UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 30

Sortiert nach

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

Journal of Virology, 2012-12, Vol.86 (23), p.12625-12642

2012

Volltextzugriff (PDF)

Population-Based Molecular Detection of Hereditary Nonpolyposis Colorectal Cancer

Journal of clinical oncology, 2000-06, Vol.18 (11), p.2193-2200

2000

Volltextzugriff (PDF)

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

The New England journal of medicine, 1998-05, Vol.338 (21), p.1481-1487

1998

Volltextzugriff (PDF)

Molecular Screening for Hereditary Nonpolyposis Colorectal Cancer: A Prospective, Population-Based Study

Journal of clinical oncology, 2001-10, Vol.19 (19), p.3944-3950

2001

Volltextzugriff (PDF)

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

Pediatrics (Evanston), 2002-03, Vol.109 (3), p.441

2002

Volltextzugriff (PDF)

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

Environmental microbiology, 2011-12, Vol.13 (12), p.3114-3127

2011

Volltextzugriff (PDF)

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

Cancer research (Chicago, Ill.), 2001-06, Vol.61 (11), p.4545-4549

2001

Volltextzugriff (PDF)

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

Nature (London), 1998-01, Vol.391 (6663), p.184-187

1998

Volltextzugriff (PDF)

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

Gene, 1998-07, Vol.214 (1), p.87-93

1998

Volltextzugriff (PDF)

Semiautomated assessment of loss of heterozygosity and replication error in tumors

Cancer research (Chicago, Ill.), 1996-07, Vol.56 (14), p.3331-3337

1996

Volltextzugriff (PDF)

Founding mutations and Alu-mediated recombination in hereditary colon cancer

Nature medicine, 1995-11, Vol.1 (11), p.1203-1206

1995

Volltextzugriff (PDF)

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

Molecular vision, 2003-05, Vol.9, p.217-222

2003

Volltextzugriff (PDF)

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

Nature (London), 1998-01, Vol.391 (6663), p.184-187

1998

Volltextzugriff (PDF)

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

The American journal of pathology, 1999-12, Vol.155 (6), p.1849-1853

1999

Volltextzugriff (PDF)

Ultrastructural and Chromosomal Studies on Manganese Superoxide Dismutase in Malignant Mesothelioma

American journal of respiratory cell and molecular biology, 2004-08, Vol.31 (2), p.147-153

2004

Volltextzugriff (PDF)

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

Oncogene, 1998-07, Vol.17 (2), p.157-163

1998

Volltextzugriff (PDF)

SMAD genes in juvenile polyposis

Genes chromosomes & cancer, 1999-09, Vol.26 (1), p.54-61

1999

Volltextzugriff (PDF)

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

Ophthalmic genetics, 2005-03, Vol.26 (1), p.17-23

2005

Volltextzugriff (PDF)

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

Yeast (Chichester, England), 1994-12, Vol.10 (12), p.1559-1568

1994

Volltextzugriff (PDF)

Hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay

Diseases of the colon & rectum, 2000-03, Vol.43 (3), p.353-360

2000

Volltextzugriff (PDF)

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

European journal of biochemistry, 1996-04, Vol.237 (1), p.240-246

1996

Volltextzugriff (PDF)

Invited editorial

Diseases of the colon & rectum, 2000-03, Vol.43 (3), p.360-362

2000

Volltextzugriff (PDF)

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

Human mutation, 1998, Vol.11 (6), p.482-483

1998

Volltextzugriff (PDF)

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

Nucleic acids research, 1981-10, Vol.9 (20), p.5383-5398

1981

Volltextzugriff (PDF)

Ovomucoid intervening sequences specify functional domains and generate protein polymorphism

Cell, 1980-10, Vol.21 (3), p.681-687

1980

Volltextzugriff (PDF)

1 – 25 von 30

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(30)
Mit Volltextzugriff
(28)

Publikationsform

Artikel
(30)

Sprache

Englisch
(30)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(24)
Science & Technology
(24)
Humans
(19)
Base Sequence
(12)
Middle Aged
(11)
Adult
(10)
Biochemistry & Molecular Biology
(10)
Biological And Medical Sciences
(10)
Female
(10)
Aged
(9)
Male
(9)
Medical Sciences
(8)
Molecular Sequence Data
(8)
Animals
(7)
Cloning, Molecular
(7)
Colorectal Neoplasms, Hereditary Nonpolyposis - Genetics
(7)
Mutation
(7)
Polymerase Chain Reaction
(7)
Genes
(6)
Germ-Line Mutation
(6)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

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

Population-Based Molecular Detection of Hereditary Nonpolyposis Colorectal Cancer

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

Molecular Screening for Hereditary Nonpolyposis Colorectal Cancer: A Prospective, Population-Based Study

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

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

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

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

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

Semiautomated assessment of loss of heterozygosity and replication error in tumors

Founding mutations and Alu-mediated recombination in hereditary colon cancer

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

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

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

Ultrastructural and Chromosomal Studies on Manganese Superoxide Dismutase in Malignant Mesothelioma

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

SMAD genes in juvenile polyposis

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

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

Hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay

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

Invited editorial

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

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

Ovomucoid intervening sequences specify functional domains and generate protein polymorphism

Suchergebnisse filtern