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Biotin helps regulate proteins in the blood, which may explain its role in hair growth.

The KRTAP36-2 gene in sheep affects wool yield.

PGA-4HGF may help treat hair loss by activating hair growth pathways and extending the hair growth phase.

miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

The Gsdma3 gene is essential for normal hair development in mice.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

5% topical minoxidil improves hair density and quality in monilethrix patients.

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

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Proper care and diet are crucial to prevent health issues in gerbils.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Cyclooxygenase-2 overexpression in mice skin causes hair loss like human androgenetic alopecia.

Researchers found a new mutation causing total hair loss from birth.

Stem cells control their future role by changing ERK signal timing, affecting tissue regeneration and cancer.

Mutations in specific llama genes may affect fiber quality for textiles.

Human stem cells can help form hair follicles in mice.

Activin helps skin growth and healing mainly through stromal cells and affects keratinocytes based on its amount.

FGF13 gene changes cause excessive hair growth in a rare condition.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Specialized ribosomes affect aging in human skin cells.

Homeopathic treatment can help manage alopecia areata in children.