| Year |
Citation |
Score |
| 2009 |
Guo X, Tu L, Gumper I, Plesken H, Novak EK, Chintala S, Swank RT, Pastores G, Torres P, Izumi T, Sun TT, Sabatini DD, Kreibich G. Involvement of vps33a in the fusion of uroplakin-degrading multivesicular bodies with lysosomes. Traffic (Copenhagen, Denmark). 10: 1350-61. PMID 19566896 DOI: 10.1111/J.1600-0854.2009.00950.X |
0.449 |
|
| 2009 |
Chintala S, Novak EK, Spernyak JA, Mazurchuk R, Torres G, Patel S, Busch K, Meeder BA, Horowitz JM, Vaughan MM, Swank RT. The Vps33a gene regulates behavior and cerebellar Purkinje cell number. Brain Research. 1266: 18-28. PMID 19254700 DOI: 10.1016/J.Brainres.2009.02.035 |
0.439 |
|
| 2008 |
Chan WT, Sherer NM, Uchil PD, Novak EK, Swank RT, Mothes W. Murine leukemia virus spreading in mice impaired in the biogenesis of secretory lysosomes and Ca2+-regulated exocytosis. Plos One. 3: e2713. PMID 18629000 DOI: 10.1371/Journal.Pone.0002713 |
0.392 |
|
| 2007 |
Chintala S, Tan J, Gautam R, Rusiniak ME, Guo X, Li W, Gahl WA, Huizing M, Spritz RA, Hutton S, Novak EK, Swank RT. The Slc35d3 gene, encoding an orphan nucleotide sugar transporter, regulates platelet-dense granules Blood. 109: 1533-1540. PMID 17062724 DOI: 10.1182/Blood-2006-08-040196 |
0.568 |
|
| 2006 |
Gautam R, Novak EK, Tan J, Wakamatsu K, Ito S, Swank RT. Interaction of Hermansky-Pudlak Syndrome genes in the regulation of lysosome-related organelles Traffic. 7: 779-792. PMID 16787394 DOI: 10.1111/J.1600-0854.2006.00431.X |
0.514 |
|
| 2005 |
Chintala S, Li W, Lamoreux ML, Ito S, Wakamatsu K, Sviderskaya EV, Bennett DC, Park YM, Gahl WA, Huizing M, Spritz RA, Ben S, Novak EK, Tan J, Swank RT. Slc7a11 gene controls production of pheomelanin pigment and proliferation of cultured cells Proceedings of the National Academy of Sciences of the United States of America. 102: 10964-10969. PMID 16037214 DOI: 10.1073/Pnas.0502856102 |
0.434 |
|
| 2005 |
Guttentag SH, Akhtar A, Tao JQ, Atochina E, Rusiniak ME, Swank RT, Bates SR. Defective surfactant secretion in a mouse model of Hermansky-Pudlak syndrome. American Journal of Respiratory Cell and Molecular Biology. 33: 14-21. PMID 15790974 DOI: 10.1165/Rcmb.2004-0293Oc |
0.431 |
|
| 2005 |
Gautam R, Rusiniak ME, Chintala S, Tan J, Li W, Novak EK, Reddington M, Swank RT, McGarry MP. A New Gene Which Regulates Platelet Dense Granules. Blood. 106: 2177-2177. DOI: 10.1182/Blood.V106.11.2177.2177 |
0.575 |
|
| 2004 |
Li W, Rusiniak ME, Chintala S, Gautam R, Novak EK, Swank RT. Murine Hermansky-Pudlak syndrome genes: regulators of lysosome-related organelles. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 26: 616-28. PMID 15170859 DOI: 10.1002/Bies.20042 |
0.577 |
|
| 2004 |
Gautam R, Chintala S, Li W, Zhang Q, Tan J, Novak EK, Di Pietro SM, Dell'Angelica EC, Swank RT. The Hermansky-Pudlak Syndrome 3 (Cocoa) Protein Is a Component of the Biogenesis of Lysosome-related Organelles Complex-2 (BLOC-2) Journal of Biological Chemistry. 279: 12935-12942. PMID 14718540 DOI: 10.1074/Jbc.M311311200 |
