Congenital absence of kidney

Known as: Missing kidney, Renal Agenesis, agenesis renal 
A congenital abnormality characterized by the absence of one or both kidneys.
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
Glial cell line–derived neurotrophic factor signaling through the Ret receptor tyrosine kinase is crucial for ureteric bud… (More)
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Highly Cited
2007
Highly Cited
2007
Pax genes are important regulators of kidney development. In the mouse, homozygous Pax2 inactivation results in renal agenesis, a… (More)
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Review
2005
Review
2005
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome affects at least 1 out of 4500 women and has for a long time been considered… (More)
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Highly Cited
2005
Highly Cited
2005
The study was performed to evaluate the prevalence of prenatal ultrasound diagnoses for renal anomalies in 20 registries of 12… (More)
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Highly Cited
2001
Highly Cited
2001
OBJECTIVE The association of idiopathic hypogonadotrophic hypogonadism (IHH) with congenital olfactory deficit defines Kallmann's… (More)
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Highly Cited
1998
Highly Cited
1998
Heparan sulfate proteoglycans have been implicated in the presentation of a number of secreted signaling molecules to their… (More)
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Highly Cited
1996
Highly Cited
1996
GLIAL-CELL-LINE-DERIVED neurotrophic factor (GDNF)1 is a potent survival factor for dopaminergic neurons and motor neurons in… (More)
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Highly Cited
1996
Highly Cited
1996
The c-ret gene encodes a receptor tyrosine kinase that is expressed in the Wolffian duct and ureteric bud of the developing… (More)
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Highly Cited
1994
Highly Cited
1994
RECEPTOR tyrosine kinases (RTKs) are cell-surface molecules that transduce signals for cell growth and differentiation1. The RTK… (More)
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Highly Cited
1983
Highly Cited
1983
Using the population-based data from the Metropolitan Atlanta Congenital Defects Program, the interrelation of the six defects… (More)
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