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1,25-dihydroxyvitamin D3 helps melanocyte precursors from hair follicles grow and produce melanin, aiding vitiligo treatment understanding.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

Acne not improved by usual treatments may indicate a genetic disorder.

A specific metabolite, not a receptor protein, triggers the production of certain kidney enzymes, but this process is disrupted in mice with a mutation causing testicular feminization.

Transamidases are present in the epidermis but their exact role is unclear.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

A new gene mutation is linked to monilethrix in the studied family.

Increasing isoleucine intake improved skin and health issues in an infant with maple syrup urine disease.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Higher CSF 5-HIAA levels may predict better response to serotonin re-uptake inhibitors in trichotillomania.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

Ornithine decarboxylase is crucial for human hair growth and the hair cycle.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Enzymes that change arginine to citrulline are important for skin barrier and hair formation, and their malfunction can lead to skin conditions and hair disorders.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

Specific keratin gene mutations can cause monilethrix.

Glucocorticoids and thyroid hormones together are essential for fetal fat development.

The enzyme 17β-HSD type 2 mainly performs oxidation in human sebaceous glands, which may help protect against acne.

A genetic variant in the KRT25 gene causes tightly curled hair.

Mitochondrial reactive oxygen species are essential for skin and hair development.