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

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Different levels of microRNAs in different parts of the scalp can cause male pattern baldness.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

Retinoic acid changes skin cells to mucosal cells with goblet cells, needing TG2/Gh, Gbx1, and TGF-beta.

Endoglin is important for proper hair growth cycles and stem cell activation in hair follicles.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Promising cancer treatments were found, but the manufacturer closed.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.

Recombinant thymosin β4 promotes blood vessel growth and reduces muscle damage.

Hair follicle samples effectively show how well the drug MK-0752 targets and engages with the Notch pathway.

Melatonin helps hair grow by activating the RORα receptor in goats.

Seasonal changes affect gene activity linked to hair growth in Angora goats.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Two new gene clusters important for hair formation were found on human chromosome 11.

Melatonin helps hair grow by activating a specific signaling pathway.

hHbl gene is active in hair shaft cells and some pilomatricomas.

Transit-amplifying cells are crucial for tissue repair and can contribute to cancer when they malfunction.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

A gene mutation causes woolly hair in a Syrian patient.

Cells with active Wnt signaling are less likely to turn into cancer when exposed to a cancer-causing gene.

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

WNT10B affects hair growth by altering gene activity in hair cells.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

New LSS gene variants help understand congenital hypotrichosis 14 better.