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miR-22, a type of microRNA, controls hair growth and its overproduction can cause hair loss, while its absence can speed up hair growth.

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

CD2 might be a new treatment target for patchy alopecia areata.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

The antibacterial toner can effectively kill acne-causing bacteria by penetrating skin plugs.

Peripilar keratin casts are a helpful sign for diagnosing traction alopecia.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

A 2-year-old girl had a hair disorder not shared by her identical twin.

Milia may come from the outer part of the hair follicle.

PEI diffuses into hair at a constant rate, and urea speeds up this process.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Researchers isolated and identified structural components of human hair follicles, providing a model for studying hair formation.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

An apple-based supplement was found to stimulate hair protein production, which may help with hair growth.

A specific type of skin cell creates an opening for hair to grow out, and problems with this process can lead to skin conditions.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Polyomavirus A2 infection in newborn mice caused hair follicle tumors.

A 69-year-old woman has a fast-growing hand lesion that didn't improve with salicylic acid.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

Human hair strength and health are linked to sulfur compounds that can be reduced by stress but improved with sulfur supplements.

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

Melanin density affects hair color, and this method can help in cosmetic assessments and diagnosing hair diseases.

Nestin-expressing cells turn into a specific type of skin cell in hair follicles during development and in adults.

Nestin marks cells that can become a specific type of skin cell in hair follicles of both developing and adult mice.

The four patients have a unique type of ichthyosis affecting hair follicles.