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Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

Thyroid disease can cause skin, hair, and nail problems, and treating the thyroid condition often improves these symptoms.

Lipin-1 is important for skin cell differentiation and skin barrier function.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

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

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

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

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Mutations in the KRT85 gene cause hair and nail problems.

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

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

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A device was made in 2008 to measure hair loss severity. Other findings include: frizzy mutation in mice isn't related to Fgfr2, C/EBPx marks preadipocytes, Cyclosporin A speeds up hair growth in mice, blocking plasmin and metalloproteinases hinders healing, hyperbaric oxygen helps ischemic wound healing, amniotic membranes heal wounds better than polyurethane foam, rhVEGF165 from a fibrin matrix improves tissue flap viability and induces VEGF-R2 expression, and bFGF enhances wound healing and reduces scarring in rabbits.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

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

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

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.

Keratin proteins in epithelial cells are dynamic and crucial for cell processes and disease understanding.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

Chemotherapy improved a girl's painful foot condition linked to pachyonychia congenita.

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

Using special RNA to target a mutant gene fixed hair problems in mice.

Chicken feather gene mutation helps understand human hair disorders.

The review found that different stem cell types in the skin are crucial for repair and could help treat skin diseases and cancer.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.