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Items: 33

1.

Characterization of the genome, proteome, and structure of yersiniophage ϕR1-37.

Skurnik M, Hyytiäinen HJ, Happonen LJ, Kiljunen S, Datta N, Mattinen L, Williamson K, Kristo P, Szeliga M, Kalin-Mänttäri L, Ahola-Iivarinen E, Kalkkinen N, Butcher SJ.

J Virol. 2012 Dec;86(23):12625-42. doi: 10.1128/JVI.01783-12. Epub 2012 Sep 12.

2.

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

Laukkanen-Ninios R, Didelot X, Jolley KA, Morelli G, Sangal V, Kristo P, Brehony C, Imori PF, Fukushima H, Siitonen A, Tseneva G, Voskressenskaya E, Falcao JP, Korkeala H, Maiden MC, Mazzoni C, Carniel E, Skurnik M, Achtman M.

Environ Microbiol. 2011 Dec;13(12):3114-27. doi: 10.1111/j.1462-2920.2011.02588.x. Epub 2011 Sep 27.

3.

Penetrance and phenotype of the Thr377Met Myocilin mutation in a large Finnish family with juvenile- and adult-onset primary open-angle glaucoma.

Puska P, Lemmelä S, Kristo P, Sankila EM, Järvelä I.

Ophthalmic Genet. 2005 Mar;26(1):17-23.

PMID:
15823921
4.

Ultrastructural and chromosomal studies on manganese superoxide dismutase in malignant mesothelioma.

Kinnula VL, Torkkeli T, Kristo P, Sormunen R, Soini Y, Pääkkö P, Ollikainen T, Kahlos K, Hirvonen A, Knuutila S.

Am J Respir Cell Mol Biol. 2004 Aug;31(2):147-53. Epub 2004 Mar 23.

PMID:
15039138
5.

The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study.

Forsman E, Lemmelä S, Varilo T, Kristo P, Forsius H, Sankila EM, Järvelä I.

Mol Vis. 2003 May 30;9:217-22.

6.

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 LA.

Gut. 2002 Jul;51(1):56-9.

7.

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.

J Med Genet. 2002 Apr;39(4):292-6. No abstract available.

8.

Genetic screening for maternal uniparental disomy of chromosome 7 in prenatal and postnatal growth retardation of unknown cause.

Hannula K, Lipsanen-Nyman M, Kristo P, Kaitila I, Simola KO, Lenko HL, Tapanainen P, Holmberg C, Kere J.

Pediatrics. 2002 Mar;109(3):441-8.

PMID:
11875139
9.

Molecular screening for hereditary nonpolyposis colorectal cancer: a prospective, population-based study.

Percesepe A, Borghi F, Menigatti M, Losi L, Foroni M, Di Gregorio C, Rossi G, Pedroni M, Sala E, Vaccina F, Roncucci L, Benatti P, Viel A, Genuardi M, Marra G, Kristo P, Peltomäki P, Ponz de Leon M.

J Clin Oncol. 2001 Oct 1;19(19):3944-50.

PMID:
11579115
10.

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

Loukola A, Eklin K, Laiho P, Salovaara R, Kristo P, Järvinen H, Mecklin JP, Launonen V, Aaltonen LA.

Cancer Res. 2001 Jun 1;61(11):4545-9.

11.

Population-based molecular detection of hereditary nonpolyposis colorectal cancer.

Salovaara R, Loukola A, Kristo P, Kääriäinen H, Ahtola H, Eskelinen M, Härkönen N, Julkunen R, Kangas E, Ojala S, Tulikoura J, Valkamo E, Järvinen H, Mecklin JP, Aaltonen LA, de la Chapelle A.

J Clin Oncol. 2000 Jun;18(11):2193-200. Erratum in: J Clin Oncol 2000 Oct 1;18(19):3456.

PMID:
10829038
12.

Hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay.

Sarroca C, Alfano N, Bendin GT, Della Valle A, Dominguez A, Quadrelli R, Vaglio A, Mechoso B, Tinley ST, Harty AE, Lynch JF, Franklin BA, Kristo P, Smyrk TC, Peltomäki P, Lynch HT.

Dis Colon Rectum. 2000 Mar;43(3):353-60; discussion 360-2.

PMID:
10733117
13.

Microsatellite instability in adenomas as a marker for hereditary nonpolyposis colorectal cancer.

Loukola A, Salovaara R, Kristo P, Moisio AL, Kääriäinen H, Ahtola H, Eskelinen M, Härkönen N, Julkunen R, Kangas E, Ojala S, Tulikoura J, Valkamo E, Järvinen H, Mecklin JP, de la Chapelle A, Aaltonen LA.

Am J Pathol. 1999 Dec;155(6):1849-53.

14.

SMAD genes in juvenile polyposis.

Roth S, Sistonen P, Salovaara R, Hemminki A, Loukola A, Johansson M, Avizienyte E, Cleary KA, Lynch P, Amos CI, Kristo P, Mecklin JP, Kellokumpu I, Järvinen H, Aaltonen LA.

Genes Chromosomes Cancer. 1999 Sep;26(1):54-61.

