Works by Rocchi, Mariano

Results: 64

Refinement of macaque synteny arrangement with respect to the official rheMac2 macaque sequence assembly.

Published in:

Chromosome Research, 2008, v. 16, n. 7, p. 977, doi. 10.1007/s10577-008-1255-1

By:

Roberta Roberto;
Doriana Misceo;
Pietro D’Addabbo;
Nicoletta Archidiacono;
Mariano Rocchi

Publication type:

Article

Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2.

Published in:

Human Mutation, 2007, v. 28, n. 5, p. 459, doi. 10.1002/humu.20465

By:

Giorda, Roberto;
Ciccone, Roberto;
Gimelli, Giorgio;
Pramparo, Tiziano;
Beri, Silvana;
Bonaglia, Maria Clara;
Giglio, Sabrina;
Genuardi, Maurizio;
Argente, Jesùs;
Rocchi, Mariano;
Zuffardi, Orsetta

Publication type:

Article

A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 10, p. 797, doi. 10.1038/sj.ejhg.5201203

By:

Zollino, Marcella;
Lecce, Rosetta;
Selicorni, Angelo;
Murdolo, Marina;
Mancuso, Irene;
Marangi, Giuseppe;
Zampino, Giuseppe;
Garavelli, Livia;
Ferrarini, Alessandra;
Rocchi, Mariano;
Opitz, John M;
Neri, Giovanni

Publication type:

Article

Inverted duplications: how many of them are mosaic?

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 9, p. 713, doi. 10.1038/sj.ejhg.5201240

By:

Pramparo, Tiziano;
Giglio, Sabrina;
Gregato, Giuliana;
De Gregori, Manuela;
Patricelli, Maria Grazia;
Ciccone, Roberto;
Scappaticci, Susi;
Mannino, Gaetano;
Lombardi, Claudio;
Pirola, Barbara;
Giorda, Roberto;
Rocchi, Mariano;
Zuffardi, Orsetta

Publication type:

Article

Saturating density of STSs (1/6 kb) in a 1.1 Mb region on 3q28-q29: a valuable resource for cloning of disease genes.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 4, p. 307, doi. 10.1038/sj.ejhg.5200630

By:

Alexander, Christiane;
Bernstein, Steven L;
Rocchi, Mariano;
Auburger, Georg

Publication type:

Article

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome.

Published in:

Nature Genetics, 2001, v. 27, n. 2, p. 159, doi. 10.1038/84781

By:

Crisponi, Laura;
Deiana, Manila;
Loi, Angela;
Chiappe, Francesca;
Uda, Manuela;
Amati, Patrizia;
Bisceglia, Luigi;
Zelante, Leopoldo;
Nagaraja, Ramaiah;
Porcu, Susanna;
Serafina Ristaldi, M.;
Marzella, Rosalia;
Rocchi, Mariano;
Nicolino, Marc;
Lienhardt-Roussie, Anne;
Nivelon, Annie;
Verloes, Alain;
Schlessinger, David;
Gasparini, Paolo

Publication type:

Article

DDXIIL: a novel transcript family emerging from human subtelomeric regions.

Published in:

BMC Genomics, 2009, v. 10, p. 250, doi. 10.1186/1471-2164-10-250

By:

Costa, Valerio;
Casamassimi, Amelia;
Roberto, Roberta;
Gianfrancesco, Fernando;
Matarazzo, Maria R.;
D'Urso, Michele;
D'Esposito, Maurizio;
Rocchi, Mariano;
Ciccodicola, Alfredo

Publication type:

Article

Translocation–excision–deletion–amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1This text presents research results of the Belgian program of Interuniversity Poles of attraction initiated by the Belgian State, Prime Minister's Office, Science Policy Programming (IUAP).

Published in:

Genes, Chromosomes & Cancer, 2006, v. 45, n. 2, p. 107, doi. 10.1002/gcc.20272

By:

Nadine Van Roy;
Jo Vandesompele;
Björn Menten;
Helén Nilsson;
Els De Smet;
Mariano Rocchi;
Anne De Paepe;
Sven Påhlman;
Frank Speleman

Publication type:

Article

Insertions generating the 5′RUNX1/3′CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints.

