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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Epiregulin can help hair grow and may be useful for treating hair loss.

ILC1-like cells can cause alopecia areata by themselves.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

New therapies and trials are needed for Merkel cell carcinoma, a tough skin cancer.

A new type of nerve cell involved in itch perception was discovered.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Blocking certain immune signals can reduce skin damage from radiation therapy.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

EREG therapy may help treat hair loss by promoting hair growth.

Skin cancer often starts from Lgr5+ progenitor cells.

EFFC might be common but underreported.

Higher CRHR1 levels in AA patients lead to increased inflammation.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.