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The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

Specific keratin gene mutations can cause monilethrix.

A new method accurately measures molecular movement without complex modeling.

RCS-01 therapy is safe and may improve skin structure by affecting gene expression.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Krox20 (Egr2) is important for the function of epithelial stem cells.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Trps1 plays a key role in hair follicle development and cycling.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

Double-stranded RNA helps regenerate hair follicles by increasing retinoic acid production and signaling.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

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

Auxin helps root hairs grow in high phosphate by affecting ROS and involving RSL2 and RSL4.

A mutation in the KRTHB5 gene causes hair and nail issues.

ROS and calcium oscillations are essential for root hair growth in plants.

R-spondins and their receptors help increase bone growth and may be used to treat bone loss diseases.

The model explains how mammal ear hair cells respond to sound and adapt.

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

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.