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IL-9 increases skin cell movement but decreases their ability to invade, and this effect is controlled by cell contractility, not by MMPs.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Sunlight exposure improved a patient's skin condition, and there may be a link between a certain disease and skin growths; a leukemia treatment caused changes in hair color and growth.

GLI1 RNA CISH effectively identifies basal cell carcinoma but is less specific for benign follicular tumors.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

ILC1-like cells may contribute to hair loss in alopecia areata.

Miz1 is essential for proper hair structure and growth.

Patched1 helps prevent tumors by controlling cell growth.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

Edar signaling is crucial for proper hair follicle development and function.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

The vector successfully directed specific gene expression in hair follicles.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

An infant had two different natural hair colors on the scalp with no health issues.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

Early diagnosis and multidisciplinary care, including orthopedic surgery, can prevent long-term disability in IFAP syndrome.

Targeting THY1 can improve skin repair and healing.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Claudin 6 is crucial for normal skin and hair development.

Hair follicle dermal stem cells help control hair growth timing by regulating signals at the hair germ–dermal papilla interface.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

NFIC helps rat dental cells grow and turn into bone-like cells.