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

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

FGF5 gene mutations cause long hair in domestic cats.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

Glutathione helps Arabidopsis roots adapt to low phosphate by regulating a specific growth pathway.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

HDAC6 helps keep ovarian follicles dormant, extending female fertility.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Polycystic ovary syndrome, a disorder causing menstrual issues and infertility, can be treated with lifestyle changes, medication, herbal remedies, surgery, and assisted reproductive techniques like artificial insemination and IVF.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Normal skin cell renewal doesn't need RAR signaling, but vitamin A-related skin thickening does.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

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

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

CDP is crucial for lung and hair follicle cell development.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Androgen self-administration might be controlled by membrane receptors, not nuclear ones.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.