| Year |
Citation |
Score |
| 2023 |
Kemmler CL, Smolikova J, Moran HR, Mannion BJ, Knapp D, Lim F, Czarkwiani A, Aguayo VH, Rapp V, Fitch OE, Bötschi S, Selleri L, Farley E, Braasch I, Yun M, et al. Conserved enhancer logic controls the notochord expression of vertebrate . Biorxiv : the Preprint Server For Biology. PMID 37131681 DOI: 10.1101/2023.04.20.536761 |
0.343 |
|
| 2020 |
Long HK, Osterwalder M, Welsh IC, Hansen K, Davies JOJ, Liu YE, Koska M, Adams AT, Aho R, Arora N, Ikeda K, Williams RM, Sauka-Spengler T, Porteus MH, Mohun T, ... ... Selleri L, et al. Loss of Extreme Long-Range Enhancers in Human Neural Crest Drives a Craniofacial Disorder. Cell Stem Cell. PMID 32991838 DOI: 10.1016/j.stem.2020.09.001 |
0.309 |
|
| 2020 |
Cozzitorto C, Mueller L, Ruzittu S, Mah N, Willnow D, Darrigrand JF, Wilson H, Khosravinia D, Mahmoud AA, Risolino M, Selleri L, Spagnoli FM. A Specialized Niche in the Pancreatic Microenvironment Promotes Endocrine Differentiation. Developmental Cell. PMID 32857951 DOI: 10.1016/J.Devcel.2020.08.003 |
0.368 |
|
| 2020 |
Rajendiran S, Smith-Berdan S, Kunz L, Risolino M, Selleri L, Schroeder T, Forsberg EC. Ubiquitous overexpression of CXCL12 confers radiation protection and enhances mobilization of hematopoietic stem and progenitor cells. Stem Cells (Dayton, Ohio). PMID 32442338 DOI: 10.1002/Stem.3205 |
0.354 |
|
| 2019 |
Alankarage D, Szot JO, Pachter N, Slavotinek A, Selleri L, Shieh JT, Winlaw D, Giannoulatou E, Chapman G, Dunwoodie SL. Functional characterisation of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease. Human Molecular Genetics. PMID 31625560 DOI: 10.1093/Hmg/Ddz231 |
0.38 |
|
| 2019 |
Selleri L, Zappavigna V, Ferretti E. 'Building a perfect body': control of vertebrate organogenesis by PBX-dependent regulatory networks. Genes & Development. 33: 258-275. PMID 30824532 DOI: 10.1101/Gad.318774.118 |
0.377 |
|
| 2019 |
Young M, Selleri L, Capellini TD. Genetics of scapula and pelvis development: An evolutionary perspective. Current Topics in Developmental Biology. 132: 311-349. PMID 30797513 DOI: 10.1016/Bs.Ctdb.2018.12.007 |
0.365 |
|
| 2018 |
Welsh IC, Hart J, Brown JM, Hansen K, Rocha Marques M, Aho RJ, Grishina I, Hurtado R, Herzlinger D, Ferretti E, Garcia-Garcia MJ, Selleri L. Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface. Journal of Anatomy. PMID 29797482 DOI: 10.1111/Joa.12821 |
0.441 |
|
| 2018 |
Losa M, Risolino M, Li B, Hart J, Quintana L, Grishina I, Yang H, Choi IF, Lewicki P, Khan S, Aho R, Feenstra J, Vincent CT, Brown AMC, Ferretti E, ... ... Selleri L, et al. Face morphogenesis is promoted by Pbx-dependent EMT via regulation of Snail1 during frontonasal prominence fusion. Development (Cambridge, England). PMID 29437830 DOI: 10.1242/Dev.157628 |
0.38 |
|
| 2018 |
