Douglas Marchuk - Publications

Affiliations: 
Genetics and Genomics Duke University, Durham, NC 
Area:
Genetics, Molecular Biology, Microbiology Biology

131 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
2021 Ren AA, Snellings DA, Su YS, Hong CC, Castro M, Tang AT, Detter MR, Hobson N, Girard R, Romanos S, Lightle R, Moore T, Shenkar R, Benavides C, Beaman MM, ... ... Marchuk DA, et al. PIK3CA and CCM mutations fuel cavernomas through a cancer-like mechanism. Nature. PMID 33910229 DOI: 10.1038/s41586-021-03562-8  0.32
2020 Li W, Shenkar R, Detter MR, Moore T, Benavides CR, Lightle R, Girard R, Hobson N, Cao Y, Li Y, Griffin E, Gallione C, Zabramski JM, Ginsberg MH, Marchuk DA, et al. Propranolol inhibits cavernous vascular malformations by β1 adrenergic receptor antagonism. The Journal of Clinical Investigation. PMID 33301422 DOI: 10.1172/JCI144893  0.32
2020 Detter MR, Shenkar R, Benavides CR, Neilson CA, Moore T, Lightle R, Hobson N, Shen L, Cao Y, Girard R, Zhang D, Griffin E, Gallione CJ, Awad IA, Marchuk DA. Novel Murine Models of Cerebral Cavernous Malformations. Angiogenesis. PMID 32710309 DOI: 10.1007/S10456-020-09736-8  0.32
2020 Hong CC, Tang AT, Detter MR, Choi JP, Wang R, Yang X, Guerrero AA, Wittig CF, Hobson N, Girard R, Lightle R, Moore T, Shenkar R, Polster SP, Goddard LM, ... ... Marchuk DA, et al. Cerebral cavernous malformations are driven by ADAMTS5 proteolysis of versican. The Journal of Experimental Medicine. 217. PMID 32648916 DOI: 10.1084/Jem.20200140  0.32
2019 Tang AT, Sullivan KR, Hong CC, Goddard LM, Mahadevan A, Ren A, Pardo H, Peiper A, Griffin E, Tanes C, Mattei LM, Yang J, Li L, Mericko-Ishizuka P, Shen L, ... ... Marchuk DA, et al. Distinct cellular roles for PDCD10 define a gut-brain axis in cerebral cavernous malformation. Science Translational Medicine. 11. PMID 31776290 DOI: 10.1126/Scitranslmed.Aaw3521  0.32
2019 Snellings DA, Gallione CJ, Clark DS, Vozoris NT, Faughnan ME, Marchuk DA. Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1. American Journal of Human Genetics. PMID 31630786 DOI: 10.1016/j.ajhg.2019.09.010  0.32
2019 Lee HK, Widmayer SJ, Huang MN, Aylor DL, Marchuk DA. Novel Neuroprotective Loci Modulating Ischemic Stroke Volume in Wild-Derived Inbred Mouse Strains. Genetics. PMID 31488517 DOI: 10.1534/Genetics.119.302555  0.32
2019 McKerracher L, Shenkar R, Abbinanti M, Cao Y, Peiper A, Liao JK, Lightle R, Moore T, Hobson N, Gallione C, Ruschel J, Koskimäki J, Girard R, Rosen K, Marchuk DA, et al. A Brain-Targeted Orally Available ROCK2 Inhibitor Benefits Mild and Aggressive Cavernous Angioma Disease. Translational Stroke Research. PMID 31446620 DOI: 10.1007/S12975-019-00725-8  0.32
2019 Koskimäki J, Zhang D, Li Y, Saadat L, Moore T, Lightle R, Polster SP, Carrión-Penagos J, Lyne SB, Zeineddine HA, Shi C, Shenkar R, Romanos S, Avner K, Srinath A, ... ... Marchuk DA, et al. Transcriptome clarifies mechanisms of lesion genesis versus progression in models of Ccm3 cerebral cavernous malformations. Acta Neuropathologica Communications. 7: 132. PMID 31426861 DOI: 10.1186/S40478-019-0789-0  0.32
2019 Lyne SB, Girard R, Koskimäki J, Zeineddine HA, Zhang D, Cao Y, Li Y, Stadnik A, Moore T, Lightle R, Shi C, Shenkar R, Carrión-Penagos J, Polster SP, Romanos S, ... ... Marchuk DA, et al. Biomarkers of cavernous angioma with symptomatic hemorrhage. Jci Insight. 4. PMID 31217347 DOI: 10.1172/Jci.Insight.128577  0.32
2019 Shenkar R, Peiper A, Pardo H, Moore T, Lightle R, Girard R, Hobson N, Polster SP, Koskimäki J, Zhang D, Lyne SB, Cao Y, Chaudagar K, Saadat L, Gallione C, ... ... Marchuk D, et al. Rho Kinase Inhibition Blunts Lesion Development and Hemorrhage in Murine Models of Aggressive Pdcd10/Ccm3 Disease. Stroke. STROKEAHA118024058. PMID 30744543 DOI: 10.1161/Strokeaha.118.024058  0.32
2019 Koskimäki J, Girard R, Li Y, Saadat L, Zeineddine HA, Lightle R, Moore T, Lyne S, Avner K, Shenkar R, Cao Y, Shi C, Polster SP, Zhang D, Carrión-Penagos J, ... ... Marchuk DA, et al. Comprehensive transcriptome analysis of cerebral cavernous malformation across multiple species and genotypes. Jci Insight. 4. PMID 30728328 DOI: 10.1172/Jci.Insight.126167  0.32
2018 Zeineddine HA, Girard R, Saadat L, Shen L, Lightle R, Moore T, Cao Y, Hobson N, Shenkar R, Avner K, Chaudager K, Koskimäki J, Polster SP, Fam MD, Shi C, ... ... Marchuk DA, et al. Phenotypic characterization of murine models of cerebral cavernous malformations. Laboratory Investigation; a Journal of Technical Methods and Pathology. PMID 29946133 DOI: 10.1038/S41374-018-0030-Y  0.32
2018 Lee HK, Koh S, Lo DC, Marchuk DA. Neuronal IL-4Rα modulates neuronal apoptosis and cell viability during the acute phases of cerebral ischemia. The Febs Journal. PMID 29756681 DOI: 10.1111/febs.14498  0.32
