Search

everythinglearnresearchcommunity

for

Search:↓

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

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

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Ponatinib can cause a rare skin reaction that resolves with topical treatment and temporary drug discontinuation.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A mutation in mice causes hair loss and immune problems.

TCDD changes skin cell growth and keratin production in mice.

ZNF750 and MPZL3 are important in causing seborrheic dermatitis.

Targeting mTOR in myeloid cells may help reduce psoriasis symptoms.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

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.

p120-catenin helps control skin inflammation by regulating cadherin levels.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Abnormal contraction of connective tissue in hair follicles causes hair loss by killing off important cells, and treating this could improve hair growth.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.