Permanent diabetes during the first year of life: multiple gene screening in 54 patients
出版年份 2011 全文链接
标题
Permanent diabetes during the first year of life: multiple gene screening in 54 patients
作者
关键词
-
出版物
DIABETOLOGIA
Volume 54, Issue 7, Pages 1693-1701
出版商
Springer Nature
发表日期
2011-03-10
DOI
10.1007/s00125-011-2094-8
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Further evidence that mutations in INScan be a rare cause of Maturity-Onset Diabetes of the Young (MODY)
- (2010) Trine W Boesgaard et al. BMC Medical Genetics
- Rfx6 directs islet formation and insulin production in mice and humans
- (2010) Stuart B. Smith et al. NATURE
- Defective Secretion of Islet Hormones in Chromogranin-B Deficient Mice
- (2010) Stefanie Obermüller et al. PLoS One
- Molecular Diagnosis of Neonatal Diabetes Mellitus Using Next-Generation Sequencing of the Whole Exome
- (2010) Amélie Bonnefond et al. PLoS One
- Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis
- (2010) I. Garin et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- SlC30A8 Is a Major Target of Humoral Autoimmunity in Type 1 Diabetes and a Predictive Marker in Prediabetes
- (2009) Janet M. Wenzlau et al. Annals of the New York Academy of Sciences
- Detailed transcriptome atlas of the pancreatic beta cell
- (2009) Burak Kutlu et al. BMC Medical Genomics
- A Novel Hypomorphic PDX1 Mutation Responsible for Permanent Neonatal Diabetes With Subclinical Exocrine Deficiency
- (2009) M. Nicolino et al. DIABETES
- Mutations inIAPPandNEUROG3genes are not a common cause of permanent neonatal/infancy/childhood-onset diabetes
- (2009) V. Nocerino et al. DIABETIC MEDICINE
- Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births
- (2009) A. S. Slingerland et al. DIABETOLOGIA
- High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?
- (2009) Laura Bernardini et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Analysis of Two KCNJ11 Neonatal Diabetes Mutations, V59G and V59A, and the Analogous KCNJ8 I60G Substitution
- (2009) Marcus Winkler et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
- (2009) Murim Choi et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 Diabetes
- (2008) A. Molven et al. DIABETES
- Insulin Gene Mutations as Cause of Diabetes in Children Negative for Five Type 1 Diabetes Autoantibodies
- (2008) R. Bonfanti et al. DIABETES CARE
- Neonatal Diabetes Mellitus
- (2008) Lydia Aguilar-Bryan et al. ENDOCRINE REVIEWS
- Update of mutations in the genes encoding the pancreatic beta-cell KATPchannel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism
- (2008) Sarah E. Flanagan et al. HUMAN MUTATION
- Diagnosis and treatment of neonatal diabetes: an United States experience†
- (2008) Julie Støy et al. PEDIATRIC DIABETES
- Clinical implications of a molecular genetic classification of monogenic β-cell diabetes
- (2008) Rinki Murphy et al. Nature clinical practice. Endocrinology & metabolism
- The G53D Mutation in Kir6.2 (KCNJ11) Is Associated with Neonatal Diabetes and Motor Dysfunction in Adulthood that Is Improved with Sulfonylurea Therapy
- (2007) Joseph C. Koster et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
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