Search

everythinglearnresearchcommunity

for

Search:↓

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

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

S1PR1 helps control inflammation in blood vessel cells by affecting gene activity differently in various cell types and locations.

PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

Different PADI isoforms help cells develop diverse functions.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Keratin 2e shows a unique pattern in developing fetal skin, different from other keratins.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

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

ASC-CM is more effective than EV for treating osteoarthritis.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Collagen XVIII is crucial for maintaining tissue structure and function in the brain, kidneys, and hair.

ARQ-234, a protein designed to treat atopic dermatitis, shows increased effectiveness in early testing.

MAP-2 is crucial for the structure of hair follicles and nails.

JAM-A helps hair regrowth in alopecia areata by protecting VCAN in skin cells.

Defective protein folding due to a mutation is key in ANE syndrome.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

CD2 might be a new treatment target for patchy alopecia areata.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

The CD44-CD49d complex boosts T cell activation and survival in autoimmune disease.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Type IV collagen chains vary in different parts of human skin, with specific patterns linked to melanocytes.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

S100A4 and NMIIA promote tumor growth in glioblastoma by enhancing blood vessel functions.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.