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The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

Certain immune cells are linked to non-scarring hair loss, suggesting potential for immune-targeted treatments.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Genes and hormones cause hair loss, with four genes contributing equally.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

FGF5 gene mutations cause long hair in domestic cats.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

A new gene mutation linked to a skin condition was found in a Spanish family.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Hair loss needs more research for better treatments.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

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

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.