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ROXY proteins help plants respond to nitrate shortage by affecting nutrient sensing and growth.

The type 3 IP3 receptor is important for controlling hair loss and growth.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

The research identified various cell types in mouse and human teeth, which could help in developing dental regenerative treatments.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Different combinations of human hair keratins affect how hair fibers form.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A specific immune response helps control mite populations on the skin, maintaining healthy hair follicles.

Dutasteride is more efficient than finasteride, but individual results vary.

Intravital imaging helps us better understand stem cells in their natural environment and could improve knowledge of organ regeneration and cancer development.

Vitamin D boosts a specific gene activity in kidney cells that could improve heart and kidney function.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Mitochondrial therapy and platelet-rich plasma therapy both stimulated hair regrowth in aging mice, with mitochondrial therapy showing similar effectiveness to plasma therapy.

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

Urokinase, a type of protein, helps skin cells multiply faster, especially in newborn mice.

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.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

A girl with type 1 diabetes developed a serious eye condition very early, suggesting the need for earlier eye checks and that early treatment can work well.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

The document concludes that MGRN1 affects mouse fur color by interfering with a receptor's signaling, but its full role in the body is still unknown.

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

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

HGF/SF increases skin melanocytes but doesn't change melanin type or amount.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.