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Fasting in hens affects thyroid hormones, which regulate feather and hair growth.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Methylprednisolone helps skin cells stick together better in pemphigus vulgaris.

Understanding proteins in skin structures like claws and hair is crucial for future research.

Trichohyalin is also found in the outer layers of normal human skin.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

Patients with severe alopecia areata have higher levels of MIF, which decrease after successful treatment.

The May issue discussed publishing agreements and four studies on cholesterol in hair, cancer cell changes, hormones in the uterus, and skin protein effects.

Tongue cancer cells show more plectin-1 than non-cancer cells, but both have similar levels of trichohyalin.

A protein called desmoglein 3 is important for keeping hair follicle stem cells inactive and helps in their regeneration.

The document concludes that the skin is a complex organ providing protection, sensation, and healing, with challenges in treating conditions like itchiness.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

A 7-year-old dog with a rare autoimmune disease was euthanized due to severe anemia and poor prognosis.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The exam tested knowledge on various skin-related topics for CME credit.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The document explains various skin conditions and their treatments.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Neurohormones help control skin health and could treat skin disorders.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Keratins are important for skin cell health and their problems can cause diseases.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

Claudin-1 is important for the barrier function and growth of hair.