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

The study found potential new DNA patterns in fertility genes, but further testing is needed.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Mutant stem cells adapt their metabolism differently to outcompete normal cells in the skin.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

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

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

A specific gene variation in goats is linked to better growth traits.

Hairless gene not strongly linked to baldness.

Loose anagen hair syndrome may be caused by keratin gene mutations.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

GLABRA 2 controls ethylene production to help root hair growth during nutrient deficiency.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Transgenic sheep embryos with a specific promoter were successfully created, but more research is needed for gene expression in hair follicles.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.