2017 McClung JM, McCord TJ, Ryan TE, Schmidt CA, Green TD, Southerland KW, Reinardy JL, Mueller SB, Venkatraman TN, Lascola CD, Keum S, Marchuk DA, Spangenburg EE, Dokun AO, Annex BH, et al. A BAG3 Coding Variant in Mice Determines Susceptibility to Ischemic Limb Muscle Myopathy by Directing Autophagy. Circulation. PMID 28442482 DOI: 10.1161/Circulationaha.116.024873  1
2016 Shenkar R, Shi C, Austin C, Moore T, Lightle R, Cao Y, Zhang L, Wu M, Zeineddine HA, Girard R, McDonald DA, Rorrer A, Gallione C, Pytel P, Liao JK, ... Marchuk DA, et al. RhoA Kinase Inhibition With Fasudil Versus Simvastatin in Murine Models of Cerebral Cavernous Malformations. Stroke. PMID 27879448 DOI: 10.1161/Strokeaha.116.015013  0.32
2016 Lee HK, Keum S, Sheng H, Warner DS, Lo DC, Marchuk DA. Natural allelic variation of the IL-21 receptor modulates ischemic stroke infarct volume. The Journal of Clinical Investigation. PMID 27400126 DOI: 10.1172/Jci84491  1
2016 Girard R, Zeineddine HA, Orsbon C, Tan H, Moore T, Hobson N, Shenkar R, Lightle R, Shi C, Fam MD, Cao Y, Shen L, Neander AI, Rorrer A, Gallione C, ... ... Marchuk DA, et al. Micro-Computed Tomography in Murine Models of Cerebral Cavernous Malformations as a Paradigm for Brain Disease. Journal of Neuroscience Methods. PMID 27345427 DOI: 10.1016/J.Jneumeth.2016.06.021  1
2016 Shi C, Shenkar R, Zeineddine HA, Girard R, Fam MD, Austin C, Moore T, Lightle R, Zhang L, Wu M, Cao Y, Gunel M, Louvi A, Rorrer A, Gallione C, ... Marchuk DA, et al. B-Cell Depletion Reduces the Maturation of Cerebral Cavernous Malformations in Murine Models. Journal of Neuroimmune Pharmacology : the Official Journal of the Society On Neuroimmune Pharmacology. PMID 27086141 DOI: 10.1007/S11481-016-9670-0  1
2015 Dokun AO, Chen L, Okutsu M, Farber CR, Hazarika S, Jones WS, Craig D, Marchuk DA, Lye RJ, Shah SH, Annex BH. ADAM12: A Genetic Modifier of Pre-clinical Peripheral Arterial Disease. American Journal of Physiology. Heart and Circulatory Physiology. ajpheart.00803.2014. PMID 26163448 DOI: 10.1152/ajpheart.00803.2014  1
2015 Shenkar R, Shi C, Rebeiz T, Stockton RA, McDonald DA, Mikati AG, Zhang L, Austin C, Akers AL, Gallione CJ, Rorrer A, Gunel M, Min W, Marcondes de Souza J, Lee C, ... Marchuk DA, et al. Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 188-96. PMID 25122144 DOI: 10.1038/Gim.2014.97  1
2014 Shen F, Degos V, Chu PL, Han Z, Westbroek EM, Choi EJ, Marchuk D, Kim H, Lawton MT, Maze M, Young WL, Su H. Endoglin deficiency impairs stroke recovery. Stroke; a Journal of Cerebral Circulation. 45: 2101-6. PMID 24876084 DOI: 10.1161/Strokeaha.114.005115  0.92
2014 McDonald DA, Shi C, Shenkar R, Gallione CJ, Akers AL, Li S, De Castro N, Berg MJ, Corcoran DL, Awad IA, Marchuk DA. Lesions from patients with sporadic cerebral cavernous malformations harbor somatic mutations in the CCM genes: evidence for a common biochemical pathway for CCM pathogenesis. Human Molecular Genetics. 23: 4357-70. PMID 24698976 DOI: 10.1093/Hmg/Ddu153  1
2014 Abraham DM, Marchuk DA. Inhibition of the cardiomyocyte-specific troponin I-interacting kinase limits oxidative stress, injury, and adverse remodeling due to ischemic heart disease. Circulation Research. 114: 938-40. PMID 24625723 DOI: 10.1161/CIRCRESAHA.113.303238  1
2014 Poe JC, Kountikov EI, Lykken JM, Natarajan A, Marchuk DA, Tedder TF. EndoU is a novel regulator of AICD during peripheral B cell selection. The Journal of Experimental Medicine. 211: 57-69. PMID 24344237 DOI: 10.1084/Jem.20130648  1
2013 Keum S, Lee HK, Chu PL, Kan MJ, Huang MN, Gallione CJ, Gunn MD, Lo DC, Marchuk DA. Natural genetic variation of integrin alpha L (Itgal) modulates ischemic brain injury in stroke. Plos Genetics. 9: e1003807. PMID 24130503 DOI: 10.1371/Journal.Pgen.1003807  1
2013 Comi AM, Marchuk DA, Pevsner J. A needle in a haystack: Sturge-Weber syndrome gene discovery. Pediatric Neurology. 49: 391-2. PMID 24075845 DOI: 10.1016/J.Pediatrneurol.2013.07.009  1
2013 Chu PL, Keum S, Marchuk DA. A novel genetic locus modulates infarct volume independently of the extent of collateral circulation. Physiological Genomics. 45: 751-63. PMID 23800850 DOI: 10.1152/Physiolgenomics.00063.2013  1
2013 Shirley MD, Tang H, Gallione CJ, Baugher JD, Frelin LP, Cohen B, North PE, Marchuk DA, Comi AM, Pevsner J. Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ. The New England Journal of Medicine. 368: 1971-9. PMID 23656586 DOI: 10.1056/Nejmoa1213507  1
2013 Tang H, Xiao K, Mao L, Rockman HA, Marchuk DA. Overexpression of TNNI3K, a cardiac-specific MAPKKK, promotes cardiac dysfunction. Journal of Molecular and Cellular Cardiology. 54: 101-11. PMID 23085512 DOI: 10.1016/J.Yjmcc.2012.10.004  1
