UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 58

Sortiert nach

Phagocytosis-initiated tumor hybrid cells acquire a c-Myc-mediated quasi-polarization state for immunoevasion and distant dissemination

Nature communications, 2023-10, Vol.14 (1), p.6569-6569, Article 6569

2023

Volltextzugriff (PDF)

Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences

Journal of medical genetics, 2023-06, Vol.60 (6), p.547

2023

Volltextzugriff (PDF)

Is 5q deletion in de novo Acute Myelogenous Leukemia (AML) with excess blasts a surrogate marker for the cryptic t(7;21)(p22;q22)? A case report and review of literature

Cancer genetics, 2022-04, Vol.262-263, p.30-34

2022

Volltextzugriff (PDF)

Oxidatively modified low‐density lipoproteins are potential mediators of proteasome inhibitor resistance in multiple myeloma

International journal of cancer, 2021-06, Vol.148 (12), p.3032-3040

2021

Volltextzugriff (PDF)

Abstract 4902: Oxidized low-density lipoprotein is a potentially potent mediator of proteasome inhibitor resistance in multiple myeloma

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.4902-4902

2018

Volltextzugriff (PDF)

Identification of Chromothripsis in Biopsy Using SNP-Based Microarray

Methods in molecular biology (Clifton, N.J.), 2018, Vol.1769, p.85

2018

Volltextzugriff (PDF)

Myelodysplasia and Mast Cell Leukemia with t(9;22)

Case reports in oncological medicine, 2017, Vol.2017, p.9249302-9249302

2017

Volltextzugriff (PDF)

Myelodysplasia and Mast Cell Leukemia with t(9;22)

Case reports in oncological medicine, 2017-01, Vol.2017, p.9249302-5

2017

Volltextzugriff (PDF)

Cytogenetic abnormalities precede morphological abnormalities in developing malignant conditions: Report of 2 cases

Experimental and molecular pathology, 2013-02, Vol.94 (1), p.98-102

2013

Volltextzugriff (PDF)

Fetoplacental Discrepancy with Normal Karyotype in Amniotic Fluid and Two Different Cell Lines in Placenta

Case reports in genetics, 2013-01, Vol.2013, p.951710-4

2013

Volltextzugriff (PDF)

A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma

Cancer genetics, 2011-12, Vol.204 (12), p.666-670

2011

Volltextzugriff (PDF)

A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia

European journal of medical genetics, 2011-07, Vol.54 (4), p.e394-e398

2011

Volltextzugriff (PDF)

Pericentric inversion, inv(14)(p11.2q22.3), in a 9-month old with features of Goldenhar syndrome

Clinical dysmorphology, 2010-10, Vol.19 (4), p.185

2010

Volltextzugriff (PDF)

Amplification of the RARA gene in acute myeloid leukemia: significant finding or coincidental observation?

Cancer genetics and cytogenetics, 2010-10, Vol.202 (1), p.33-37

2010

Volltextzugriff (PDF)

Fusion of HMGA2 to COG5 in uterine leiomyoma

Cancer genetics and cytogenetics, 2010-10, Vol.202 (1), p.11-16

2010

Volltextzugriff (PDF)

A case of Down syndrome with mirror-image duplication of chromosome 21

American journal of medical genetics. Part A, 2010-06, Vol.152A (6), p.1580-1582

2010

Volltextzugriff (PDF)

The phenotypic spectrum of trisomy 2: report of two new cases

Clinical dysmorphology, 2009-10, Vol.18 (4), p.201

2009

Volltextzugriff (PDF)

Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3‐month‐old with severe pediatric gastroesophageal reflux

American journal of medical genetics. Part A, 2009-04, Vol.149A (4), p.751-754

2009

Volltextzugriff (PDF)

First report of an interstitial deletion, del(5)(q33.1q35.1) in a girl with primary amenorrhea, seizures, and severe behavioral and developmental deficiencies

American journal of medical genetics. Part A, 2008-10, Vol.146A (19), p.2578-2582

2008

Volltextzugriff (PDF)

Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family

Indian journal of pediatrics, 2008-09, Vol.75 (9), p.956-960

2008

Volltextzugriff (PDF)

Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features

American journal of medical genetics. Part A, 2008-09, Vol.146A (17), p.2234-2241

2008

Volltextzugriff (PDF)

Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement

American journal of medical genetics. Part A, 2008-05, Vol.146A (9), p.1166-1172

2008

Volltextzugriff (PDF)

Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?

