Search

everythinglearnresearchcommunity

for

Search:↓

Patients with acute and subacute skin lupus respond faster to belimumab than those with chronic skin lupus.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Squaric acid dibutylester for alopecia areata can cause benign skin lymphoid growths.

Identified genes linked to male-pattern baldness may help develop new treatments.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

A special receptor in sensory nerve endings helps control how they respond to stretching.

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

Presynaptic inhibition of certain nerve fibers in cats is mainly controlled by GABA and glycine.

Trps1 is essential for proper hair follicle development.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Lower SMAD2/3 activation predicts more severe skin cancer.

The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

Pyrene excimer nucleic acid probes are promising for detecting biomolecules accurately with potential for biological research and drug screening.

Botulinum toxin type A helps treat hair loss by stopping cell death in hair follicles through a process involving certain non-coding RNAs and a protein called Bax.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A specific gene mutation causes different hair defects in Indian monilethrix families.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

The "spade sign" is a highly specific indicator for diagnosing acne keloidalis.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Ptprq has multiple forms that change during inner ear development.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Bexxar treatment led to a high response rate in patients with advanced-stage, treatment-resistant follicular lymphoma.

Raman micro-spectroscopy can help distinguish basal cell carcinoma from hair follicles in skin tissue.