2012 Lodder EM, Scicluna BP, Milano A, Sun AY, Tang H, Remme CA, Moerland PD, Tanck MW, Pitt GS, Marchuk DA, Bezzina CR. Dissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conduction. Plos Genetics. 8: e1003113. PMID 23236294 DOI: 10.1371/Journal.Pgen.1003113  1
2012 McClung JM, McCord TJ, Keum S, Johnson S, Annex BH, Marchuk DA, Kontos CD. Skeletal muscle-specific genetic determinants contribute to the differential strain-dependent effects of hindlimb ischemia in mice. The American Journal of Pathology. 180: 2156-69. PMID 22445571 DOI: 10.1016/J.Ajpath.2012.01.032  1
2012 Lo W, Marchuk DA, Ball KL, Juhász C, Jordan LC, Ewen JB, Comi A. Updates and future horizons on the understanding, diagnosis, and treatment of Sturge-Weber syndrome brain involvement. Developmental Medicine and Child Neurology. 54: 214-23. PMID 22191476 DOI: 10.1111/J.1469-8749.2011.04169.X  1
2012 McDonald DA, Shi C, Shenkar R, Stockton RA, Liu F, Ginsberg MH, Marchuk DA, Awad IA. Fasudil decreases lesion burden in a murine model of cerebral cavernous malformation disease. Stroke; a Journal of Cerebral Circulation. 43: 571-4. PMID 22034008 DOI: 10.1161/Strokeaha.111.625467  1
2011 Gallione CJ, Solatycki A, Awad IA, Weber JL, Marchuk DA. A founder mutation in the Ashkenazi Jewish population affecting messenger RNA splicing of the CCM2 gene causes cerebral cavernous malformations. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 662-6. PMID 21543988 DOI: 10.1097/GIM.0b013e318211ff8b  1
2011 McDonald DA, Shenkar R, Shi C, Stockton RA, Akers AL, Kucherlapati MH, Kucherlapati R, Brainer J, Ginsberg MH, Awad IA, Marchuk DA. A novel mouse model of cerebral cavernous malformations based on the two-hit mutation hypothesis recapitulates the human disease. Human Molecular Genetics. 20: 211-22. PMID 20940147 DOI: 10.1093/Hmg/Ddq433  1
2010 Ahn SH, Deshmukh H, Johnson N, Cowell LG, Rude TH, Scott WK, Nelson CL, Zaas AK, Marchuk DA, Keum S, Lamlertthon S, Sharma-Kuinkel BK, Sempowski GD, Fowler VG. Two genes on A/J chromosome 18 are associated with susceptibility to Staphylococcus aureus infection by combined microarray and QTL analyses. Plos Pathogens. 6: e1001088. PMID 20824097 DOI: 10.1371/Journal.Ppat.1001088  1
2010 Du F, Ozdowski EF, Kotowski IK, Marchuk DA, Sherwood NT. Functional conservation of human Spastin in a Drosophila model of autosomal dominant-hereditary spastic paraplegia. Human Molecular Genetics. 19: 1883-96. PMID 20154342 DOI: 10.1093/Hmg/Ddq064  1
2010 Gallione C, Aylsworth AS, Beis J, Berk T, Bernhardt B, Clark RD, Clericuzio C, Danesino C, Drautz J, Fahl J, Fan Z, Faughnan ME, Ganguly A, Garvie J, Henderson K, ... ... Marchuk DA, et al. Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP-HHT syndrome. American Journal of Medical Genetics. Part A. 152: 333-9. PMID 20101697 DOI: 10.1002/Ajmg.A.33206  1
2009 Keum S, Marchuk DA. A locus mapping to mouse chromosome 7 determines infarct volume in a mouse model of ischemic stroke. Circulation. Cardiovascular Genetics. 2: 591-8. PMID 20031639 DOI: 10.1161/Circgenetics.109.883231  1
2009 Wheeler FC, Tang H, Marks OA, Hadnott TN, Chu PL, Mao L, Rockman HA, Marchuk DA. Tnni3k modifies disease progression in murine models of cardiomyopathy. Plos Genetics. 5: e1000647. PMID 19763165 DOI: 10.1371/Journal.Pgen.1000647  1
2009 Fernandez L, Marchuk DA, Moran JL, Beier DR, Rockman HA. An N-ethyl-N-nitrosourea mutagenesis recessive screen identifies two candidate regions for murine cardiomyopathy that map to chromosomes 1 and 15. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 20: 296-304. PMID 19387734 DOI: 10.1007/S00335-009-9184-7  1
2009 Whitehead KJ, Chan AC, Navankasattusas S, Koh W, London NR, Ling J, Mayo AH, Drakos SG, Jones CA, Zhu W, Marchuk DA, Davis GE, Li DY. The cerebral cavernous malformation signaling pathway promotes vascular integrity via Rho GTPases. Nature Medicine. 15: 177-84. PMID 19151728 DOI: 10.1038/nm.1911  1
2009 Akers AL, Johnson E, Steinberg GK, Zabramski JM, Marchuk DA. Biallelic somatic and germline mutations in cerebral cavernous malformations (CCMs): evidence for a two-hit mechanism of CCM pathogenesis. Human Molecular Genetics. 18: 919-30. PMID 19088123 DOI: 10.1093/Hmg/Ddn430  1
2008 Kim H, Marchuk DA, Pawlikowska L, Chen Y, Su H, Yang GY, Young WL. Genetic considerations relevant to intracranial hemorrhage and brain arteriovenous malformations Acta Neurochirurgica, Supplementum. 199-206. PMID 19066109 DOI: 10.1007/978-3-211-09469-3_38  1