Published in:

Genes, Chromosomes & Cancer, 2004, v. 41, n. 1, p. 86, doi. 10.1002/gcc.20061

By:

Giorgina Specchia;
Francesco Albano;
Luisa Anelli;
Antonella Zagaria;
Arcangelo Liso;
Roberta La Starza;
Marco Mancini;
Lucia Sebastio;
Emilia Giugliano;
Giuseppe Saglio;
Vincenzo Liso;
Mariano Rocchi

Publication type:

Article

Heterogeneous pattern of chromosomal breakpoints involving the MYC locus in multiple myeloma.

Published in:

Genes, Chromosomes & Cancer, 2003, v. 37, n. 3, p. 261, doi. 10.1002/gcc.10211

By:

Sonia Fabris;
Clelia Tiziana Storlazzi;
Luca Baldini;
Lucia Nobili;
Luigia Lombardi;
Anna Teresa Maiolo;
Mariano Rocchi;
Antonino Neri

Publication type:

Article

Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases.

Published in:

Genes, Chromosomes & Cancer, 2003, v. 36, n. 4, p. 353, doi. 10.1002/gcc.10183

By:

Francesco Albano;
Giorgina Specchia;
Luisa Anelli;
Antonella Zagaria;
Clelia Tiziana Storlazzi;
Caterina Buquicchio;
Maria Grazia Roberti;
Vincenzo Liso;
Mariano Rocchi

Publication type:

Article

Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients.

Published in:

Genes, Chromosomes & Cancer, 2002, v. 35, n. 3, p. 271, doi. 10.1002/gcc.10116

By:

Storlazzi, Clelia T.;
Specchia, Giorgina;
Anelli, Luisa;
Albano, Francesco;
Pastore, Domenico;
Zagaria, Antonella;
Rocchi, Mariano;
Liso, Vincenzo

Publication type:

Article

The nm23 gene maps to human chromosome band 17q22 and shows a restriction fragment length polymorphism with bg/II.

Published in:

Genes, Chromosomes & Cancer, 1992, v. 4, n. 1, p. 84, doi. 10.1002/gcc.2870040113

By:

Varesco, Lillana;
Caligo, Maria A.;
Nardini, Vincenzo;
Bevilacqua, Generoso;
Casarino, Lucia;
Ferrar, Giovanbattista;
Simi, Paolo;
Rocchi, Mariano;
Black, Donald M.;
Solomon, Ellen

Publication type:

Article

Derivative Chromosome 9 Deletions in Chronic Myeloid Leukemia are Associated with Loss of Tumor Suppressor Genes.

Published in:

Leukemia & Lymphoma, 2004, v. 45, n. 4, p. 689, doi. 10.1080/10428190310001623900

By:

Specchia, Giorgina;
Albano, Francesco;
Anelli, Luisa;
Storlazzi, Clelia Tiziana;
Zagaria, Antonella;
Liso, Arcangelo;
Pannunzio, Alessandra;
Pastore, Domenico;
Mestice, Anna;
Greco, Giuseppina;
Liso, Vincenzo;
Rocchi, Mariano

Publication type:

Article

De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup(15)s.

Published in:

PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0039180

By:

Rossi, Elena;
Giorda, Roberto;
Bonaglia, Maria Clara;
Di Candia, Stefania;
Grechi, Elena;
Franzese, Adriana;
Soli, Fiorenza;
Rivieri, Francesca;
Patricelli, Maria Grazia;
Saccilotto, Donatella;
Bonfante, Aldo;
Giglio, Sabrina;
Beri, Silvana;
Rocchi, Mariano;
Zuffardi, Orsetta

Publication type:

Article

Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication.

Published in:

1995

By:

Uncini, Antonio;
Di Guglielmo, Giovanni;
Di Muzio, Antonio;
Gambi, Domenico;
Sabatelli, Mario;
Mignogna, Teresa;
Tonali, Pietro;
Marzella, Rosalia;
Finelli, Palma;
Archidiacono, Nicoletta;
Rocchi, Mariano;
Uncini, A;
Di Guglielmo, G;
Di Muzio, A;
Gambi, D;
Sabatelli, M;
Mignogna, T;
Tonali, P;
Marzella, R;
Finelli, P

Publication type:

journal article

Human centromere repositioning activates transcription and opens chromatin fibre structure.

