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...

MPL mutations in myeloproliferative disorders: analysis of the PT-1 cohort

Blood, 2008-07, Vol.112 (1), p.141-149

2008

Volltextzugriff (PDF)

Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study

The Lancet (British edition), 2005-12, Vol.366 (9501), p.1945-1953

2005

Volltextzugriff (PDF)

Molecular diagnosis of the myeloproliferative neoplasms: UK guidelines for the detection of JAK2 V617F and other relevant mutations

British journal of haematology, 2013-01, Vol.160 (1), p.25-34

2013

Volltextzugriff (PDF)

Clinical utility of routine MPL exon 10 analysis in the diagnosis of essential thrombocythaemia and primary myelofibrosis

British journal of haematology, 2010-04, Vol.149 (2), p.250-257

2010

Volltextzugriff (PDF)

Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

The Lancet (British edition), 2005-03, Vol.365 (9464), p.1054-1061

2005

Volltextzugriff (PDF)

Mutation of JAK2 in the myeloproliferative disorders: timing, clonality studies, cytogenetic associations, and role in leukemic transformation

Blood, 2006-11, Vol.108 (10), p.3548-3555

2006

Volltextzugriff (PDF)

Effects of the JAK2 mutation on the hematopoietic stem and progenitor compartment in human myeloproliferative neoplasms

Blood, 2011-07, Vol.118 (1), p.177-181

2011

Volltextzugriff (PDF)

High resolution melting analysis for detection of BRAF exon 15 mutations in hairy cell leukaemia and other lymphoid malignancies

British journal of haematology, 2011-12, Vol.155 (5), p.609-612

2011

Volltextzugriff (PDF)

Phospho‐STAT5 and phospho‐Akt expression in chronic myeloproliferative neoplasms

British journal of haematology, 2009-11, Vol.147 (4), p.495-506

2009

Volltextzugriff (PDF)

Methylation of the suppressor of cytokine signaling 3 gene (SOCS3) in myeloproliferative disorders

Haematologica (Roma), 2008-11, Vol.93 (11), p.1635-1644

2008

Volltextzugriff (PDF)

A practical strategy for the routine use of BIOMED‐2 PCR assays for detection of B‐ and T‐cell clonality in diagnostic haematopathology

British journal of haematology, 2007-07, Vol.138 (1), p.31-43

2007

Volltextzugriff (PDF)

Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions

The Journal of clinical investigation, 2013-05, Vol.123 (5), p.2169-2182

2013

Volltextzugriff (PDF)

Clonal diversity in the myeloproliferative neoplasms: independent origins of genetically distinct clones

British journal of haematology, 2009-03, Vol.144 (6), p.904-908

2009

Volltextzugriff (PDF)

Deletions of the derivative chromosome 9 occur at the time of the Philadelphia translocation and provide a powerful and independent prognostic indicator in chronic myeloid leukemia

Blood, 2001-09, Vol.98 (6), p.1732-1738

2001

Volltextzugriff (PDF)

Prevalance of JAK2 V617F and exon 12 mutations in polycythaemia vera

British journal of haematology, 2007-11, Vol.139 (3), p.511-512

2007

Volltextzugriff (PDF)

Imprinting of the Human L3MBTL Gene, a Polycomb Family Member Located in a Region of Chromosome 20 Deleted in Human Myeloid Malignancies

Proceedings of the National Academy of Sciences - PNAS, 2004-05, Vol.101 (19), p.7341-7346

2004

Volltextzugriff (PDF)

Analysis of vertebrate SCL loci identifies conserved enhancers

Nature biotechnology, 2000-02, Vol.18 (2), p.181-186

2000

Volltextzugriff (PDF)

Chromosome 20 deletions in myeloid malignancies : reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes

Oncogene, 2000-08, Vol.19 (34), p.3902-3913

2000

Volltextzugriff (PDF)

Quantification of PRV-1 mRNA distinguishes polycythemia vera from secondary erythrocytosis

Blood, 2003-11, Vol.102 (10), p.3569-3574

2003

Volltextzugriff (PDF)

Can cytoplasmic nucleophosmin be detected by immunocytochemical staining of cell smears in acute myeloid leukemia?

