UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 267

Sortiert nach

1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis

Journal of medical genetics, 1998-12, Vol.35 (12), p.993-996

1998

Volltextzugriff (PDF)

Aberrant 3′ oligoadenylation of spliceosomal U6 small nuclear RNA in poikiloderma with neutropenia

Blood, 2013-02, Vol.121 (6), p.1028-1038

2013

Volltextzugriff (PDF)

Aberrant activation of stress-response pathways leads to TNF-α oversecretion in Fanconi anemia. Commentary

Blood, 2008, Vol.111 (4)

2008

Volltextzugriff (PDF)

Abstract 1107: Precision phosphoproteomic analysis in Chr22q11.2 amplified NSCLC cells reveals distinct signaling corruption and response to Aurora kinase B inhibition

Cancer research (Chicago, Ill.), 2021-07, Vol.81 (13_Supplement), p.1107-1107

2021

Volltextzugriff (PDF)

Abstract IA19: Dyskeratosis congenita and related syndromes

Cancer research (Chicago, Ill.), 2014-12, Vol.74 (23_Supplement), p.IA19-IA19

Dokal, Inderjeet

2014

Volltextzugriff (PDF)

Abstract LBA013: Phosphoproteomics reveals active drug targets on pathways of resistance and predicts response to midostaurin plus chemotherapy in FLT3 mutant-positive acute myeloid leukemia

Molecular cancer therapeutics, 2021-12, Vol.20 (12_Supplement), p.LBA013-LBA013

2021

Volltextzugriff (PDF)

Acquired somatic variants in inherited myeloid malignancies

Leukemia, 2022-05, Vol.36 (5), p.1377-1381

2022

Volltextzugriff (PDF)

Adult onset of acute myeloid leukaemia (M6) in patients with Shwachman‐Diamond syndrome

British journal of haematology, 1997-10, Vol.99 (1), p.171-173

1997

Volltextzugriff (PDF)

Advances in the understanding of dyskeratosis congenita

British journal of haematology, 2009-04, Vol.145 (2), p.164-172

2009

Volltextzugriff (PDF)

ALLOGENEIC BONE MARROW TRANSPLANTATION FOR PRIMARY MYELOFIBROSIS

British journal of haematology, 1989-01, Vol.71 (1), p.158-160

1989

Volltextzugriff (PDF)

Allogeneic stem cell transplantation for Fanconi Anaemia

Bone marrow transplantation (Basingstoke), 1998-04, Vol.21, p.S24-S27

1998

Volltextzugriff (PDF)

Allogeneic stem cell transplantation for Fanconi Anaemia. Severe Aplastic Anaemia Working Party of the EBMT and EUFAR. European Group for Blood and Marrow Transplantation

Bone marrow transplantation (Basingstoke), 1998-04, Vol.21 Suppl 2, p.S24-S27

1998

Volltextzugriff (PDF)

Analysis of chimaerism in thalassaemic children undergoing stem cell transplantation

British journal of haematology, 2001-07, Vol.114 (1), p.219-225

2001

Volltextzugriff (PDF)

Anti-CD20 Monoclonal Antibodies Hijack the B-Cell Receptor Signaling Cascade Thereby Activating the NOTCH1 Signaling Pathway

Blood, 2018-11, Vol.132 (Supplement 1), p.588-588

2018

Volltextzugriff (PDF)

Approaches to identify kinase dependencies in cancer signalling networks

FEBS letters, 2017-09, Vol.591 (17), p.2577-2592

2017

Volltextzugriff (PDF)

Association between aplastic anaemia and mutations in telomerase RNA

The Lancet (British edition), 2002-06, Vol.359 (9324), p.2168-2170

2002

Volltextzugriff (PDF)

Association of complementation group and mutation type with clinical outcome in Fanconi anemia

Blood, 2000-12, Vol.96 (13), p.4064-4070

2000

Volltextzugriff (PDF)

Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group

Blood, 2000-12, Vol.96 (13), p.4064

2000

Volltextzugriff (PDF)

Ataxia and pancytopenia caused by a mutation in TINF2

Human genetics, 2008-12, Vol.124 (5), p.507-513

2008

Volltextzugriff (PDF)

