Patrick G. Starremans

Author

Brigham and Women's Hospital

Also Known As

P. Starremans, P.G. Starremans, Patrick G. Starremans, Patrick G.J.F. Starremans, Patrick Starremans

Publications

703

Citations

H-Index

Concepts

All Affiliations

Brigham and Women's Hospital Harvard University Radboud University Medical Center Radboud University Nijmegen

About

Patrick G. Starremans is an author at Brigham and Women's Hospital specializing in medicine, urology, and chronic kidney disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	588
2	Natural Sciences	2	2	226
3	Engineering	1	1	14
4	Biochemistry	1	1	14
5	Biomolecular Engineering	1	1	14

Patrick G. Starremans

Publications

683

Citations

H-Index

Page 1

	Year	Citations
Polycystin-1 and polycystin-2 regulate the cell cycle through the helix–loop–helix inhibitor Id2 Xiaogang Li, Ying Luo, Patrick G. Starremans, Nature Cell Biology Transcriptional RegulationCell RegulationCell DivisionHelix–loop–helix Inhibitor Id2Cell Signaling	2005	212
Fibrocystin/Polyductin, Found in the Same Protein Complex with Polycystin-2, Regulates Calcium Responses in Kidney Epithelia Shixuan Wang, Jingjing Zhang, Surya M. Nauli, Molecular and Cellular Biology Regulates Calcium ResponsesRenal PathologyRenal InflammationPathologyFlow Sensation	2007	186
A mouse model for polycystic kidney disease through a somatic in-frame deletion in the 5′ end of Pkd1 Patrick G. Starremans, X. Li, P.E. Finnerty, Kidney International Renal PathologyRenal InflammationPathologyNephrologyCellular Physiology	2008	86
Mutations in the Human Na-K-2Cl Cotransporter (NKCC2) Identified in Bartter Syndrome Type I Consistently Result in Nonfunctional Transporters Patrick G. Starremans, Ferry F.J. Kersten, Nine V.A.M. Knoers, Journal of the American Society of Nephrology Electrolyte DisorderXenopus Laevis OocytesGeneticsPathologyBartter Syndrome	2003	76
Dimeric Architecture of the Human Bumetanide-Sensitive Na-K-Cl Co-transporter Patrick G. Starremans, Ferry F.J. Kersten, Lambertus P. van den Heuvel, Journal of the American Society of Nephrology	2003	52
Co‐inheritance of a PKD1 mutation and homozygous PKD2 variant: a potential modifier in autosomal dominant polycystic kidney disease George Dedoussis, Yang Luo, Patrick G. Starremans, European Journal of Clinical Investigation	2008	29
Functional implications of mutations in the human renal outer medullary potassium channel (ROMK2) identified in Bartter syndrome Patrick G. Starremans, Annemiete W. van der Kemp, Nine V.A.M. Knoers, Pflügers Archiv - European Journal of Physiology ChannelopathiesUrologyHyperpolarization (Biology)MedicinePhysiology	2002	28
Well-Defined Aminooxy Terminated <i>N</i>-(2-Hydroxypropyl) Methacrylamide Macromers for Site Specific Bioconjugation of Glycoproteins Pradeep K. Dhal, Steven C. Polomoscanik, Diego A. Gianolio, Bioconjugate Chemistry EngineeringSite Specific BioconjugationGlycobiologyMolecular BiologyOrganic Chemistry	2013	14

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