PMID:
10441006
15.

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 RB, Mecklin JP, Järvinen H, de la Chapelle A, Nyström-Lahti M, Peltomäki P.

Hum Mutat. 1998;11(6):482.

PMID:
10200055
16.

Genomic structure of the human congenital chloride diarrhea (CLD) gene.

Haila S, Höglund P, Scherer SW, Lee JR, Kristo P, Coyle B, Trembath R, Holmberg C, de la Chapelle A, Kere J.

Gene. 1998 Jul 3;214(1-2):87-93.

PMID:
9729124
17.

Mismatch repair genes and mononucleotide tracts as mutation targets in colorectal tumors with different degrees of microsatellite instability.

Percesepe A, Kristo P, Aaltonen LA, Ponz de Leon M, de la Chapelle A, Peltomäki P.

Oncogene. 1998 Jul 16;17(2):157-63.

18.

Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease.

Aaltonen LA, Salovaara R, Kristo P, Canzian F, Hemminki A, Peltomäki P, Chadwick RB, Kääriäinen H, Eskelinen M, Järvinen H, Mecklin JP, de la Chapelle A.

N Engl J Med. 1998 May 21;338(21):1481-7.

19.

A missense mutation in the BRCA2 gene in three siblings with ovarian cancer.

Roth S, Kristo P, Auranen A, Shayehgi M, Seal S, Collins N, Barfoot R, Rahman N, Klemi PJ, Grénman S, Sarantaus L, Nevanlinna H, Butzow R, Ashworth A, Stratton MR, Aaltonen LA.

Br J Cancer. 1998 Apr;77(8):1199-202.

20.

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 Dec;11(12):2097-104.

PMID:
9447826
21.

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

Hemminki A, Markie D, Tomlinson I, Avizienyte E, Roth S, Loukola A, Bignell G, Warren W, Aminoff M, Höglund P, Järvinen H, Kristo P, Pelin K, Ridanpää M, Salovaara R, Toro T, Bodmer W, Olschwang S, Olsen AS, Stratton MR, de la Chapelle A, Aaltonen LA.

Nature. 1998 Jan 8;391(6663):184-7.

PMID:
9428765
22.

Semiautomated assessment of loss of heterozygosity and replication error in tumors.

Canzian F, Salovaara R, Hemminki A, Kristo P, Chadwick RB, Aaltonen LA, de la Chapelle A.

Cancer Res. 1996 Jul 15;56(14):3331-7.

23.

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

Kristo P, Saarelainen R, Fagerström R, Aho S, Korhola M.

Eur J Biochem. 1996 Apr 1;237(1):240-6.

24.

Founding mutations and Alu-mediated recombination in hereditary colon cancer.

Nyström-Lahti M, Kristo P, Nicolaides NC, Chang SY, Aaltonen LA, Moisio AL, Järvinen HJ, Mecklin JP, Kinzler KW, Vogelstein B, et al.

Nat Med. 1995 Nov;1(11):1203-6.

PMID:
7584997
26.

Small N-terminal deletion by splicing in cerebellar alpha 6 subunit abolishes GABAA receptor function.

Korpi ER, Kuner T, Kristo P, Köhler M, Herb A, Lüddens H, Seeburg PH.

J Neurochem. 1994 Sep;63(3):1167-70.

PMID:
8051560
27.

Molecular cloning and nucleotide sequence of chicken avidin-related genes 1-5.

Keinänen RA, Wallén MJ, Kristo PA, Laukkanen MO, Toimela TA, Helenius MA, Kulomaa MS.

Eur J Biochem. 1994 Mar 1;220(2):615-21.

28.

Molecular cloning of the chicken avidin cDNA.

Gope ML, Keinänen RA, Kristo PA, Conneely OM, Beattie WG, Zarucki-Schulz T, O'Malley BW, Kulomaa MS.

Nucleic Acids Res. 1987 Apr 24;15(8):3595-606.

29.

Characterization of three chicken pseudogenes for U1 RNA.

Kristo P, Tsai MJ, O'Malley BW.

DNA. 1984 Aug;3(4):281-6.

PMID:
6207998
30.

A chicken middle-repetitive DNA sequence which shares homology with mammalian ubiquitous repeats.

Stumph WE, Kristo P, Tsai MJ, O'Malley BW.

Nucleic Acids Res. 1981 Oct 24;9(20):5383-97.

31.

Structure and expression of a chicken gene coding for U1 RNA.

Roop DR, Kristo P, Stumph WE, Tsai MJ, O'Malley BW.

Cell. 1981 Mar;23(3):671-80.

PMID:
6164492
32.

Primary sequence of ovomucoid messenger RNA as determined from cloned complementary DNA.

Catterall JF, Stein JP, Kristo P, Means AR, O'Malley BW.

J Cell Biol. 1980 Nov;87(2 Pt 1):480-7.

33.

Ovomucoid intervening sequences specify functional domains and generate protein polymorphism.

Stein JP, Catterall JF, Kristo P, Means AR, O'Malley BW.

Cell. 1980 Oct;21(3):681-7.

PMID:
7438205

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