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The new treatment using tiny lipid carriers to deliver minoxidil and latanoprost directly to hair follicles shows promise for alopecia.

Nothopanax scutellarium leaves can promote hair growth but may mildly irritate the skin.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

The document concludes that the new expert system can assess the risk of PCOS effectively despite uncertainties in diagnosis.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

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

Using LC-MS/MS for hormone measurement can prevent false high testosterone results and avoid unnecessary tests.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Hair follicle cells change their DNA packaging during growth cycles and when grown in the lab.

Older age increases positive hair alcohol test results, and chest hair is a good alternative for testing; season affects results, with higher levels in winter.

The document concludes that understanding hair's chemical makeup is key to creating effective hair growth products that also improve social confidence.

5% topical minoxidil improves hair density and quality in monilethrix patients.

The document concludes that better targeted treatments are needed for wound healing, and single-cell technologies may improve cell-based therapies.

Fibroblasts are crucial for tissue repair and inflammation, and understanding them can help treat fibrotic diseases.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

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

PXX is an effective and affordable photocatalyst for creating new chemical bonds in organic synthesis.

The research maps the complex development of early mouse skin, identifying diverse cell types and their roles in forming skin layers and structures.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

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

Hair strength is similar across different scalp areas, and not affected by age, gender, or hair thickness.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

The research reveals how early embryonic mouse skin develops from simple to complex structures, identifying various cell types and their roles in this process.

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

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

The document concludes that while some organisms can regenerate body parts, mammals generally cannot, and cancer progression is complex, involving mutations rather than a strict stem cell hierarchy.