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Glomerulocystic kidney disease

Known as: Glomerulocystic Disease 
A condition characterized by dilatation of the Bowman space and affecting more than 5% of the glomeruli.(NICHD)
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2009
Review
2009
  • M. Gunay‐Aygun
  • American journal of medical genetics. Part C…
  • 2009
  • Corpus ID: 2529774
Hepatorenal fibrocystic diseases (HRFCDs) are among the most common inherited human disorders. The discovery that proteins… Expand
Highly Cited
2007
Highly Cited
2007
Wwtr1 is a widely expressed 14-3-3-binding protein that regulates the activity of several transcription factors involved in… Expand
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Highly Cited
2006
Highly Cited
2006
Background: Hepatocyte nuclear factor-1 beta (HNF-1β) is a widely distributed transcription factor which plays a critical role in… Expand
Highly Cited
2005
Highly Cited
2005
BACKGROUND Autosomal dominant medullary cystic kidney disease type 2 (MCKD2), familial juvenile hyperuricemic nephropathy (FJHN… Expand
Review
2004
Review
2004
Glomerulocystic kidneys can be categorized into three major groups: (1) glomerulocystic kidney disease, comprising nonsyndromal… Expand
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Highly Cited
2003
Highly Cited
2003
The disease complex medullary cystic disease/familial juvenile hyperuricemic nephropathy (MCKD/FJHN) is characterized by… Expand
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Highly Cited
2001
Highly Cited
2001
Familial glomerulocystic kidney disease (GCKD) is a dominantly inherited condition characterized by glomerular cysts and variable… Expand
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
1989
1989
Autosomal dominant (or possibly X-linked) inheritance of familial hypoplastic glomerulocystic kidneys is described in a mother… Expand
Review
1987
Review
1987
To determine the frequency of autosomal recessive and autosomal dominant polycystic kidney disease (PKD) in infants and to… Expand