UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 96

Sortiert nach

Identification of a Gene, MLL, that Spans the Breakpoint in 11q23 Translocations Associated with Human Leukemias

Proceedings of the National Academy of Sciences - PNAS, 1991-12, Vol.88 (23), p.10735-10739

1991

Volltextzugriff (PDF)

Chromosomal instability in chromosome band 12p13: multiple breaks leading to complex rearrangements including cytogenetically undetectable sub-clones

Leukemia, 2001-08, Vol.15 (8), p.1193-1202

2001

Volltextzugriff (PDF)

Replication of a Common Fragile Site, FRA3B, Occurs Late in S Phase and is Delayed Further Upon Induction: Implications for the Mechanism of Fragile Site Induction

Human molecular genetics, 1998-04, Vol.7 (4), p.755-761

1998

Volltextzugriff (PDF)

axl, a transforming gene isolated from primary human myeloid leukemia cells, encodes a novel receptor tyrosine kinase

Molecular and Cellular Biology, 1991-10, Vol.11 (10), p.5016-5031

1991

Volltextzugriff (PDF)

Cytogenetic and Molecular Delineation of the Smallest Commonly Deleted Region of Chromosome 5 in Malignant Myeloid Diseases

Proceedings of the National Academy of Sciences - PNAS, 1993-06, Vol.90 (12), p.5484-5488

1993

Volltextzugriff (PDF)

Human and rat brain-derived neurotrophic factor and neurotrophin-3: Gene structures, distributions, and chromosomal localizations

Genomics (San Diego, Calif.), 1991-07, Vol.10 (3), p.558-568

1991

Volltextzugriff (PDF)

Mapping Chromosome Band 11q23 in Human Acute Leukemia with Biotinylated Probes: Identification of 11q23 Translocation Breakpoints with a Yeast Artificial Chromosome

Proceedings of the National Academy of Sciences - PNAS, 1990-12, Vol.87 (23), p.9358-9362

1990

Volltextzugriff (PDF)

TAL2, A Helix-Loop-Helix Gene Activated by the (7;9)(q34;q32) Translocation in Human T-Cell Leukemia

Proceedings of the National Academy of Sciences - PNAS, 1991-12, Vol.88 (24), p.11416-11420

1991

Volltextzugriff (PDF)

Refinement of the Smallest Commonly Deleted Segment of Chromosome 20 in Malignant Myeloid Diseases and Development of a PAC-Based Physical and Transcription Map

Genomics (San Diego, Calif.), 2000-07, Vol.67 (1), p.28-39

2000

Volltextzugriff (PDF)

Preferential Integration of Marker DNA into the Chromosomal Fragile Site at 3p14: An Approach to Cloning Fragile Sites

Proceedings of the National Academy of Sciences - PNAS, 1991-08, Vol.88 (15), p.6657-6661

1991

Volltextzugriff (PDF)

Characterization of the human pleiotrophin gene. Promoter region and chromosomal localization

The Journal of biological chemistry, 1992-12, Vol.267 (36), p.26011-26016

1992

Volltextzugriff (PDF)

Human CDC23 : cDNA cloning, mapping to 5q31, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias

Genomics (San Diego, Calif.), 1998-10, Vol.53 (2), p.184-190

1998

Volltextzugriff (PDF)

ERK8, a New Member of the Mitogen-activated Protein Kinase Family

The Journal of biological chemistry, 2002-05, Vol.277 (19), p.16733-16743

2002

Volltextzugriff (PDF)

A physical and genetic linkage map of the distal long arm of human chromosome 5

Cytogenetics and cell genetics, 1992, Vol.59 (1), p.27

1992

Volltextzugriff (PDF)

The human mitochondrial citrate transporter gene (SLC20A3) maps to chromosome band 22q11 within a region implicated in DiGeorge syndrome, velo-cardio-facial syndrome and schizophrenia

Human genetics, 1996-07, Vol.98 (1), p.113-115

1996

Volltextzugriff (PDF)

HEN1 and HEN2: A Subgroup of Basic Helix-Loop-Helix Genes That are Coexpressed in a Human Neuroblastoma

Proceedings of the National Academy of Sciences - PNAS, 1992-09, Vol.89 (18), p.8492-8496

1992

Volltextzugriff (PDF)

Physical localization of 70 polymorphic markers to human chromosome 5 by fluorescence in situ hybridization

Cytogenetics and cell genetics, 1993, Vol.62 (4), p.207

1993

Volltextzugriff (PDF)

Amplification and Overexpression of Peroxisome Proliferator-Activated Receptor Binding Protein (PBP/PPARBP) Gene in Breast Cancer

Proceedings of the National Academy of Sciences - PNAS, 1999-09, Vol.96 (19), p.10848-10853

1999

Volltextzugriff (PDF)

Cytogenetic and Molecular Delineation of a Region of Chromosome 7 Commonly Deleted in Malignant Myeloid Diseases

Blood, 1996-09, Vol.88 (6), p.1930-1935

1996

Volltextzugriff (PDF)

Molecular Delineation of the Smallest Commonly Deleted Region of Chromosome 5 in Malignant Myeloid Diseases to 1-1.5 Mb and Preparation of a PAC-Based Physical Map

Proceedings of the National Academy of Sciences - PNAS, 1997-06, Vol.94 (13), p.6948-6953

1997

Volltextzugriff (PDF)

