UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 873

Sortiert nach

Dual-color fluorescence in situ hybridization reveals an association of chromosome 8q22 but not 8p21 imbalance with high grade invasive breast carcinoma

PloS one, 2013-07, Vol.8 (7), p.e70790

2013

Link zum Volltext

Verfügbarkeit prüfen

Familial Mutations of the Transcription Factor RUNX1 (AML1, CBFA2) Predispose to Acute Myeloid Leukemia

Leukemia & lymphoma, 2004-01, Vol.45 (1), p.1-10

2004

Link zum Volltext

Verfügbarkeit prüfen

Historical Aspects of Formal Education at APL

Johns Hopkins APL technical digest, 2018-03, Vol.34 (2), p.275

2018

Link zum Volltext

Verfügbarkeit prüfen

Double complex mutations involving F8 and FUNDC2 caused by distinct break-induced replication

Human mutation, 2007-12, Vol.28 (12), p.1198-1206

2007

Link zum Volltext

Verfügbarkeit prüfen

Polyploidy in myelofibrosis: analysis by cytogenetic and SNP array indicates association with advancing disease

Molecular cytogenetics, 2013-12, Vol.6 (1), p.59-59

2013

Link zum Volltext

Verfügbarkeit prüfen

Refined physical map of the human PAX2/HOX11/NFKB2 cancer gene region at 10q24 and relocalization of the HPV6AI1 viral integration site to 14q13.3-q21.1

BMC genomics, 2003-03, Vol.4 (1), p.9-9, Article 9

2003

Link zum Volltext

Verfügbarkeit prüfen

Array of hope for high-resolution genetic screening services in New Zealand

New Zealand medical journal, 2010-07, Vol.123 (1318), p.6-11

2010

Link zum Volltext

Verfügbarkeit prüfen

Genotyping the factor VIII intron 22 inversion locus using fluorescent in situ hybridization

Blood cells, molecules, & diseases, 2011-02, Vol.46 (2), p.151-158

2011

Link zum Volltext

Verfügbarkeit prüfen

Association of chromosome band 8q22 copy number gain with high grade invasive breast carcinomas by assessment of core needle biopsies

Genes chromosomes & cancer, 2008-05, Vol.47 (5), p.405-417

2008

Link zum Volltext

Verfügbarkeit prüfen

A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia

British journal of haematology, 2002-06, Vol.117 (4), p.878-881

2002

Link zum Volltext

Verfügbarkeit prüfen

Chronic myeloid leukemia: cytogenetic methods and applications for diagnosis and treatment

Methods in molecular biology (Clifton, N.J.), 2011, Vol.730, p.33

Morris, Christine M

2011

Link zum Volltext

Verfügbarkeit prüfen

cDNA cloning of human DEC-205, a putative antigen-uptake receptor on dendritic cells

Immunogenetics (New York), 1998-05, Vol.47 (6), p.442-450

1998

Link zum Volltext

Verfügbarkeit prüfen

Integration of human herpesvirus 6 genome in human chromosomes

The Lancet (British edition), 1998-11, Vol.352 (9141), p.1707-1707

1998

Link zum Volltext

Verfügbarkeit prüfen

A full-length and potentially active LINE element is integrated polymorphically within the IGL locus in a genomically unstable region of chromosome 22

Human genetics, 2001-12, Vol.109 (6), p.628-637

2001

Link zum Volltext

Verfügbarkeit prüfen

Cloning, Sequence Analysis, and Chromosomal Localization of the Novel Human Integrin α11 Subunit (ITGA11)

Genomics (San Diego, Calif.), 1999-09, Vol.60 (2), p.179-187

1999

Link zum Volltext

Verfügbarkeit prüfen

Abstract 1146: Three-color array CGH differentiates constitutional from acquired CNVs in cancer genomes

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.1146-1146

2010

Link zum Volltext

Verfügbarkeit prüfen

Genomic diversity correlates with clinical variation in Ph′-negative chronic myeloid leukaemia

Nature (London), 1986-03, Vol.320 (6059), p.281-283

1986

Link zum Volltext

Verfügbarkeit prüfen

The BCR Gene Recombines Preferentially with Alu Elements in Complex BCR-ABL Translocations of Chronic Myeloid Leukaemia

