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There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A specific gene variation in goats is linked to better growth traits.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

KRT81 gene variations in sheep affect wool weight but not fiber length or thickness.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

A new method can detect mutations in mice by observing changes in hair follicle cells.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Inherited color dilution in rabbits is linked to DNA methylation changes.

Researchers found 15 new genetic links to skin traits in Japanese women.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

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

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.