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A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Desmocollin 1 helps maintain skin structure during fetal development.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Paneth cells help support stem cells and aid tissue regeneration after injury.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

Certain peptides can prevent hair loss in young rats caused by a cancer drug.

Keratin 15 helps maintain skin cell growth and repair.

Desmosomal adhesion is essential for healthy skin structure and function.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

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

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

The cerium-polypeptide hydrogel effectively heals drug-resistant bacterial wounds by fighting bacteria, reducing inflammation, and promoting tissue repair.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The extracellular matrix affects where tumors can start in the body.

CAP7.1 is generally safe at 200 mg/m²/day, but can cause fatigue, nausea, hair loss, fever, and blood-related issues.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Lipin-1 is important for skin cell differentiation and skin barrier function.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Claudin 6 is crucial for normal skin and hair development.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.