Shen Y, Jung J, Rahmanto YS, Selleri L, Shih I, Chuang C, Wang T. Abstract 1966: A novel small-molecule compound targeting PBX1-DNA interaction impedes cancer cell survival and carboplatin resistance Cancer Research. 78: 1966-1966. DOI: 10.1158/1538-7445.Am2018-1966 |
0.353 |
|
| 2017 |
McCulley DJ, Wienhold MD, Hines EA, Hacker TA, Rogers A, Pewowaruk RJ, Zewdu R, Chesler NC, Selleri L, Sun X. PBX transcription factors drive pulmonary vascular adaptation to birth. The Journal of Clinical Investigation. PMID 29251627 DOI: 10.1172/Jci93395 |
0.335 |
|
| 2017 |
Slavotinek A, Risolino M, Losa M, Cho MT, Monaghan KG, Schneidman-Duhovny D, Parisotto S, Herkert JC, Stegmann APA, Miller K, Shur N, Chui J, Muller E, DeBrosse S, Szot JO, ... ... Selleri L, et al. De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects. Human Molecular Genetics. PMID 29036646 DOI: 10.1093/Hmg/Ddx363 |
0.417 |
|
| 2016 |
Selleri L, Bartolomei MS, Bickmore WA, He L, Stubbs L, Reik W, Barsh GS. A Hox-Embedded Long Noncoding RNA: Is It All Hot Air? Plos Genetics. 12: e1006485. PMID 27977680 DOI: 10.1371/Journal.Pgen.1006485 |
0.339 |
|
| 2016 |
Jung JG, Shih IM, Park JT, Gerry E, Kim TH, Ayhan A, Handschuh K, Davidson B, Nickles Fader A, Selleri L, Wang TL. Ovarian cancer chemoresistance relies on the the stem cell reprogramming factor PBX1. Cancer Research. PMID 27590741 DOI: 10.1158/0008-5472.Can-16-0980 |
0.352 |
|
| 2016 |
Hanley O, Zewdu R, Cohen LJ, Jung H, Lacombe J, Philippidou P, Lee DH, Selleri L, Dasen JS. Parallel Pbx-Dependent Pathways Govern the Coalescence and Fate of Motor Columns. Neuron. PMID 27568519 DOI: 10.1016/J.Neuron.2016.07.043 |
0.313 |
|
| 2016 |
Villaescusa JC, Li B, Toledo EM, Rivetti di Val Cervo P, Yang S, Stott SR, Kaiser K, Islam S, Gyllborg D, Laguna-Goya R, Landreh M, Lönnerberg P, Falk A, Bergman T, Barker RA, ... ... Selleri L, et al. A PBX1 transcriptional network controls dopaminergic neuron development and is impaired in Parkinson's disease. The Embo Journal. PMID 27354364 DOI: 10.15252/Embj.201593725 |
0.564 |
|
| 2016 |
Grebbin BM, Hau AC, Groß A, Anders-Maurer M, Schramm J, Koss M, Wille C, Mittelbronn M, Selleri L, Schulte D. Pbx1 is required for adult SVZ neurogenesis. Development (Cambridge, England). PMID 27226325 DOI: 10.1242/Dev.128033 |
0.753 |
|
| 2016 |
Zewdu R, Risolino M, Barbulescu A, Ramalingam P, Butler JM, Selleri L. Spleen hypoplasia leads to abnormal stress hematopoiesis in mice with loss of Pbx homeoproteins in splenic mesenchyme. Journal of Anatomy. PMID 27075259 DOI: 10.1111/Joa.12479 |
0.375 |
|
| 2015 |
Prescott SL, Srinivasan R, Marchetto MC, Grishina I, Narvaiza I, Selleri L, Gage FH, Swigut T, Wysocka J. Enhancer Divergence and cis-Regulatory Evolution in the Human and Chimp Neural Crest. Cell. 163: 68-83. PMID 26365491 DOI: 10.1016/J.Cell.2015.08.036 |
0.344 |
|
| 2014 |
