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...

Morphologic Features in Congenital Pulmonary Airway Malformations and Pulmonary Sequestrations Correlate With Mutation Status: A Mechanistic Approach to Classification

The American journal of surgical pathology, 2023-05, Vol.47 (5), p.568-579

2023

Volltextzugriff (PDF)

Mucinous Cell Clusters in Infantile Congenital Pulmonary Airway Malformations Mimic Adult Mucinous Adenocarcinoma But Are Not Associated With Poor Outcomes When Appropriately Resected

The American journal of surgical pathology, 2020-08, Vol.44 (8), p.1118-1129

2020

Volltextzugriff (PDF)

Bugs in inflammatory bowel disease — A questionable therapy

Digestive and liver disease, 2019-02, Vol.51 (2), p.323-323

2019

Volltextzugriff (PDF)

Defining the spatial landscape of KRAS mutated congenital pulmonary airway malformations: a distinct entity with a spectrum of histopathologic features

Modern pathology, 2022-12, Vol.35 (12), p.1870-1881

2022

Volltextzugriff (PDF)

Kikuchi-Fujimoto disease is mediated by an aberrant type I interferon response

Modern pathology, 2022-04, Vol.35 (4), p.462-469

2022

Volltextzugriff (PDF)

Extrathyroidal Extension is an Important Predictor of Regional Lymph Node Metastasis in Pediatric Differentiated Thyroid Cancer

Thyroid (New York, N.Y.), 2020-07, Vol.30 (7), p.1037-1043

2020

Volltextzugriff (PDF)

Helicobacter pylori Antigen But Not the Organism Is Occasionally Present Within Germinal Centers: Implications for Patient Management and Biology

The American journal of surgical pathology, 2020-11, Vol.44 (11), p.1528-1534

2020

Volltextzugriff (PDF)

The C-Terminal Extension Unique to the Long Isoform of the Shelterin Component TIN2 Enhances Its Interaction with TRF2 in a Phosphorylation- and Dyskeratosis Congenita Cluster-Dependent Fashion

Molecular and cellular biology, 2018-06, Vol.38 (12)

2018

Volltextzugriff (PDF)

Rapid fluorescence in situ hybridisation optimises induction therapy for acute myeloid leukaemia

British journal of haematology, 2020-12, Vol.191 (5), p.935-938

2020

Volltextzugriff (PDF)

Thrombopoietin Measurement as a Key Component in the Evaluation of Pediatric Thrombocytosis

Pediatric blood & cancer, 2016-08, Vol.63 (8), p.1484-1487

2016

Volltextzugriff (PDF)

Characterization of Plasmacytoid Dendritic Cells, Microbial Sequences, and Identification of a Candidate Public T-Cell Clone in Kikuchi-Fujimoto Disease

Pediatric and developmental pathology, 2021-06, Vol.24 (3), p.193-205

2021

Volltextzugriff (PDF)

Dyskeratosis congenita as a disorder of telomere maintenance

Mutation research, 2012-02, Vol.730 (1-2), p.43-51

2012

Volltextzugriff (PDF)

Three novel truncating TINF2 mutations causing severe dyskeratosis congenita in early childhood

Clinical genetics, 2012-05, Vol.81 (5), p.470-478

2012

Volltextzugriff (PDF)

Thrombopoietin Measurement as a Key Component in the Evaluation of Pediatric Thrombocytosis: THPO 5′ UTR Mutations in Sporadic Thrombocytosis

Pediatric blood & cancer, 2016-08, Vol.63 (8), p.1484-1487

2016

Volltextzugriff (PDF)

Book Review

Human Pathology, 2020, Vol.97, p.8

2020

Volltextzugriff (PDF)

Pathology of Heart Disease in the Fetus, Infant, and Child: Autopsy, Surgical, and Molecular Pathology. Michael T. Ashworth, Cambridge: Cambridge University Press. doi:https://doi.org/10.1017/9781316337073

Human Pathology, 2020, Vol.97, p.8-8

2020

Volltextzugriff (PDF)

1 – 16 von 16

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(15)
Mit Volltextzugriff
(12)

Publikationsform

Artikel
(14)
Reviews
(2)

Sprache

Englisch
(16)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(12)
Science & Technology
(12)
Humans
(11)
Male
(5)
Pathology
(5)
Female
(4)
Mutation
(4)
Dyskeratosis Congenita
(3)
Dyskeratosis Congenita - Genetics
(3)
Infant
(3)
Telomere
(3)
Telomere-Binding Proteins - Genetics
(3)
Adenocarcinoma, Mucinous - Pathology
(2)
Adolescent
(2)
Amino Acid Substitution
(2)
Cell Line
(2)
Child
(2)
Child, Preschool
(2)
Congenital Pulmonary Airway Malformation
(2)
Cystic Adenomatoid Malformation Of Lung, Congenital - Pathology
(2)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Morphologic Features in Congenital Pulmonary Airway Malformations and Pulmonary Sequestrations Correlate With Mutation Status: A Mechanistic Approach to Classification

Mucinous Cell Clusters in Infantile Congenital Pulmonary Airway Malformations Mimic Adult Mucinous Adenocarcinoma But Are Not Associated With Poor Outcomes When Appropriately Resected

Bugs in inflammatory bowel disease — A questionable therapy

Defining the spatial landscape of KRAS mutated congenital pulmonary airway malformations: a distinct entity with a spectrum of histopathologic features

Kikuchi-Fujimoto disease is mediated by an aberrant type I interferon response

Extrathyroidal Extension is an Important Predictor of Regional Lymph Node Metastasis in Pediatric Differentiated Thyroid Cancer

Helicobacter pylori Antigen But Not the Organism Is Occasionally Present Within Germinal Centers: Implications for Patient Management and Biology

The C-Terminal Extension Unique to the Long Isoform of the Shelterin Component TIN2 Enhances Its Interaction with TRF2 in a Phosphorylation- and Dyskeratosis Congenita Cluster-Dependent Fashion

Rapid fluorescence in situ hybridisation optimises induction therapy for acute myeloid leukaemia

Thrombopoietin Measurement as a Key Component in the Evaluation of Pediatric Thrombocytosis

Characterization of Plasmacytoid Dendritic Cells, Microbial Sequences, and Identification of a Candidate Public T-Cell Clone in Kikuchi-Fujimoto Disease

Dyskeratosis congenita as a disorder of telomere maintenance

Three novel truncating TINF2 mutations causing severe dyskeratosis congenita in early childhood

Thrombopoietin Measurement as a Key Component in the Evaluation of Pediatric Thrombocytosis: THPO 5′ UTR Mutations in Sporadic Thrombocytosis

Book Review

Pathology of Heart Disease in the Fetus, Infant, and Child: Autopsy, Surgical, and Molecular Pathology. Michael T. Ashworth, Cambridge: Cambridge University Press. doi:https://doi.org/10.1017/9781316337073

Suchergebnisse filtern