Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees (Q46963852)

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scientific article published on 25 February 2006

Language	Label	Description	Also known as
English	Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees	scientific article published on 25 February 2006

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scholarly article

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees (English)

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

phenotypic heterogeneity

1 reference

based on heuristic

inferred from title

2

object named as

G I Bell

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

author name string

S S Fajans

1

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

publication date

25 February 2006

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

49

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

5

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

1106-1108

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

https://scigraph.springernature.com/pub.10.1007/s00125-006-0158-y

0 references

Are glucokinase mutations associated with low triglycerides?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16502298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic abnormality in the beta cell determines the response to an oral glucose load

1 reference

https://pubmed.ncbi.nlm.nih.gov/16502298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucokinase (GCK) mutations in hyper- and hypoglycemia: Maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16502298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Scope and heterogeneous nature of MODY.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16502298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the HNF-4alpha gene affects insulin secretion and triglyceride metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16502298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4α mutations in a large European collection

1 reference

https://pubmed.ncbi.nlm.nih.gov/16502298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16502298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16502298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16502298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype/phenotype relationships in HNF-4alpha/MODY1: haploinsufficiency is associated with reduced apolipoprotein (AII), apolipoprotein (CIII), lipoprotein(a), and triglyceride levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/16502298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00125-006-0158-Y

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/16502298

ResearchGate publication ID

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