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Limited expression of cytochrome p450 17α-hydroxylase/17,20-lyase in prostate cancer cell lines.

Korean journal of urology

Jeong CW, Yoon CY, Jeong SJ, Hong SK, Byun SS, Lee SE.
PMID: 21860772
Korean J Urol. 2011 Jul;52(7):494-7. doi: 10.4111/kju.2011.52.7.494. Epub 2011 Jul 24.

PURPOSE: Cytochrome P450 17α-hydroxylase/17,20-lyase (CYP17A1) is a key enzyme in the androgen biosynthesis pathway. CYP17A1 has been focused on because of the promising results of a potent CYP17A1 inhibitor in the treatment of castration-resistant prostate cancer (CRPC). A hypothesis...

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Jeong CW, Yoon CY, Jeong SJ, et al. Limited expression of cytochrome p450 17α-hydroxylase/17,20-lyase in prostate cancer cell lines. Korean J Urol. 2011;52(7):494-7doi: 10.4111/kju.2011.52.7.494.
Jeong, C. W., Yoon, C. Y., Jeong, S. J., Hong, S. K., Byun, S. S., & Lee, S. E. (2011). Limited expression of cytochrome p450 17α-hydroxylase/17,20-lyase in prostate cancer cell lines. Korean journal of urology, 52(7), 494-7. https://doi.org/10.4111/kju.2011.52.7.494
Jeong, Chang Wook, et al. "Limited expression of cytochrome p450 17α-hydroxylase/17,20-lyase in prostate cancer cell lines." Korean journal of urology vol. 52,7 (2011): 494-7. doi: https://doi.org/10.4111/kju.2011.52.7.494
Jeong CW, Yoon CY, Jeong SJ, Hong SK, Byun SS, Lee SE. Limited expression of cytochrome p450 17α-hydroxylase/17,20-lyase in prostate cancer cell lines. Korean J Urol. 2011 Jul;52(7):494-7. doi: 10.4111/kju.2011.52.7.494. Epub 2011 Jul 24. PMID: 21860772; PMCID: PMC3151639.
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Seventeen Alpha-Hydroxylase Deficiency Associated with Absent Gonads and Myelolipoma: A Case Report and Review of Literature.

Iranian journal of medical sciences

Soveid M, Rais-Jalali GA.
PMID: 27853336
Iran J Med Sci. 2016 Nov;41(6):543-547.

Congenital adrenal hyperplasia comprises a group of disorders resulting from defects in enzymes required for the synthesis of cortisol. The clinical presentation depends on the specific enzyme defect. We report a rare case of congenital adrenal hyperplasia due to...

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Soveid M, Rais-Jalali GA. Seventeen Alpha-Hydroxylase Deficiency Associated with Absent Gonads and Myelolipoma: A Case Report and Review of Literature. Iran J Med Sci. 2016;41(6):543-547
Soveid, M., & Rais-Jalali, G. A. (2016). Seventeen Alpha-Hydroxylase Deficiency Associated with Absent Gonads and Myelolipoma: A Case Report and Review of Literature. Iranian journal of medical sciences, 41(6), 543-547.
Soveid, Mahmood, and Rais-Jalali, Ghanbar Ali. "Seventeen Alpha-Hydroxylase Deficiency Associated with Absent Gonads and Myelolipoma: A Case Report and Review of Literature." Iranian journal of medical sciences vol. 41,6 (2016): 543-547.
Soveid M, Rais-Jalali GA. Seventeen Alpha-Hydroxylase Deficiency Associated with Absent Gonads and Myelolipoma: A Case Report and Review of Literature. Iran J Med Sci. 2016 Nov;41(6):543-547. PMID: 27853336; PMCID: PMC5106571.
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Functional Identification of Compound Heterozygous Mutations in the .

Endocrinology and metabolism (Seoul, Korea)

Mo EY, Lee JY, Kim SY, Kim MJ, Kim ES, Lee S, Han JH, Moon SD.
PMID: 30229581
Endocrinol Metab (Seoul). 2018 Sep;33(3):413-422. doi: 10.3803/EnM.2018.33.3.413.

BACKGROUND: We previously reported a patient with congenital adrenal hyperplasia (CAH) with compound heterozygous mutations in the cytochrome P450 17A1 (METHODS: To understand how p.His373Leu and p.Glu383fsX36 affect P450c17 enzymatic activity, wild type and mutant RESULTS: Production of the...

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Mo EY, Lee JY, Kim SY, et al. Functional Identification of Compound Heterozygous Mutations in the . Endocrinol Metab (Seoul). 2018;33(3):413-422doi: 10.3803/EnM.2018.33.3.413.
Mo, E. Y., Lee, J. Y., Kim, S. Y., Kim, M. J., Kim, E. S., Lee, S., Han, J. H., & Moon, S. D. (2018). Functional Identification of Compound Heterozygous Mutations in the . Endocrinology and metabolism (Seoul, Korea), 33(3), 413-422. https://doi.org/10.3803/EnM.2018.33.3.413
Mo, Eun Yeong, et al. "Functional Identification of Compound Heterozygous Mutations in the ." Endocrinology and metabolism (Seoul, Korea) vol. 33,3 (2018): 413-422. doi: https://doi.org/10.3803/EnM.2018.33.3.413
Mo EY, Lee JY, Kim SY, Kim MJ, Kim ES, Lee S, Han JH, Moon SD. Functional Identification of Compound Heterozygous Mutations in the . Endocrinol Metab (Seoul). 2018 Sep;33(3):413-422. doi: 10.3803/EnM.2018.33.3.413. PMID: 30229581; PMCID: PMC6145962.
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