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The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

Anti-IL-12/IL-23 antibody therapy effectively treats psoriasiform skin lesions in IBD patients.

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

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

The EDAR gene greatly affects hair thickness in Asian populations.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

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

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Genes and hormones cause hair loss, with four genes contributing equally.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

Two gene areas linked to male pattern baldness found, more research needed.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Men with baldness have higher levels of specific proteins, suggesting local hormone production may play a role in hair loss.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Hairless gene not strongly linked to baldness.