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A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Guasha changed rat skin appearance and blood vessels temporarily without affecting certain nerve proteins or fiber structure.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Certain gene variations may increase the risk and severity of alopecia areata.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

Nestin-expressing hair follicle cells may be useful for nerve repair and regeneration.

PDO, PLLA, and PCL threads increase collagen in ageing skin but don't change MMP1 gene expression.

CT60 polymorphism might increase the risk of Alopecia Areata.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

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

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Longer CAG repeat lengths in the androgen receptor gene are linked to higher testosterone levels in women with PCOS.

Mutations in the KRT85 gene cause hair and nail problems.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

KAP8.1 gene variations affect cashmere weight in Inner Mongolian goats.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

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