Search

everythinglearnresearchcommunity

for

Search:↓

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

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

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

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

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

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.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

Minoxidil, a common alopecia medication, might cause eye changes due to its properties and lack of tissue selectivity.

Terbinafine can cause hair loss.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

miR-29 is a key factor that accelerates aging.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The document explains the genetic causes and characteristics of inherited hair disorders.

Female pattern hair loss involves thinning hair on crown and frontal scalp, diagnosed by hair ratio, and treated with minoxidil, antiandrogens, or hair transplantation.

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

NF-κB signaling is crucial in many diseases and can be targeted for new treatments.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Understanding skin structure and development helps diagnose and treat skin disorders.

PCOS and related metabolic issues often run in families.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Twist2 is essential for scarless skin healing and hair growth in mouse fetuses.

Twist2 is essential for proper skin healing and hair growth in developing mice.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.