0.541 |
|
| 2004 |
Swank RT. The light side of platelet dense granules Blood. 104: 3006-3006. DOI: 10.1182/Blood-2004-08-3256 |
0.375 |
|
| 2004 |
Swank RT, Chintala S, Lamoreux ML, Li W, Wakamatsu K, Ito S, Sviderskaya EV, Bennett DC. Abnormal regulation of Pheomelanin in the subtle gray (SUT) mouse. Pigment Cell Research. 17: 437-438. DOI: 10.1111/J.1600-0749.2004.00175_34.X |
0.355 |
|
| 2003 |
Li W, Zhang Q, Oiso N, Novak EK, Gautam R, O'Brien EP, Tinsley CL, Blake DJ, Spritz RA, Copeland NG, Jenkins NA, Amato D, Roe BA, Starcevic M, Dell'Angelica EC, ... ... Swank RT, et al. Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1). Nature Genetics. 35: 84-9. PMID 12923531 DOI: 10.1038/Ng1229 |
0.556 |
|
| 2003 |
Tiwari S, Italiano JE, Barral DC, Mules EH, Novak EK, Swank RT, Seabra MC, Shivdasani RA. A role for Rab27b in NF-E2-dependent pathways of platelet formation. Blood. 102: 3970-9. PMID 12907454 DOI: 10.1182/Blood-2003-03-0977 |
0.453 |
|
| 2003 |
Chiang PW, Oiso N, Gautam R, Suzuki T, Swank RT, Spritz RA. The Hermansky-Pudlak syndrome 1 (HPS1) and HPS4 proteins are components of two complexes, BLOC-3 and BLOC-4, involved in the biogenesis of lysosome-related organelles Journal of Biological Chemistry. 278: 20332-20337. PMID 12663659 DOI: 10.1074/Jbc.M300090200 |
0.501 |
|
| 2003 |
Zhang Q, Zhao B, Li W, Oiso N, Novak EK, Rusiniak ME, Gautam R, Chintala S, O'Brien EP, Zhang Y, Roe BA, Elliott RW, Eicher EM, Liang P, Kratz C, ... ... Swank RT, et al. Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6. Nature Genetics. 33: 145-53. PMID 12548288 DOI: 10.1038/Ng1087 |
0.548 |
|
| 2003 |
Suzuki T, Oiso N, Gautam R, Novak EK, Panthier JJ, Suprabha PG, Vida T, Swank RT, Spritz RA. The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation Proceedings of the National Academy of Sciences of the United States of America. 100: 1146-1150. PMID 12538872 DOI: 10.1073/Pnas.0237292100 |
0.528 |
|
| 2003 |
Swank RT. Novel genes for specialized organelles Blood. 101: 4229-4229. DOI: 10.1182/Blood-2003-03-0859 |
0.446 |
|
| 2002 |
Nguyen T, Novak EK, Kermani M, Fluhr J, Peters LL, Swank RT, Wei ML. Melanosome morphologies in murine models of hermansky-pudlak syndrome reflect blocks in organelle development. The Journal of Investigative Dermatology. 119: 1156-64. PMID 12445206 DOI: 10.1046/J.1523-1747.2002.19535.X |
0.399 |
|
| 2002 |
Novak EK, Gautam R, Reddington M, Collinson LM, Copeland NG, Jenkins NA, McGarry MP, Swank RT. The regulation of platelet-dense granules by Rab27a in the ashen mouse, a model of Hermansky-Pudlak and Griscelli syndromes, is granule-specific and dependent on genetic background. Blood. 100: 128-35. PMID 12070017 DOI: 10.1182/Blood.V100.1.128 |
0.426 |
|
| 2002 |
McGarry MP, Borchers M, Novak EK, Lee NA, Ohtake PJ, Lee JJ, Swank RT. Pulmonary pathologies in pallid mice result from nonhematopoietic defects. Experimental and Molecular Pathology. 72: 213-20. PMID 12009785 DOI: 10.1006/Exmp.2002.2431 |
