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The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The protein ER71/ETV2 helps regrow hair after chemotherapy by improving the growth of new blood vessels.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

The XBB lineage of the Omicron variant spread rapidly in Southeastern Wisconsin.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

PCFCL may have unrecognized subtypes and needs more research.

The research found that chickenpox virus spreads in skin through blood then to skin cells, while shingles virus moves from nerves to hair follicle areas before infecting skin cells.

HPV-150 and HPV-151 are rare skin viruses linked to warts and some skin cancers.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Somatic BHD mutations are rare in Japanese renal tumors.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

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.

A calf in Scotland likely had Schmallenberg virus from its mother.

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

Eclipta alba has a genome size of 4.27 billion base pairs, and Aloe barbadensis has 4.42 billion base pairs.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

SVpgC2a cells show abnormal growth and keratin changes, modeling early cancer development.

Merkel cell polyomavirus can infect and persist in skin cells, evading the immune system, but certain treatments can control it.

HPV16 oncogenes disrupt the normal activity of hair follicle stem cells.

Epidermolysis bullosa in calves was not caused by mutations in the keratin genes bKRT5 and bKRT14.

A small group of slow-growing cells causes basal cell carcinoma to return after treatment.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Blocking Hedgehog signaling offers new treatment options for advanced basal cell carcinoma.