Andreas P. Russ, MD - Publications

Affiliations: 
Biochemistry University of Oxford, Oxford, United Kingdom 
Area:
Neurogenetics, Developmental genetics

49 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
2012 Prömel S, Frickenhaus M, Hughes S, Mestek L, Staunton D, Woollard A, Vakonakis I, Schöneberg T, Schnabel R, Russ AP, Langenhan T. The GPS motif is a molecular switch for bimodal activities of adhesion class G protein-coupled receptors. Cell Reports. 2: 321-31. PMID 22938866 DOI: 10.1016/J.Celrep.2012.06.015  1
2012 Prömel S, Waller-Evans H, Dixon J, Zahn D, Colledge WH, Doran J, Carlton MB, Grosse J, Schöneberg T, Russ AP, Langenhan T. Characterization and functional study of a cluster of four highly conserved orphan adhesion-GPCR in mouse. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 241: 1591-602. PMID 22837050 DOI: 10.1002/Dvdy.23841  1
2012 Johns MA, Russ A, Fu H. Current drug targets and the druggable genome Chemical Genomics. 320-333. DOI: 10.1017/CBO9781139021500.029  1
2011 Strotmann R, Schröck K, Böselt I, Stäubert C, Russ A, Schöneberg T. Evolution of GPCR: Change and continuity Molecular and Cellular Endocrinology. 331: 170-178. PMID 20708652 DOI: 10.1016/J.Mce.2010.07.012  1
2010 Langenhan T, Russ AP. Latrophilin signalling in tissue polarity and morphogenesis. Advances in Experimental Medicine and Biology. 706: 37-48. PMID 21618824 DOI: 10.1007/978-1-4419-7913-1_3  1
2010 Waller-Evans H, Prömel S, Langenhan T, Dixon J, Zahn D, Colledge WH, Doran J, Carlton MB, Davies B, Aparicio SA, Grosse J, Russ AP. The orphan adhesion-GPCR GPR126 is required for embryonic development in the mouse. Plos One. 5: e14047. PMID 21124978 DOI: 10.1371/Journal.Pone.0014047  1
2010 Schöneberg T, Schröck K, Stäubert C, Russ A. The evolution of the repertoire and structure of G protein-coupled receptors G Protein-Coupled Receptors: Structure, Signaling, and Physiology. 5-31. DOI: 10.1017/CBO9780511760334.002  1
2009 Langenhan T, Prömel S, Mestek L, Esmaeili B, Waller-Evans H, Hennig C, Kohara Y, Avery L, Vakonakis I, Schnabel R, Russ AP. Latrophilin signaling links anterior-posterior tissue polarity and oriented cell divisions in the C. elegans embryo. Developmental Cell. 17: 494-504. PMID 19853563 DOI: 10.1016/J.Devcel.2009.08.008  1
2008 Vakonakis I, Langenhan T, Prömel S, Russ A, Campbell ID. Solution structure and sugar-binding mechanism of mouse latrophilin-1 RBL: a 7TM receptor-attached lectin-like domain. Structure (London, England : 1993). 16: 944-53. PMID 18547526 DOI: 10.1016/J.Str.2008.02.020  1
2008 Cash JL, Hart R, Russ A, Dixon JP, Colledge WH, Doran J, Hendrick AG, Carlton MB, Greaves DR. Synthetic chemerin-derived peptides suppress inflammation through ChemR23. The Journal of Experimental Medicine. 205: 767-75. PMID 18391062 DOI: 10.1084/Jem.20071601  1
2007 Barbaric I, Wells S, Russ A, Dear TN. Spectrum of ENU-induced mutations in phenotype-driven and gene-driven screens in the mouse Environmental and Molecular Mutagenesis. 48: 124-142. PMID 17295309 DOI: 10.1002/Em.20286  1
2007 Russ AP, Grosse J. Mouse genetics in drug target discovery and validation: No simple answers to complex problems Expert Opinion On Drug Discovery. 2: 1379-1387. DOI: 10.1517/17460441.2.10.1379  1