Human molecular genetics, 1998-05, Vol.7 (5), p.767-776

1998

Link zum Volltext

Verfügbarkeit prüfen

Nonrandom distribution of interspersed repeat elements in the BCR and ABL1 genes and its relation to breakpoint cluster regions

Genes chromosomes & cancer, 2001-10, Vol.32 (2), p.144-154

2001

Link zum Volltext

Verfügbarkeit prüfen

Cytokeratin KRT8/18 expression differentiates distinct subtypes of grade 3 invasive ductal carcinoma of the breast

Cancer genetics and cytogenetics, 2007-10, Vol.178 (2), p.94-103

2007

Link zum Volltext

Verfügbarkeit prüfen

Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia

Cancer genetics and cytogenetics, 2004-03, Vol.149 (2), p.125-130

2004

Link zum Volltext

Verfügbarkeit prüfen

Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy 7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia

Cancer genetics and cytogenetics, 2004-03, Vol.149 (2), p.125-130

2004

Link zum Volltext

Verfügbarkeit prüfen

Translocation (5;10)(q22;q24) in a case of acute lymphoblastic leukemia

Cancer genetics and cytogenetics, 2006-02, Vol.165 (1), p.36-40

2006

Link zum Volltext

Verfügbarkeit prüfen

Identification of Amplified Genes in a Patient with Acute Myeloid Leukemia and Double Minute Chromosomes

Cancer genetics and cytogenetics, 1999-09, Vol.113 (2), p.126-133

1999

Link zum Volltext

Verfügbarkeit prüfen

The small GTPase RAC3 gene is located within chromosome band 17q25.3 outside and telomeric of a region commonly deleted in breast and ovarian tumours

Cytogenetics and cell genetics, 2000, Vol.89 (1-2), p.18

2000

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 873

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(764)
Mit Volltextzugriff
(764)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Dual-color fluorescence in situ hybridization reveals an association of chromosome 8q22 but not 8p21 imbalance with high grade invasive breast carcinoma

Familial Mutations of the Transcription Factor RUNX1 (AML1, CBFA2) Predispose to Acute Myeloid Leukemia

Historical Aspects of Formal Education at APL

Double complex mutations involving F8 and FUNDC2 caused by distinct break-induced replication

Polyploidy in myelofibrosis: analysis by cytogenetic and SNP array indicates association with advancing disease

Refined physical map of the human PAX2/HOX11/NFKB2 cancer gene region at 10q24 and relocalization of the HPV6AI1 viral integration site to 14q13.3-q21.1

Array of hope for high-resolution genetic screening services in New Zealand

Genotyping the factor VIII intron 22 inversion locus using fluorescent in situ hybridization

Association of chromosome band 8q22 copy number gain with high grade invasive breast carcinomas by assessment of core needle biopsies

A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia

Chronic myeloid leukemia: cytogenetic methods and applications for diagnosis and treatment

cDNA cloning of human DEC-205, a putative antigen-uptake receptor on dendritic cells

Integration of human herpesvirus 6 genome in human chromosomes

A full-length and potentially active LINE element is integrated polymorphically within the IGL locus in a genomically unstable region of chromosome 22

Cloning, Sequence Analysis, and Chromosomal Localization of the Novel Human Integrin α11 Subunit (ITGA11)

Abstract 1146: Three-color array CGH differentiates constitutional from acquired CNVs in cancer genomes

Genomic diversity correlates with clinical variation in Ph′-negative chronic myeloid leukaemia

The BCR Gene Recombines Preferentially with Alu Elements in Complex BCR-ABL Translocations of Chronic Myeloid Leukaemia

Nonrandom distribution of interspersed repeat elements in the BCR and ABL1 genes and its relation to breakpoint cluster regions

Cytokeratin KRT8/18 expression differentiates distinct subtypes of grade 3 invasive ductal carcinoma of the breast

Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia

Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy 7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia

Translocation (5;10)(q22;q24) in a case of acute lymphoblastic leukemia

Identification of Amplified Genes in a Patient with Acute Myeloid Leukemia and Double Minute Chromosomes

The small GTPase RAC3 gene is located within chromosome band 17q25.3 outside and telomeric of a region commonly deleted in breast and ovarian tumours

Suchergebnisse filtern