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A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Polycystic Ovary Syndrome (PCOS) affects Iranian women's feelings of femininity and self-image.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

New treatments for male hair loss show promise but need more research for safety and effectiveness.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

No link found between aromatase gene and female hair loss.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Finasteride side effects in young men may be linked to specific gene variations.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Haplogroup X found in Altaian population supports Amerindian origin.

Older men should openly discuss sexual health with doctors to improve their quality of life.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

A substance called TCQA could potentially darken hair by activating certain genes and increasing melanin.

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.

A specific gene mutation causes Olmsted syndrome.

Juvéderm Ultra Plus is safe and effective for treating severe nasolabial folds in Chinese subjects.

A gene mutation causes woolly hair in a Syrian patient.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

A new mouse mutation causes skin and hair defects due to a gene change.

Night shift work disrupts the body's natural clock genes.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

Eating collagen peptides may help with skin and hair growth.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Fox genes are important for hair growth and development in cashmere goats.