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

The HCR gene contributes to psoriasis risk.

The research updated the skin cell profile, finding new skin cell markers and showing fibroblasts' key role in skin health.

The PML protein helps prevent skin cancer in mice.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Basal cell carcinomas likely originate from hair follicle cells or stem cells.

The Walleye dermal sarcoma virus cyclin causes excessive skin cell growth in mice.

Researchers found certain genes are overactive and others are underactive in men with early balding, which could help create new treatments.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

Young donor, early passage stem cells have the highest stemness.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Increasing EGR1 levels makes hair root cells grow faster.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.

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

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

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

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.