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Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

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

Genetic screening can help diagnose and manage infertility in Slovenian couples.

C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

A new DSG4 gene mutation causes hair defects in a young girl.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

OsPHR2 gene in rice enhances root growth and phosphorus accumulation.

Ezh2 controls skin development by balancing signals for dermal and epidermal growth.

Activating the Nrf2 pathway reduces inflammation and cell activation in human hair follicles, suggesting a potential treatment for certain hair loss conditions.

The three estrogen receptor genes are highly expressed in zebrafish neuromasts during development.

RORA may help regulate hair growth by affecting hair follicle stem cells.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

RORA boosts autophagy in hair follicle stem cells, potentially aiding hair growth.

Certain long non-coding RNAs are important for controlling hair growth cycles in sheep.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Krox20 is important for maintaining stem cells in the skin and affects hair growth and color.

Transglutaminase 2 may control sebocyte maturation and lipid metabolism.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Certain genes are linked to wool follicle structure and function, but not hair cycle regulation.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

H3K4me3 helps control RSPO3 to influence hair growth and development.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.