Published in:

Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33426-2

By:

Naughton, Catherine;
Huidobro, Covadonga;
Catacchio, Claudia R.;
Buckle, Adam;
Grimes, Graeme R.;
Nozawa, Ryu-Suke;
Purgato, Stefania;
Rocchi, Mariano;
Gilbert, Nick

Publication type:

Article

Organization and Evolution of Primate Centromeric DNA from Whole-Genome Shotgun Sequence Data.

Published in:

PLoS Computational Biology, 2007, v. 3, n. 9, p. 1807, doi. 10.1371/journal.pcbi.0030181

By:

Alkan, Can;
Ventura, Mario;
Archidiacono, Nicoletta;
Rocchi, Mariano;
Sahinalp, S. Cenk;
Eichler, Evan E.

Publication type:

Article

Episomal amplification of MYCN in a case of medulloblastoma.

Published in:

Virchows Archiv: European Journal of Pathology, 2008, v. 452, n. 5, p. 491

By:

Florence Pedeutour;
Domenico Trombetta;
Fanny Burel-Vandenbos;
Mariano Rocchi;
Clelia Storlazzi

Publication type:

Article

Direct duplication 12p11.21–p13.31 mediated by segmental duplications: a new recurrent rearrangement?

Published in:

Human Genetics, 2005, v. 118, n. 2, p. 207, doi. 10.1007/s00439-005-0008-x

By:

De Gregori, Manuela;
Pramparo, Tiziano;
Memo, Luigi;
Gimelli, Giorgio;
Messa, Jole;
Rocchi, Mariano;
Patricelli, Maria Grazia;
Ciccone, Roberto;
Giorda, Roberto;
Zuffardi, Orsetta

Publication type:

Article

Reciprocal translocations: a trap for cytogenetists?

Published in:

Human Genetics, 2005, v. 117, n. 6, p. 571, doi. 10.1007/s00439-005-1324-x

By:

Ciccone, Roberto;
Giorda, Roberto;
Gregato, Giuliana;
Guerrini, Renzo;
Giglio, Sabrina;
Carrozzo, Romeo;
Bonaglia, Maria Clara;
Priolo, Emanuela;
Laganà, Carmelo;
Tenconi, Romano;
Rocchi, Mariano;
Pramparo, Tiziano;
Zuffardi, Orsetta;
Rossi, Elena

Publication type:

Article

AcroM fluorescent in situ hybridization analyses of marker chromosomes.

Published in:

Human Genetics, 2001, v. 109, n. 2, p. 152, doi. 10.1007/s004390100571

By:

Langer, Sabine;
Fauth, Christine;
Rocchi, Mariano;
Murken, Jan;
Speicher, Michael R.

Publication type:

Article

A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 199, doi. 10.1007/s004390100459

By:

Nietzel, Angela;
Rocchi, Mariano;
Starke, Heike;
Heller, Anita;
Fiedler, Wolfgang;
Wlodarska, Iwona;
Loncarevic, Ivan F.;
Beensen, Volkmar;
Claussen, Uwe;
Liehr, Thomas

Publication type:

Article

The Hidden Genomic and Transcriptomic Plasticity of Giant Marker Chromosomes in Cancer.

Published in:

Genetics, 2018, v. 208, n. 3, p. 951, doi. 10.1534/genetics.117.300552

By:

Macchia, Gemma;
Severgnini, Marco;
Purgato, Stefania;
Tolomeo, Doron;
Casciaro, Hilen;
Cifola, Ingrid;
L'Abbate, Alberto;
Loverro, Anna;
Palumbo, Orazio;
Carella, Massimo;
Bianchini, Laurence;
Perini, Giovanni;
De Bellis, Gianluca;
Mertens, Fredrik;
Rocchi, Mariano;
Storlazzi, Clelia Tiziana

Publication type:

Article

Epigenetic origin of evolutionary novel centromeres.

