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Epimorphin, a protein, plays a key role in the development of hair follicles in human fetuses, but it doesn't help in maintaining the stem cell population of the follicular skin layer.

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

Gene therapy shows promise for enhancing physical traits but faces ethical, safety, and regulatory challenges.

A gene mutation causes woolly hair in a Syrian patient.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Lack of cystatin M/E causes thin hair and dry skin.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Certain gene variations might be linked to severe acne in women but not in men.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

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

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

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

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.