0.448 |
|
| 2002 |
Zhang Q, Zhen L, Li W, Novak EK, Collinson LM, Jang EK, Haslam RJ, Elliott RW, Swank RT. Cell-specific abnormal prenylation of Rab proteins in platelets and melanocytes of the gunmetal mouse. British Journal of Haematology. 117: 414-23. PMID 11972527 DOI: 10.1046/J.1365-2141.2002.03444.X |
0.49 |
|
| 2002 |
Zhang Q, Li W, Novak EK, Karim A, Mishra VS, Kingsmore SF, Roe BA, Suzuki T, Swank RT. The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking. Human Molecular Genetics. 11: 697-706. PMID 11912185 DOI: 10.1093/Hmg/11.6.697 |
0.552 |
|
| 2002 |
Feng L, Novak EK, Hartnell LM, Bonifacino JS, Collinson LM, Swank RT. The Hermansky-Pudlak syndrome 1 (HPS1) and HPS2 genes independently contribute to the production and function of platelet dense granules, melanosomes, and lysosomes Blood. 99: 1651-1658. PMID 11861280 DOI: 10.1182/Blood.V99.5.1651.H8001651_1651_1658 |
0.73 |
|
| 2002 |
Suzuki T, Li W, Zhang Q, Karim A, Novak EK, Sviderskaya EV, Hill SP, Bennett DC, Levin AV, Nieuwenhuiss HK, Fong CT, Castellan C, Miterski B, Swank RT, Spritz RA. Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene Nature Genetics. 30: 321-324. PMID 11836498 DOI: 10.1038/Ng835 |
0.56 |
|
| 2001 |
Suzuki T, Li W, Zhang Q, Novak EK, Sviderskaya EV, Wilson A, Bennett DC, Roe BA, Swank RT, Spritz RA. The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human hermansky-pudlak syndrome-3 gene Genomics. 78: 30-37. PMID 11707070 DOI: 10.1006/Geno.2001.6644 |
0.576 |
|
| 2001 |
Anikster Y, Huizing M, White J, Shevchenko YO, Fitzpatrick DL, Touchman JW, Compton JG, Bale SJ, Swank RT, Gahl WA, Toro JR. Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto Rico. Nature Genetics. 28: 376-80. PMID 11455388 DOI: 10.1038/Ng576 |
0.528 |
|
| 2001 |
Li W, Detter JC, Weiss HJ, Cramer EM, Zhang Q, Novak EK, Favier R, Kingsmore SF, Swank RT. 5'-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) gene. Molecular Genetics and Metabolism. 71: 599-608. PMID 11136552 DOI: 10.1006/Mgme.2000.3091 |
0.446 |
|
| 2000 |
Gwynn B, Ciciotte SL, Hunter SJ, Washburn LL, Smith RS, Andersen SG, Swank RT, Dell'Angelica EC, Bonifacino JS, Eicher EM, Peters LL. Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism. Blood. 96: 4227-35. PMID 11110696 DOI: 10.1182/Blood.V96.13.4227.H8004227_4227_4235 |
0.573 |
|
| 2000 |
Feng L, Rigatti BW, Novak EK, Gorin MB, Swank RT. Genomic structure of the mouse Ap3b1 gene in normal and pearl mice. Genomics. 69: 370-9. PMID 11056055 DOI: 10.1006/Geno.2000.6350 |
0.63 |
|
| 2000 |
Swank RT, Novak EK, McGarry MP, Zhang Y, Li W, Zhang Q, Feng L. Abnormal vesicular trafficking in mouse models of Hermansky-Pudlak syndrome. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 13: 59-67. PMID 11041359 DOI: 10.1034/J.1600-0749.13.S8.12.X |
0.72 |
|
| 2000 |