2008 Shenkar R, Venkatasubramanian PN, Wyrwicz AM, Zhao JC, Shi C, Akers A, Marchuk DA, Awad IA. Advanced magnetic resonance imaging of cerebral cavernous malformations: part II. Imaging of lesions in murine models. Neurosurgery. 63: 790-7; discussion 79. PMID 18981891 DOI: 10.1227/01.Neu.0000315862.24920.49  1
2008 Dokun AO, Keum S, Hazarika S, Li Y, Lamonte GM, Wheeler F, Marchuk DA, Annex BH. A quantitative trait locus (LSq-1) on mouse chromosome 7 is linked to the absence of tissue loss after surgical hindlimb ischemia. Circulation. 117: 1207-15. PMID 18285563 DOI: 10.1161/Circulationaha.107.736447  1
2008 Williams RB, Marchuk DA, Siegler IC, Barefoot JC, Helms MJ, Brummett BH, Surwit RS, Lane JD, Kuhn CM, Gadde KM, Ashley-Koch A, Svenson IK, Schanberg SM. Childhood socioeconomic status and serotonin transporter gene polymorphism enhance cardiovascular reactivity to mental stress. Psychosomatic Medicine. 70: 32-9. PMID 18158371 DOI: 10.1097/Psy.0B013E31815F66C3  1
2007 Hale LP, Perera D, Gottfried MR, Maggio-Price L, Srinivasan S, Marchuk D. Neonatal co-infection with helicobacter species markedly accelerates the development of inflammation-associated colonic neoplasia in IL-10(-/-) mice. Helicobacter. 12: 598-604. PMID 18001399 DOI: 10.1111/J.1523-5378.2007.00552.X  1
2007 Salzler HR, Griffiths R, Ruiz P, Chi L, Frey C, Marchuk DA, Rockman HA, Le TH. Hypertension and albuminuria in chronic kidney disease mapped to a mouse chromosome 11 locus. Kidney International. 72: 1226-32. PMID 17851470 DOI: 10.1038/Sj.Ki.5002519  1
2007 Young WL, Kwok PY, Pawlikowska L, Lawton MT, Kim H, Hysi PG, Marchuk DA. Arteriovenous malformation. Journal of Neurosurgery. 106: 731-2; author reply . PMID 17432733 DOI: 10.3171/jns.2007.106.4.731  1
2007 Liquori CL, Berg MJ, Squitieri F, Leedom TP, Ptacek L, Johnson EW, Marchuk DA. Deletions in CCM2 are a common cause of cerebral cavernous malformations. American Journal of Human Genetics. 80: 69-75. PMID 17160895 DOI: 10.1086/510439  1
2007 Donahue MP, Marchuk DA, Rockman HA. Reply Journal of the American College of Cardiology. 49: 1106-1107. DOI: 10.1016/J.Jacc.2006.12.019  1
2006 Donahue MP, Marchuk DA, Rockman HA. Redefining heart failure: the utility of genomics. Journal of the American College of Cardiology. 48: 1289-98. PMID 17010784 DOI: 10.1016/J.Jacc.2006.05.062  1
2006 Pittman KM, Losken HW, Kleinman ME, Marcus JR, Blei F, Gurtner GC, Marchuk DA. No evidence for maternal-fetal microchimerism in infantile hemangioma: a molecular genetic investigation. The Journal of Investigative Dermatology. 126: 2533-8. PMID 16902414 DOI: 10.1038/sj.jid.5700516  1
2006 Carlson KM, Yamaga KM, Reinker KA, Hsia YE, Carpenter C, Abe LM, Perry AK, Person DA, Marchuk DA, Raney EM. Precocious osteoarthritis in a family with recurrent COL2A1 mutation. The Journal of Rheumatology. 33: 1133-6. PMID 16755660  1
2006 Pawlikowska L, Poon KY, Achrol AS, McCulloch CE, Ha C, Lum K, Zaroff JG, Ko NU, Johnston SC, Sidney S, Marchuk DA, Lawton MT, Kwok PY, Young WL. Apolipoprotein E epsilon 2 is associated with new hemorrhage risk in brain arteriovenous malformations. Neurosurgery. 58: 838-43; discussion 8. PMID 16639317 DOI: 10.1227/01.Neu.0000209605.18358.E5  1
2006 Shianna KV, Marchuk DA, Strand MK. Genomic characterization of POS5, the Saccharomyces cerevisiae mitochondrial NADH kinase. Mitochondrion. 6: 94-101. PMID 16621727 DOI: 10.1016/j.mito.2006.02.003  1
2006 Gallione CJ, Richards JA, Letteboer TG, Rushlow D, Prigoda NL, Leedom TP, Ganguly A, Castells A, Ploos van Amstel JK, Westermann CJ, Pyeritz RE, Marchuk DA. SMAD4 mutations found in unselected HHT patients. Journal of Medical Genetics. 43: 793-7. PMID 16613914 DOI: 10.1136/jmg.2006.041517  1
2006 Plummer NW, Squire TL, Srinivasan S, Huang E, Zawistowski JS, Matsunami H, Hale LP, Marchuk DA. Neuronal expression of the Ccm2 gene in a new mouse model of cerebral cavernous malformations. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 119-28. PMID 16465592 DOI: 10.1007/S00335-005-0098-8  1
2006 Liquori CL, Berg MJ, Squitieri F, Ottenbacher M, Sorlie M, Leedom TP, Cannella M, Maglione V, Ptacek L, Johnson EW, Marchuk DA. Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus. Human Mutation. 27: 118. PMID 16329096 DOI: 10.1002/Humu.9389  1
2006 Achrol AS, Pawlikowska L, McCulloch CE, Poon KY, Ha C, Zaroff JG, Johnston SC, Lee C, Lawton MT, Sidney S, Marchuk DA, Kwok PY, Young WL. Tumor necrosis factor-alpha-238G>A promoter polymorphism is associated with increased risk of new hemorrhage in the natural course of patients with brain arteriovenous malformations. Stroke; a Journal of Cerebral Circulation. 37: 231-4. PMID 16322490 DOI: 10.1161/01.Str.0000195133.98378.4B  1
