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Finasteride, at doses of 5mg or higher, may negatively affect male fertility by reducing the expression of certain genes involved in sperm production.

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

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Finasteride effectively treats BPH but requires continuous use to maintain benefits.

Finasteride reduces sperm count and quality and alters hormone levels in mice.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Two distinct pathways direct proteins to vacuoles in Arabidopsis, affecting root hair growth and protein targeting.

Skin-derived stem cells can become various cell types, including germ cell-like and oocyte-like cells.

Key genes linked to important traits in Chinese sheep and goats have been identified, but challenges remain in breeding improvements.

PCOS may be influenced by factors in the blood, not just the ovaries.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

SOCS1 and SOCS3 help control skin inflammation and are important for developing treatments for skin diseases.

Defects in certain proteins cause major heart abnormalities during early development.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

S100A3 protein is crucial for hair shaft formation in mice.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

S100A3 protein is mainly found in specific parts of human hair cells.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.