Wilson SM, Yip R, Swing DA, O'Sullivan TN, Zhang Y, Novak EK, Swank RT, Russell LB, Copeland NG, Jenkins NA. A mutation in Rab27a causes the vesicle transport defects observed in ashen mice. Proceedings of the National Academy of Sciences of the United States of America. 97: 7933-8. PMID 10859366 DOI: 10.1073/Pnas.140212797 |
0.488 |
|
| 1999 |
McGarry MP, Reddington M, Jackson CW, Zhen L, Novak EK, Swank RT. Increased incidence and analysis of emperipolesis in megakaryocytes of the mouse mutant gunmetal. Experimental and Molecular Pathology. 66: 191-200. PMID 10486237 DOI: 10.1006/Exmp.1999.2270 |
0.438 |
|
| 1999 |
Richards-Smith B, Novak EK, Jang EK, He P, Haslam RJ, Castle D, Whiteheart SW, Swank RT. Analyses of proteins involved in vesicular trafficking in platelets of mouse models of Hermansky Pudlak syndrome. Molecular Genetics and Metabolism. 68: 14-23. PMID 10479478 DOI: 10.1006/Mgme.1999.2891 |
0.597 |
|
| 1999 |
Zhen L, Jiang S, Feng L, Bright NA, Peden AA, Seymour AB, Novak EK, Elliott R, Gorin MB, Robinson MS, Swank RT. Abnormal expression and subcellular distribution of subunit proteins of the AP-3 adaptor complex lead to platelet storage pool deficiency in the pearl mouse. Blood. 94: 146-55. PMID 10381507 DOI: 10.1182/Blood.V94.1.146.413K39_146_155 |
0.697 |
|
| 1999 |
McGarry MP, Reddington M, Novak EK, Swank RT. Survival and lung pathology of mouse models of Hermansky-Pudlak syndrome and Chediak-Higashi syndrome. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 220: 162-8. PMID 10193444 DOI: 10.1046/J.1525-1373.1999.D01-24.X |
0.451 |
|
| 1999 |
Ji W, Herron B, Jones JM, Jenkins NA, Gilbert DJ, Copeland NG, Swank R, Flaherty L, Meisler MH. Identification of genes within the Krd deletion on mouse chromosome 19. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 399-401. PMID 10087301 DOI: 10.1007/S003359901010 |
0.433 |
|
| 1999 |
Feng L, Seymour AB, Jiang S, To A, Peden AA, Novak EK, Zhen L, Rusiniak ME, Eicher EM, Robinson MS, Gorin MB, Swank RT. The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness. Human Molecular Genetics. 8: 323-30. PMID 9931340 DOI: 10.1093/Hmg/8.2.323 |
0.726 |
|
| 1998 |
Swank RT, Novak EK, McGarry MP, Rusiniak ME, Feng L. Mouse models of Hermansky Pudlak syndrome: a review. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 11: 60-80. PMID 9585243 DOI: 10.1111/J.1600-0749.1998.Tb00713.X |
0.708 |
|
| 1996 |
Mohlke KL, Nichols WC, Westrick RJ, Novak EK, Cooney KA, Swank RT, Ginsburg D. A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11 Proceedings of the National Academy of Sciences of the United States of America. 93: 15352-15357. PMID 8986815 DOI: 10.1073/Pnas.93.26.15352 |
0.448 |
|
| 1996 |
Rusiniak ME, O'Brien EP, Novak EK, Barone SM, McGarry MP, Reddington M, Swank RT. Molecular markers near the mouse brachymorphic (bm) gene, which affects connective tissues and bleeding time. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 98-102. PMID 8835524 DOI: 10.1007/S003359900027 |
0.517 |
|
| 1996 |
