Search

everythinglearnresearchcommunity

for

Search:↓

c-Maf positive macrophages help form hypertrophic scars by affecting fibroblasts and collagen production.

Rapamycin treatment helps reduce brain inflammation and symptoms of mitochondrial disease by blocking specific pathways in mice.

Mutations in the hairless protein gene cause hair loss.

JMJD3 and NF-κB activate Notch1, which is essential for skin cell movement and wound healing.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

Acne patients have higher levels of mTOR in their skin, which could be linked to future metabolic disease.

Targeting CD169+ skin macrophages may help treat psoriasis.

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

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

BLMP-1 is important for regular molting and gene expression cycles in worms.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Deleting TNFα gene reduces skin cancer risk in certain mice.

CD271 is crucial for maintaining healthy skin and preventing inflammation.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

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

The Celsr1 gene is crucial for normal hair patterning in mice.

MicroRNAs could help assess and manage multiple chronic diseases.

Targeting mTOR in myeloid cells may help reduce psoriasis symptoms.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A new portable microscope can effectively monitor skin wound healing in real-time.

The LMNA mutation affects skin structure even in asymptomatic carriers.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Ribonucleotide excision repair is crucial to prevent skin cancer.

DNMT1 helps turn hair follicle stem cells into fat cells by blocking a specific microRNA.