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

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

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.

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

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

A man experienced hair loss from radiotherapy, which can be temporary or permanent depending on radiation dose, with potential treatments available.

The X5 Hairlaser might help treat male hair loss, but more research is needed.

Gintonin-enriched fraction promotes hair growth and could be a potential alopecia treatment.

The document concludes that understanding hair follicles requires more research using computational methods and an integrative approach, considering the current limitations in hair treatment products.

Future hair cosmetics will be safer and more effective.

sPLA2-X is crucial for normal hair growth and follicle health.

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

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

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

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.

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

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

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.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

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.

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

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

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