Published in:

Scientific Reports, 2017, p. 41980, doi. 10.1038/srep41980

By:

Tolomeo, Doron;
Capozzi, Oronzo;
Stanyon, Roscoe R.;
Archidiacono, Nicoletta;
D'Addabbo, Pietro;
Catacchio, Claudia R.;
Purgato, Stefania;
Perini, Giovanni;
Schempp, Werner;
Huddleston, John;
Malig, Maika;
Eichler, Evan E.;
Rocchi, Mariano

Publication type:

Article

Two murine and human homologs of mab-21, a cell fate determination gene involved in neural development.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 13, p. 2397, doi. 10.1093/hmg/8.13.2397

By:

Mariani, Margherita;
Baldessari, Danila;
Francisconi, Simona;
Viggiano, Luigi;
Rocchi, Mariano;
Zappavigna, Vincenzo;
Malgaretti, Nicoletta;
Consalez, G. Giacomo

Publication type:

Article

Differential Expression Pattern of XqPAR-Linked Genes SYBL1 and IL9R Correlates with the Structure and Evolution of the Region.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 11, p. 1917, doi. 10.1093/hmg/6.11.1917

By:

D'Esposito, Maurizio;
Matarazzo, Maria Rosaria;
Ciccodicola, Alfredo;
Strazzullo, Maria;
Mazzarella, Richard;
Quaderi, Nandita A.;
Fujiwara, Hiroyuki;
Ko, Minoru S. H.;
Rowe, Lucy B.;
Ricco, Angela;
Archidiacono, Nicoletta;
Rocchi, Mariano;
Schlessinger, David;
D'Urso, Michele

Publication type:

Article

Interchromosomal Duplications of the Adrenoleukodystrophy Locus: A Phenomenon of Pericentromeric Plasticity.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 7, p. 991, doi. 10.1093/hmg/6.7.991

By:

Eichler, Evan E.;
Budarf, Marcia L.;
Rocchi, Mariano;
Deaven, Larry L.;
Doggett, Norman A.;
Baldini, Antonio;
Nelson, David L.;
Mohrenweiser, Harvey W.

Publication type:

Article

Identification of the Gene Encoding the Human Mitochondrial RNA Polymerase (h-mtRPOL) by Cyberscreening of the Expressed Sequence Tags Database.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 4, p. 615, doi. 10.1093/hmg/6.4.615

By:

Tiranti, Valeria;
Savoia, Anna;
Forti, Francesca;
D'Apolito, Maria-Felicia;
Centra, Marta;
Rocchi, Mariano;
Zeviani, Massimo

Publication type:

Article

Characterization of a Cluster of Sulfatase Genes on Xp22.3 Suggests Gene Duplications in an Ancestral Pseudoautosomal Region.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 4, p. 423, doi. 10.1093/hmg/5.4.423

By:

Meroni, Germana;
Franco, Brunella;
Archidiacono, Nicoletta;
Messali, Silvia;
Andolfi, Grazia;
Rocchi, Mariano;
Ballabio, Andrea

Publication type:

Article

Localization of a new highly repeated DNA sequence of Lemurcatta (Lemuridae, Strepsirhini).

Published in:

Genome, 2002, v. 45, n. 5, p. 973, doi. 10.1139/g02-048

By:

Boniotto, Michele;
Ventura, Mario;
Cardone, Maria Francesca;
Boaretto, Francesca;
Archidiacono, Nicoletta;
Rocchi, Mariano;
Crovella, Sergio

Publication type:

Article

22q11.2 Low Copy Repeats Expanded in the Human Lineage.

Published in:

Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.706641

By:

Vervoort, Lisanne;
Dierckxsens, Nicolas;
Pereboom, Zjef;
Capozzi, Oronzo;
Rocchi, Mariano;
Shaikh, Tamim H.;
Vermeesch, Joris R.

