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Chronological age affects the mouse auditory cortex more than hearing loss, and the brain may be less sensitive to mitochondrial dysfunction.

Prostaglandin D2 blocks new hair growth after skin injury through the Gpr44 receptor.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

ERβ has potential in treating prostate cancer and neurodegenerative diseases, but human studies are needed before clinical use.

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

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

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

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

New treatments for prostate cancer are less toxic and show promise, but more research is needed to enhance their effectiveness and reduce side effects.

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

Peppercorn's rich cultural and historical significance was reduced to just a flavor by 20th-century chemists.

Otter rabbit, mink, and blue fox fur can be identified by their unique hair structures.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

Mutations in the DSG4 gene cause specific hair and scalp issues.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.

Hair follicles can be used to study gene mutations in Stargardt disease.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

Omega-3 fatty acids may not help and could harm hair loss improvement in middle-aged or elderly men.

The dataset includes detailed genetic information from mouse skin cells before and after injury.

The dataset includes detailed genetic information from mouse skin cells before and after injury.

Curry leaves can be used to make effective herbal hair oil for promoting hair growth.

The new rabbit model better mimics human acne symptoms.

Some herbal treatments are effective for skin disorders, but more research and regulation are needed.

Mutations in the SNRPE gene cause hereditary hair loss.