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

Keratin-based hydrogels with calcium are effective for delivering anti-fibrotic drugs.

Recombinant keratins can form useful structures for medical applications, overcoming natural keratin limitations.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

α-Ketoglutaric acid improves hair growth, rabbit performance, and antioxidant levels.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Radiation damages hair stem cells and changes keratin expression, with Krt5 as a potential marker for radiation effects.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

TEDAR is crucial for skin cell differentiation and barrier formation.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

YAP and TAZ proteins control skin cell growth and repair.

A genetic variant in the KRT25 gene causes tightly curled hair.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Certain genetic variants in keratins increase the risk of tooth decay.

Inward rectifier potassium channels are important in many body functions and diseases, and could be potential drug targets.

A kidney transplant patient developed pink skin bumps with spiny centers on her face and limbs.

Runx1 helps control the KAP5 gene in human hair follicles.

The research helps in creating genetically modified animals to study hair growth.

The prototype for analyzing skin aging works technically and clinically.