Member of the Association of American Physicians
Peter Igarashi mainly investigates Kidney, Cell biology, Internal medicine, Endocrinology and Polycystic kidney disease. His Kidney research incorporates elements of Reperfusion injury, Molecular biology, Acute kidney injury and Pathology. The study incorporates disciplines such as Genetics, Gene, Tubule and Kidney morphogenesis in addition to Cell biology.
His Internal medicine research integrates issues from Sodium–hydrogen antiporter, Brush border and Transcellular. His Endocrinology study combines topics from a wide range of disciplines, such as Fibrosis, Intracellular pH and Phosphorylation. His Polycystic kidney disease study integrates concerns from other disciplines, such as Cyst, Kidney disease, Pathogenesis, Cilium and Regulation of gene expression.
Kidney, Molecular biology, Cell biology, Internal medicine and Endocrinology are his primary areas of study. His Kidney research is multidisciplinary, incorporating elements of Cancer research, Transgene, Pathology, Intracellular pH and Acute kidney injury. His biological study spans a wide range of topics, including Epithelium, Gene expression, Hepatocyte nuclear factors, Biochemistry and Complementary DNA.
His studies deal with areas such as Regulation of gene expression, Transcription factor and Alternative splicing as well as Gene expression. His Cell biology research incorporates themes from Cleavage, Gene, Cellular differentiation and Kidney development. The concepts of his Polycystic kidney disease study are interwoven with issues in Cyst, Kidney cysts, Cilium and Pathogenesis.
His primary scientific interests are in Internal medicine, Cell biology, Endocrinology, Hepatocyte nuclear factors and Cystic kidney. His is involved in several facets of Internal medicine study, as is seen by his studies on Kidney, Polycystic kidney disease, Kidney disease and Nephrology. The Kidney study combines topics in areas such as Creatinine, Organogenesis and Mutant.
His work deals with themes such as Cyst, Kidney cysts, Autosomal dominant polycystic kidney disease and Cilium, which intersect with Polycystic kidney disease. His Cell biology research focuses on subjects like Gene, which are linked to Embryo and Stem cell. His studies in Molecular biology integrate themes in fields like Regulation of gene expression and Genetically modified mouse.
The scientist’s investigation covers issues in Internal medicine, Endocrinology, Autosomal dominant polycystic kidney disease, Polycystic kidney disease and Cystic kidney. His Internal medicine research focuses on Kidney, Cystic kidney disease and Fibrosis. His Kidney study combines topics in areas such as Nephrology and Mutant, Gene.
His Endocrinology research focuses on Cancer research and how it connects with Nephronophthisis. The PKD1 study which covers Mutation that intersects with Cell biology. Peter Igarashi combines subjects such as Cilium and microRNA with his study of Cyst.
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Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease
Fangming Lin;Thomas Hiesberger;Kimberly Cordes;Angus M. Sinclair.
Proceedings of the National Academy of Sciences of the United States of America (2003)
Genetics and Pathogenesis of Polycystic Kidney Disease
Peter Igarashi;Stefan Somlo.
Journal of The American Society of Nephrology (2002)
Intrarenal cells, not bone marrow–derived cells, are the major source for regeneration in postischemic kidney
Fangming Lin;Ashley Moran;Peter Igarashi.
Journal of Clinical Investigation (2005)
HOXA10 is expressed in response to sex steroids at the time of implantation in the human endometrium.
H S Taylor;A Arici;D Olive;P Igarashi.
Journal of Clinical Investigation (1998)
Hematopoietic Stem Cells Contribute to the Regeneration of Renal Tubules after Renal Ischemia-Reperfusion Injury in Mice
Fangming Lin;Kimberly Cordes;Linheng Li;Leroy Hood.
Journal of The American Society of Nephrology (2003)
A conserved Hox axis in the mouse and human female reproductive system: late establishment and persistent adult expression of the Hoxa cluster genes.
Hugh S. Taylor;Gregory B. Vanden Heuvel;Peter Igarashi.
Biology of Reproduction (1997)
NHE3: a Na+/H+ exchanger isoform of renal brush border
Daniel Biemesderfer;John Pizzonia;Ali Abu-Alfa;Markus Exner.
American Journal of Physiology-renal Physiology (1993)
Wnt9b signaling regulates planar cell polarity and kidney tubule morphogenesis
Courtney M. Karner;Rani Chirumamilla;Shigehisa Aoki;Shigehisa Aoki;Peter Igarashi.
Nature Genetics (2009)
Epithelial-specific Cre/lox recombination in the developing kidney and genitourinary tract
Xinli Shao;Stefan Somlo;Peter Igarashi.
Journal of The American Society of Nephrology (2002)
Primary cilia regulate mTORC1 activity and cell size through Lkb1
Christopher Boehlke;Fruzsina Kotsis;Vishal Patel;Simone Braeg.
Nature Cell Biology (2010)
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