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HPV infection is linked to better survival in advanced anal cancer, higher radiation doses improve survival, especially in HPV-negative patients, and prostaglandin E₂ pretreatment can protect mouse hair follicles from radiation damage.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

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

Genetic variants in specific genes cause a type of hair loss.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

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

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Keratin 15 cells from hair follicles help develop and maintain skin tumors in mice.

HPV8 causes skin cancer by expanding specific skin stem cells.

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

Radiotherapy effectively treated a large scalp tumor in an elderly woman, avoiding surgery.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

New cancer treatments show promise in reducing tumor growth and improving skin regeneration in mice.

Removing p16INK4a from skin cells can lead to faster and more clumped growth, which might help with hair growth.

Increasing SSAT makes skin more prone to cancer.

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

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.