2005 Sweet K, Willis J, Zhou XP, Gallione C, Sawada T, Alhopuro P, Khoo SK, Patocs A, Martin C, Bridgeman S, Heinz J, Pilarski R, Lehtonen R, Prior TW, Frebourg T, ... ... Marchuk DA, et al. Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis. Jama. 294: 2465-73. PMID 16287957 DOI: 10.1001/Jama.294.19.2465  1
2005 Pawlikowska L, Tran MN, Achrol AS, Ha C, Burchard E, Choudhry S, Zaroff J, Lawton MT, Castro R, McCulloch CE, Marchuk D, Kwok PY, Young WL. Polymorphisms in transforming growth factor-beta-related genes ALK1 and ENG are associated with sporadic brain arteriovenous malformations. Stroke; a Journal of Cerebral Circulation. 36: 2278-80. PMID 16179574 DOI: 10.1161/01.Str.0000182253.91167.Fa  1
2005 Plummer NW, Zawistowski JS, Marchuk DA. Genetics of cerebral cavernous malformations. Current Neurology and Neuroscience Reports. 5: 391-6. PMID 16131422 DOI: 10.1007/S11910-005-0063-7  0.8
2005 Wheeler FC, Fernandez L, Carlson KM, Wolf MJ, Rockman HA, Marchuk DA. QTL mapping in a mouse model of cardiomyopathy reveals an ancestral modifier allele affecting heart function and survival. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 414-23. PMID 16075368 DOI: 10.1007/S00335-005-2468-7  1
2005 Zawistowski JS, Stalheim L, Uhlik MT, Abell AN, Ancrile BB, Johnson GL, Marchuk DA. CCM1 and CCM2 protein interactions in cell signaling: implications for cerebral cavernous malformations pathogenesis. Human Molecular Genetics. 14: 2521-31. PMID 16037064 DOI: 10.1093/Hmg/Ddi256  1
2005 Svenson IK, Kloos MT, Jacon A, Gallione C, Horton AC, Pericak-Vance MA, Ehlers MD, Marchuk DA. Subcellular localization of spastin: implications for the pathogenesis of hereditary spastic paraplegia. Neurogenetics. 6: 135-41. PMID 15891913 DOI: 10.1007/S10048-005-0219-2  1
2005 Taylor WD, Steffens DC, Payne ME, MacFall JR, Marchuk DA, Svenson IK, Krishnan KR. Influence of serotonin transporter promoter region polymorphisms on hippocampal volumes in late-life depression. Archives of General Psychiatry. 62: 537-44. PMID 15867107 DOI: 10.1001/Archpsyc.62.5.537  1
2005 Lux A, Beil C, Majety M, Barron S, Gallione CJ, Kuhn HM, Berg JN, Kioschis P, Marchuk DA, Hafner M. Human retroviral gag- and gag-pol-like proteins interact with the transforming growth factor-beta receptor activin receptor-like kinase 1. The Journal of Biological Chemistry. 280: 8482-93. PMID 15611116 DOI: 10.1074/jbc.M409197200  0.32
2004 Plummer NW, Gallione CJ, Srinivasan S, Zawistowski JS, Louis DN, Marchuk DA. Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformations. The American Journal of Pathology. 165: 1509-18. PMID 15509522 DOI: 10.1016/S0002-9440(10)63409-8  1
2004 Pawlikowska L, Tran MN, Achrol AS, McCulloch CE, Ha C, Lind DL, Hashimoto T, Zaroff J, Lawton MT, Marchuk DA, Kwok PY, Young WL. Polymorphisms in genes involved in inflammatory and angiogenic pathways and the risk of hemorrhagic presentation of brain arteriovenous malformations. Stroke; a Journal of Cerebral Circulation. 35: 2294-300. PMID 15331795 DOI: 10.1161/01.Str.0000141932.44613.B1  1
2004 Verlaan DJ, Laurent SB, Rochefort DL, Liquori CL, Marchuk DA, Siegel AM, Rouleau GA. CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations. Annals of Neurology. 55: 757-8. PMID 15122722 DOI: 10.1002/Ana.20112  1
2004 Abdalla SA, Gallione CJ, Barst RJ, Horn EM, Knowles JA, Marchuk DA, Letarte M, Morse JH. Primary pulmonary hypertension in families with hereditary haemorrhagic telangiectasia. The European Respiratory Journal. 23: 373-7. PMID 15065824 DOI: 10.1183/09031936.04.00085504  1
2004 Gallione CJ, Repetto GM, Legius E, Rustgi AK, Schelley SL, Tejpar S, Mitchell G, Drouin E, Westermann CJ, Marchuk DA. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). Lancet (London, England). 363: 852-9. PMID 15031030 DOI: 10.1016/S0140-6736(04)15732-2  0.36
2004 Whitehead KJ, Plummer NW, Adams JA, Marchuk DA, Li DY. Ccm1 is required for arterial morphogenesis: implications for the etiology of human cavernous malformations. Development (Cambridge, England). 131: 1437-48. PMID 14993192 DOI: 10.1242/dev.01036  0.8
2004 Hashimoto T, Lawton MT, Wen G, Yang GY, Chaly T, Stewart CL, Dressman HK, Barbaro NM, Marchuk DA, Young WL. Gene microarray analysis of human brain arteriovenous malformations. Neurosurgery. 54: 410-23; discussion 4. PMID 14744289  1
2004 Le TH, Fogo AB, Salzler HR, Vinogradova T, Oliverio MI, Marchuk DA, Coffman TM. Modifier locus on mouse chromosome 3 for renal vascular pathology in AT1A receptor-deficiency. Hypertension. 43: 445-51. PMID 14718357 DOI: 10.1161/01.Hyp.0000112423.28987.00  1
2003 Liquori CL, Berg MJ, Siegel AM, Huang E, Zawistowski JS, Stoffer T, Verlaan D, Balogun F, Hughes L, Leedom TP, Plummer NW, Cannella M, Maglione V, Squitieri F, Johnson EW, ... ... Marchuk DA, et al. Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations. American Journal of Human Genetics. 73: 1459-64. PMID 14624391 DOI: 10.1086/380314  1