Vierstra J, Rynes E, Sandstrom R, Zhang M, Canfield T, Hansen RS, Stehling-Sun S, Sabo PJ, Byron R, Humbert R, Thurman RE, Johnson AK, Vong S, Lee K, Bates D, ... ... Selleri L, et al. Mouse regulatory DNA landscapes reveal global principles of cis-regulatory evolution. Science (New York, N.Y.). 346: 1007-12. PMID 25411453 DOI: 10.1126/Science.1246426 |
0.344 |
|
| 2014 |
Yue F, Cheng Y, Breschi A, Vierstra J, Wu W, Ryba T, Sandstrom R, Ma Z, Davis C, Pope BD, Shen Y, Pervouchine DD, Djebali S, Thurman RE, Kaul R, ... ... Selleri L, et al. A comparative encyclopedia of DNA elements in the mouse genome. Nature. 515: 355-64. PMID 25409824 DOI: 10.1038/Nature13992 |
0.382 |
|
| 2014 |
Handschuh K, Feenstra J, Koss M, Ferretti E, Risolino M, Zewdu R, Sahai MA, Bénazet JD, Peng XP, Depew MJ, Quintana L, Sharpe J, Wang B, Alcorn H, Rivi R, ... ... Selleri L, et al. ESCRT-II/Vps25 constrains digit number by endosome-mediated selective modulation of FGF-SHH signaling. Cell Reports. 9: 674-87. PMID 25373905 DOI: 10.1016/J.Celrep.2014.09.019 |
0.718 |
|
| 2014 |
Li W, Lin CY, Shang C, Han P, Xiong Y, Lin CJ, Yang J, Selleri L, Chang CP. Pbx1 activates Fgf10 in the mesenchyme of developing lungs. Genesis (New York, N.Y. : 2000). 52: 399-407. PMID 24591256 DOI: 10.1002/Dvg.22764 |
0.34 |
|
| 2013 |
Hall KC, Hill D, Otero M, Plumb DA, Froemel D, Dragomir CL, Maretzky T, Boskey A, Crawford HC, Selleri L, Goldring MB, Blobel CP. ADAM17 controls endochondral ossification by regulating terminal differentiation of chondrocytes. Molecular and Cellular Biology. 33: 3077-90. PMID 23732913 DOI: 10.1128/Mcb.00291-13 |
0.365 |
|
| 2013 |
Bolze A, Mahlaoui N, Byun M, Turner B, Trede N, Ellis SR, Abhyankar A, Itan Y, Patin E, Brebner S, Sackstein P, Puel A, Picard C, Abel L, Quintana-Murci L, ... ... Selleri L, et al. Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia. Science (New York, N.Y.). 340: 976-8. PMID 23579497 DOI: 10.1126/Science.1234864 |
0.315 |
|
| 2012 |
Feldhahn N, Ferretti E, Robbiani DF, Callen E, Deroubaix S, Selleri L, Nussenzweig A, Nussenzweig MC. The hSSB1 orthologue Obfc2b is essential for skeletogenesis but dispensable for the DNA damage response in vivo. The Embo Journal. 31: 4045-56. PMID 22940690 DOI: 10.1038/Emboj.2012.247 |
0.342 |
|
| 2012 |
Koss M, Bolze A, Brendolan A, Saggese M, Capellini TD, Bojilova E, Boisson B, Prall OW, Elliott DA, Solloway M, Lenti E, Hidaka C, Chang CP, Mahlaoui N, Harvey RP, ... ... Selleri L, et al. Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module. Developmental Cell. 22: 913-26. PMID 22560297 DOI: 10.1016/J.Devcel.2012.02.009 |
0.729 |
|
| 2012 |
Hernandez K, Selleri L, Spector J, Pino A, Reiffel A, Ferretti E. Abstract 106: Time Course and Gene Expression Analysis of Infant Mouse Model of Re-Synostosis Plastic and Reconstructive Surgery. 130: 77. DOI: 10.1097/01.Prs.0000416189.67993.6C |
0.306 |
|
| 2012 |
