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

IGFBP-rP1 could be a new treatment for a common type of hair loss.