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...

Mutation patterns of 16 genes in primary and secondary acute myeloid leukemia (AML) with normal cytogenetics

PloS one, 2012-08, Vol.7 (8), p.e42334-e42334

2012

Volltextzugriff (PDF)

TET2 mutations are associated with specific 5-methylcytosine and 5-hydroxymethylcytosine profiles in patients with chronic myelomonocytic leukemia

PloS one, 2012-02, Vol.7 (2), p.e31605-e31605

2012

Volltextzugriff (PDF)

Identification of Gene Expression–Based Prognostic Markers in the Hematopoietic Stem Cells of Patients With Myelodysplastic Syndromes

Journal of clinical oncology, 2013-10, Vol.31 (28), p.3557-3564

2013

Volltextzugriff (PDF)

MicroRNA expression in multiple myeloma is associated with genetic subtype, isotype and survival

Biology direct, 2011-05, Vol.6 (1), p.23-23, Article 23

2011

Volltextzugriff (PDF)

The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts

PloS one, 2008-04, Vol.3 (4), p.e1970-e1970

2008

Volltextzugriff (PDF)

5q- syndrome

Current pharmaceutical design, 2012, Vol.18 (22), p.3180-3183

2012

Volltextzugriff (PDF)

Presence of fetal DNA in maternal plasma and serum

The Lancet (British edition), 1997-08, Vol.350 (9076), p.485-487

1997

Volltextzugriff (PDF)

A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q– syndrome

Nature medicine, 2010-01, Vol.16 (1), p.59-66

2010

Volltextzugriff (PDF)

Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype

PloS one, 2011-06, Vol.6 (6), p.e20607-e20607

2011

Volltextzugriff (PDF)

Activation of the mTOR pathway by the amino acid l-leucine in the 5q- syndrome and other ribosomopathies

Advances in biological regulation, 2013-01, Vol.53 (1), p.8-17

2013

Volltextzugriff (PDF)

Clonality in the myelodysplastic syndromes

International journal of hematology, 2001-06, Vol.73 (4), p.411-415

2001

Volltextzugriff (PDF)

Haploinsufficiency of ribosomal proteins and p53 activation in anemia: Diamond-Blackfan anemia and the 5q- syndrome

Advances in biological regulation, 2012-01, Vol.52 (1), p.196-203

2012

Volltextzugriff (PDF)

Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

American journal of human genetics, 1998-04, Vol.62 (4), p.768-775

1998

Volltextzugriff (PDF)

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

Nature genetics, 2003-08, Vol.34 (4), p.446-449

2003

Volltextzugriff (PDF)

The role of cell-free DNA size distribution in the management of prostate cancer

Oncology research, 2006, Vol.16 (1), p.35-41

2006

Volltextzugriff (PDF)

Transcription Mapping of the 5q− Syndrome Critical Region: Cloning of Two Novel Genes and Sequencing, Expression, and Mapping of a Further Six Novel cDNAs

Genomics (San Diego, Calif.), 2000-05, Vol.66 (1), p.26-34

2000

Volltextzugriff (PDF)

The HumanPOP2Gene: Identification, Sequencing, and Mapping to the Critical Region of the 5q- Syndrome

Genomics (San Diego, Calif.), 1999-02, Vol.56 (1), p.134-136

1999

Volltextzugriff (PDF)

Novel Genes Mapping to the Critical Region of the 5q− Syndrome

Genomics (San Diego, Calif.), 1997-10, Vol.45 (1), p.88-96

1997

Volltextzugriff (PDF)

Mutation Patterns of 16 Genes in Primary and Secondary Acute Myeloid Leukemia

PloS one, 2012-08, Vol.7 (8), p.e42334

2012

Volltextzugriff (PDF)

Activation of the mTOR pathway by the amino acid (L)-leucine in the 5q- syndrome and other ribosomopathies

Advances in biological regulation, 2013-01, Vol.53 (1), p.8

2013

Volltextzugriff (PDF)

