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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Young donor, early passage stem cells have the highest stemness.

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

More research and guidelines are needed for managing prostate cancer in people with high-risk genetic mutations.

Stem cell treatment from umbilical cords reduces symptoms of atopic dermatitis and may help hair growth.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

Hair samples can be used to create stem cells easily and non-invasively.

Different gene mutations cause different types of ichthyosis, with some new mutations found.

Vitamin D Receptor is crucial for hair follicle shrinkage and cell death, affecting hair growth.

Bioavailable quercetin may help improve aging signs by positively affecting gut health.

Mechanotransduction aids healthy wound healing by promoting specific fibroblasts.

A temporary capillary cell type helps skin repair after radiation by promoting blood vessel growth.

Increased EGFR gene variations may predict chemotherapy outcomes in small cell lung cancer patients.

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

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

The study improved understanding of gene roles in cashmere goat hair growth, aiding future cashmere production.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Sunscreen technology is improving with new ingredients and methods to better protect skin from sun damage.

EDA2R is a key gene linked to ageing and diseases, and targeting it may help treat conditions like hair loss and chronic diseases.

PRP may help with aging and osteoarthritis, improving tissue repair and reducing surgery risk.

High levels of ERK activity are key for tissue regeneration in spiny mice, and activating ERK can potentially redirect scar-forming healing towards regenerative healing in mammals.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

Lysine carboxymethyl cysteinate (LCC) protects skin from UVB damage by activating autophagy.

Four new FGF5 gene variants cause long hair in dogs.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Comprehensive genetic testing and international collaboration are crucial for better understanding and managing Ehlers-Danlos syndromes.

Interleukin-1 increases keratin K6 production in skin cells.