Publication type:

Article

Characterization and evolution of the novel gene family FAM90A in primates originated by multiple duplication and rearrangement events.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 21, p. 2572, doi. 10.1093/hmg/ddm209

By:

Bosch, Nina;
Cáceres, Mario;
Cardone, Maria Francesca;
Carreras, Anna;
Ballana, Ester;
Rocchi, Mariano;
Armengol, Lluís;
Estivill, Xavier

Publication type:

Article

Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 14, p. 1479, doi. 10.1093/hmg/ddh164

By:

Storlazzi, Clelia T.;
Fioretos, Thoas;
Paulsson, Kajsa;
Strömbeck, Bodil;
Lassen, Carin;
Ahlgren, Tomas;
Juliusson, Gunnar;
Mitelman, Felix;
Rocchi, Mariano;
Johansson, Bertil

Publication type:

Article

Linkage analysis conditionalon HLA status in a large North American pedigree supports the presenceof a multiple sclerosis susceptibility locus on chromosome 12p12.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 3, p. 295, doi. 10.1093/hmg/11.3.295

By:

Vitale, Emilia;
Cook, Stuart;
Sun, Rong;
Specchia, Claudia;
Subramanian, Kavitha;
Rocchi, Mariano;
Nathanson, Douglas;
Schwalb, Marvin;
Devoto, Marcella;
Rohowsky-Kochan, Christine

Publication type:

Article

Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1->qter in prenatal diagnosis: a case report.

Published in:

Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 1, doi. 10.1186/s13039-014-0069-4

By:

Altieri, Vincenzo;
Capozzi, Oronzo;
Marzano, Maria Cristina;
Catapano, Oriana;
Di Biase, Immacolata;
Rocchi, Mariano;
De Tollis, Giuliana

Publication type:

Article

The double deceit generated by an insertion mechanism in chronic myeloid leukemia with t(9;9;22).

Published in:

2008

By:

Albano, Francesco;
Zagaria, Antonella;
Anelli, Luisa;
Pannunzio, Alessandra;
Manodoro, Floriana;
Coccaro, Nicoletta;
Russo Rossi, Antonella;
Liso, Vincenzo;
Rocchi, Mariano;
Specchia, Giorgina

Publication type:

Letter

Molecular cytogenetic findings supporting the evidence of a biclonal origin in acute myeloid leukemia.

Published in:

2006

By:

Albano, Francesco;
Specchia, Giorgina;
Anelli, Luisa;
Zagaria, Antonella;
Archidiacono, Nicoletta;
Liso, Vincenzo;
Rocchi, Mariano

Publication type:

Letter

Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case.

Published in:

2001

By:

Specchia, Giorgina;
Storlazzi, Clelia;
Cuneo, Antonio;
Surace, Cecilia;
Mestice, Anna;
Pannunzio, Alessandra;
Rocchi, Mariano;
Liso, Vincenzo

Publication type:

Erratum

Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case.

Published in:

2001

By:

Specchia, Giorgina;
Tiziana Storlazzi, Clelia;
Cuneo, Antonio;
Surace, Cecilia;
Mestice, Anna;
Pannunzio, Alessandra;
Rocchi, Mariano;
Liso, Vincenzo;
Specchia, G;
Storlazzi, C T;
Cuneo, A;
Surace, C;
Mestice, A;
Pannunzio, A;
Rocchi, M;
Liso, V

Publication type:

journal article

Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas.

Published in:

Genes, Chromosomes & Cancer, 2015, v. 54, n. 3, p. 156, doi. 10.1002/gcc.22228

By:

Macchia, Gemma;
Nord, Karolin H.;
Zoli, Monica;
Purgato, Stefania;
D'Addabbo, Pietro;
Whelan, Christopher W.;
Carbone, Lucia;
Perini, Giovanni;
Mertens, Fredrik;
Rocchi, Mariano;
Storlazzi, Clelia Tiziana

Publication type:

Article

MIRN199B downregulation in chronic myeloid leukaemia is associated with deletions on der(9).

Published in:

2009

By:

Albano, Francesco;
Anelli, Luisa;
Zagaria, Antonella;
Liso, Vincenzo;
Rocchi, Mariano;
Specchia, Giorgina

Publication type:

Letter

The structure and evolution of centromeric transition regions within the human genome.

