Search

everythinglearnresearchcommunity

for

Search:↓

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Thrombospondin-1 is crucial for hair follicle regression and reduced blood vessel growth during the catagen phase.

Basement membrane changes are crucial for hair follicle development.

Vitamin D and its receptor regulate skin functions like cell growth, immunity, hair cycle, and tumor prevention.

Acid can block TRPV3 from outside the cell but boost its function from inside.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

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

Lack of FPR2 slows hair growth by affecting hair cell activity.

The enzyme is crucial for skin cell development and can be activated without proteolytic activation.

MOTILIPERM may help treat male infertility by reducing stress in cells.

Mitochondrial genes help predict breast cancer outcomes and spread.

A gene mutation in mice causes skin defects and early death.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Beta-HPV and MCPyV are linked to certain skin cancers, with ongoing research and vaccine development.

Specific mutations in a receptor cause facial abnormalities and hair loss.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Lack of vitamin D receptor increases skin tumor risk by boosting hedgehog signaling.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

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

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Acne patients have higher mTOR gene expression.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Beer yeast vesicles may improve hair follicle health.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

Vitamin D receptor gene variations are not linked to alopecia areata.