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the [alpha]-thalassemia myelodysplasia syndrome (ATMDS)

Nature genetics, 2003-08, Vol.34 (4), p.446

2003

Volltextzugriff (PDF)

The human POP2 gene : Identification, sequencing, and mapping to the critical region of the 5q- syndrome

Genomics (San Diego, Calif.), 1999-02, Vol.56 (1), p.134-136

1999

Volltextzugriff (PDF)

Prenatal sex determination from maternal peripheral blood using the polymerase chain reaction

Human genetics, 1993, Vol.90 (5), p.483-488

1993

Volltextzugriff (PDF)

Detection of susceptability alleles to insulin-dependent diabetes mellitus at the DQB1 locus by artificial PCR-RFLP

Immunogenetics (New York), 1992-07, Vol.36 (4), p.264-265

1992

Volltextzugriff (PDF)

Translocation 1;7 in hematologic disorders—A report of three further cases

Cancer genetics and cytogenetics, 1991-05, Vol.53 (1), p.91-95

1991

Volltextzugriff (PDF)

1 – 25 von 28

Suche als RSS-Feed

Aktive Filter

KollektionIngenta

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(26)
Mit Volltextzugriff
(25)

Publikationsform

Artikel
(28)

Sprache

Englisch
(28)

Erscheinungsjahr

n.n

Thema

Humans
(20)
Science & Technology
(19)
Life Sciences & Biomedicine
(13)
Biological And Medical Sciences
(10)
Male
(10)
Female
(9)
Medical Sciences
(9)
Genetics
(7)
Myelodysplastic Syndromes - Genetics
(7)
Genetic Aspects
(6)
Genetics & Heredity
(6)
Hematology
(6)
Mutation
(6)
Aged
(5)
Chromosome Deletion
(5)
Deoxyribonucleic Acid
(5)
Dna
(5)
Gene Expression
(5)
Genes
(5)
Hematologic And Hematopoietic Diseases
(5)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mutation patterns of 16 genes in primary and secondary acute myeloid leukemia (AML) with normal cytogenetics

TET2 mutations are associated with specific 5-methylcytosine and 5-hydroxymethylcytosine profiles in patients with chronic myelomonocytic leukemia

Identification of Gene Expression–Based Prognostic Markers in the Hematopoietic Stem Cells of Patients With Myelodysplastic Syndromes

MicroRNA expression in multiple myeloma is associated with genetic subtype, isotype and survival

The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts

5q- syndrome

Presence of fetal DNA in maternal plasma and serum

A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q– syndrome

Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype

Activation of the mTOR pathway by the amino acid l-leucine in the 5q- syndrome and other ribosomopathies

Clonality in the myelodysplastic syndromes

Haploinsufficiency of ribosomal proteins and p53 activation in anemia: Diamond-Blackfan anemia and the 5q- syndrome

Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

The role of cell-free DNA size distribution in the management of prostate cancer

Transcription Mapping of the 5q− Syndrome Critical Region: Cloning of Two Novel Genes and Sequencing, Expression, and Mapping of a Further Six Novel cDNAs

The HumanPOP2Gene: Identification, Sequencing, and Mapping to the Critical Region of the 5q- Syndrome

Novel Genes Mapping to the Critical Region of the 5q− Syndrome

Mutation Patterns of 16 Genes in Primary and Secondary Acute Myeloid Leukemia

Activation of the mTOR pathway by the amino acid (L)-leucine in the 5q- syndrome and other ribosomopathies

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the [alpha]-thalassemia myelodysplasia syndrome (ATMDS)

The human POP2 gene : Identification, sequencing, and mapping to the critical region of the 5q- syndrome

Prenatal sex determination from maternal peripheral blood using the polymerase chain reaction

Detection of susceptability alleles to insulin-dependent diabetes mellitus at the DQB1 locus by artificial PCR-RFLP

Translocation 1;7 in hematologic disorders—A report of three further cases

Aktive Filter

Suchergebnisse filtern