The biology and management of dyskeratosis congenita and related disorders of telomeres

Expert review of hematology, 2022-08, Vol.15 (8), p.685-696

2022

Volltextzugriff (PDF)

Bone Manifestations of Neurofibromatosis Type 1

Global pediatric health, 2022, Vol.9, p.2333794X221101771-2333794X221101771

2022

Volltextzugriff (PDF)

Bone Manifestations of Neurofibromatosis Type 1

Global pediatric health, 2022, Vol.9, p.2333794X221101771

2022

Volltextzugriff (PDF)

Bone marrow failure syndromes

Stiehm's Immune Deficiencies, 2020, p.411-441

Second Edition, 2020

Volltextzugriff (PDF)

Bone marrow transplantation for (beta)-thalassaemia major: The UK experience in two paediatric centres

British journal of haematology, 2003-01, Vol.120 (2), p.289

2003

Volltextzugriff (PDF)

Bone marrow transplantation for Fanconi's anaemia: conditioning with reduced doses of cyclophosphamide without radiation

British journal of haematology, 1996-08, Vol.94 (2), p.423

1996

Volltextzugriff (PDF)

1 – 25 von 267

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(235)
Mit Volltextzugriff
(234)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(163)
Humans
(157)
Life Sciences & Biomedicine
(155)
Hematology
(95)
Male
(88)
Biological And Medical Sciences
(80)
Female
(78)
Medical Sciences
(76)
Dyskeratosis Congenita - Genetics
(64)
Mutation
(58)
Adult
(53)
Dyskeratosis Congenita
(49)
Adolescent
(44)
Child
(44)
Hematologic And Hematopoietic Diseases
(41)
Pedigree
(38)
Telomerase - Genetics
(36)
Dermatology
(35)
Telomerase
(35)
Child, Preschool
(34)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis

Aberrant 3′ oligoadenylation of spliceosomal U6 small nuclear RNA in poikiloderma with neutropenia

Aberrant activation of stress-response pathways leads to TNF-α oversecretion in Fanconi anemia. Commentary

Abstract 1107: Precision phosphoproteomic analysis in Chr22q11.2 amplified NSCLC cells reveals distinct signaling corruption and response to Aurora kinase B inhibition

Abstract IA19: Dyskeratosis congenita and related syndromes

Abstract LBA013: Phosphoproteomics reveals active drug targets on pathways of resistance and predicts response to midostaurin plus chemotherapy in FLT3 mutant-positive acute myeloid leukemia

Acquired somatic variants in inherited myeloid malignancies

Adult onset of acute myeloid leukaemia (M6) in patients with Shwachman‐Diamond syndrome

Advances in the understanding of dyskeratosis congenita

ALLOGENEIC BONE MARROW TRANSPLANTATION FOR PRIMARY MYELOFIBROSIS

Allogeneic stem cell transplantation for Fanconi Anaemia

Allogeneic stem cell transplantation for Fanconi Anaemia. Severe Aplastic Anaemia Working Party of the EBMT and EUFAR. European Group for Blood and Marrow Transplantation

Analysis of chimaerism in thalassaemic children undergoing stem cell transplantation

Anti-CD20 Monoclonal Antibodies Hijack the B-Cell Receptor Signaling Cascade Thereby Activating the NOTCH1 Signaling Pathway

Approaches to identify kinase dependencies in cancer signalling networks

Association between aplastic anaemia and mutations in telomerase RNA

Association of complementation group and mutation type with clinical outcome in Fanconi anemia

Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group

Ataxia and pancytopenia caused by a mutation in TINF2

The biology and management of dyskeratosis congenita and related disorders of telomeres

Bone Manifestations of Neurofibromatosis Type 1

Bone Manifestations of Neurofibromatosis Type 1

Bone marrow failure syndromes

Bone marrow transplantation for (beta)-thalassaemia major: The UK experience in two paediatric centres

Bone marrow transplantation for Fanconi's anaemia: conditioning with reduced doses of cyclophosphamide without radiation

Suchergebnisse filtern