Significant biomarkers for predicting 1-month changes in IGF-1 in growth hormone-deficient children following r-hGH therapy
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China Science Publishing & Media Ltd.
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https://engine.scichina.com/doi/pdf/EB74718C17DC4965BBEECBD5CCDFAAD5
Reference10 articles.
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2. Lu W, Shen S, Luo X, Gong C, Gu X, Li Y, Du M. Comparative evaluation of short-term biomarker response to treatment for growth hormone deficiency in Chinese children with growth hormone deficiency born small for or appropriate for gestational age: a randomized phase IV open-label study. Ther Adv Endocrinol, 2013, 4: 41-49.
3. Mullis PE, Deladoëy J, Dannies PS. Molecular and cellular basis of isolated dominant-negative growth hormone deficiency, IGHD type II: insights on the secretory pathway of peptide hormones. Horm Res Paediatr, 2002, 58: 53-66.
4. Stevens A, Murray P, Wojcik J, Raelson J, Koledova E, Chatelain P, Clayton P. Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study. Eur J Endocrinol, 2016, 175: 633-643.
5. Payankaulam S, Raicu AM, Arnosti DN. Transcriptional regulation of INSR, the insulin receptor gene. Genes, 2019, 10:
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