Search Results - "Ni, Shining"
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Polyethylene glycol recombinant human growth hormone in Chinese prepubertal slow-growing short children: doses reported in a multicenter real-world study
Published in BMC endocrine disorders (09-08-2022)“…Abstract Background To evaluate the effectiveness of individualized-dose polyethylene glycol recombinant human growth hormone (PEG-rhGH) for short stature…”
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BiOI/BiVO4 Two-Dimensional Heteronanostructures for Visible-Light Photocatalytic Degradation of Rhodamine B
Published in ACS applied nano materials (28-09-2018)“…By virtue of the facile anion-exchange technique, smart BiOI/BiVO4 two-dimensional (2D) heteronanostructure (HNS) photocatalysts targeted for the degradation…”
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Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study
Published in Diabetes care (01-08-2019)“…Type 1 diabetes (T1D) is a highly heritable disease with much lower incidence but more adult-onset cases in the Chinese population. Although genome-wide…”
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Sn4+-doped TiO2 nanorod array film with enhanced visible light photocatalytic activity
Published in Bulletin of materials science (01-08-2018)“…Sn 4 + -doped TiO 2 nanorod array film (NAF) on the fluorine-doped tin oxide (FTO) conducting glass was successfully synthesized using the facile hydrothermal…”
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hbox {Sn}^{4+}$$ Sn 4 + -doped $$\hbox {TiO}_{2}$$ TiO 2 nanorod array film with enhanced visible light photocatalytic activity
Published in Bulletin of materials science (01-08-2018)Get full text
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Long-term Pegylated GH for Children With GH Deficiency: A Large, Prospective, Real-world Study
Published in The journal of clinical endocrinology and metabolism (01-08-2023)“…Abstract Context The evidence of long-term polyethylene glycol recombinant human GH (PEG-rhGH) in pediatric GH deficiency (GHD) is limited. Objective This…”
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BiOI/BiVO 4 Two-Dimensional Heteronanostructures for Visible-Light Photocatalytic Degradation of Rhodamine B
Published in ACS applied nano materials (28-09-2018)Get full text
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Clinical characteristics and mutation analysis of two Chinese children with 17a-hydroxylase/17,20-lyase deficiency
Published in International journal of clinical and experimental medicine (01-01-2015)“…Combined with the literature, recognize the clinical features and molecular genetic mechanism of the disease. 17a-hydroxylase/17,20-lyase deficiency, a rare…”
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Effect of the pregnant mice with Graves’ disease on thyroid function in the offspring
Published in International journal of pediatric endocrinology (03-10-2013)Get full text
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