O’Brien EP, Zhen L, Jiang SY, Novak EK, Swank RT. High-resolution genetic mapping of the gunmetal gene which regulates platelet production. Mammalian Genome. 7: 206-208. PMID 8833241 DOI: 10.1007/S003359900055 |
0.491 |
|
| 1996 |
Seymour AB, Yanak BL, O'Brien EP, Rusiniak ME, Novak EK, Pinto LH, Swank RT, Gorin MB. An integrated genetic map of the pearl locus of mouse chromosome 13. Genome Research. 6: 538-44. PMID 8828042 DOI: 10.1101/Gr.6.6.538 |
0.35 |
|
| 1996 |
Poirier C, O'Brien EP, Bueno Brunialti AL, Chambard JC, Swank RT, Guénet JL. The gene encoding the thrombin receptor (Cf2r) maps to mouse Chromosome 13 Mammalian Genome. 7: 322. PMID 8661713 DOI: 10.1007/Bf03035441 |
0.343 |
|
| 1995 |
Zhen L, Rusiniak ME, Swank RT. The -Glucuronidase Propeptide Contains a Serpin-related Octamer Necessary for Complex Formation with Egasyn Esterase and for Retention within the Endoplasmic Reticulum Journal of Biological Chemistry. 270: 11912-11920. PMID 7744842 DOI: 10.1074/Jbc.270.20.11912 |
0.308 |
|
| 1995 |
O'Brien EP, Novak EK, Zhen L, Manly KF, Stephenson D, Swank RT. Molecular markers near two mouse Chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD) Mammalian Genome. 6: 19-24. PMID 7719021 DOI: 10.1007/Bf00350888 |
0.478 |
|
| 1995 |
Novak EK, Reddington M, Zhen L, Stenberg PE, Jackson CW, McGarry MP, Swank RT. Inherited thrombocytopenia caused by reduced platelet production in mice with the gunmetal pigment gene mutation. Blood. 85: 1781-1789. DOI: 10.1182/Blood.V85.7.1781.Bloodjournal8571781 |
0.542 |
|
| 1994 |
Nichols WC, Cooney KA, Mohlke KL, Ballew JD, Yang A, Bruck ME, Reddington M, Novak EK, Swank RT, Ginsburg D. von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene. Blood. 83: 3225-31. PMID 8193357 DOI: 10.1182/Blood.V86.6.2461.Bloodjournal8662461 |
0.436 |
|
| 1991 |
Swank RT, Sweet HO, Davisson MT, Reddington M, Novak EK. Sandy: a new mouse model for platelet storage pool deficiency. Genetical Research. 58: 51-62. PMID 1936982 DOI: 10.1017/S0016672300029608 |
0.515 |
|
| 1991 |
Swank R, Reddington M, Howlett O, Novak E. Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha Blood. 78: 2036-2044. DOI: 10.1182/Blood.V78.8.2036.Bloodjournal7882036 |
0.525 |
|
| 1990 |
Sweeney J, Novak E, Reddington M, Takeuchi K, Swank R. The RIIIS/J inbred mouse strain as a model for von Willebrand disease. Blood. 76: 2258-2265. DOI: 10.1182/Blood.V76.11.2258.2258 |
0.432 |
|
| 1987 |
Reddington M, Novak E, Hurley E, Medda C, McGarry M, Swank R. Immature dense granules in platelets from mice with platelet storage pool disease. Blood. 69: 1300-1306. DOI: 10.1182/Blood.V69.5.1300.Bloodjournal6951300 |
0.485 |
|
| 1985 |
Novak E, McGarry M, Swank R. Correction of symptoms of platelet storage pool deficiency in animal models for Chediak-Higashi syndrome and Hermansky-Pudlak syndrome. Blood. 66: 1196-1201. DOI: 10.1182/Blood.V66.5.1196.1196 |
0.492 |
|
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