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 t(1;12)(q21;p13) Translocation of Human Acute Myeloblastic Leukemia Results in a TEL-ARNT Fusion

Proceedings of the National Academy of Sciences - PNAS, 2000-06, Vol.97 (12), p.6757-6762

2000

Volltextzugriff (PDF)

Involvement of a Human Gene Related to the Drosophila spen Gene in the Recurrent t(1;22) Translocation of Acute Megakaryocytic Leukemia

Proceedings of the National Academy of Sciences - PNAS, 2001-05, Vol.98 (10), p.5776-5779

2001

Volltextzugriff (PDF)

Chromosome 21 abnormalities with AML1 amplification in acute lymphoblastic leukemia

Genes chromosomes & cancer, 2001-11, Vol.32 (3), p.244-249

2001

Volltextzugriff (PDF)

Transcriptional Analysis of the Orphan Nuclear Receptor Constitutive Androstane Receptor (NR1I3) Gene Promoter: Identification of a Distal Glucocorticoid Response Element

Molecular endocrinology (Baltimore, Md.), 2003-01, Vol.17 (1), p.42-55

2003

Volltextzugriff (PDF)

Recurrence of OTT-MAL fusion in t(1;22) of infant AML-M7

Genes chromosomes & cancer, 2002-01, Vol.33 (1), p.22-28

2002

Volltextzugriff (PDF)

The TEL gene products: nuclear phosphoproteins with DNA binding properties

Oncogene, 1997-01, Vol.14 (3), p.349-357

1997

Volltextzugriff (PDF)

Analysis of TEL proteins in human leukemias

Oncogene, 1998-06, Vol.16 (22), p.2895-2903

1998

Volltextzugriff (PDF)

Cytogenetic Studies in Acute Promyelocytic Leukemia: A Survey of Secondary Chromosomal Abnormalities

Genes chromosomes & cancer, 1991-09, Vol.3 (5), p.332-337

1991

Volltextzugriff (PDF)

HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis

Blood, 2002-08, Vol.100 (3), p.991-997

2002

Volltextzugriff (PDF)

AF6q21, a Novel Partner of the MLL Gene in t(6; 11)(q21; q23), Defines a Forkhead Transcriptional Factor Subfamily

Blood, 1997-11, Vol.90 (9), p.3714-3719

1997

Volltextzugriff (PDF)

The characterization of murine BCMA gene defines it as a new member of the tumor necrosis factor receptor superfamily

International immunology, 1998-11, Vol.10 (11), p.1693-1702

1998

Volltextzugriff (PDF)

t( 12;21): A new recurrent translocation in acute lymphoblastic leukemia

Genes chromosomes & cancer, 1994-03, Vol.9 (3), p.186-191

1994

Volltextzugriff (PDF)

Breakpoint heterogeneity in t(10;11) translocation in AML-M4/M5 resulting in fusion of AF10 and MLL is resolved by fluorescent in situ hybridization analysis

Cancer research (Chicago, Ill.), 1995-10, Vol.55 (19), p.4220-4224

1995

Volltextzugriff (PDF)

Chromosomal alterations during metastasis formation of head and neck squamous cell carcinoma

Genes chromosomes & cancer, 2002-01, Vol.33 (1), p.29-35

2002

Volltextzugriff (PDF)

Double trisomy 8 and 21 in acute myelocytic leukemias, one with rearrangement of the RUNX1 gene

Cancer genetics and cytogenetics, 2003-04, Vol.142 (2), p.158-161

2003

Volltextzugriff (PDF)

A new case of translocation t(6;11)(q21;q23) in a therapy-related acute myeloid leukemia resulting in anMLL–AF6q21 fusion

Genes chromosomes & cancer, 1998-07, Vol.22 (3), p.221-224

1998

Volltextzugriff (PDF)

Acute megakaryocytic leukaemia with acquired polysomy 21 and translocation t(1;21)

Annales de génétique, 2000-04, Vol.43 (2), p.99-104

2000

Volltextzugriff (PDF)

A new case of translocation t(6;11)(q21;q23) in a therapy-related acute myeloid leukemia resulting in an MLL-AF6q21 fusion

Genes chromosomes & cancer, 1998-07, Vol.22 (3), p.221-224

1998

Volltextzugriff (PDF)

Chromosome abnormalities in bone marrow of Fanconi anemia patients

Cancer genetics and cytogenetics, 1993, Vol.65 (1), p.47-50

1993

Volltextzugriff (PDF)

