Search

everythinglearnresearchcommunity

for

Search:↓

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

A gene called HDAC9 might be a new factor in male-pattern baldness.

ROP GTPase helps control the growth of pollen tubes and root hairs by managing cell structure and movement.

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

The gene Prss53 affects hair shape and bone development in rabbits.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Fgf9 helps create new hair follicles after injury through skin T cells.

The Itpr3 gene causes a specific hair pattern in mice.

ISX9 helps regrow hair by activating a specific cell signaling pathway.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

IL-9/IL-9R signaling can negatively affect human hair growth and may be a target for treating hair loss conditions.

The FRZB gene slows hair growth in rabbits.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Mutations in the SNRPE gene cause hereditary hair loss.

Nexin 1 may help control hair growth.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

RORA affects hair follicle stem cells' structure and movement, potentially helping treat hair loss.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.