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A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Chicken feather gene mutation helps understand human hair disorders.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

The WIF1 gene is crucial for hair growth in Angora rabbits.

The SOSTDC1 gene is crucial for determining sheep wool type.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

The FRZB gene slows hair growth in rabbits.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Certain gene variations are linked to the thickness of cashmere goat hair.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The Hairless gene is crucial for healthy skin and hair growth.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

miR-31 regulates hair growth by controlling gene expression in hair follicles.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

A new gene, JMJD1C, may affect testosterone levels in men.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

HOXC13 is essential for hair and nail development by regulating Foxn1.