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Raghu Kalluri

Researcher at University of Texas MD Anderson Cancer Center

Publications -  325
Citations -  89851

Raghu Kalluri is an academic researcher from University of Texas MD Anderson Cancer Center. The author has contributed to research in topics: Cancer & Angiogenesis. The author has an hindex of 115, co-authored 306 publications receiving 71127 citations. Previous affiliations of Raghu Kalluri include Beth Israel Deaconess Medical Center & Baylor College of Medicine.

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Stage-Specific Action of Matrix Metalloproteinases Influences Progressive Hereditary Kidney Disease

TL;DR: It is suggested that preserving GBM/extracellular matrix integrity before the onset of proteinuria leads to significant disease protection, but if this window of opportunity is lost, MMP-inhibition at the later stages of Alport disease leads to accelerated glomerular and interstitial fibrosis.
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Discovery of Double-Stranded Genomic DNA in Circulating Exosomes

TL;DR: The discovery of exosomal DNA, studies related to the origin of genomic DNA in exosomes, and its utility in cancer diagnosis and disease monitoring are focused on.
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Matrix metalloproteinase-9 deficiency phenocopies features of preeclampsia and intrauterine growth restriction

TL;DR: It is shown that matrix metalloproteinase-9 (MMP9) deficiency causes physiological and placental abnormalities in mice, which mimic features of PE, and that fetal and maternal MMP9 play a role in the development of PE.
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Blocking Angiotensin II Synthesis/Activity Preserves Glomerular Nephrin in Rats with Severe Nephrosis

TL;DR: In this paper, the authors used an accelerated model of experimental nephrosis to assess nephrin gene and protein expression in the kidney and the possible modulating effect of drugs that block angiotensin II (AII) synthesis/activity.
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Glomerular expression of nephrin and synaptopodin, but not podocin, is decreased in kidney sections from women with preeclampsia

TL;DR: It is concluded that down-regulation of nephrin and synaptopodin is associated with proteinuria in women with preeclampsia, further supporting a possible role of sFlt-1 in the dysregulation of podocyte foot-process proteins.