Search

everythinglearnresearchcommunity

for

Search:↓

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

A new gene mutation causes insulin resistance in a girl and her mother.

Researchers developed new compounds that target the androgen receptor effectively with fewer side effects.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Some men's prostate tissues have low enzyme levels due to genetic changes, possibly affecting treatment for prostate enlargement.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

A new DSG4 gene mutation causes hair defects in a young girl.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

Different enzymes are active in different parts of developing mouse organs.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

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

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.

The new particle system could be a promising treatment for diseases related to the 5-α reductase enzyme.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

PAD type III enzyme is specific to rat skin and hair follicles.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

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

The B2 genes are crucial for hair growth in rats.

The discovery of 5α-reductase deficiency in guevedoces led to the development of important urologic medications.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.