Search

everythinglearnresearchcommunity

for

Search:↓

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

LPA3 is crucial for embryo implantation and links LPA to prostaglandin signaling.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

Specific gene variants affect wool traits in Chinese Tan sheep.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

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

The hair keratin variant is mostly found in Caucasians.

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

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

The fuzzy gene is crucial for controlling hair growth cycles.

Genetic differences affect COVID-19 severity and treatment effectiveness.

Two gene variants cause white spots in cattle.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

Vitamin D receptor gene variations are not linked to alopecia areata.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Black hairs have more pigment-related genes, while gray hairs have more keratin-related genes.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Nociplastic pain is a complex, heritable trait with genetic links to chronic and neuropathic pain.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.