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Pathogenesis and treatment of microalbuminuria in patients with diabetes: the road ahead.
Genome-wide identification of microRNA expression quantitative trait loci.
Prevention, Diagnosis, and Treatment of Postthrombotic Syndrome.
Protein Kinase C-theta
Observational Studies as Topic
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Glucokinase mutations, insulin secretion, and diabetes mellitus.
Academic Article
Why?
Insulin gene mutations as a cause of permanent neonatal diabetes.
Academic Article
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Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.
Academic Article
Why?
Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene.
Academic Article
Why?
In celebration of a century with insulin - Update of insulin gene mutations in diabetes.
Academic Article
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Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.
Academic Article
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Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
Academic Article
Why?
Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.
Academic Article
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Successful transition from insulin to sulfonylurea therapy in a patient with monogenic neonatal diabetes owing to a KCNJ11 F333L [corrected] mutation.
Academic Article
Why?
Insulin promoter factor-1 mutations and diabetes in Trinidad: identification of a novel diabetes-associated mutation (E224K) in an Indo-Trinidadian family.
Academic Article
Why?
Use of in vitro DNA amplification to screen family members for an insulin gene mutation.
Academic Article
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Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12.
Academic Article
Why?
Type 2 (non-insulin-dependent) diabetes mellitus associated with a mutation of the glucokinase gene in a Japanese family.
Academic Article
Why?
Characterization of Japanese families with early-onset type 2 (non-insulin dependent) diabetes mellitus and screening for mutations in the glucokinase and mitochondrial tRNA(Leu(UUR)) genes.
Academic Article
Why?
Mutations in the glucokinase gene are not a major cause of late-onset type 2 (non-insulin-dependent) diabetes mellitus in Japanese subjects.
Academic Article
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