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Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

Acitretin is effective for severe skin conditions but has significant side effects and requires careful monitoring.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Enzymes involved in Vitamin A metabolism affect hair growth and type in mice.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

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.

Genetic factors and diet significantly increase the risk of male pattern baldness.

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

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

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.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

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.