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ERK activation spreads between cells in mouse skin, linked to cell division and influenced by TPA and EGF receptors.

Certain human skin cells marked by CD44 and ALDH are rich in stem cells capable of long-term skin renewal.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Overexpression of the glucocorticoid receptor in mice causes developmental defects similar to ectodermal dysplasia.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Electrical impedance spectroscopy improves biopsy accuracy and efficiency for skin lesions.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Certain genetic variants in keratins increase the risk of tooth decay.

People with advanced chronic kidney disease often have skin problems, which can be treated with various medications and procedures to improve their quality of life.

A rare gene variant causes hair and nail issues in a family.

Epithelial-derived Pop-Up Keratinocytes (ePUKs) may enhance wound healing in regenerative medicine.

The improved EczemaNet more reliably and clearly identifies and assesses the severity of atopic dermatitis from photos.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

C-scores can help predict gain-of-function and loss-of-function mutations.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Dermoscopy helps accurately diagnose and treat benign skin cysts.

The ginseng cicada decoction effectively reduces atopic dermatitis symptoms and improves quality of life safely.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Patients with central centrifugal cicatricial alopecia benefit from shared decision-making with their doctors.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Epidermolysis bullosa in calves was not caused by mutations in the keratin genes bKRT5 and bKRT14.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

cDermo-1 causes dense skin, feathers, and scales in chickens.