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Researchers developed a new way to measure gene activity in single hair follicles and found that a specific gene's activity changes with different amounts and times of treatment.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

KGF and its receptor are found in enlarged prostate tissue and KGF strongly increases cell growth.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A KRT32 gene variant causes loose anagen hair syndrome.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Normal human melanocytes can avoid cell death through multiple pathways.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

PI3K/Akt pathway is crucial for hair growth and regeneration.

The enzyme pyruvate kinase M2 helps hair regrowth and could be a potential treatment for hair loss.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Targeting mitophagy may help treat alopecia areata by reducing inflammasome activation.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

EGFR helps control how hair grows and forms without needing p53 protein.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Inhibiting the PI3K/Akt pathway may help prevent radiation-induced liver injury.

ING5 is crucial for stem cell maintenance and preventing certain cancers.

Certain genes control the color of human hair by affecting pigment production.

The Exfoliate-Dissolve-Repair skincare approach may effectively treat keratosis pilaris and reduce the need for corticosteroids.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

KAP6 genes are conserved across species and active in hair follicles.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

A specific enzyme is crucial for the bean plant's relationship with certain beneficial soil bacteria and fungi.

Dickkopf-related Protein 2 can help hair grow by activating a specific cell pathway.

Keratinocyte growth factor significantly alters skin and tissue development.

K15 gene is mainly active in the basal layers of hair follicles and epithelia, aiding early skin cell development.

PP-PTKL may help treat hair greying, but more testing is needed.