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The study found that androgen receptors in skin cells mainly affect the focal adhesion pathway and control the caveolin-1 gene, with implications for new treatments for related diseases.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

Loss of TET2 increases the risk of skin and oral cancer.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Removing EGFR in skin causes inflammation and abnormal hair growth.

Sea cucumbers have unique genes that help them regenerate their intestines.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

Suppressing very long chain fatty acids is linked to skin cancer.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

17β-estradiol boosts APE1/Ref-1 secretion in cells and mice via a calcium-dependent pathway.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

ROR2 is crucial for hair follicle stem cell maintenance and self-renewal.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The protein ER71/ETV2 helps regrow hair after chemotherapy by improving the growth of new blood vessels.

A new one-step test can quickly identify skin cancer during surgery.

Gene variation affects prostate issues and hair loss.

A rare EGFR mutation in newborns leads to severe health issues and early death.

UVB exposure affects retinoid metabolism, which is important for skin cancer progression and treatment.

BerEP4 and CD34 staining can help tell apart tricholemmoma from basal cell carcinoma.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Involucrin is a useful marker for keratinocyte differentiation in mice.

Atopic dermatitis shows a link between skin layers in inflammation, detectable with detailed gene analysis.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.