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A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

New genetic mutations causing hair loss were found in a Chinese family.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

The topical inhibitor CUR61414 was not effective in treating basal cell carcinoma in human trials.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

Cepharanthine may help treat gastric cancer by causing cancer cell death and affecting energy use.

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

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Corin speeds up wound healing by helping skin cells move and grow.

CCCA and LPP may be related hair loss conditions influenced by genetics and environment, needing early treatment.

Nexin 1 may help control hair growth.

Dermal EZH2 controls skin cell development and hair growth in mice.

m6A-circHECA may affect cashmere goat hair growth and is possibly controlled by gene promoter methylation.

BMP receptor IA is essential for proper hair cell differentiation in mice.

Cyclosporin A, a drug, reduces TGF-β2 expression in skin cells, potentially causing excessive hair growth through a process involving the calcineurin/NFAT pathway.

Trichohyalin is also found in the outer layers of normal human skin.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

miR-200c-3p could help diagnose and treat alopecia areata.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

S100A6 is important for cell functions and can help diagnose and treat diseases.

Nucleic acids trigger chemokine production in skin cells, affecting skin inflammation.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Calreticulin has roles in healing, immune response, and disease beyond its known functions in the endoplasmic reticulum.

A missing mK6irs1 gene causes hair loss in mice.