2003 Le Corvoisier P, Park HY, Carlson KM, Marchuk DA, Rockman HA. Multiple quantitative trait loci modify the heart failure phenotype in murine cardiomyopathy. Human Molecular Genetics. 12: 3097-107. PMID 14519689 DOI: 10.1093/Hmg/Ddg333  1
2003 Le Corvoisier P, Park HY, Carlson KM, Donahue MP, Marchuk DA, Rockman HA. Impact of genetic polymorphisms on heart failure prognosis. Archives Des Maladies Du Coeur Et Des Vaisseaux. 96: 197-206. PMID 12722550  1
2003 Marchuk DA, Srinivasan S, Squire TL, Zawistowski JS. Vascular morphogenesis: tales of two syndromes. Human Molecular Genetics. 12: R97-112. PMID 12668602 DOI: 10.1093/Hmg/Ddg103  0.8
2003 Williams RB, Marchuk DA, Gadde KM, Barefoot JC, Grichnik K, Helms MJ, Kuhn CM, Lewis JG, Schanberg SM, Stafford-Smith M, Suarez EC, Clary GL, Svenson IK, Siegler IC. Serotonin-related gene polymorphisms and central nervous system serotonin function. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 28: 533-41. PMID 12629534 DOI: 10.1038/Sj.Npp.1300054  1
2003 Srinivasan S, Hanes MA, Dickens T, Porteous ME, Oh SP, Hale LP, Marchuk DA. A mouse model for hereditary hemorrhagic telangiectasia (HHT) type 2. Human Molecular Genetics. 12: 473-82. PMID 12588795 DOI: 10.1093/hmg/ddg050  0.44
2002 Suzuki M, Carlson KM, Marchuk DA, Rockman HA. Genetic modifier loci affecting survival and cardiac function in murine dilated cardiomyopathy. Circulation. 105: 1824-9. PMID 11956126 DOI: 10.1161/01.Cir.0000014926.32463.89  1
2002 Zawistowski JS, Serebriiskii IG, Lee MF, Golemis EA, Marchuk DA. KRIT1 association with the integrin-binding protein ICAP-1: a new direction in the elucidation of cerebral cavernous malformations (CCM1) pathogenesis. Human Molecular Genetics. 11: 389-96. PMID 11854171 DOI: 10.1093/Hmg/11.4.389  0.8
2002 Walter JW, North PE, Waner M, Mizeracki A, Blei F, Walker JW, Reinisch JF, Marchuk DA. Somatic mutation of vascular endothelial growth factor receptors in juvenile hemangioma. Genes, Chromosomes & Cancer. 33: 295-303. PMID 11807987 DOI: 10.1002/gcc.10028  1
2001 Ashley-Koch A, Bonner ER, Gaskell PC, West SG, Tim R, Wolpert CM, Jones R, Farrell CD, Nance M, Svenson IK, Marchuk DA, Boustany RM, Vance JM, Scott WK, Pericak-Vance MA. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia. Neurogenetics. 3: 91-7. PMID 11354831 DOI: 10.1007/S100480000098  1
2001 Svenson IK, Ashley-Koch AE, Gaskell PC, Riney TJ, Cumming WJ, Kingston HM, Hogan EL, Boustany RM, Vance JM, Nance MA, Pericak-Vance MA, Marchuk DA. Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia. American Journal of Human Genetics. 68: 1077-85. PMID 11309678 DOI: 10.1086/320111  1
2001 Williams RB, Marchuk DA, Gadde KM, Barefoot JC, Grichnik K, Helms MJ, Kuhn CM, Lewis JG, Schanberg SM, Stafford-Smith M, Suarez EC, Clary GL, Svenson IK, Siegler IC. Central nervous system serotonin function and cardiovascular responses to stress. Psychosomatic Medicine. 63: 300-5. PMID 11292279 DOI: 10.1097/00006842-200103000-00016  1
2001 Berg JN, Walter JW, Thisanagayam U, Evans M, Blei F, Waner M, Diamond AG, Marchuk DA, Porteous ME. Evidence for loss of heterozygosity of 5q in sporadic haemangiomas: are somatic mutations involved in haemangioma formation? Journal of Clinical Pathology. 54: 249-52. PMID 11253142 DOI: 10.1136/jcp.54.3.249  1
2001 Calvert JT, Burns S, Riney TJ, Sahoo T, Orlow SJ, Nevin NC, Haisley-Royster C, Prose N, Simpson SA, Speer MC, Marchuk DA. Additional glomangioma families link to chromosome 1p: no evidence for genetic heterogeneity. Human Heredity. 51: 180-2. PMID 11173970 DOI: 10.1159/000053340  1
2001 Sahoo T, Goenaga-Diaz E, Serebriiskii IG, Thomas JW, Kotova E, Cuellar JG, Peloquin JM, Golemis E, Beitinjaneh F, Green ED, Johnson EW, Marchuk DA. Computational and experimental analyses reveal previously undetected coding exons of the KRIT1 (CCM1) gene. Genomics. 71: 123-6. PMID 11161805 DOI: 10.1006/Geno.2000.6426  1
1999 Sahoo T, Johnson EW, Thomas JW, Kuehl PM, Jones TL, Dokken CG, Touchman JW, Gallione CJ, Lee-Lin SQ, Kosofsky B, Kurth JH, Louis DN, Mettler G, Morrison L, Gil-Nagel A, ... ... Marchuk DA, et al. Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1). Human Molecular Genetics. 8: 2325-33. PMID 10545614 DOI: 10.1093/Hmg/8.12.2325  1
1999 Calvert JT, Riney TJ, Kontos CD, Cha EH, Prieto VG, Shea CR, Berg JN, Nevin NC, Simpson SA, Pasyk KA, Speer MC, Peters KG, Marchuk DA. Allelic and locus heterogeneity in inherited venous malformations. Human Molecular Genetics. 8: 1279-89. PMID 10369874 DOI: 10.1093/Hmg/8.7.1279  1
