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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

HLD10 can include increased body hair and Mongolian spots.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

A gene called HDAC9 might be a new factor in male-pattern baldness.

A specific gene variant may increase the risk of developing Alopecia Areata.

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

A specific gene mutation causes congenital hair loss.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

A specific gene mutation causes a severe skin disorder in a family.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Certain gene variations may increase the risk and severity of alopecia areata.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

The HR protein's role as a repressor is essential for controlling hair growth.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

A specific gene mutation causes sparse, brittle hair in a family.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.