UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 70

Sortiert nach

Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients

Journal of medical genetics, 2007-12, Vol.44 (12), p.750-762

2007

Volltextzugriff (PDF)

Twenty years of the Italian Fanconi Anemia Registry: where we stand and what remains to be learned

Haematologica (Roma), 2016-03, Vol.101 (3), p.319

2016

Volltextzugriff (PDF)

A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia

Leukemia, 2007, Vol.21 (1), p.72-78

2007

Volltextzugriff (PDF)

Transferable clastogenic activity in plasma from patients with Fanconi anemia

Human genetics, 1995-07, Vol.96 (1), p.14-20

1995

Volltextzugriff (PDF)

Mitomycin C–Induced DNA Damage in Fanconi Anemia: Cross-Linking or Redox-Mediated Effects?

Blood, 1999-02, Vol.93 (3), p.1116-1117

1999

Volltextzugriff (PDF)

In vitro hypersensitivity to oxygen of Fanconi anemia (FA) cells is linked to ex vivo evidence for oxidative stress in FA homozygotes and heterozygotes

Blood, 1997-02, Vol.89 (3), p.1111-1111

1997

Volltextzugriff (PDF)

Oxidative stress as a multiple effector in Fanconi anaemia clinical phenotype

European journal of haematology, 2005-08, Vol.75 (2), p.93-100

2005

Volltextzugriff (PDF)

Congenital disorders sharing oxidative stress and cancer proneness as phenotypic hallmarks: prospects for joint research in pharmacology

Medical hypotheses, 1998-09, Vol.51 (3), p.253-266

1998

Volltextzugriff (PDF)

Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases

Genes chromosomes & cancer, 2002-01, Vol.33 (1), p.93-97

2002

Volltextzugriff (PDF)

In vivo prooxidant state in Werner syndrome (WS): Results from three WS patients and two WS heterozygotes

Free radical research, 2005-05, Vol.39 (5), p.529-533

2005

Volltextzugriff (PDF)

Identification and treatment of late onset Fanconi's anemia

Haematologica (Roma), 1995-11, Vol.80 (6), p.535

1995

Volltextzugriff (PDF)

Gender- and age-related distinctions for the in vivo prooxidant state in Fanconi anaemia patients

Carcinogenesis (New York), 2004-10, Vol.25 (10), p.1899-1909

2004

Volltextzugriff (PDF)

Fanconi anaemia proteins: Major roles in cell protection against oxidative damage

BioEssays, 2003-06, Vol.25 (6), p.589-595

2003

Volltextzugriff (PDF)

Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy

Human genetics, 2005-11, Vol.118 (1), p.76-81

2005

Volltextzugriff (PDF)

Multiple involvement of oxidative stress in Werner syndrome phenotype

Biogerontology (Dordrecht), 2005-09, Vol.6 (4), p.233-243

2005

Volltextzugriff (PDF)

In vivo accumulation of 8-hydroxy-2'-deoxyguanosine in DNA correlates with release of reactive oxygen species in Fanconi's anaemia families

Carcinogenesis (New York), 1995-04, Vol.16 (4), p.735-742

1995

Volltextzugriff (PDF)

Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9

European journal of human genetics : EJHG, 2000-11, Vol.8 (11), p.861-868

2000

Volltextzugriff (PDF)

Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis

American journal of medical genetics, 2004-06, Vol.127A (2), p.144-148

2004

Volltextzugriff (PDF)

Cytoskeleton alterations of erythrocytes from patients with Fanconi’s anemia

FEBS letters, 2000-02, Vol.468 (2), p.125-128

2000

Volltextzugriff (PDF)

Spectrin Changes Occur in Erythrocytes from Patients with Fanconi's Anemia and Their Parents

Biochemical and biophysical research communications, 2000-07, Vol.273 (3), p.899-901

2000

Volltextzugriff (PDF)

Resistance to apoptosis in Fanconi's anaemia: An ex vivo study in peripheral blood mononuclear cells

FEBS letters, 1997-06, Vol.409 (3), p.365-369

1997

Volltextzugriff (PDF)

Multiple endocrine neoplasia type 2 (Sipple's syndrome): clinical and cytogenetic analysis of a kindred

Journal of medical genetics, 1984-04, Vol.21 (2), p.108-111

1984

Volltextzugriff (PDF)

Fanconi anaemia in Italy : high prevalence of complementation group A in two geographic clusters

Human genetics, 1996-05, Vol.97 (5), p.599-603

1996

Volltextzugriff (PDF)

Il Registro Italiano Anemia di Fanconi: Prevenzione dei fattori di rischio della salute materno-infantile

Annali dell'Istituto superiore di sanità, 1999, Vol.35 (2), p.233-235

1999

Volltextzugriff (PDF)

The Italian Fanconi Anemia Registry

Annali dell'Istituto superiore di sanità, 1999, Vol.35 (2), p.233-235

1999

Volltextzugriff (PDF)

1 – 25 von 70

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(69)
Mit Volltextzugriff
(65)

Publikationsform

Artikel
(70)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Blood
(5)
Human Genetics
(5)
Annali Dell'istituto Superiore Di Sanità
(4)
Carcinogenesis
(3)
Cells
(3)
Febs Letters
(3)
International Journal Of Molecular Sciences
(3)
Biogerontology
(2)
Clinical Biochemistry
(2)
Clinical Epigenetics
(2)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients

Twenty years of the Italian Fanconi Anemia Registry: where we stand and what remains to be learned

A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia

Transferable clastogenic activity in plasma from patients with Fanconi anemia

Mitomycin C–Induced DNA Damage in Fanconi Anemia: Cross-Linking or Redox-Mediated Effects?

In vitro hypersensitivity to oxygen of Fanconi anemia (FA) cells is linked to ex vivo evidence for oxidative stress in FA homozygotes and heterozygotes

Oxidative stress as a multiple effector in Fanconi anaemia clinical phenotype

Congenital disorders sharing oxidative stress and cancer proneness as phenotypic hallmarks: prospects for joint research in pharmacology

Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases

In vivo prooxidant state in Werner syndrome (WS): Results from three WS patients and two WS heterozygotes

Identification and treatment of late onset Fanconi's anemia

Gender- and age-related distinctions for the in vivo prooxidant state in Fanconi anaemia patients

Fanconi anaemia proteins: Major roles in cell protection against oxidative damage

Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy

Multiple involvement of oxidative stress in Werner syndrome phenotype

In vivo accumulation of 8-hydroxy-2'-deoxyguanosine in DNA correlates with release of reactive oxygen species in Fanconi's anaemia families

Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9

Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis

Cytoskeleton alterations of erythrocytes from patients with Fanconi’s anemia

Spectrin Changes Occur in Erythrocytes from Patients with Fanconi's Anemia and Their Parents

Resistance to apoptosis in Fanconi's anaemia: An ex vivo study in peripheral blood mononuclear cells

Multiple endocrine neoplasia type 2 (Sipple's syndrome): clinical and cytogenetic analysis of a kindred

Fanconi anaemia in Italy : high prevalence of complementation group A in two geographic clusters

Il Registro Italiano Anemia di Fanconi: Prevenzione dei fattori di rischio della salute materno-infantile

The Italian Fanconi Anemia Registry

Suchergebnisse filtern