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Certain gene variations might increase the risk of a hair loss condition in Koreans.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

Abnormal gene expression related to keratin causes hair loss in certain mice.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Defective nuclear transport may cause gene expression changes in Progeria.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

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

Four new FGF5 gene variants cause long hair in dogs.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Lack of KSR1 stops certain skin tumors in mice.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

Targeting Keratin 17 may help overcome cancer therapy resistance.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Researchers found two new genetic variants linked to Alzheimer's disease.

Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.