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The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Two genetic variations in Moa buffalo help them adapt to heat.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

Transgenic sheep embryos with a specific promoter were successfully created, but more research is needed for gene expression in hair follicles.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

Altering SSAT affects fat metabolism and body fat in mice.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

SQSTM1 is linked to increased risk of alopecia areata.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Pangenome analysis reveals key genes for pig adaptation and traits, aiding genetic improvement.

Different PADI isoforms help cells develop diverse functions.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

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

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.

New LSS gene variants help understand congenital hypotrichosis 14 better.