Search

everythinglearnresearchcommunity

for

Search:↓

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

Mutation in hairless gene may increase hair loss risk.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

Alopecia areata involves unique activation of certain immune cells.

miR-22 helps skin cancer grow and spread by activating specific cell signals.

Mice with alopecia areata had wider lymphatic vessels in their skin.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Mutation in hairless gene may increase hair loss risk.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

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

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

Gene linked to common hair loss found, may lead to new treatments.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Certain VDR gene changes can affect melanoma risk.