Search

everythinglearnresearchcommunity

for

Search:↓

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

AP-2α and AP-2β are crucial for healthy skin and hair.

Keratin 19 forms less stable and shorter filaments than keratin 14, giving unique traits to certain skin cells.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

miR-218-5p helps skin and hair growth by targeting SFRP2 and activating a specific signaling pathway.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

KAP8.1 protein is crucial for hair structure and interacts with keratin 85.

TMPRSS2 affects COVID-19 severity and treatment options.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

PP2Acα is essential for proper hair and skin development.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

KAP6 genes are conserved across species and active in hair follicles.

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

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

Researchers found a non-functional sheep keratin gene due to mutations.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Two specific genes are more active during hair growth in mice.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.