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The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Minoxidil foam helps hair growth by increasing good proteins and decreasing bad pathways in men with hair loss.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Overexpressing SIMK in alfalfa boosts root hair growth, nodule clustering, and shoot biomass.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Ptprq has multiple forms that change during inner ear development.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

The main enzyme found in pubic skin that could be targeted to treat excessive hair growth is 5 alpha-R2.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Possible link between androgens and COVID-19 severity; more research needed.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Certain gene variations are linked to better memory in healthy Chinese women.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Keratin 33A is a key protein in goat winter coats, especially in high-producing breeds.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

CD61 is important for mouse tooth cell growth and works through Lgr5.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Testosterone is crucial for development, growth, and various body functions in mammals.

COVID-19 may worsen with androgens; anti-androgen drugs could help.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

The Itpr3 gene causes a specific hair pattern in mice.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.