Haematologica (Roma), 2010-04, Vol.95 (4), p.670-673

2010

Volltextzugriff (PDF)

Chromosomal Abnormalities and Molecular Markers in Myeloproliferative Disorders

Seminars in hematology, 2005-10, Vol.42 (4), p.196-205

2005

Volltextzugriff (PDF)

Size matters: the prognostic implications of large and small deletions of the derivative 9 chromosome in chronic myeloid leukemia

Haematologica (Roma), 2006-07, Vol.91 (7), p.952

2006

Volltextzugriff (PDF)

Derivative chromosome 9 deletions in chronic myeloid leukemia: poor prognosis is not associated with loss of ABL-BCR expression, elevated BCR-ABL levels, or karyotypic instability

Blood, 2002-06, Vol.99 (12), p.4547-4553

2002

Volltextzugriff (PDF)

Methods for detecting mutations in the human JAK2 gene

Methods in molecular biology (Clifton, N.J.), 2013, Vol.967, p.115

2013

Volltextzugriff (PDF)

1 – 25 von 76

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(66)
Mit Volltextzugriff
(68)

Publikationsform

Sprache

Englisch
(75)
Japanisch
(17)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(45)
Humans
(42)
Life Sciences & Biomedicine
(42)
Hematology
(33)
Biological And Medical Sciences
(28)
Hematologic And Hematopoietic Diseases
(23)
Medical Sciences
(23)
Leukemias. Malignant Lymphomas. Malignant Reticulosis. Myelofibrosis
(21)
Mutation
(15)
Female
(14)
Myeloproliferative Disorders - Genetics
(14)
Male
(11)
Janus Kinase 2 - Genetics
(9)
Middle Aged
(9)
Aged
(8)
Base Sequence
(8)
Chromosome Deletion
(8)
Polycythemia Vera - Genetics
(8)
Animals
(7)
Adult
(6)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Blood
(16)
British Journal Of Haematology
(16)
Genomics
(3)
Haematologica
(3)
Hematology
(3)
Oncogene
(3)
The Lancet
(3)
Best Practice & Research. Clinical Haematology
(2)
Clinical Chemistry And Laboratory Medicine
(2)
Physical Review Letters
(2)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

MPL mutations in myeloproliferative disorders: analysis of the PT-1 cohort

Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study

Molecular diagnosis of the myeloproliferative neoplasms: UK guidelines for the detection of JAK2 V617F and other relevant mutations

Clinical utility of routine MPL exon 10 analysis in the diagnosis of essential thrombocythaemia and primary myelofibrosis

Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

Development and validation of a comprehensive genomic diagnostic tool for myeloid malignancies

Mutation of JAK2 in the myeloproliferative disorders: timing, clonality studies, cytogenetic associations, and role in leukemic transformation

Effects of the JAK2 mutation on the hematopoietic stem and progenitor compartment in human myeloproliferative neoplasms

High resolution melting analysis for detection of BRAF exon 15 mutations in hairy cell leukaemia and other lymphoid malignancies

Phospho‐STAT5 and phospho‐Akt expression in chronic myeloproliferative neoplasms

Methylation of the suppressor of cytokine signaling 3 gene (SOCS3) in myeloproliferative disorders

A practical strategy for the routine use of BIOMED‐2 PCR assays for detection of B‐ and T‐cell clonality in diagnostic haematopathology

Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions

Clonal diversity in the myeloproliferative neoplasms: independent origins of genetically distinct clones

Deletions of the derivative chromosome 9 occur at the time of the Philadelphia translocation and provide a powerful and independent prognostic indicator in chronic myeloid leukemia

Prevalance of JAK2 V617F and exon 12 mutations in polycythaemia vera

Imprinting of the Human L3MBTL Gene, a Polycomb Family Member Located in a Region of Chromosome 20 Deleted in Human Myeloid Malignancies

Analysis of vertebrate SCL loci identifies conserved enhancers

Chromosome 20 deletions in myeloid malignancies : reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes

Quantification of PRV-1 mRNA distinguishes polycythemia vera from secondary erythrocytosis

Can cytoplasmic nucleophosmin be detected by immunocytochemical staining of cell smears in acute myeloid leukemia?

Chromosomal Abnormalities and Molecular Markers in Myeloproliferative Disorders

Size matters: the prognostic implications of large and small deletions of the derivative 9 chromosome in chronic myeloid leukemia

Derivative chromosome 9 deletions in chronic myeloid leukemia: poor prognosis is not associated with loss of ABL-BCR expression, elevated BCR-ABL levels, or karyotypic instability

Methods for detecting mutations in the human JAK2 gene

Suchergebnisse filtern