Partial chromosome 21 amplification in a child with acute lymphoblastic leukemia

Genes chromosomes & cancer, 1995-11, Vol.14 (3), p.204-209

1995

Volltextzugriff (PDF)

Chromosomal localization of the human D3 dopamine receptor gene

Human genetics, 1991-09, Vol.87 (5), p.618-620

1991

Volltextzugriff (PDF)

Loss of the TEL/ETV6 gene by a second translocation in ALL patients with t(12;21)

Leukemia research, 1999-10, Vol.23 (10), p.895-899

1999

Volltextzugriff (PDF)

Genomic Organization of the Human ERM (ETV5) Gene, a PEA3 Group Member of ETS Transcription Factors

Genomics (San Diego, Calif.), 1996-07, Vol.35 (1), p.236-240

1996

Volltextzugriff (PDF)

Chromosomal localization of the human histamine H1-receptor gene

Human genetics, 1994-08, Vol.94 (2), p.186-188

1994

Volltextzugriff (PDF)

The 5-HT2B Receptor Gene Maps to 2q36.3–2q37.1

Genomics (San Diego, Calif.), 1996-02, Vol.32 (1), p.172-173

1996

Volltextzugriff (PDF)

1 – 25 von 73

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(40)
Mit Volltextzugriff
(70)

Publikationsform

Artikel
(73)

Sprache

Englisch
(73)

Erscheinungsjahr

n.n

Thema

Humans
(62)
Science & Technology
(62)
Life Sciences & Biomedicine
(60)
Genetics & Heredity
(51)
Oncology
(42)
Biological And Medical Sciences
(41)
Male
(36)
Female
(35)
Medical Sciences
(31)
Adult
(28)
Hematologic And Hematopoietic Diseases
(26)
Karyotyping
(24)
Leukemias. Malignant Lymphomas. Malignant Reticulosis. Myelofibrosis
(24)
Child
(21)
Chromosome Aberrations
(19)
In Situ Hybridization, Fluorescence
(19)
Translocation, Genetic
(18)
Child, Preschool
(14)
Middle Aged
(14)
Adolescent
(13)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The t(1;12)(q21;p13) Translocation of Human Acute Myeloblastic Leukemia Results in a TEL-ARNT Fusion

Involvement of a Human Gene Related to the Drosophila spen Gene in the Recurrent t(1;22) Translocation of Acute Megakaryocytic Leukemia

Chromosome 21 abnormalities with AML1 amplification in acute lymphoblastic leukemia

Transcriptional Analysis of the Orphan Nuclear Receptor Constitutive Androstane Receptor (NR1I3) Gene Promoter: Identification of a Distal Glucocorticoid Response Element

Recurrence of OTT-MAL fusion in t(1;22) of infant AML-M7

The TEL gene products: nuclear phosphoproteins with DNA binding properties

Analysis of TEL proteins in human leukemias

Cytogenetic Studies in Acute Promyelocytic Leukemia: A Survey of Secondary Chromosomal Abnormalities

HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis

AF6q21, a Novel Partner of the MLL Gene in t(6; 11)(q21; q23), Defines a Forkhead Transcriptional Factor Subfamily

The characterization of murine BCMA gene defines it as a new member of the tumor necrosis factor receptor superfamily

t( 12;21): A new recurrent translocation in acute lymphoblastic leukemia

Breakpoint heterogeneity in t(10;11) translocation in AML-M4/M5 resulting in fusion of AF10 and MLL is resolved by fluorescent in situ hybridization analysis

Chromosomal alterations during metastasis formation of head and neck squamous cell carcinoma

Double trisomy 8 and 21 in acute myelocytic leukemias, one with rearrangement of the RUNX1 gene

A new case of translocation t(6;11)(q21;q23) in a therapy-related acute myeloid leukemia resulting in anMLL–AF6q21 fusion

Acute megakaryocytic leukaemia with acquired polysomy 21 and translocation t(1;21)

A new case of translocation t(6;11)(q21;q23) in a therapy-related acute myeloid leukemia resulting in an MLL-AF6q21 fusion

Chromosome abnormalities in bone marrow of Fanconi anemia patients

Partial chromosome 21 amplification in a child with acute lymphoblastic leukemia

Chromosomal localization of the human D3 dopamine receptor gene

Loss of the TEL/ETV6 gene by a second translocation in ALL patients with t(12;21)

Genomic Organization of the Human ERM (ETV5) Gene, a PEA3 Group Member of ETS Transcription Factors

Chromosomal localization of the human histamine H1-receptor gene

The 5-HT2B Receptor Gene Maps to 2q36.3–2q37.1

Suchergebnisse filtern