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

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

The Itpr3 gene causes a specific hair pattern in mice.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

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

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

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

Dihydrotestosterone (DHT) is crucial for conditions like male-pattern baldness and acne, and measuring a byproduct, androstanediol glucuronide, is a better way to assess DHT's effects than DHT blood levels.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Gray hair can potentially be reversed, leading to new treatments.

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

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

A specific genetic deletion in goats affects cashmere yield and thickness.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

People with Down's syndrome are more likely to have syringomas.

The Third World Congress of the International Academy of Cosmetic Dermatology discussed various topics like hair disorders, skin conditions, wound healing, shampoo technology, acne treatment, and the use of lasers in dermatology.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.