UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

The Genetic Defect Causing Familial Alzheimer's Disease Maps on Chromosome 21

Science (American Association for the Advancement of Science), 1987-02, Vol.235 (4791), p.885-890

1987

Volltextzugriff (PDF)

A polymorphic DNA marker genetically linked to Huntington's disease

Nature (London), 1983-11, Vol.306 (5940), p.234-238

1983

Volltextzugriff (PDF)

Evidence for Reduced Recombination on the Nondisjoined Chromosomes 21 in Down Syndrome

Science (American Association for the Advancement of Science), 1987-08, Vol.237 (4815), p.652-654

1987

Volltextzugriff (PDF)

Amyloid $\beta $ Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage near the Alzheimer Locus

Science (American Association for the Advancement of Science), 1987-02, Vol.235 (4791), p.880-884

1987

Volltextzugriff (PDF)

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8

Nature (London), 1990-06, Vol.345 (6277), p.736-739

1990

Volltextzugriff (PDF)

Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin

The New England journal of medicine, 1990-10, Vol.323 (15), p.1046-1050

1990

Volltextzugriff (PDF)

Absence of Duplication of Chromosome 21 Genes in Familial and Sporadic Alzheimer's Disease

Science (American Association for the Advancement of Science), 1987-10, Vol.238 (4827), p.664-666

1987

Volltextzugriff (PDF)

Rapid Detection of Human Chromosome 21 Aberrations by in situ Hybridization

Proceedings of the National Academy of Sciences - PNAS, 1988-12, Vol.85 (24), p.9664-9668

1988

Volltextzugriff (PDF)

Critical Role of the D21S55 Region on Chromosome 21 in the Pathogenesis of Down Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1989-08, Vol.86 (15), p.5958-5962

1989

Volltextzugriff (PDF)

Rapid and efficient cloning of Alu-PCR products using uracil DNA glycosylase

Genome research, 1991, Vol.1 (2), p.120-123

1991

Volltextzugriff (PDF)

Molecular genetic approach to the characterization of the “Down syndrome region” of chromosome 21

Genomics (San Diego, Calif.), 1989-08, Vol.5 (2), p.325-331

1989

Volltextzugriff (PDF)

A genetic linkage map of human chromosome 21 : analysis of recombination as a function of sex and age

American journal of human genetics, 1992-03, Vol.50 (3), p.551-558

1992

Volltextzugriff (PDF)

AMLI fusion transcripts in t(3;21) positive leukemia: Evidence of molecular heterogeneity and usage of splicing sites frequently involved in the generation of normal AMLI transcripts

Genes chromosomes & cancer, 1994-12, Vol.11 (4), p.226-236

1994

Volltextzugriff (PDF)

Comparative Mapping of DNA Markers from the Familial Alzheimer Disease and Down Syndrome Regions of Human Chromosome 21 to Mouse Chromosomes 16 and 17

Proceedings of the National Academy of Sciences - PNAS, 1988-08, Vol.85 (16), p.6032-6036

1988

Volltextzugriff (PDF)

Isolation of Exons from Cloned DNA by Exon Trapping

Current Protocols in Human Genetics, 2001-05, Vol.3 (1), p.6.1.1-6.1.27

2001

Volltextzugriff (PDF)

The exon trapping assay partly discriminates against alternatively spliced exons

Nucleic acids research, 1993-05, Vol.21 (9), p.2217-2221

1993

Volltextzugriff (PDF)

Genetic linkage map of human chromosome 21

Genomics (San Diego, Calif.), 1988-08, Vol.3 (2), p.129-136

1988

Volltextzugriff (PDF)

Molecular Cloning of the cDNA for Human Erythrocyte β-Spectrin

Blood, 1988-07, Vol.72 (1), p.328-334

1988

Volltextzugriff (PDF)

Protocols for trapping internal and 3'-terminal exons

Genome research, 1994-08, Vol.4 (1), p.S24-S39

1994

Volltextzugriff (PDF)

Isolation of polymorphic DNA segments from human chromosome 21

Nucleic acids research, 1985-09, Vol.13 (17), p.6075-6088

1985

Volltextzugriff (PDF)

Analysis of DNA Haplotypes Suggests a Genetic Predisposition to Trisomy 21 Associated with DNA Sequences on Chromosome 21

Proceedings of the National Academy of Sciences - PNAS, 1985-05, Vol.82 (10), p.3360-3364

