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1
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Artigo
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Population structure of the Yersinia pseudotuberculosis complex according to multilocus sequence typing

Riikka Laukkanen-Ninios Xavier Didelot; Keith A Jolley; Giovanna Morelli; Vartul Sangal; Paula Kristo; Carina Brehony; Priscilla F. M Imori; Hiroshi Fukushima; Anja Siitonen; Galina Tseneva; Ekaterina Voskressenskaya; Juliana Pfrimer Falcão; Hannu Korkeala; Martin C. J Maiden; Camila Mazzoni; Elisabeth Carniel; Mikael Skurnik; Mark Achtman

Environmental Microbiology Oxford v. 13, n. 12, p. 3114-3127, 2011

Oxford 2011

Localização: FCFRP - Fac. Ciên. Farm. Ribeirão Preto    (pcd 2290882 Estantes Deslizantes )(Acessar)

2
Microsatellite marker analysis in screening for hereditary nonpolyposis colorectal cancer (HNPCC)
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Microsatellite marker analysis in screening for hereditary nonpolyposis colorectal cancer (HNPCC)

LOUKOLA, Anu ; EKLIN, Katja ; LAIHO, Päivi ; SALOVAARA, Reijo ; KRISTO, Paula ; JÄRVINEN, Heikki ; MECKLIN, Jukka-Pekka ; LAUNONEN, Virpi ; AALTONEN, Lauri A

Cancer research (Chicago, Ill.), 2001-06, Vol.61 (11), p.4545-4549 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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3
Frequent loss of SMAD4/DPC4 protein in colorectal cancers
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Frequent loss of SMAD4/DPC4 protein in colorectal cancers

Salovaara, R ; Roth, S ; Loukola, A ; Launonen, V ; Sistonen, P ; Avizienyte, E ; Kristo, P ; Järvinen, H ; Souchelnytskyi, S ; Sarlomo-Rikala, M ; Aaltonen, L A

Gut, 2002-07, Vol.51 (1), p.56-59 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and British Society of Gastroenterology

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4
Four novel mutations in the OFD1 (Cxorf5) gene in Finnish patients with oral-facial-digital syndrome 1
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Four novel mutations in the OFD1 (Cxorf5) gene in Finnish patients with oral-facial-digital syndrome 1

Rakkolainen, A ; Ala-Mello, S ; Kristo, P ; Orpana, A ; Järvelä, I

Journal of medical genetics, 2002-04, Vol.39 (4), p.292-296 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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5
Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease
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Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

Aaltonen, Lauri A ; Salovaara, Reijo ; Kristo, Paula ; Canzian, Federico ; Hemminki, Akseli ; Peltomäki, Päivi ; Chadwick, Robert B ; Kääriäinen, Helena ; Eskelinen, Matti ; Järvinen, Heikki ; Mecklin, Jukka-Pekka ; de la Chapelle, Albert ; Percesepe, Antonio ; Ahtola, Heikki ; Härkönen, Niilo ; Julkunen, Risto ; Kangas, Eero ; Ojala, Seppo ; Tulikoura, Jukka ; Valkamo, Erkki

The New England journal of medicine, 1998-05, Vol.338 (21), p.1481-1487 [Periódico revisado por pares]

Boston, MA: Massachusetts Medical Society

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6
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
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A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

Aaltonen, Lauri A ; Hemminki, Akseli ; Markie, David ; Tomlinson, Ian ; Avizienyte, Egle ; Roth, Stina ; Loukola, Anu ; Bignell, Graham ; Warren, William ; Aminoff, Maria ; Höglund, Pia ; Järvinen, Heikki ; Kristo, Paula ; Pelin, Katarina ; Ridanpää, Maaret ; Salovaara, Reijo ; Toro, Tumi ; Bodmer, Walter ; Olschwang, Sylviane ; Olsen, Anne S ; Stratton, Michael R ; de la Chapelle, Albert

Nature (London), 1998-01, Vol.391 (6663), p.184-187 [Periódico revisado por pares]

London: Nature Publishing

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7
Mutation sharing, predominant involvement of the MLH1 gene and description of four novel mutations in hereditary nonpolyposis colorectal cancer. Mutations in brief no. 144. Online
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Mutation sharing, predominant involvement of the MLH1 gene and description of four novel mutations in hereditary nonpolyposis colorectal cancer. Mutations in brief no. 144. Online

Holmberg, M ; Kristo, P ; Chadwicks, R B ; Mecklin, J P ; Järvinen, H ; de la Chapelle, A ; Nyström-Lahti, M ; Peltomäki, P

Human mutation, 1998, Vol.11 (6), p.482-482 [Periódico revisado por pares]

United States

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8
Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm
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Artigo
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Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm

KIURU-KUHLEFELT, S ; KRISTO, P ; RUUTU, T ; KNUUTILA, S ; KERE, J

Leukemia, 1997-12, Vol.11 (12), p.2097-2104 [Periódico revisado por pares]

London: Nature Publishing

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9
Semiautomated assessment of loss of heterozygosity and replication error in tumors
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Artigo
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Semiautomated assessment of loss of heterozygosity and replication error in tumors

CANZIAN, F ; SALOVAARA, R ; HEMMINKI, A ; KRISTO, P ; CHADWICK, R. B ; AALTONEN, L. A ; DE LA CHAPELLE, A

Cancer research (Chicago, Ill.), 1996-07, Vol.56 (14), p.3331-3337 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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10
Protein purification, and cloning and characterization of the cDNA and gene for xylose isomerase of barley
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Artigo
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Protein purification, and cloning and characterization of the cDNA and gene for xylose isomerase of barley

Kristo, P ; Saarelainen, R ; Fagerstrom, R ; Aho, S ; Korhola, M

European journal of biochemistry, 1996-04, Vol.237 (1), p.240-246 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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Deste Autor:

  1. Mazzoni, C
  2. Falcão, J
  3. Korkeala, H
  4. Kristo, P
  5. Skurnik, M

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