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ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

New genetic mutations linked to rare skin disorders were found in three newborns.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

Certain transporters are found in human hair follicles and may affect hair growth and loss.

Cholesterol transport in hair follicles decreases from growth to regression phase.

Jieduquyuziyin prescription helps treat SLE with atherosclerosis by improving cholesterol removal and reducing inflammation.

Researchers found 15 new genetic links to skin traits in Japanese women.

ABCG2 protein marks stem-like skin cells in human epidermis.

Hair follicles play a crucial role in regulating skin barrier function.

Androgens increase cervical cancer risk and affect its development.

Men with Addison disease should be screened for X-linked adrenoleukodystrophy if they have hair loss.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Chemotherapy patients don't all lose their hair due to factors like hair growth rates, age, genetics, and the type of drugs used.

Docetaxel often causes hair loss, with limited effective treatments and no cure for permanent hair loss.

Hair follicles are crucial for maintaining skin barrier function.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

Hair follicle development involves specific cells and genes, crucial for understanding severe skin diseases like harlequin ichthyosis.

Toll-like receptor 3 helps repair the skin barrier after UV damage.

Bone growth is controlled by both internal and external signals, involving stem cells and tissue interactions.

A new gene mutation linked to a skin condition was found in a Spanish family.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Vitamin D may help regulate cholesterol and influence prostate cancer development.

The May issue discussed publishing agreements and four studies on cholesterol in hair, cancer cell changes, hormones in the uterus, and skin protein effects.