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The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

Human hair keratin fibers have a detailed nano-scale structure that changes with different conditions.

The vitamin D receptor is involved in multiple body functions beyond calcium regulation, including immune response and rapid reactions not related to gene activity.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Hair structure changes immediately during perm treatment, with initial damage partially restored later.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Collagen is crucial for health and treating certain diseases, and supplements can improve skin, nails, and hair conditions.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

New compounds with carborane showed anti-androgen effects similar to flutamide.

The HR protein's role as a repressor is essential for controlling hair growth.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Human hair keratin might be good for filtering out harmful substances from water.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Hair strength is similar across different scalp areas, and not affected by age, gender, or hair thickness.

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

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

Melanocytes are important for skin and hair color and protect the skin from UV damage.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

Minoxidil can reduce functions related to androgen receptors.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

pH, calcium, and reactive oxygen species regulate plant cell growth, with key roles for NADPH oxidases and plasma membrane H+-ATPases.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Hair and nail cells share similar proteins, indicating a common differentiation pathway.

The vitamin D receptor helps maintain hair and bone health even without binding vitamin D.

Dermal EZH2 controls skin cell development and hair growth in mice.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.