Ferretti E, Hernandez KA, Reiffel AJ, Hart J, Spector JA, Selleri L. Repair of cleft lip in utero by reactivation of craniofacial developmental programs Journal of the American College of Surgeons. 215. DOI: 10.1016/J.Jamcollsurg.2012.06.097 |
0.365 |
|
| 2011 |
Ferretti E, Li B, Zewdu R, Wells V, Hebert JM, Karner C, Anderson MJ, Williams T, Dixon J, Dixon MJ, Depew MJ, Selleri L. A conserved Pbx-Wnt-p63-Irf6 regulatory module controls face morphogenesis by promoting epithelial apoptosis. Developmental Cell. 21: 627-41. PMID 21982646 DOI: 10.1016/J.Devcel.2011.08.005 |
0.395 |
|
| 2011 |
Gordon JA, Hassan MQ, Koss M, Montecino M, Selleri L, van Wijnen AJ, Stein JL, Stein GS, Lian JB. Epigenetic regulation of early osteogenesis and mineralized tissue formation by a HOXA10-PBX1-associated complex. Cells, Tissues, Organs. 194: 146-50. PMID 21597276 DOI: 10.1159/000324790 |
0.747 |
|
| 2011 |
Vitobello A, Ferretti E, Lampe X, Vilain N, Ducret S, Ori M, Spetz JF, Selleri L, Rijli FM. Hox and Pbx factors control retinoic acid synthesis during hindbrain segmentation. Developmental Cell. 20: 469-82. PMID 21497760 DOI: 10.1016/J.Devcel.2011.03.011 |
0.344 |
|
| 2011 |
Capellini TD, Handschuh K, Quintana L, Ferretti E, Di Giacomo G, Fantini S, Vaccari G, Clarke SL, Wenger AM, Bejerano G, Sharpe J, Zappavigna V, Selleri L. Control of pelvic girdle development by genes of the Pbx family and Emx2. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 240: 1173-89. PMID 21455939 DOI: 10.1002/Dvdy.22617 |
0.393 |
|
| 2011 |
Capellini TD, Zappavigna V, Selleri L. Pbx homeodomain proteins: TALEnted regulators of limb patterning and outgrowth. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 240: 1063-86. PMID 21416555 DOI: 10.1002/Dvdy.22605 |
0.415 |
|
| 2010 |
Capellini TD, Vaccari G, Ferretti E, Fantini S, He M, Pellegrini M, Quintana L, Di Giacomo G, Sharpe J, Selleri L, Zappavigna V. Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1. Development (Cambridge, England). 137: 2559-69. PMID 20627960 DOI: 10.1242/Dev.048819 |
0.4 |
|
| 2009 |
Mercader N, Selleri L, Criado LM, Pallares P, Parras C, Cleary ML, Torres M. Ectopic Meis1 expression in the mouse limb bud alters P-D patterning in a Pbx1-independent manner. The International Journal of Developmental Biology. 53: 1483-94. PMID 19247936 DOI: 10.1387/Ijdb.072430Nm |
0.392 |
|
| 2008 |
Capellini TD, Dunn MP, Passamaneck YJ, Selleri L, Di Gregorio A. Conservation of notochord gene expression across chordates: insights from the Leprecan gene family. Genesis (New York, N.Y. : 2000). 46: 683-96. PMID 18798549 DOI: 10.1002/Dvg.20406 |
0.415 |
|
| 2008 |
Stankunas K, Shang C, Twu KY, Kao SC, Jenkins NA, Copeland NG, Sanyal M, Selleri L, Cleary ML, Chang CP. Pbx/Meis deficiencies demonstrate multigenetic origins of congenital heart disease. Circulation Research. 103: 702-9. PMID 18723445 DOI: 10.1161/Circresaha.108.175489 |
0.331 |
|
| 2008 |
