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Cytarabine can cause multiple organ toxicities, especially neurotoxicity, but better research methods are needed to fully understand and predict these effects.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

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

Mutations in the hairless protein gene cause hair loss.

Beta-catenin is crucial for skin cell growth, development, and cancer formation.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Increasing PDCD4 protein may help prevent or treat some skin cancers.

FLCN helps control iron levels in cells.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

Biglycan helps regulate hair growth and regeneration.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

The research shows how certain drug molecules form stable structures with polymers, which could help create new drug forms.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

The research found a way to develop hair growth materials by targeting a specific signaling pathway.

Blocking β-catenin in skin cells improves hair growth during wound healing.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Activating c-Myc in skin causes rapid cell growth and changes, but these effects are reversible.

Scientists made new substances that can block an enzyme linked to prostate issues and hair loss, with potential for creating a new treatment.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

Changing light exposure can affect hair growth timing in goats, possibly due to a key gene, CSDC2.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.