Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

TMPRSS2 is crucial for COVID-19 infection and is a potential target for treatment.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

CRTH2 antagonists might be useful for treating many conditions because they play a role in immune and inflammation responses.

ATP-sensitive potassium channels are important for hair growth.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

PPAR-γ may be a key target for treating alopecia areata and other skin conditions.

Polygenic Score can help predict severe psoriasis and psoriatic arthritis.

Genetic variations may affect how well finasteride works for BPH patients.

The B2 genes are crucial for hair growth in rats.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

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

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

PDRN helps repair tissue and improve wound healing with a high safety profile.

Ptprq has multiple forms that change during inner ear development.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

The Itpr3 gene causes a specific hair pattern in mice.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

A unique gene mutation was found in a family with monilethrix.

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

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

Environmental factors affect reproductive traits by altering the SRD5A1 gene.

CD2 might be a new treatment target for patchy alopecia areata.

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

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.