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The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

Some skin growths with mucin can form hair follicles and resemble skin cancer, but a special stain can help tell them apart.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

ZNF750 and MPZL3 are important in causing seborrheic dermatitis.

Alopecia can be caused by multicentric reticulohistiocytosis.

Laminin α5 is essential for skin communication and health.

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

PP2Acα is essential for proper hair and skin development.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

Mutations in the LIPH gene cause woolly hair in a child.

KLHL24-mutant stem cells help understand skin and heart disease.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

CCCA is a scarring hair loss condition mainly in African descent women, possibly caused by genetics and hairstyling, treated with gentle hair care and medications.

Mutations in claudin-1 and claudin-3 cause hair loss in baby mice.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

Mitf plays a key role in melanoma progression and is linked to disease stage.