Capellini TD, Zewdu R, Di Giacomo G, Asciutti S, Kugler JE, Di Gregorio A, Selleri L. Pbx1/Pbx2 govern axial skeletal development by controlling Polycomb and Hox in mesoderm and Pax1/Pax9 in sclerotome. Developmental Biology. 321: 500-14. PMID 18691704 DOI: 10.1016/J.Ydbio.2008.04.005 |
0.41 |
|
| 2007 |
Chung EY, Liu J, Homma Y, Zhang Y, Brendolan A, Saggese M, Han J, Silverstein R, Selleri L, Ma X. Interleukin-10 expression in macrophages during phagocytosis of apoptotic cells is mediated by homeodomain proteins Pbx1 and Prep-1. Immunity. 27: 952-64. PMID 18093541 DOI: 10.1016/J.Immuni.2007.11.014 |
0.335 |
|
| 2007 |
Yeh N, Miller JP, Gaur T, Capellini TD, Nikolich-Zugich J, de la Hoz C, Selleri L, Bromage TG, van Wijnen AJ, Stein GS, Lian JB, Vidal A, Koff A. Cooperation between p27 and p107 during endochondral ossification suggests a genetic pathway controlled by p27 and p130. Molecular and Cellular Biology. 27: 5161-71. PMID 17502351 DOI: 10.1128/Mcb.02431-06 |
0.345 |
|
| 2007 |
Sanyal M, Tung JW, Karsunky H, Zeng H, Selleri L, Weissman IL, Herzenberg LA, Cleary ML. B-cell development fails in the absence of the Pbx1 proto-oncogene. Blood. 109: 4191-9. PMID 17244677 DOI: 10.1182/Blood-2006-10-054213 |
0.34 |
|
| 2007 |
Brendolan A, Rosado MM, Carsetti R, Selleri L, Dear TN. Development and function of the mammalian spleen. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 29: 166-77. PMID 17226804 DOI: 10.1002/Bies.20528 |
0.36 |
|
| 2006 |
Zhang X, Rowan S, Yue Y, Heaney S, Pan Y, Brendolan A, Selleri L, Maas RL. Pax6 is regulated by Meis and Pbx homeoproteins during pancreatic development. Developmental Biology. 300: 748-57. PMID 17049510 DOI: 10.1016/J.Ydbio.2006.06.030 |
0.378 |
|
| 2006 |
Ferretti E, Villaescusa JC, Di Rosa P, Fernandez-Diaz LC, Longobardi E, Mazzieri R, Miccio A, Micali N, Selleri L, Ferrari G, Blasi F. Hypomorphic mutation of the TALE gene Prep1 (pKnox1) causes a major reduction of Pbx and Meis proteins and a pleiotropic embryonic phenotype. Molecular and Cellular Biology. 26: 5650-62. PMID 16847320 DOI: 10.1128/Mcb.00313-06 |
0.405 |
|
| 2006 |
Capellini TD, Di Giacomo G, Salsi V, Brendolan A, Ferretti E, Srivastava D, Zappavigna V, Selleri L. Pbx1/Pbx2 requirement for distal limb patterning is mediated by the hierarchical control of Hox gene spatial distribution and Shh expression. Development (Cambridge, England). 133: 2263-73. PMID 16672333 DOI: 10.1242/Dev.02395 |
0.422 |
|
| 2006 |
Moens CB, Selleri L. Hox cofactors in vertebrate development. Developmental Biology. 291: 193-206. PMID 16515781 DOI: 10.1016/J.Ydbio.2005.10.032 |
0.349 |
|
| 2006 |
Di Giacomo G, Koss M, Capellini TD, Brendolan A, Pöpperl H, Selleri L. Spatio-temporal expression of Pbx3 during mouse organogenesis. Gene Expression Patterns : Gep. 6: 747-57. PMID 16434237 DOI: 10.1016/J.Modgep.2005.12.002 |
0.752 |
|
| 2005 |
