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Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Low-dose acitretin helps nail psoriasis, stem cells may treat scarring alopecia, Chinese men have lower baldness rates, lateral foldplasty is good for ingrown toenails, hair diameter helps diagnose female baldness, childhood trauma linked to alopecia areata, certain hair-weaving leads to scalp conditions in African American women, and new methods for hair research and understanding hair and sweat gland development were introduced.

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.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Future hair cosmetics will be safer and more effective.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Hair shaft disorders are diagnosed through examination and history, with general care and some treatments offering improvement.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

LPA3 is crucial for embryo implantation and links LPA to prostaglandin signaling.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

Finding functions for unknown GPCRs is hard but key for making new drugs.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Different scaffold patterns improve wound healing and immune response in mouse skin, with aligned patterns being particularly effective.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

ATP increases melanin production in skin after UV exposure, with the P2X7 receptor being crucial for this process.

Chemotherapy can cause brain inflammation and damage, and understanding this process could help manage side effects.

The study found new details about human hair growth and suggests that preventing a specific biological pathway could potentially treat hair graying.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

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

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Minoxidil solution applied twice daily improved hair growth in patients with Woolly Hair/Hypotrichosis due to LIPH gene issues, with mild side effects.