2006 Gray SL, Dalla Nora E, Grosse J, Manieri M, Stoeger T, Medina-Gomez G, Burling K, Wattler S, Russ A, Yeo GSH, Chatterjee VK, O'Rahilly S, Voshol PJ, Cinti S, Vidal-Puig A. Leptin deficiency unmasks the deleterious effects of impaired peroxisome proliferator-activated receptor γ function (P465L PPARγ) in mice Diabetes. 55: 2669-2677. PMID 17003330 DOI: 10.2337/Db06-0389  1
2006 Rudelius M, Osanger A, Kohlmann S, Augustin M, Piontek G, Heinzmann U, Jennen G, Russ A, Matiasek K, Stumm G, Schlegel J. A missense mutation in the WD40 domain of murine Lyst is linked to severe progressive Purkinje cell degeneration Acta Neuropathologica. 112: 267-276. PMID 16791600 DOI: 10.1007/S00401-006-0092-6  1
2006 Pfister KK, Shah PR, Hummerich H, Russ A, Cotton J, Annuar AA, King SM, Fisher EMC. Genetic analysis of the cytoplasmic dynein subunit families Plos Genetics. 2: e1. PMID 16440056 DOI: 10.1371/Journal.Pgen.0020001  1
2005 Russ AP, Lampel S. The druggable genome: an update. Drug Discovery Today. 10: 1607-10. PMID 16376820 DOI: 10.1016/S1359-6446(05)03666-4  1
2005 Intlekofer AM, Takemoto N, Wherry EJ, Longworth SA, Northrup JT, Palanivel VR, Mullen AC, Gasink CR, Kaech SM, Miller JD, Gapin L, Ryan K, Russ AP, Lindsten T, Orange JS, et al. Effector and memory CD8+ T cell fate coupled by T-bet and eomesodermin. Nature Immunology. 6: 1236-44. PMID 16273099 DOI: 10.1038/Ni1268  1
2005 Yu P, Constien R, Dear N, Katan M, Hanke P, Bunney TD, Kunder S, Quintanilla-Martinez L, Huffstadt U, Schröder A, Jones NP, Peters T, Fuchs H, de Angelis MH, Nehls M, ... ... Russ A, et al. Autoimmunity and inflammation due to a gain-of-function mutation in phospholipase C gamma 2 that specifically increases external Ca2+ entry. Immunity. 22: 451-65. PMID 15845450 DOI: 10.1016/J.Immuni.2005.01.018  1
2004 Ryan K, Russ AP, Levy RJ, Wehr DJ, You J, Easterday MC. Modulation of eomes activity alters the size of the developing heart: implications for in utero cardiac gene therapy. Human Gene Therapy. 15: 842-55. PMID 15353039 DOI: 10.1089/Hum.2004.15.842  1
2004 Challis BG, Coll AP, Yeo GS, Pinnock SB, Dickson SL, Thresher RR, Dixon J, Zahn D, Rochford JJ, White A, Oliver RL, Millington G, Aparicio SA, Colledge WH, Russ AP, et al. Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY(3-36). Proceedings of the National Academy of Sciences of the United States of America. 101: 4695-700. PMID 15070780 DOI: 10.1073/Pnas.0306931101  1
2004 Paffenholz R, Bergstrom RA, Pasutto F, Wabnitz P, Munroe RJ, Jagla W, Heinzmann U, Marquardt A, Bareiss A, Laufs J, Russ A, Stumm G, Schimenti JC, Bergstrom DE. Vestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidase. Genes & Development. 18: 486-91. PMID 15014044 DOI: 10.1101/Gad.1172504  1
2004 Candille SI, Van Raamsdonk CD, Chen C, Kuijper S, Chen-Tsai Y, Russ A, Meijlink F, Barsh GS. Dorsoventral patterning of the mouse coat by Tbx15. Plos Biology. 2: E3. PMID 14737183 DOI: 10.1371/Journal.Pbio.0020003  1
2003 Peters T, Sedlmeier R, Büssow H, Runkel F, Lüers GH, Korthaus D, Fuchs H, Hrabé de Angelis M, Stumm G, Russ AP, Porter RM, Augustin M, Franz T. Alopecia in a novel mouse model RCO3 is caused by mK6irs1 deficiency. The Journal of Investigative Dermatology. 121: 674-80. PMID 14632181 DOI: 10.1046/J.1523-1747.2003.12491.X  1
2003 Peters T, Thaete C, Wolf S, Popp A, Sedlmeier R, Grosse J, Nehls MC, Russ A, Schlueter V. A mouse model for cystinuria type I Human Molecular Genetics. 12: 2109-2120. PMID 12923163 DOI: 10.1093/hmg/ddg189  1