Brendolan A, Ferretti E, Salsi V, Moses K, Quaggin S, Blasi F, Cleary ML, Selleri L. A Pbx1-dependent genetic and transcriptional network regulates spleen ontogeny. Development (Cambridge, England). 132: 3113-26. PMID 15944191 DOI: 10.1242/Dev.01884 |
0.425 |
|
| 2004 |
Manley NR, Selleri L, Brendolan A, Gordon J, Cleary ML. Abnormalities of caudal pharyngeal pouch development in Pbx1 knockout mice mimic loss of Hox3 paralogs. Developmental Biology. 276: 301-12. PMID 15581866 DOI: 10.1016/J.Ydbio.2004.08.030 |
0.412 |
|
| 2004 |
Rhee JW, Arata A, Selleri L, Jacobs Y, Arata S, Onimaru H, Cleary ML. Pbx3 deficiency results in central hypoventilation. The American Journal of Pathology. 165: 1343-50. PMID 15466398 DOI: 10.1016/S0002-9440(10)63392-5 |
0.428 |
|
| 2004 |
Selleri L, DiMartino J, van Deursen J, Brendolan A, Sanyal M, Boon E, Capellini T, Smith KS, Rhee J, Pöpperl H, Grosveld G, Cleary ML. The TALE homeodomain protein Pbx2 is not essential for development and long-term survival. Molecular and Cellular Biology. 24: 5324-31. PMID 15169896 DOI: 10.1128/Mcb.24.12.5324-5331.2004 |
0.414 |
|
| 2003 |
Schnabel CA, Selleri L, Cleary ML. Pbx1 is essential for adrenal development and urogenital differentiation. Genesis (New York, N.Y. : 2000). 37: 123-30. PMID 14595835 DOI: 10.1002/Gene.10235 |
0.453 |
|
| 2001 |
DiMartino JF, Selleri L, Traver D, Firpo MT, Rhee J, Warnke R, O'Gorman S, Weissman IL, Cleary ML. The Hox cofactor and proto-oncogene Pbx1 is required for maintenance of definitive hematopoiesis in the fetal liver. Blood. 98: 618-26. PMID 11468159 DOI: 10.1182/Blood.V98.3.618 |
0.395 |
|
| 2001 |
Schnabel CA, Selleri L, Jacobs Y, Warnke R, Cleary ML. Expression of Pbx1b during mammalian organogenesis Mechanisms of Development. 100: 131-135. PMID 11118899 DOI: 10.1016/S0925-4773(00)00516-5 |
0.444 |
|
| 1999 |
Wlodarska I, Selleri L, Starza RL, Paternotte C, Evans GA, Boogaerts M, Berghe HVd, Mecucci C. Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation. Genes, Chromosomes and Cancer. 24: 199-206. PMID 10451699 DOI: 10.1002/(Sici)1098-2264(199903)24:3<199::Aid-Gcc4>3.0.Co;2-V |
0.301 |
|
| 1997 |
Velcich A, Palumbo L, Selleri L, Evans G, Augenlicht L. Organization and Regulatory Aspects of the Human Intestinal Mucin Gene (MUC2) Locus Journal of Biological Chemistry. 272: 7968-7976. PMID 9065467 DOI: 10.1074/Jbc.272.12.7968 |
0.434 |
|
| 1995 |
Tsang P, Gilles F, Yuan L, Kuo Y, Lupu F, Samara G, Moosikasuwan J, Goye A, Zelenetz AD, Selleri L, Tycko B. A novel L23-related gene 40 kb downstream of the imprinted H19 gene is biallelically expressed in mid-fetal and adult human tissues Human Molecular Genetics. 4: 1499-1507. PMID 8541832 DOI: 10.1093/Hmg/4.9.1499 |
0.396 |
|
| 1994 |
Selleri L, Giovannini M, Romo A, Zucman J, Delattre O, Thomas G, Evans GA. Cloning of the entire FLI1 gene, disrupted by the Ewing's sarcoma translocation breakpoint on 11q24, in a yeast artificial chromosome. Cytogenetic and Genome Research. 67: 129-136. PMID 8039423 DOI: 10.1159/000133813 |