European journal of haematology, 2007-02, Vol.78 (2), p.152-156

2007

Volltextzugriff (PDF)

Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?

European Journal of Haematology, 2007, Vol.78 (2), p.152-156

2007

Volltextzugriff (PDF)

Cytogenetic and molecular studies of an unusual case of multiple primary alveolar rhabdomyosarcomas: Low-level chromosomal instability and reciprocal translocation t(6;11)

Experimental and molecular pathology, 2007-02, Vol.82 (1), p.58-62

2007

Volltextzugriff (PDF)

1 – 25 von 58

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(35)
Mit Volltextzugriff
(53)

Publikationsform

Artikel
(56)
Berichte
(2)

Sprache

Englisch
(57)
Japanisch
(3)

Erscheinungsjahr

n.n

Thema

Humans
(49)
Science & Technology
(46)
Life Sciences & Biomedicine
(45)
Genetics & Heredity
(35)
Biological And Medical Sciences
(31)
Karyotyping
(30)
Medical Sciences
(30)
Female
(27)
Male
(22)
In Situ Hybridization, Fluorescence
(21)
Chromosome Aberrations
(20)
Medical Genetics
(16)
Adult
(15)
Translocation, Genetic
(14)
Oncology
(13)
Chromosome Deletion
(12)
Abnormalities, Multiple - Genetics
(10)
Child
(10)
Fish
(10)
Infant
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Phagocytosis-initiated tumor hybrid cells acquire a c-Myc-mediated quasi-polarization state for immunoevasion and distant dissemination

Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences

Is 5q deletion in de novo Acute Myelogenous Leukemia (AML) with excess blasts a surrogate marker for the cryptic t(7;21)(p22;q22)? A case report and review of literature

Oxidatively modified low‐density lipoproteins are potential mediators of proteasome inhibitor resistance in multiple myeloma

Abstract 4902: Oxidized low-density lipoprotein is a potentially potent mediator of proteasome inhibitor resistance in multiple myeloma

Identification of Chromothripsis in Biopsy Using SNP-Based Microarray

Myelodysplasia and Mast Cell Leukemia with t(9;22)

Myelodysplasia and Mast Cell Leukemia with t(9;22)

Cytogenetic abnormalities precede morphological abnormalities in developing malignant conditions: Report of 2 cases

Fetoplacental Discrepancy with Normal Karyotype in Amniotic Fluid and Two Different Cell Lines in Placenta

A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma

A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia

Pericentric inversion, inv(14)(p11.2q22.3), in a 9-month old with features of Goldenhar syndrome

Amplification of the RARA gene in acute myeloid leukemia: significant finding or coincidental observation?

Fusion of HMGA2 to COG5 in uterine leiomyoma

A case of Down syndrome with mirror-image duplication of chromosome 21

The phenotypic spectrum of trisomy 2: report of two new cases

Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3‐month‐old with severe pediatric gastroesophageal reflux

First report of an interstitial deletion, del(5)(q33.1q35.1) in a girl with primary amenorrhea, seizures, and severe behavioral and developmental deficiencies

Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family

Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features

Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement

Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?

Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?

Cytogenetic and molecular studies of an unusual case of multiple primary alveolar rhabdomyosarcomas: Low-level chromosomal instability and reciprocal translocation t(6;11)

Suchergebnisse filtern