Transient neonatal diabetes: Widening the understanding of the etiopathogenesis of diabetes

Diabetes

Volumn 49, Issue 8, 2000, Pages 1359-1366

  Temple, I K ^a   Gardner, R J ^a   Mackay, D J G ^a   Barber, J C K ^a   Robinson, D O ^a   Shield, J P H ^a  

^a PRINCESS ANNE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 6; CHROMOSOME ABERRATION; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; CLINICAL ARTICLE; CONTROLLED STUDY; CPG ISLAND; DIABETES MELLITUS; DISEASE PREDISPOSITION; FEMALE; HUMAN; MALE; NEWBORN; NEWBORN DISEASE; NON INSULIN DEPENDENT DIABETES MELLITUS; PRIORITY JOURNAL;

EID: 0033860008     PISSN: 00121797     EISSN: None     Source Type: Journal    
DOI: 10.2337/diabetes.49.8.1359     Document Type: Article

References (37)

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2. Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence
3. Insulin promoter factor-1 gene mutation linked to early-onset type 2 diabetes mellitus directs expression of a dominant negative isoprotein
4. Aetiopathology and genetic basis of neonatal diabetes
5. Is transient neonatal diabetes a risk factor for diabetes in later life?
6. Neonatal diabetes
7. An imprinted gene(s) for diabetes?
8. Paternal uniparental disomy for chromosome 6 causes transient neonatal diabetes
9. Paternal uniparental isodisomy of chromosome 6 in transient neonatal diabetes mellitus
10. Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitus
11. Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitus
12. Refinement of the 6q chromosome region implicated in transient neonatal diabetes
13. Isodisomy of chromosome 6 in a newborn with methyl-malonic acidaemia and agenesis of pancreatic beta cells causing diabetes mellitus
14. Uniparental isodisomy 6 associated with deficiency of the fourth component of complement
15. Fortuitous detection of uniparental disomy of chromosome 6
16. Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23
17. Transient neonatal diabetes mellitus in a child with invdup (6)(q22-q23) of paternal origin
18. Partial duplication of the long arm of chromosome 6: A clinically recognisable syndrome
19. Uniparental maternal disomy 6 in a renal transplant patient
20. Partial trisomy of chromosome 6q: An interstitial duplication of the long arm
21. An imprinted locus associated with transient neonatal diabetes mellitus
22. The cell cycle control gene ZAC/PLAGL1 is imprinted: A strong candidate gene for transient neonatal diabetes
23. Fluorescence in situ hybridisation with human chromosome specific libraries: Detection of trisomy 21 and translocation of chromosome 4
24. A simple salting out procedure for extracting DNA from human nucleated cells
25. Isolation and chromosome assignment of 100 highly informative human simple sequence repeat polymorphisms
26. Determination of gene dosage at the PMP22 and androgen receptor loci by quantitative PCR
27. Duplication of 7p12.1-p13, including GRB10 and IGFBP1 in a mother and daughter with features of Silver Russell syndrome
28. Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis
29. Metabolic and growth patterns in transient neonatal diabetes
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31. Aetiology of transient neonatal diabetes
32. Two interesting cases of transient neonatal diabetes mellitus
33. Transient neonatal diabetes mellitus in a pair of twins
34. Prevalence and incidence of NIDDM in Europe
35. Long-term course of neonatal diabetes
36. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
37. Mutations in the glucokinase gene of the fetus result in reduced birth weight