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A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

FOXN1 duplication can cause excessive hair growth.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

The study found nine new hair protein genes in human hair follicles.

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 genetic change in the EDAR gene causes the unique hair traits found in East Asians.

The study identified key genes and pathways linked to hair disorders, aiding precision medicine.

Werner's syndrome causes early aging and increases cancer risk, requiring early diagnosis and symptom management.

The study found 65 intermediate filament genes, including new keratins, and suggested updating keratin naming.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

Mutant stem cells adapt their metabolism differently to outcompete normal cells in the skin.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

The type of tumor suppressor affects the form of skin cancer from hair follicle stem cells.

Hairless gene not strongly linked to baldness.