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

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Dutasteride is more efficient than finasteride, but individual results vary.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Gene differences may affect baldness treatment response in Korean men.

Testosterone and dihydrotestosterone treatments can help with penile growth in males with 5α-reductase type 2 deficiency, with dihydrotestosterone being more effective in infancy.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

South American camelids should be sheared early, fleece type affects fiber quality, and the S/P follicle ratio doesn't distinguish between Bolivian llama genotypes.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Male hormones and their interactions are crucial for male sexual development and characteristics.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

Melanocyte stem cells in hair follicles are key for hair color and could help treat greying and pigment disorders.

The KRTAP21-2 gene affects wool length and quality in sheep.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Chemotherapy and radiation therapy cause skin and hair damage by altering gene expression and signaling pathways.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

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

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Notch1 signaling is crucial for improving wound healing and skin regeneration by affecting stem cell behavior.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Researchers developed a way to study human body clocks using hair tissue, which works similarly in both healthy and dementia patients.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.