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Molecular Endocrinology (Baltimore, Md.)|November 29, 2013
GATA factors promote ER integrity and β-cell survival and contribute to type 1 diabetes riskDaniel J Sartori, Christopher J Wilbur, Simon Y Long, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|February 18, 2025
The genetic landscape of pediatric postural orthostatic tachycardia syndromeHuiqi Qu, Jingchun Qu, Xiao Chang, et al.
Neurology. Clinical Practice|May 1, 2024
Expanding the Spectrum of Congenital Myopathy Linked to Variants in the MYBPC1 Gene: A Clinical ReportPierre-Louis Lanvin, Dong Li, Solène Conrad, et al.
Clinical Epigenetics|October 11, 2025
DNA methylation and machine learning: challenges and perspective toward enhanced clinical diagnosticsErfan Aref-Eshghi, Arash B Abadi, Mohammad-Erfan Farhadieh, et al.
American Journal of Obstetrics & Gynecology MFM|December 21, 2020
Detection of maternal X chromosome abnormalities using single nucleotide polymorphism-based noninvasive prenatal testingKimberly A Martin, Carole A Samango-Sprouse, Valerie Kantor, et al.
Scientific Reports|August 7, 2021
Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patientsJingchun Qu, Hui-Qi Qu, Jonathan P Bradfield, et al.
Communications Biology|July 24, 2021
Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported lociHui-Qi Qu, Jingchun Qu, Jonathan Bradfield, et al.
Science Signaling|January 18, 2018
Learning-dependent chromatin remodeling highlights noncoding regulatory regions linked to autismJohn N Koberstein, Shane G Poplawski, Mathieu E Wimmer, et al.
Journal of Paediatrics and Child Health|August 9, 2020
High prevalence of elevated serum liver enzymes in Chinese children suggests metabolic syndrome as a common risk factorJinling Wang, Hui-Qi Qu, Ke Huang, et al.
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