Mammalian Neurotrophin-4: Structure, Chromosomal Localization, Tissue Distribution, and Receptor Specificity

Proceedings of the National Academy of Sciences - PNAS, 1992-04, Vol.89 (7), p.3060-3064

1992

Volltextzugriff (PDF)

Sequence-independent amplification and labeling of yeast artificial chromosomes for fluorescence in situ hybridization

Cytogenetics and cell genetics, 1994-01, Vol.65 (1-2), p.108

1994

Volltextzugriff (PDF)

Identification of the Gene Associated with the Recurring Chromosomal Translocations t(3;14)(q27;q32) and t(3;22)(q27;q11) in B-Cell Lymphomas

Proceedings of the National Academy of Sciences - PNAS, 1993-06, Vol.90 (11), p.5262-5266

1993

Volltextzugriff (PDF)

Transcript Map and Comparative Analysis of the 1.5-Mb Commonly Deleted Segment of Human 5q31 in Malignant Myeloid Diseases with a del(5q)

Genomics (San Diego, Calif.), 2001-01, Vol.71 (2), p.235-245

2001

Volltextzugriff (PDF)

cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young

Human molecular genetics, 1993-01, Vol.2 (1), p.1-4

1993

Volltextzugriff (PDF)

1 – 25 von 96

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(94)
Mit Volltextzugriff
(80)

Publikationsform

Artikel
(94)
Bücher
(2)

Sprache

Englisch
(95)
Japanisch
(13)

Erscheinungsjahr

n.n

Thema

Humans
(80)
Science & Technology
(69)
Biological And Medical Sciences
(64)
Life Sciences & Biomedicine
(54)
Chromosome Mapping
(49)
Molecular Sequence Data
(43)
Base Sequence
(39)
Fundamental And Applied Biological Sciences. Psychology
(35)
In Situ Hybridization, Fluorescence
(33)
Genetics & Heredity
(31)
Genes
(30)
Medical Sciences
(30)
Animals
(29)
Female
(22)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(22)
Human
(22)
Male
(22)
Classical Genetics, Quantitative Genetics, Hybrids
(21)
Translocation, Genetic
(19)
Amino Acid Sequence
(18)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Identification of a Gene, MLL, that Spans the Breakpoint in 11q23 Translocations Associated with Human Leukemias

Chromosomal instability in chromosome band 12p13: multiple breaks leading to complex rearrangements including cytogenetically undetectable sub-clones

Replication of a Common Fragile Site, FRA3B, Occurs Late in S Phase and is Delayed Further Upon Induction: Implications for the Mechanism of Fragile Site Induction

axl, a transforming gene isolated from primary human myeloid leukemia cells, encodes a novel receptor tyrosine kinase

Cytogenetic and Molecular Delineation of the Smallest Commonly Deleted Region of Chromosome 5 in Malignant Myeloid Diseases

Human and rat brain-derived neurotrophic factor and neurotrophin-3: Gene structures, distributions, and chromosomal localizations

Mapping Chromosome Band 11q23 in Human Acute Leukemia with Biotinylated Probes: Identification of 11q23 Translocation Breakpoints with a Yeast Artificial Chromosome

TAL2, A Helix-Loop-Helix Gene Activated by the (7;9)(q34;q32) Translocation in Human T-Cell Leukemia

Refinement of the Smallest Commonly Deleted Segment of Chromosome 20 in Malignant Myeloid Diseases and Development of a PAC-Based Physical and Transcription Map

Preferential Integration of Marker DNA into the Chromosomal Fragile Site at 3p14: An Approach to Cloning Fragile Sites

Characterization of the human pleiotrophin gene. Promoter region and chromosomal localization

Human CDC23 : cDNA cloning, mapping to 5q31, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias

ERK8, a New Member of the Mitogen-activated Protein Kinase Family

A physical and genetic linkage map of the distal long arm of human chromosome 5

The human mitochondrial citrate transporter gene (SLC20A3) maps to chromosome band 22q11 within a region implicated in DiGeorge syndrome, velo-cardio-facial syndrome and schizophrenia

HEN1 and HEN2: A Subgroup of Basic Helix-Loop-Helix Genes That are Coexpressed in a Human Neuroblastoma

Physical localization of 70 polymorphic markers to human chromosome 5 by fluorescence in situ hybridization

Amplification and Overexpression of Peroxisome Proliferator-Activated Receptor Binding Protein (PBP/PPARBP) Gene in Breast Cancer

Cytogenetic and Molecular Delineation of a Region of Chromosome 7 Commonly Deleted in Malignant Myeloid Diseases

Molecular Delineation of the Smallest Commonly Deleted Region of Chromosome 5 in Malignant Myeloid Diseases to 1-1.5 Mb and Preparation of a PAC-Based Physical Map

Mammalian Neurotrophin-4: Structure, Chromosomal Localization, Tissue Distribution, and Receptor Specificity

Sequence-independent amplification and labeling of yeast artificial chromosomes for fluorescence in situ hybridization

Identification of the Gene Associated with the Recurring Chromosomal Translocations t(3;14)(q27;q32) and t(3;22)(q27;q11) in B-Cell Lymphomas

Transcript Map and Comparative Analysis of the 1.5-Mb Commonly Deleted Segment of Human 5q31 in Malignant Myeloid Diseases with a del(5q)

cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young

Suchergebnisse filtern