0.31 |
|
| 1994 |
Selleri L, Giovannini M, Hermanson GG, Romo A, Quackenbush J, Penny L, Khristich JV, Evans GA. Yeast Artificial Chromosome Cloning of 3.2 Megabases within Chromosomal Band 11q24 Closely Linking c-ets 1 and Fli-1 and Encompassing the Ewing Sarcoma Breakpoint Genomics. 22: 137-147. PMID 7959760 DOI: 10.1006/Geno.1994.1354 |
0.309 |
|
| 1993 |
Giovannini M, Selleri L, Hermanson GG, Evans GA. Localization of the human oncostatin M gene (OSM) to chromosome 22q12, distal to the Ewing's sarcoma breakpoint. Cytogenetics and Cell Genetics. 62: 32-4. PMID 8422753 DOI: 10.1159/000133439 |
0.325 |
|
| 1993 |
Giovannini M, Djabali M, McElligott D, Selleri L, Evans GA. Tandem linkage of genes coding for leukemia inhibitory factor (LIF) and oncostatin M (OSM) on human chromosome 22 Cytogenetic and Genome Research. 64: 240-244. PMID 8404048 DOI: 10.1159/000133586 |
0.349 |
|
| 1992 |
Eubanks JH, Djabali M, Selleri L, Grandy DK, Civelli O, McElligott DL, Evans GA. Structure and linkage of the D2 dopamine receptor and neural cell adhesion molecule genes on human chromosome 11q23. Genomics. 14: 1010-8. PMID 1478642 DOI: 10.1016/S0888-7543(05)80124-7 |
0.341 |
|
| 1992 |
Saleh M, Selleri L, Little PFR, Evans GA. Isolation and expression of linked zinc finger gene clusters on human chromosome 11q. Genomics. 14: 970-978. PMID 1339395 DOI: 10.1016/S0888-7543(05)80119-3 |
0.391 |
|
| 1992 |
Djabali M, Selleri L, Parry P, Bower M, Young BD, Evans GA. A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias. Nature Genetics. 2: 113-118. PMID 1303259 DOI: 10.1038/Ng1092-113 |
0.344 |
|
| 1990 |
Sacchi S, Artusi T, Selleri L, Temperani P, Zucchini P, Vecchi A, Emilia G, Torelli U. Sinus histiocytosis with massive lymphadenopathy: immunological, cytogenetic and molecular studies. Annals of Hematology. 60: 339-344. PMID 2375964 DOI: 10.1007/Bf01737849 |
0.305 |
|
| 1990 |
Sacchi S, Temperani P, Selleri L, Zucchini P, Morselli S, Vecchi A, Longo R, Torelli G, Emilia G, Torelli U. Extramedullary pleural blast crisis in chronic myelogenous leukemia: cytogenetic and molecular study. Acta Haematologica. 83: 198-202. PMID 2115717 DOI: 10.1159/000205213 |
0.301 |
|
| 1990 |
Selleri L, Lindern Mv, Hermans A, Meijer D, Torelli G, Grosveld G. Chronic myeloid leukemia may be associated with several bcr-abl transcripts including the acute lymphoid leukemia-type 7 kb transcript. Blood. 75: 1146-1153. DOI: 10.1182/Blood.V75.5.1146.1146 |
0.335 |
|
| 1989 |
Emilia G, Temperani P, Ferrari S, Zucchini P, Tagliafico E, Selleri L, Torelli G, Artusi T, Torelli U. Cytogenetic and molecular studies in primary myelofibrosis. Cancer Genetics and Cytogenetics. 38: 101-113. PMID 2713806 DOI: 10.1016/0165-4608(89)90170-2 |
0.339 |
|
| 1988 |
