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Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

Lithocholic acid helps hair growth and regeneration in alopecia by activating vitamin D receptors.

A new genetic mutation was found causing hair and eye issues in a boy.

Sirolimus and propranolol may reduce abnormal cell growth and improve lymphatic malformations in children.

UC.145 may be a new biomarker for predicting gastric cancer.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A new gene mutation is linked to monilethrix in the studied family.

Blocking both main energy pathways can stop hair follicle stem cell-induced skin cancer growth.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

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

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

LEF-1 boosts cell growth in goat hair follicles, aiding cashmere production.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

A 2-year-old girl had a hair disorder not shared by her identical twin.

Skin acetyl-CoA synthesis is crucial for overall lipid balance.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

New mouse models help study melanocytic cells for melanoma research.

The calcineurin/NFAT pathway plays a significant role in the development and growth of a type of skin cancer called cutaneous squamous cell carcinoma.

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

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

The method shows how hair lipids form specific patterns and their roles in hair structure.