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...

Stromal Fibroblasts Present in Invasive Human Breast Carcinomas Promote Tumor Growth and Angiogenesis through Elevated SDF-1/CXCL12 Secretion

Cell, 2005-05, Vol.121 (3), p.335-348

2005

Volltextzugriff (PDF)

Call for improvement in medical school training in genetics: results of a national survey

Genetics in medicine, 2021-06, Vol.23 (6), p.1151-1157

2021

Volltextzugriff (PDF)

Identifying the current status and future needs of clinical, educational, and laboratory genetics services in Pakistan: a web-based panel discussion

Journal of community genetics, 2023-02, Vol.14 (1), p.71-80

2023

Volltextzugriff (PDF)

Overexpression of Eg5 Causes Genomic Instability and Tumor Formation in Mice

Cancer research (Chicago, Ill.), 2007-11, Vol.67 (21), p.10138-10147

2007

Volltextzugriff (PDF)

Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q

Blood, 2008-08, Vol.112 (4), p.1042-1047

2008

Volltextzugriff (PDF)

Quantitation of Aurora Kinase A Gene Copy Number in Urine Sediments and Bladder Cancer Detection

JNCI : Journal of the National Cancer Institute, 2008-10, Vol.100 (19), p.1401-1411

2008

Volltextzugriff (PDF)

De novo mosaic and partial monosomy of chromosome 21 in a case with superior vena cava duplication

Molecular cytogenetics, 2020-09, Vol.13 (1), p.45-7, Article 45

2020

Volltextzugriff (PDF)

Myelodysplastic syndromes arising in patients with germline TP53 mutation and Li-Fraumeni syndrome

Archives of pathology & laboratory medicine (1976), 2010-07, Vol.134 (7), p.1010-1015

2010

Volltextzugriff (PDF)

Overexpression of MAGE/GAGE Genes in Paclitaxel/Doxorubicin-resistant Human Cancer Cell Lines

Clinical cancer research, 2003-07, Vol.9 (7), p.2778-2785

2003

Volltextzugriff (PDF)

Cloned transchromosomic calves producing human immunoglobulin

Nature biotechnology, 2002-09, Vol.20 (9), p.889-894

2002

Volltextzugriff (PDF)

Identifying unnecessary duplicate genetic testing in a large medical center

American journal of clinical pathology, 2021-10, Vol.156 (Supplement_1), p.S9-S10

2021

Volltextzugriff (PDF)

Pitfalls of using polymerase chain reaction-based assays for JAK2 and CALR exon 9 variant testing in myeloproliferative neoplasms: Knowing when to go the extra mile

American journal of clinical pathology, 2024-02, Vol.161 (2), p.155-161

2024

Volltextzugriff (PDF)

p53 Immunoreactivity Score Correlates With Predicted Gene Sequence Alterations of Variants Detected by Next-Generation Sequencing

Archives of pathology & laboratory medicine (1976), 2024-09, Vol.148 (9), p.E268-E268

2024

Volltextzugriff (PDF)

Clinical validation of the Ion Torrent Oncomine Myeloid Assay GX v2 on the Genexus Integrated Sequencer as a stand-alone assay for single-nucleotide variants, insertions/deletions, and fusion genes: Challenges, performance, and perspectives

American journal of clinical pathology, 2024-06

2024

Volltextzugriff (PDF)

The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program Directors

Genetics in Medicine Open, 2024, Vol.2, p.101820, Article 101820

2024

Volltextzugriff (PDF)

Medical students' self‐perceived knowledge and clinical comfort with genetics in Pakistan

Journal of genetic counseling, 2024-10, Vol.33 (5), p.1113-1125

2024

Volltextzugriff (PDF)

What Are We Missing? High Risk Human Papilloma Virus (HPV) Genotype and Cytology Correlates in a Diverse Bronx Population

Journal of the American Society of Cytopathology JASC, 2016-09, Vol.5 (5), p.S38-S38

2016

Volltextzugriff (PDF)

Developing medical genetics in a low-income country: Unveiling the journey of the Pakistani Society of Medical Genetics and Genomics (PSMG)

Genetics in Medicine Open, 2024-08, p.101883, Article 101883

2024

Volltextzugriff (PDF)

Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia

Pediatric Blood & Cancer, 2008-08, Vol.51 (2), p.171-177

2008

Volltextzugriff (PDF)

eP478: Identifying the current status and future needs of clinical, educational, and laboratory genetics services in Pakistan: A web-based panel discussion

