Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

The VDR gene polymorphism does not affect BDNF levels in autoimmune thyroiditis and hypothyroidism patients.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Increasing SSAT makes skin more prone to cancer.

Lower ghrelin levels and certain gene variations may increase acne risk.

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

Certain gene variations are not a major cause of male infertility in Nigerian men.

The ZIP13 variant is linked to abnormal hair quality.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

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

LncRNA-599554 helps hair growth in cashmere goats by boosting certain cell functions.

Enriching the French health care database with external data greatly improved its usefulness.

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

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

A girl had rickets due to a gene mutation affecting vitamin D response.

A gene mutation causes curly hair and hair loss in rats.

Vitamin D helps protect skin, PSORS1 gene's risk interval for psoriasis is expanded, hair follicles can be generated from mouse cells, and interferon-γ may cause pigmented skin lesions.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

IVIG and dupilumab effectively improved symptoms in a child with Netherton syndrome.

miR-200c-3p could help diagnose and treat alopecia areata.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.