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Christian Pawlu - Publications

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3/8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2006 Kittel RJ, Wichmann C, Rasse TM, Fouquet W, Schmidt M, Schmid A, Wagh DA, Pawlu C, Kellner RR, Willig KI, Hell SW, Buchner E, Heckmann M, Sigrist SJ. Bruchpilot promotes active zone assembly, Ca2+ channel clustering, and vesicle release. Science (New York, N.Y.). 312: 1051-4. PMID 16614170 DOI: 10.1126/Science.1126308  0.633
2004 Pawlu C, DiAntonio A, Heckmann M. Postfusional control of quantal current shape. Neuron. 42: 607-18. PMID 15157422 DOI: 10.1016/S0896-6273(04)00269-7  0.64
2003 Hallermann S, Pawlu C, Jonas P, Heckmann M. A large pool of releasable vesicles in a cortical glutamatergic synapse. Proceedings of the National Academy of Sciences of the United States of America. 100: 8975-80. PMID 12815098 DOI: 10.1073/Pnas.1432836100  0.475
Low-probability matches (unlikely to be authored by this person)
2004 Neumann HP, Pawlu C, Peczkowska M, Bausch B, McWhinney SR, Muresan M, Buchta M, Franke G, Klisch J, Bley TA, Hoegerle S, Boedeker CC, Opocher G, Schipper J, Januszewicz A, et al. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. Jama. 292: 943-51. PMID 15328326 DOI: 10.1001/Jama.292.8.943  0.254
2005 Pawlu C, Bausch B, Neumann HP. Mutations of the SDHB and SDHD genes. Familial Cancer. 4: 49-54. PMID 15883710 DOI: 10.1007/S10689-004-4227-4  0.251
2007 Bausch B, Borozdin W, Mautner VF, Hoffmann MM, Boehm D, Robledo M, Cascon A, Harenberg T, Schiavi F, Pawlu C, Peczkowska M, Letizia C, Calvieri S, Arnaldi G, Klingenberg-Noftz RD, et al. Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1. The Journal of Clinical Endocrinology and Metabolism. 92: 2784-92. PMID 17426081 DOI: 10.1210/Jc.2006-2833  0.25
2005 Schiavi F, Boedeker CC, Bausch B, Peçzkowska M, Gomez CF, Strassburg T, Pawlu C, Buchta M, Salzmann M, Hoffmann MM, Berlis A, Brink I, Cybulla M, Muresan M, Walter MA, et al. Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. Jama. 294: 2057-63. PMID 16249420 DOI: 10.1001/Jama.294.16.2057  0.246
2005 Pawlu C, Bausch B, Reisch N, Neumann HP. Genetic testing for pheochromocytoma-associated syndromes. Annales D'Endocrinologie. 66: 178-85. PMID 15988378  0.054
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