1999 Walter JW, Blei F, Anderson JL, Orlow SJ, Speer MC, Marchuk DA. Genetic mapping of a novel familial form of infantile hemangioma American Journal of Medical Genetics. 82: 77-83. PMID 9916848 DOI: 10.1002/(Sici)1096-8628(19990101)82:1<77::Aid-Ajmg15>3.0.Co;2-A  1
1998 Blei F, Walter J, Orlow SJ, Marchuk DA. Familial segregation of hemangiomas and vascular malformations as an autosomal dominant trait Archives of Dermatology. 134: 718-722. PMID 9645641 DOI: 10.1001/Archderm.134.6.718  1
1998 Gallione CJ, Klaus DJ, Yeh EY, Stenzel TT, Xue Y, Anthony KB, McAllister KA, Baldwin MA, Berg JN, Lux A, Smith JD, Vary CP, Craigen WJ, Westermann CJ, Warner ML, ... ... Marchuk DA, et al. Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles. Human Mutation. 11: 286-94. PMID 9554745 DOI: 10.1002/(SICI)1098-1004(1998)11:4<286::AID-HUMU6>3.0.CO;2-B  0.32
1998 Damji KF, Gallione CJ, Allingham RR, Slotterbeck B, Guttmacher AE, Pasyk KA, Vance JM, Pericak-Vance MA, Speer MC, Marchuk DA. Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant disease Human Genetics. 102: 207-212. PMID 9521591 DOI: 10.1007/S004390050679  1
1997 Berg JN, Gallione CJ, Stenzel TT, Johnson DW, Allen WP, Schwartz CE, Jackson CE, Porteous ME, Marchuk DA. The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2. American Journal of Human Genetics. 61: 60-7. PMID 9245985 DOI: 10.1086/513903  0.32
1997 Alberts MJ, Davis JP, Graffagnino C, McClenny C, Delong D, Granger C, Herbstreith MH, Boteva K, Marchuk DA, Roses AD. Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhage. Annals of Neurology. 41: 683-6. PMID 9153532 DOI: 10.1002/ana.410410519  1
1996 Vikkula M, Boon LM, Carraway KL, Calvert JT, Diamonti AJ, Goumnerov B, Pasyk KA, Marchuk DA, Warman ML, Cantley LC, Mulliken JB, Olsen BR. Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2 Cell. 87: 1181-1190. PMID 8980225 DOI: 10.1016/S0092-8674(00)81814-0  1
1996 Cummings LM, Trent JM, Marchuk DA. Identification and mapping of type 1 neurofibromatosis (NF1) homologous loci Cytogenetics and Cell Genetics. 73: 334-340. PMID 8751390 DOI: 10.1159/000134370  1
1996 McKeever PE, Dennis TR, Burgess AC, Meltzer PS, Marchuk DA, Trent JM. Chromosome breakpoint at 17q11.2 and insertion of DNA from three different chromosomes in a glioblastoma with exceptional glial fibrillary acidic protein expression. Cancer Genetics and Cytogenetics. 87: 41-7. PMID 8646740 DOI: 10.1016/0165-4608(95)00237-5  1
1996 Johnson DW, Berg JN, Baldwin MA, Gallione CJ, Marondel I, Yoon SJ, Stenzel TT, Speer M, Pericak-Vance MA, Diamond A, Guttmacher AE, Jackson CE, Attisano L, Kucherlapati R, Porteous ME, ... Marchuk DA, et al. Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2. Nature Genetics. 13: 189-95. PMID 8640225 DOI: 10.1038/Ng0696-189  0.32
1995 Johnson EW, Iyer LM, Rich SS, Orr HT, Gil-Nagel A, Kurth JH, Zabramski JM, Marchuk DA, Weissenbach J, Clericuzio CL, Davis LE, Hart BL, Gusella JF, Kosofsky BE, Louis DN, et al. Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig. Genome Research. 5: 368-80. PMID 8750196 DOI: 10.1101/Gr.5.4.368  1
1995 Johnson DW, Berg JN, Gallione CJ, McAllister KA, Warner JP, Helmbold EA, Markel DS, Jackson CE, Porteous ME, Marchuk DA. A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12. Genome Research. 5: 21-8. PMID 8717052 DOI: 10.1101/gr.5.1.21  0.32
1995 Marchuk DA, Gallione CJ, Morrison LA, Clericuzio CL, Hart BL, Kosofsky BE, Louis DN, Gusella JF, Davis LE, Prenger VL. A locus for cerebral cavernous malformations maps to chromosome 7q in two families. Genomics. 28: 311-4. PMID 8530042 DOI: 10.1006/Geno.1995.1147  1
1995 Greenspan DS, Northrup H, Au KS, McAllister KA, Francomano CA, Wenstrup RJ, Marchuk DA, Kwiatkowski DJ. COL5a1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers-Danlos syndrome type II Genomics. 25: 737-739. PMID 7759113 DOI: 10.1016/0888-7543(95)80021-D  1
1994 McDonald MT, Papenberg KA, Ghosh S, Glatfelter AA, Biesecker BB, Helmbold EA, Markel DS, Zolotor A, McKinnon WC, Vanderstoep JL, Jackson CE, Iannuzzi M, Collins FS, Boehnke M, Porteous ME, ... ... Marchuk DA, et al. A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34 Nature Genetics. 6: 197-204. PMID 8162075 DOI: 10.1038/Ng0294-197  1
1993 McDonald MT, Papenberg KA, Glatfelter AA, Vander-Stoep JL, Marchuk DA. Dinucleotide repeat polymorphism at the human erythropoietin receptor locus (EPOR) at 19p13 Human Molecular Genetics. 2: 619. PMID 8518819 DOI: 10.1093/hmg/2.5.619-a  1
1993 Legius E, Marchuk DA, Collins FS, Glover TW. Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis. Nature Genetics. 3: 122-6. PMID 8499945 DOI: 10.1038/Ng0293-122  1
