P. Kristo

发表

A serine/threonine kinase gene defective in Peutz–Jeghers syndrome

M. Stratton, G. Bignell, L. Aaltonen, 1998, Nature.

Characterization of the Genome, Proteome, and Structure of Yersiniophage ϕR1-37

M. Skurnik, S. Butcher, P. Kristo, 2012, Journal of Virology.

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

P. Kristo, S. Aho, M. Korhola, 1996, European journal of biochemistry.

M o l ecular S creening f or H ereditary N onpolyposis Colorectal C ancer: A P rospective, P opulation-Based S tudy

A. Viel, L. Roncucci, M. P. Leòn, 2001 .

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

P. Peltomäki, A. Viel, M. Genuardi, 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

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

A. Ashworth, S. Seal, M. Stratton, 1998, British Journal of Cancer.

Penetrance and Phenotype of the Thr377Met Myocilin Mutation in a Large Finnish Family with Juvenile- and Adult-Onset Primary Open-Angle Glaucoma

E. Sankila, I. Järvelä, P. Kristo, 2005, Ophthalmic genetics.

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

E. Sankila, I. Järvelä, T. Varilo, 2003, Molecular vision.

Consideration of the evolution of the Saccharomyces cerevisiae MEL gene family on the basis of the nucleotide sequences of the genes and their flanking regions

P. Kristo, M. Korhola, H. Turakainen, 1994, Yeast.

Hereditary nonpolyposis colorectal cancer (lynch syndrome II) in Uruguay

T. Smyrk, P. Peltomäki, H. Lynch, 2000, Diseases of the colon and rectum.

Mutation sharing, predominant involvement of the MLH1 gene and description of four novel mutations in hereditary nonpolyposis colorectal cancer

A. de la Chapelle, P. Peltomäki, J. Mecklin, 1998, Human mutation.

Molecnlar cloning of the cfakken avidin cDNA

M. Kulomaa, B. O’Malley, P. Kristo, 1987 .

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

S. Knuutila, Y. Soini, P. Kristo, 2004, American journal of respiratory cell and molecular biology.

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.

P. Peltomäki, J. Mecklin, H. Järvinen, 1998 .

SMAD genes in juvenile polyposis

L. Aaltonen, C. Amos, P. Sistonen, 1999, Genes, chromosomes & cancer.

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

C. Mazzoni, M. Achtman, A. Siitonen, 2011, Environmental microbiology.

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

S. Scherer, A. Chapelle, J. Kere, 1998, Gene.

Founding mutations and Alu-mediated recombination in hereditary colon cancer

K. Kinzler, B. Vogelstein, L. Aaltonen, 1995, Nature Medicine.

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

J. Kere, S. Knuutila, P. Kristo, 1997, Leukemia.

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

B. O’Malley, M. Tsai, P. Kristo, 1981, Nucleic acids research.

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

L. Aaltonen, P. Laiho, J. Mecklin, 2001, Cancer research.

Structure and expression of a chicken gene coding for U1 RNA

B. O’Malley, M. Tsai, D. Roop, 1981, Cell.

Characterization of three chicken pseudogenes for U1 RNA.

B. O’Malley, M. Tsai, P. Kristo, 1984, DNA.

Ovomucoid intervening sequences specify functional domains and generate protein polymorphism

A. Means, B. O’Malley, P. Kristo, 1980, Cell.

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

J. Kere, I. Kaitila, P. Kristo, 2002, Pediatrics.

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

L. Aaltonen, A. de la Chapelle, J. Mecklin, 1999, The American journal of pathology.

Short Communication Microsatellite Instability in Adenomas as a Marker for Hereditary Nonpolyposis Colorectal Cancer

L. Aaltonen, J. Mecklin, M. Eskelinen, 1999 .

Frequent loss of SMAD4/DPC4 protein in colorectal cancers

L. Aaltonen, P. Sistonen, H. Järvinen, 2002, Gut.

Frequent loss of SMAD4/DPC4 protein in colorectal cancers

L. Aaltonen, P. Sistonen, H. Järvinen, 2002 .

Population-based molecular detection of hereditary nonpolyposis colorectal cancer.

L. Aaltonen, A. de la Chapelle, J. Mecklin, 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Population-Based M olecular D etection o f H ereditary Nonpolyposis C olorectal C ancer

L. Aaltonen, J. Mecklin, M. Eskelinen, 2000 .

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

L. Aaltonen, R. Chadwick, A. de la Chapelle, 1998, The New England journal of medicine.

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

I. Järvelä, P. Kristo, A. Orpana, 2002, Journal of medical genetics.

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

L. Aaltonen, R. Chadwick, A. de la Chapelle, 1996, Cancer research.

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

A. Means, B. O’Malley, P. Kristo, 1980, The Journal of cell biology.

Molecular screening for Hereditary Non Polyposis Colorectal Cancer (HNPCC): a prospective, population-based study

P. Peltomäki, A. Viel, L. Roncucci, 2001 .

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

L. Aaltonen, P. Peltomäki, M. P. Leòn, 1998, Oncogene.

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

M. Kulomaa, M. Laukkanen, P. Kristo, 1994, European journal of biochemistry.

Small N‐Terminal Deletion by Splicing in Cerebellar α6 Subunit Abolishes GABAA Receptor Function

T. Kuner, A. Herb, M. Köhler, 1994, Journal of neurochemistry.

Frequent loss of SMAD4/DPC4 protein in colorectal cancers

L. Aaltonen, P. Sistonen, H. Järvinen, 2002, Gut.