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Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

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.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Certain IL-18 gene variations may increase the risk of alopecia areata.

Root hairs in cereal crops can grow beyond the usual zone, and using Turface® clay helps study this.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

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

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

New genetic mutations linked to rare skin disorders were found in three newborns.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Genomic research can help improve the quality and production of natural fibers in animals.

Retinoic acid affects male and female muscle energy use and function differently.

Ashwagandha may improve hormone levels and reduce hair loss in non-classical adrenal hyperplasia.

Tioconazole cream is highly effective and easy to use for treating sheep dermatophytosis.

Povidone iodine reduced skin bacteria more than chlorhexidine gluconate, but neither met FDA reduction standards.

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

New models predict male pattern baldness better than old ones but still need improvement.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

Exosome treatment for hair growth is promising but not FDA-approved and needs more research on safety and how it works.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Hair growth serums A and C can affect hair growth genes and pathways, suggesting potential for personalized hair loss treatments.