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The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

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

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

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Gene differences may affect baldness treatment response in Korean men.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

HLA-DRB5 and other genes may be linked to alopecia universalis.

A new 3D culture system helps grow and study mouse skin stem cells for a long time.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Hordenine may help hair grow by activating a specific cell growth pathway.

The cause of Frontal fibrosing alopecia, a type of hair loss, is complex, likely involving immune responses and genetics, but is not fully understood.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

The conclusion is that accurately identifying the cause of high androgen levels in women with PCOS is crucial and requires specific tests.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A new gene mutation causes long hair in some Maine Coon cats.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.