2003 Hafezparast M, Klocke R, Ruhrberg C, Marquardt A, Ahmad-Annuar A, Bowen S, Lalli G, Witherden AS, Hummerich H, Nicholson S, Morgan PJ, Oozageer R, Priestley JV, Averill S, King VR, ... ... Russ AP, et al. Mutations in dynein link motor neuron degeneration to defects in retrograde transport. Science (New York, N.Y.). 300: 808-12. PMID 12730604 DOI: 10.1126/Science.1083129  1
2002 Russ A, Stumm G, Augustin M, Sedlmeier R, Wattler S, Nehls M. Random mutagenesis in the mouse as a tool in drug discovery Drug Discovery Today. 7: 1175-1183. PMID 12547018 DOI: 10.1016/S1359-6446(02)02515-1  1
2002 Stumm G, Russ A, Nehls M. Deductive genomics: A functional approach to identify innovative drug targets in the post-genome era American Journal of Pharmacogenomics. 2: 263-271. PMID 12421097 DOI: 10.2165/00129785-200202040-00006  1
2000 Yi CH, Russ A, Brook JD. Virtual cloning and physical mapping of a human T-box gene, TBX4 Genomics. 67: 92-95. PMID 10945475 DOI: 10.1006/geno.2000.6222  1
2000 Russ AP, Aparicio SA, Carlton MB. Open-source work even more vital to genome project than to software. Nature. 404: 809. PMID 10786768 DOI: 10.1038/35009255  1
2000 Russ AP, Wattler S, Colledge WH, Aparicio SA, Carlton MB, Pearce JJ, Barton SC, Surani MA, Ryan K, Nehls MC, Wilson V, Evans MJ. Eomesodermin is required for mouse trophoblast development and mesoderm formation. Nature. 404: 95-9. PMID 10716450 DOI: 10.1038/35003601  1
1999 Winkelmann BR, Russ AP, Nauck M, Klein B, Böhm BO, Maier V, Zotz R, Matheis G, Wolf A, Wieland H, Gross W, Galton DJ, März W. Angiotensinogen M235T polymorphism is associated with plasma angiotensinogen and cardiovascular disease. American Heart Journal. 137: 698-705. PMID 10097233  1
1998 Thorey IS, Muth K, Russ AP, Otte J, Reffelmann A, von Melchner H. Selective disruption of genes transiently induced in differentiating mouse embryonic stem cells by using gene trap mutagenesis and site-specific recombination. Molecular and Cellular Biology. 18: 3081-8. PMID 9566926  1
1998 Mondorf UF, Russ A, Wiesemann A, Herrero M, Oremek G, Lenz T. Contribution of angiotensin I converting enzyme gene polymorphism and angiotensinogen gene polymorphism to blood pressure regulation in essential hypertension American Journal of Hypertension. 11: 174-183. PMID 9524045 DOI: 10.1016/S0895-7061(97)00402-0  1
1998 Wattler S, Russ A, Evans M, Nehls M. A combined analysis of genomic and primary protein structure defines the phylogenetic relationship of new members of the T-box family Genomics. 48: 24-33. PMID 9503012 DOI: 10.1006/Geno.1997.5150  1
1997 Evans MJ, Carlton MB, Russ AP. Gene trapping and functional genomics. Trends in Genetics : Tig. 13: 370-4. PMID 9287493 DOI: 10.1016/S0168-9525(97)01240-7  1
1997 Russ AP, Friedel C, Ballas K, Kalina U, Zahn D, Strebhardt K, Von Melchner H. Identification of genes induced by factor deprivation in hematopoietic cells undergoing apoptosis using gene-trap mutagenesis and site-specific recombination (Proceedings of the National Academy of Sciences of the United States of America (December 24, 1996) 93:26 (15279-15284)) Proceedings of the National Academy of Sciences of the United States of America. 94: 4233.  1
