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Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

A specific gene mutation causes complete hair loss without other health issues.

New findings suggest potential treatments for melanoma, hyperpigmentation, hair defects, and multiple sclerosis, and show skin microbiome changes don't cause atopic dermatitis.

FTase and GGTase-I are essential for skin keratinocyte health.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Too much Sonic Hedgehog protein stops hair growth in embryos.

The research mapped gene activity in developing mouse skin and found key markers for skin cell types and changes from fetal to early postnatal stages.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

Zfp462 deficiency in mice causes anxiety-like behaviors and excessive self-grooming.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Wnt5a overexpression alone doesn't cause psoriasis in mice but affects hair growth.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Mouse tail skin has different keratinization near hair follicles and scales.

Lack of KSR1 stops certain skin tumors in mice.

Multiple pregnancies prevent skin disease but worsen kidney disease in certain mice.

A mutation in the human hairless gene causes alopecia universalis.

Disrupted stem cell signals in hairpoor mice cause hair loss.

Lack of cystatin M/E causes thin hair and dry skin.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

Zinc made mice's coarse hair turn into fine hair without affecting skin structure.