Renal cysts and diabetes syndrome

Known as: Glomerulocystic kidney, familial hypoplastic, MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 5, CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT WITH DIABETES 
A condition associated with mutation(s) in the HNF1B gene or TCF2, characterized by renal cysts and early onset non-insulin dependent diabetes.(NICHD… Expand
National Institutes of Health

Papers overview

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2011
2011
BACKGROUND Hyperuricemia is an independent risk factor for renal progression in IgA nephropathy (IgAN). However, no study has… Expand
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2011
2011
Maturity-onset diabetes of the young (MODY) is a clinically heterogeneous group of monogenic disorders characterized by autosomal… Expand
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2010
2010
C53/LZAP (also named as Cdk5rap3) is a putative tumor suppressor that plays important roles in multiple cell signaling pathways… Expand
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2008
2008
CONTEXT There are interplays between the endocrine and exocrine pancreas. We recently reported an increased frequency of exocrine… Expand
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Highly Cited
2006
Highly Cited
2006
Renal hypodysplasia (RHD) is characterized by a reduced nephron number, small kidney size, and disorganized renal tissue. A… Expand
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2004
2004
AbstractAims/hypothesisMutations in the hepatocyte nuclear factor-1 beta (HNF-1β) gene result in disorders of renal development… Expand
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Highly Cited
2004
Highly Cited
2004
Mutations in cystic kidney disease genes represent a major genetic cause of end-stage renal disease. However, the molecular… Expand
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Highly Cited
2002
Highly Cited
2002
Hyperuricemia is associated with renal disease, but it is usually considered a marker of renal dysfunction rather than a risk… Expand
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Highly Cited
2001
Highly Cited
2001
Mutations in the homeobox gene vHnf1 are associated with human diseases MODY5 (maturity-onset diabetes of the young, type V) and… Expand
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2001
2001
Maturity onset diabetes of the young (MODY) is a heterogenous, monogenic disease that is characterized by an autosomal dominant… Expand
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