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LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

The method helps estimate and track skin cell growth and movement during healing.

Beta-sitosterol and stigmasterol might help prevent hair loss by blocking a specific enzyme.

C-scores can help predict gain-of-function and loss-of-function mutations.

Spironolactone works well for acne and hirsutism, isotretinoin is very effective for acne and may have antiandrogenic effects, and 5 alpha-reductase inhibitors should be considered antiandrogens.

Maintaining DNA integrity in stem cells is crucial to prevent aging and cancer.

Toxic shock syndrome is caused by a complex interaction of bacterial toxins and the immune system, and understanding this can help improve diagnosis and treatment.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

VDR regulation varies by tissue and is crucial for its biological functions.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Epigenetic mechanisms control skin development by regulating gene expression.

A new method helps detect androgen receptor movement in cells, aiding research on hair loss treatments.

Cri-du-chat syndrome can cause skin and oral lesions affecting nutrition and quality of life.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Sex neurosteroids cause different effects on hippocampal synaptic plasticity in males and females.

Prolactin levels and gene polymorphism are not linked to vitiligo severity but are related to BMI.

MED1 is essential for normal hair growth and maintaining hair follicle stem cells.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

The Androgen Receptor could be a target for treating diseases like cancer, but more research is needed to confirm the effectiveness of potential treatments.