Genetics in medicine, 2022-03, Vol.24 (3), p.S304-S305

2022

Volltextzugriff (PDF)

Hypopigmented mycosis fungoides in childhood and adolescence: a long-term retrospective study

Journal of cutaneous pathology, 2013-11, Vol.40 (11), p.924-934

2013

Volltextzugriff (PDF)

Molecular monitoring of 8p11 myeloproliferative syndrome in an infant

Journal of pediatric hematology/oncology, 2009-11, Vol.31 (11), p.879-883

2009

Volltextzugriff (PDF)

Karyotypic complexity, TP53 pathogenic variants, and increased number of variants on Next‐Generation Sequencing are associated with disease progression in a North American Adult T‐Cell Leukemia/Lymphoma cohort

International journal of laboratory hematology, 2021-08, Vol.43 (4), p.651-657

2021

Volltextzugriff (PDF)

Ameloblastoma with adenoid features: Case report with cyto‐histopathologic correlation and molecular findings

Diagnostic cytopathology, 2022-06, Vol.50 (6), p.E140-E145

2022

Volltextzugriff (PDF)

1 – 25 von 439

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(318)
Mit Volltextzugriff
(349)

Publikationsform

Sprache

Englisch
(437)
Portugiesisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(271)
Life Sciences & Biomedicine
(166)
Technology
(77)
Physical Sciences
(58)
Humans
(56)
Engineering
(44)
Female
(36)
Male
(32)
Environmental Sciences
(30)
Environmental Sciences & Ecology
(30)
Chemistry
(27)
Animals
(26)
Physics
(24)
Computer Science
(23)
Machine Learning
(23)
Materials Science
(23)
Adult
(21)
Engineering, Electrical & Electronic
(21)
Biochemistry & Molecular Biology
(20)
General & Internal Medicine
(19)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Stromal Fibroblasts Present in Invasive Human Breast Carcinomas Promote Tumor Growth and Angiogenesis through Elevated SDF-1/CXCL12 Secretion

Call for improvement in medical school training in genetics: results of a national survey

Identifying the current status and future needs of clinical, educational, and laboratory genetics services in Pakistan: a web-based panel discussion

Overexpression of Eg5 Causes Genomic Instability and Tumor Formation in Mice

Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q

Quantitation of Aurora Kinase A Gene Copy Number in Urine Sediments and Bladder Cancer Detection

De novo mosaic and partial monosomy of chromosome 21 in a case with superior vena cava duplication

Myelodysplastic syndromes arising in patients with germline TP53 mutation and Li-Fraumeni syndrome

Overexpression of MAGE/GAGE Genes in Paclitaxel/Doxorubicin-resistant Human Cancer Cell Lines

Cloned transchromosomic calves producing human immunoglobulin

Identifying unnecessary duplicate genetic testing in a large medical center

Pitfalls of using polymerase chain reaction-based assays for JAK2 and CALR exon 9 variant testing in myeloproliferative neoplasms: Knowing when to go the extra mile

p53 Immunoreactivity Score Correlates With Predicted Gene Sequence Alterations of Variants Detected by Next-Generation Sequencing

Clinical validation of the Ion Torrent Oncomine Myeloid Assay GX v2 on the Genexus Integrated Sequencer as a stand-alone assay for single-nucleotide variants, insertions/deletions, and fusion genes: Challenges, performance, and perspectives

The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program Directors

Medical students' self‐perceived knowledge and clinical comfort with genetics in Pakistan

What Are We Missing? High Risk Human Papilloma Virus (HPV) Genotype and Cytology Correlates in a Diverse Bronx Population

Developing medical genetics in a low-income country: Unveiling the journey of the Pakistani Society of Medical Genetics and Genomics (PSMG)

Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia

eP478: Identifying the current status and future needs of clinical, educational, and laboratory genetics services in Pakistan: A web-based panel discussion

Hypopigmented mycosis fungoides in childhood and adolescence: a long-term retrospective study

Molecular monitoring of 8p11 myeloproliferative syndrome in an infant

Karyotypic complexity, TP53 pathogenic variants, and increased number of variants on Next‐Generation Sequencing are associated with disease progression in a North American Adult T‐Cell Leukemia/Lymphoma cohort

Ameloblastoma with adenoid features: Case report with cyto‐histopathologic correlation and molecular findings

Atlas of Cytogenomics in Oncology and Hematology: a Platform-Neutral Clinical Cancer Genomics Database

Suchergebnisse filtern