Ferrari S, Mariano MT, Tagliafico E, Sarti M, Ceccherelli G, Selleri L, Merli F, Narni F, Donelli A, Torelli G. Myeloperoxidase gene expression in blast cells with a lymphoid phenotype in cases of acute lymphoblastic leukemia. Blood. 72: 873-876. DOI: 10.1182/Blood.V72.3.873.873 |
0.339 |
|
| 1987 |
Donelli A, Narni F, Tabilio A, Emilia G, Selleri L, Colo A, Zucchini P, Montagnani G, Torelli G, Torelli U. Establishment and characterization of a human IgA‐κ‐secreting plasma cell line (MT3) International Journal of Cancer. 40: 383-388. PMID 3114153 DOI: 10.1002/Ijc.2910400317 |
0.314 |
|
| 1987 |
Torelli UL, Torelli GM, Emilia G, Selleri L, Venturelli D, Artusi T, Donelli A, Colò A, Fornieri C. Simultaneously increased expression of the c-myc and mu chain genes in the acute blastic transformation of a chronic lymphocytic leukaemia. British Journal of Haematology. 65: 165-170. PMID 3103669 DOI: 10.1111/J.1365-2141.1987.Tb02259.X |
0.315 |
|
| 1987 |
Selleri L, Narni F, Emilia G, Colo A, Zucchini P, Venturelli D, Donelli A, Torelli U, Torelli G. Philadelphia-positive chronic myeloid leukemia with a chromosome 22 breakpoint outside the breakpoint cluster region. Blood. 70: 1659-1664. DOI: 10.1182/Blood.V70.5.1659.Bloodjournal7051659 |
0.321 |
|
| 1986 |
Emilia G, Donelli A, Ferrari S, Torelli U, Selleri L, Zucchini P, Moretti L, Venturelli D, Ceccherelli G, Torelli G. Cellular levels of mRNA from c-myc, c-myb and c-fes onc-genes in normal myeloid anderythroid precursors of human bone marrow: an in situ hybridization study British Journal of Haematology. 62: 287-292. PMID 3947550 DOI: 10.1111/J.1365-2141.1986.Tb02931.X |
0.311 |
|
| 1986 |
Torelli U, Selleri L, Venturelli D, Donelli A, Emilia G, Ceccherelli G, Turchi L, Torelli G. Differential patterns of expression of cell cycle-related genes in blast cells of acute myeloid leukemia Leukemia Research. 10: 1249-1254. PMID 3464813 DOI: 10.1016/0145-2126(86)90244-4 |
0.369 |
|
| 1985 |
Torelli G, Selleri L, Donelli A, Ferrari S, Emilia G, Venturelli D, Moretti L, Torelli U. Activation of c-myb expression by phytohemagglutinin stimulation in normal human T lymphocytes. Molecular and Cellular Biology. 5: 2874-2877. PMID 3915538 DOI: 10.1128/Mcb.5.10.2874 |
0.308 |
|
| 1985 |
Ferrari S, Torelli U, Selleri L, Donelli A, Venturelli D, Narni F, Moretti L, Torelli G. Study of the levels of expression of two oncogenes, c-myc and c-myb, in acute and chronic leukemias of both lymphoid and myeloid lineage. Leukemia Research. 9: 833-842. PMID 3860696 DOI: 10.1016/0145-2126(85)90304-2 |
0.336 |
|
| 1985 |
Ferrari S, Torelli U, Selleri L, Donelli A, Venturelli D, Moretti L, Torelli G. Expression of human c‐fes one‐gene occurs at detectable levels in myeloid but not in lymphoid cell populations British Journal of Haematology. 59: 21-25. PMID 3855647 DOI: 10.1111/J.1365-2141.1985.Tb02959.X |
0.348 |
|
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