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Blocking YAP/TAZ could be a new way to treat skin cancer.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

A new DSG4 gene mutation causes hair defects in a young girl.

SQSTM1 gene issues may increase the risk of alopecia areata.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

Genetic mutations affecting DNA repair cause early aging symptoms in progeroid syndromes.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

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

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Chromosomal differences affect how muscle cells respond to testosterone.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A stable sheep ovarian cell line was created for studying reproduction and hormones.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Injury boosts normal skin cell growth, reducing cancer cell advantage.

A specific gene mutation causes woolly hair and hair loss.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Cats with abnormal hair had DSG4 gene changes causing hair problems.