Member of the Association of American Physicians
His primary areas of study are Polycystic kidney disease, Endocrinology, Internal medicine, Autosomal dominant polycystic kidney disease and PKD1. His study in Polycystic kidney disease is interdisciplinary in nature, drawing from both Cilium, Cell biology and Pathogenesis. His Endocrinology research includes elements of Cyst, Cancer research and Bioinformatics.
His research investigates the link between Cyst and topics such as Kidney disease that cross with problems in Pathology. His Autosomal dominant polycystic kidney disease research is multidisciplinary, relying on both Metformin, Signal transduction and Protein kinase A. PKD1 is the subject of his research, which falls under Genetics.
His main research concerns Polycystic kidney disease, Autosomal dominant polycystic kidney disease, PKD1, Genetics and Internal medicine. His Polycystic kidney disease study combines topics in areas such as Cyst, Kidney cysts and Cilium. Stefan Somlo is interested in Polycystin 2, which is a branch of Autosomal dominant polycystic kidney disease.
His PKD1 research includes themes of Frameshift mutation, Allele, Cell growth and Cell biology. Stefan Somlo combines topics linked to Endocrinology with his work on Internal medicine. The study incorporates disciplines such as Triptolide and Calcium, Calcium signaling in addition to Endocrinology.
Stefan Somlo mainly focuses on Polycystic kidney disease, Autosomal dominant polycystic kidney disease, PKD1, Cilium and Internal medicine. He interconnects Cyst, Cancer research and Renal function in the investigation of issues within Polycystic kidney disease. His Autosomal dominant polycystic kidney disease study is concerned with Genetics in general.
His PKD1 research is multidisciplinary, incorporating elements of Kidney cysts, PI3K/AKT/mTOR pathway and Gene. His research in Cilium intersects with topics in Polycystin 2 and Pathogenesis. His Internal medicine research is multidisciplinary, relying on both Endocrinology, Gene knockdown and RNA interference.
Polycystic kidney disease, Autosomal dominant polycystic kidney disease, Cilium, PKD1 and Cell biology are his primary areas of study. His Polycystic kidney disease study integrates concerns from other disciplines, such as Cyst, Cancer research and Gerontology. Genetics covers Stefan Somlo research in Autosomal dominant polycystic kidney disease.
A large part of his PKD1 studies is devoted to Polycystin-1. His studies in Cell biology integrate themes in fields like Polycystin complex, Polycystin 2, Internal medicine and Endocrinology. His study in Polycystin 2 is interdisciplinary in nature, drawing from both Cystic kidney disease and Signal transduction.
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PKD2, a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein
Toshio Mochizuki;Guanqing Wu;Tomohito Hayashi;Stavroulla L. Xenophontos.
Science (1996)
Two Populations of Node Monocilia Initiate Left-Right Asymmetry in the Mouse
James McGrath;Stefan Somlo;Svetlana Makova;Xin Tian.
Cell (2003)
Polycystin-2 is an intracellular calcium release channel
Peter Koulen;Yiqiang Cai;Lin Geng;Yoshiko Maeda.
Nature Cell Biology (2002)
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)
PKD1 interacts with PKD2 through a probable coiled-coil domain
Qian F;Germino Fj;Cai Y;Zhang X.
Nature Genetics (1997)
Genetics and Pathogenesis of Polycystic Kidney Disease
Peter Igarashi;Stefan Somlo.
Journal of The American Society of Nephrology (2002)
Effective treatment of an orthologous model of autosomal dominant polycystic kidney disease.
Vicente E Torres;Xiaofang Wang;Qi Qian;Stefan Somlo.
Nature Medicine (2004)
PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats
Luiz F. Onuchic;Laszlo Furu;Yasuyuki Nagasawa;Xiaoying Hou.
American Journal of Human Genetics (2002)
Somatic Inactivation of Pkd2 Results in Polycystic Kidney Disease
Guanqing Wu;Vivette D'Agati;Yiqiang Cai;Glen Markowitz.
Cell (1998)
DCDC2 is associated with reading disability and modulates neuronal development in the brain
Haiying Meng;Shelley D. Smith;Karl Hager;Matthew Held.
Proceedings of the National Academy of Sciences of the United States of America (2005)
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