Published in:

Nature, 2004, v. 430, n. 7002, p. 857, doi. 10.1038/nature02806

By:

Xinwei She;
Horvath, Julie E.;
Zhaoshi Jiang;
Ge Liu;
Furey, Terrence S.;
Christ, Laurie;
Clark, Royden;
Graves, Tina;
Gulden, Cassy L.;
Alkan, Can;
Bailey, Jeff A.;
Sahinalp, Cenk;
Rocchi, Mariano;
Haussler, David;
Wilson, Richard K.;
Miller, Webb;
Schwartz, Stuart;
Eichler, Evan E.

Publication type:

Article

Positive selection of a gene family during the emergence of humans and African apes.

Published in:

Nature, 2001, v. 413, n. 6855, p. 514, doi. 10.1038/35097067

By:

Johnson, Matthew E.;
Viggiano, Luigi;
Bailey, Jeffrey A.;
Abdul-Rauf, Munah;
Goodwin, Graham;
Rocchi, Mariano;
Eichler, Evan E.

Publication type:

Article

t(5;6;12) associated with resistance to imatinib mesylate in chronic myeloid leukemia.

Published in:

2009

By:

Denčić-Fekete, Marija;
Đorđević, Vesna;
Storlazzi, Clelia;
Janković, Gradimir;
Bogdanović, Andrija;
Jovanović, Jelica;
Rocchi, Mariano;
Todorić-Živanović, Biljana;
Strnad, Milica;
Gotić, Mirjana;
Dencić-Fekete, Marija;
Dordević, Vesna;
Storlazzi, Clelia Tiziana;
Janković, Gradimir;
Bogdanović, Andrija;
Jovanović, Jelica;
Todorić-Zivanović, Biljana;
Gotić, Mirjana;
Denčić-Fekete, Marija;
Đorđević, Vesna

Publication type:

journal article

Non random distribution of genomic features inbreakpoint regions involved in chronic myeloidleukemia cases with variant t(9;22) or additionalchromosomal rearrangements.

Published in:

Molecular Cancer, 2010, v. 9, p. 120, doi. 10.1186/1476-4598-9-120

By:

Albano, Francesco;
Anelli, Luisa;
Zagaria, Antonella;
Coccaro, Nicoletta;
Casieri, Paola;
Rossi, Antonella Russo;
Vicari, Laura;
Liso, Vincenzo;
Rocchi, Mariano;
Specchia, Giorgina

Publication type:

Article

Evolutionary History of Chromosome 20.

Published in:

Molecular Biology & Evolution, 2005, v. 22, n. 2, p. 360

By:

Misceo, Doriana;
Cardone, Maria Francesca;
Carbone, Lucia;
D'Addabbo, Pietro;
de Jong, Pieter J.;
Rocchi, Mariano;
Archidiacono, Nicoletta

Publication type:

Article

Chromosome 6 Phylogeny in Primates and Centromere Repositioning.

Published in:

Molecular Biology & Evolution, 2003, v. 20, n. 9, p. 1506, doi. 10.1093/molbev/msg165

By:

Eder, Verena;
Ventura, Mario;
Ianigro, Massimo;
Teti, Mariagrazia;
Rocchi, Mariano;
Archidiacono, Nicoletta

Publication type:

Article

Mapping of Human Hexokinase 1 Gene to10q11→qter.

Published in:

Human Heredity, 1992, v. 42, n. 2, p. 107, doi. 10.1159/000154049

By:

Daniele, Aurora;
Altruda, Fiorella;
Ferrone, Marina;
Silengo, Lorenzo;
Romeo, Giovanni;
Archidiacond, Nicoletta;
Rocchi, Mariano

Publication type:

Article

A genome-wide comparison of recent chimpanzee and human segmental duplications.

Published in:

Nature, 2005, v. 437, n. 7055, p. 88, doi. 10.1038/nature04000

By:

Ze Cheng;
Ventura, Mario;
Xinwei She;
Khaitovich, Philipp;
Graves, Tina;
Osoegawa, Kazutoyo;
Church, Deanna;
DeJong, Pieter;
Wilson, Richard K.;
Pääbo, Svante;
Rocchi, Mariano;
Eichler, Evan E.

Publication type:

Article