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Researchers found a way to create cells from stem cells that act like human cells important for hair growth and could be used for hair regeneration treatments.

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

Cysteine-rich keratins evolved independently in mammals, reptiles, and birds for hard skin structures like hair, claws, and feathers.

White hair grows thicker and faster than black hair due to higher activity of growth-related genes and proteins.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

New treatments targeting immune pathways show promise for severe hair loss but need more research for safety and effectiveness.

Regenerative therapies show promise for treating vitiligo and alopecia areata.

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

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Changthangi goats have specific genes that help produce Pashmina wool.

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

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Trichoscopy is useful for diagnosing and monitoring alopecia areata treatment.

Eating collagen peptides may help with skin and hair growth.

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

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

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

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Human hair protein modifications could potentially indicate heart disease risk.

The study developed a method to analyze ancient hair proteins using very small samples.

STAT3 signaling is important for healthy skin and hair follicles, and its disruption can lead to skin conditions like atopic dermatitis.

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Light therapy reduces scalp inflammation, boosts hair regrowth with Minoxidil 2%.

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

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

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

The analysis aims to identify the most effective and safest treatments for alopecia areata.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

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