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The new method found new shared genetic areas linked to both Type 2 Diabetes and Prostate Cancer.

Turning off a specific gene in stem cells speeds up skin healing by helping cells move better.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

A 532 nm laser helps tendon stem cells grow and become tendon-like by increasing Nr4a1 activity, which may speed up tendon repair.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Activating the GDNF-GFRα1-RET signaling pathway could potentially promote skin and limb regeneration in humans and could be used to treat hair loss and promote wound healing.

Researchers found 15 new genetic links to skin traits in Japanese women.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

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

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

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Wnt10b helps hair follicle cells mature and produce pigment.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Transglutaminases help form strong hair by linking proteins, and can potentially alter hair properties.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

Th22 cells are essential for Tβ15-induced hair growth in mice.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

DGAT1 enzyme helps make diacylglycerols, waxes, and retinyl esters.