1993 Gutmann DH, Boguski M, Marchuk D, Wigler M, Collins FS, Ballester R. Analysis of the neurofibromatosis type 1 (NF1) GAP-related domain by site-directed mutagenesis. Oncogene. 8: 761-9. PMID 8437860  1
1993 Andersen LB, Ballester R, Marchuk DA, Chang E, Gutmann DH, Saulino AM, Camonis J, Wigler M, Collins FS. A conserved alternative splice in the von Recklinghausen neurofibromatosis (NF1) gene produces two neurofibromin isoforms, both of which have GTPase-activating protein activity. Molecular and Cellular Biology. 13: 487-95. PMID 8417346 DOI: 10.1128/Mcb.13.1.487  1
1993 Andersen LB, Tarlé SA, Marchuk DA, Legius E, Collins FS. A compound nucleotide repeat in the neurofibromatosis (NF1) gene. Human Molecular Genetics. 2: 1083. PMID 8364559 DOI: 10.1093/Hmg/2.7.1083-A  0.8
1993 Reyniers E, De Boulle K, Marchuk DA, Andersen LB, Collins FS, Willems PJ. An EcoRI RFLP in the 5' region of the human NF1 gene. Human Genetics. 92: 631. PMID 7903272 DOI: 10.1007/Bf00420953  0.8
1992 Chandrasekharappa SC, Marchuk DA, Collins FS. Analysis of yeast artificial chromosome clones. Methods in Molecular Biology (Clifton, N.J.). 12: 235-57. PMID 21409638 DOI: 10.1385/0-89603-229-9:235  0.8
1992 Marchuk DA, Tavakkol R, Wallace MR, Brownstein BH, Taillon-Miller P, Fong CT, Legius E, Andersen LB, Glover TW, Collins FS. A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis gene. Genomics. 13: 672-80. PMID 1639394 DOI: 10.1016/0888-7543(92)90140-N  0.8
1992 Legius E, Marchuk DA, Hall BK, Andersen LB, Wallace MR, Collins FS, Glover TW. NF1-related locus on chromosome 15. Genomics. 13: 1316-8. PMID 1505963 DOI: 10.1016/0888-7543(92)90055-W  0.8
1992 Kayes LM, Schroeder WT, Marchuk DA, Collins FS, Riccardi VM, Duvic M, Stephens K. The gene for a novel epidermal antigen maps near the neurofibromatosis 1 gene. Genomics. 14: 369-76. PMID 1358802 DOI: 10.1016/S0888-7543(05)80228-9  0.8
1992 Martin-Gallardo A, Marchuk DA, Gocayne J, Kerlavage AR, McCombie WR, Venter JC, Collins FS, Wallace MR. Sequencing and analysis of genomic fragments from the NF1 locus. Dna Sequence : the Journal of Dna Sequencing and Mapping. 3: 237-43. PMID 1338369 DOI: 10.3109/10425179209034023  0.8
1991 Marchuk D, Drumm M, Saulino A, Collins FS. Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products. Nucleic Acids Research. 19: 1154. PMID 2020552 DOI: 10.1093/Nar/19.5.1154  1
1991 Marchuk DA, Saulino AM, Tavakkol R, Swaroop M, Wallace MR, Andersen LB, Mitchell AL, Gutmann DH, Boguski M, Collins FS. cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene product. Genomics. 11: 931-40. PMID 1783401 DOI: 10.1016/0888-7543(91)90017-9  1
1991 Andersen LB, Wallace MR, Marchuk DA, Tavakkol R, Mitchell A, Saulino AM, Collins FS. A highly polymorphic cDNA probe in the NF1 gene. Nucleic Acids Research. 19: 3754. PMID 1677185 DOI: 10.1093/Nar/19.13.3754  0.8
1991 Andersen LB, Wallace MR, Marchuk DA, Cawthon RM, Odeh HM, Letcher R, White RL, Collins FS. A polymorphic cDNA probe on chromosome 17q11.2 located within the NF1 gene [D17S376]. Nucleic Acids Research. 19: 197. PMID 1672744 DOI: 10.1093/nar/19.1.197-a  1
1990 Wallace MR, Andersen LB, Fountain JW, Odeh HM, Viskochil D, Marchuk DA, O'Connell P, White R, Collins FS. A chromosome jump crosses a translocation breakpoint in the von Recklinghausen neurofibromatosis region. Genes, Chromosomes & Cancer. 2: 271-7. PMID 2176541 DOI: 10.1002/Gcc.2870020404  1
1990 Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, Fountain JW, Brereton A, Nicholson J, Mitchell AL, Brownstein BH, Collins FS. Type 1 neurofibromatosis gene: Identification of a large transcript disrupted in three NF1 patients Science. 249: 181-186. PMID 2134734 DOI: 10.1126/Science.2134734  1
1990 Ballester R, Marchuk D, Boguski M, Saulino A, Letcher R, Wigler M, Collins F. The NF1 locus encodes a protein functionally related to mammalian GAP and yeast IRA proteins. Cell. 63: 851-9. PMID 2121371 DOI: 10.1016/0092-8674(90)90151-4  1
1988 Marchuk D, Collins FS. pYAC-RC, a yeast artificial chromosome vector for cloning DNA cut with infrequently cutting restriction endonucleases. Nucleic Acids Research. 16: 7743. PMID 3045765 DOI: 10.1093/Nar/16.15.7743  1
1987 Fuchs E, Tyner AL, Giudice GJ, Marchuk D, RayChaudhury A, Rosenberg M. The human keratin genes and their differential expression Current Topics in Developmental Biology. 22: 5-34. PMID 2443316 DOI: 10.1016/S0070-2153(08)60097-6  1
1985 Fuchs E, Hanukoglu I, Marchuk D, Grace MP, Kim KH. The nature and significance of differential keratin gene expression. Annals of the New York Academy of Sciences. 455: 436-50. PMID 2417525 DOI: 10.1111/J.1749-6632.1985.Tb50427.X  1
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