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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Overexpressing ovine β-catenin in mice skin increases hair follicle density and growth.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Mutations in the KRT85 gene cause hair and nail problems.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Placental growth factor may help treat hair loss.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A new mutation in the HR gene causes hair loss in a specific family.

Certain drugs change freshwater snail shells to a "banana" shape.

A gene mutation causes woolly hair in a Syrian patient.

Genetic variants affect minoxidil hair loss treatment success.

Certain gene variations might be linked to severe acne in women but not in men.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.