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Finasteride users have higher odds of certain health issues and lower odds of specific lifestyle factors compared to nonusers.

Endocrine disruptors may cause early hair loss.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

A new skin disease in four Labrador retrievers responded well to immunosuppressive treatment.

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

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Using mesenchymal stem cells or their exosomes is safe for COVID-19 patients and helps improve lung healing and oxygen levels.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

Plant-derived vesicles from Ayurvedic plants may improve treatment delivery for hair growth and other conditions.

Excessive scalp massage after using minoxidil can cause hair damage, but reducing massage and using MSC exosomes can help.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

A specific gene mutation causes a severe skin disorder in a family.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

Certain genetic changes in the STX17 and KRT82 genes contribute to hair loss in alopecia areata.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

DPC-Exos can help regenerate hair follicles and heal wounds by activating the Wnt/β-catenin pathway.