1996 Russ AP, Friedel C, Ballas K, Kalina U, Zahn D, Strebhardt K, von Melchner H. Identification of genes induced by factor deprivation in hematopoietic cells undergoing apoptosis using gene-trap mutagenesis and site-specific recombination. Proceedings of the National Academy of Sciences of the United States of America. 93: 15279-84. PMID 8986802 DOI: 10.1073/pnas.93.26.15279  1
1996 Atta J, Martin H, Bruecher J, Elsner S, Wassmann B, Rode C, Russ A, Kvalheim G, Hoelzer D. Residual leukemia and immunomagnetic bead purging in patients with BCR-ABL-positive acute lymphoblastic leukemia Bone Marrow Transplantation. 18: 541-548. PMID 8879615  1
1996 Russ AP, Friedel C, Grez M, von Melchner H. Self-deleting retrovirus vectors for gene therapy. Journal of Virology. 70: 4927-32. PMID 8763996  1
1996 Winkelmann BR, Nauck M, Klein B, Russ AP, Böhm BO, Siekmeier R, Ihnken K, Verho M, Gross W, März W. Deletion polymorphism of the angiotensin I-converting enzyme gene is associated with increased plasma angiotensin-converting enzyme activity but not with increased risk for myocardial infarction and coronary artery disease. Annals of Internal Medicine. 125: 19-25. PMID 8644984  1
1996 Atta J, Russ A, Martin H. Bcr-abl inhibits apoptosis induced by wortmannin in murine cell lines Experimental Hematology. 24: 1085.  1
1994 DeGregori J, Russ A, Von Melchner H, Rayburn H, Priyaranjan P, Jenkins NA, Copeland NG, Ruley HE. A murine homolog of the yeast RNA1 gene is required for postimplantation development Genes and Development. 8: 265-276. PMID 8314081 DOI: 10.1101/Gad.8.3.265  1
1993 Russ AP, Maerz W, Ruzicka V, Stein U, Gross W. Rapid detection of the hypertension-associated Met235-->Thr allele of the human angiotensinogen gene. Human Molecular Genetics. 2: 609-10. PMID 8518804 DOI: 10.1093/hmg/2.5.609  1
1993 März W, Ruzicka V, Fisher E, Russ AP, Schneider W, Gross W. Typing of the 3' hypervariable region of the apolipoprotein B gene: approaches, pitfalls, and applications. Electrophoresis. 14: 169-73. PMID 8486126  1
1993 Ruzicka V, Marz W, Russ A, Gross W, Sano T, Smith CL, Cantor CR. Immuno-PCR with a commercially available avidin system Science. 260: 698-699. PMID 8480182  1
1993 März W, Baumstark MW, Scharnagl H, Ruzicka V, Buxbaum S, Herwig J, Pohl T, Russ A, Schaaf L, Berg A, Böhles HJ, Usadel KH, Groß W. Accumulation of "small dense" Low Density Lipoproteins (LDL) in a homozygous patient with familial defective apolipoprotein B-100 results from heterogenous interaction of LDL subfractions with the LDL receptor Journal of Clinical Investigation. 92: 2922-2933. PMID 8254047  1
1993 Ruzicka V, Marz W, Russ A, Fisher E, Mondorf W, Gross W. Characterization of the gene for apolipoprotein E5-Frankfurt (Gln81 -> Lys, Cys112 -> Arg) by polymerase chain reaction, restriction isotyping, and temperature gradient gel electrophoresis Electrophoresis. 14: 1032-1037. PMID 8125051  1
1992 Ruzicka V, Marz W, Russ A, Gross W. Apolipoprotein B(Arg3500 → Gln) allele specific polymerase chain reaction: Large-scale screening of pooled blood samples Journal of Lipid Research. 33: 1563-1567. PMID 1431580  1
1992 Russ AP, Ruzicka V, Maerz W, Appelhans H, Gross W. Amplification and direct sequencing of a cDNA encoding human cytosolic 3-hydroxy-3-methylglutaryl-coenzyme A synthase. Biochimica Et Biophysica Acta. 1132: 329-31. PMID 1358203 DOI: 10.1016/0167-4781(92)90172-V  1
Show low-probability matches.