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The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

Scientists found cells in hair that are key for growth and color.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

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

CDP is crucial for lung and hair follicle cell development.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

β-catenin is essential for stem cell activation and proliferation in hair follicles.

Applying a DNA vaccine to skin with active hair growth boosts immune response and protection against anthrax in mice.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The document explains how to identify different hair problems using a microscope.

Manipulating the catagen and telogen phases of hair growth could lead to treatments for hair disorders.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Shift work disrupts the body's natural clock, leading to health problems.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.