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Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

lncRNAs play a key role in hair follicle development, affecting cashmere quality and yield.

Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

CT60 polymorphism might increase the risk of Alopecia Areata.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

Calreticulin has roles in healing, immune response, and disease beyond its known functions in the endoplasmic reticulum.

Hair loss gene linked to prostate issues.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

The study found key long non-coding RNAs involved in yak hair growth cycles.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

Noncoding dsRNA helps produce exosomes that aid in skin regeneration.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Egfl6 is not needed for zebrafish face development.

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

Septin4 helps kill colon cancer cells by working with the protein BAX.

FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Some people have a genetic variation that makes them less effective at breaking down drugs.

An extremely low-birthweight infant had a rare genetic skin disease and died despite treatment.