1985

Volltextzugriff (PDF)

Generation of 19 STS markers that can be anchored at specific sites on human chromosome 21

Genomics (San Diego, Calif.), 1992-09, Vol.14 (1), p.185-187

1992

Volltextzugriff (PDF)

DNA sequence and regional assignment of the human follicle-stimulating hormone beta-subunit gene to the short arm of human chromosome 11

DNA (New York, N.Y.), 1987-06, Vol.6 (3), p.205-212

1987

Volltextzugriff (PDF)

Regional assignment of the erythropoietin gene to human chromosome region 7pter----q22

Cytogenetic and genome research, 1986-01, Vol.42 (4), p.214-218

1986

Volltextzugriff (PDF)

Transcriptionally active chimeric gene derived from the fusion of the AML1 gene and a novel gene on chromosome 8 in t(8;21) leukemic cells

Cancer genetics and cytogenetics, 1992-10, Vol.63 (2), p.81-88

1992

Volltextzugriff (PDF)

1 – 25 von 640

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(565)
Mit Volltextzugriff
(523)

Publikationsform

Artikel
(587)
Buchkapitel
(29)
Bücher
(15)
Reviews
(9)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(441)
Life Sciences & Biomedicine
(375)
Humans
(363)
Female
(210)
Male
(203)
Biological And Medical Sciences
(133)
Middle Aged
(112)
Medical Sciences
(105)
Aged
(104)
Animals
(102)
Adult
(99)
Risk Factors
(61)
Genetics & Heredity
(56)
Mice
(55)
Neurosciences & Neurology
(53)
Science & Technology - Other Topics
(47)
Multidisciplinary Sciences
(46)
Medicin Och Hälsovetenskap
(43)
Cardiovascular System & Cardiology
(42)
Fundamental And Applied Biological Sciences. Psychology
(39)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Nature Genetics
(17)
Neurology
(16)
Blood
(14)
The New England Journal Of Medicine
(14)
Plos One
(12)
Clinical Pharmacology And Therapeutics
(9)
Proceedings Of The National Academy Of Sciences - Pnas
(9)
Science
(9)
Brain Imaging And Behavior
(8)
Cancer Research
(8)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

The Genetic Defect Causing Familial Alzheimer's Disease Maps on Chromosome 21

A polymorphic DNA marker genetically linked to Huntington's disease

Evidence for Reduced Recombination on the Nondisjoined Chromosomes 21 in Down Syndrome

Amyloid $\beta $ Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage near the Alzheimer Locus

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8

Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin

Absence of Duplication of Chromosome 21 Genes in Familial and Sporadic Alzheimer's Disease

Rapid Detection of Human Chromosome 21 Aberrations by in situ Hybridization

Critical Role of the D21S55 Region on Chromosome 21 in the Pathogenesis of Down Syndrome

Rapid and efficient cloning of Alu-PCR products using uracil DNA glycosylase

Molecular genetic approach to the characterization of the “Down syndrome region” of chromosome 21

A genetic linkage map of human chromosome 21 : analysis of recombination as a function of sex and age

AMLI fusion transcripts in t(3;21) positive leukemia: Evidence of molecular heterogeneity and usage of splicing sites frequently involved in the generation of normal AMLI transcripts

Comparative Mapping of DNA Markers from the Familial Alzheimer Disease and Down Syndrome Regions of Human Chromosome 21 to Mouse Chromosomes 16 and 17

Isolation of Exons from Cloned DNA by Exon Trapping

The exon trapping assay partly discriminates against alternatively spliced exons

Genetic linkage map of human chromosome 21

Molecular Cloning of the cDNA for Human Erythrocyte β-Spectrin

Protocols for trapping internal and 3'-terminal exons

Isolation of polymorphic DNA segments from human chromosome 21

Analysis of DNA Haplotypes Suggests a Genetic Predisposition to Trisomy 21 Associated with DNA Sequences on Chromosome 21

Generation of 19 STS markers that can be anchored at specific sites on human chromosome 21

DNA sequence and regional assignment of the human follicle-stimulating hormone beta-subunit gene to the short arm of human chromosome 11

Regional assignment of the erythropoietin gene to human chromosome region 7pter----q22

Transcriptionally active chimeric gene derived from the fusion of the AML1 gene and a novel gene on chromosome 8 in t(8;21) leukemic cells

Suchergebnisse filtern