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Blue light can help hair grow by affecting certain receptors in hair follicles.

The gene Endothelin 3 makes mice's fur darker by increasing pigment cells and pigment levels.

Proteins like aPKC and PDGF-AA, substances like adenosine and ATP, and adipose-derived stem cells all play important roles in hair growth and health, and could potentially be used to treat hair loss and skin conditions.

Scientists developed tools to observe hair regeneration in real time and assess skin health, using glowing mice and light-controlled genes.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Wnt ligands are crucial for hair growth and repair.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Male hormones like testosterone may make COVID-19 worse, and testing for sensitivity to these hormones could help predict how severe a patient's symptoms might be. Treatments that reduce these hormones are being explored.

Melanocytes are crucial for skin pigmentation and can affect conditions like melanoma, vitiligo, and albinism, as well as hair color and hearing.

Genes and hormones cause hair loss, with four genes contributing equally.

GmMAX3b gene in soybeans boosts nodulation and affects hormone levels.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

PDGF signaling is crucial for maintaining and renewing hair follicle stem cells, which could help treat hair loss.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

The Gsdma3 gene is essential for normal hair development in mice.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

SCF and ET-1 together significantly increase skin pigmentation and melanin production.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

Using neurohormones to control keratin can lead to new skin disease treatments.

Blocking Wnt/β-catenin signaling with EGF receptor is necessary for proper hair growth.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

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

The gel made of minoxidil and hydroxypropyl-β-cyclodextrin improves hair growth and is good for long-term use.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.