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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.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

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

Specific genes influence hair and cashmere growth in Laiwu black goats.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Melatonin affects cashmere growth in goats by influencing stem cell and certain signaling pathways.

The document concludes that hair loss is complex, affects many people, has limited treatments, and requires more research on its causes and psychological impact.

Swiss Holstein cattle with curly, short hair carry genes from the Simmental breed.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

A new gene mutation causes insulin resistance in a girl and her mother.

A new gene variant causes glucocorticoid resistance in a mother and son.

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

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

Skin grafting can help repigment vitiligo, but it's less effective for widespread cases due to the Koebner phenomenon.