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...

Improving Performance Estimation for FPGA-Based Accelerators for Convolutional Neural Networks

Applied Reconfigurable Computing. Architectures, Tools, and Applications, p.3-13

Volltextzugriff (PDF)

Two lines of defense in the pupas of ichneumonid wasp parasitoids associated with spider hosts

Frontiers in ecology and evolution, 2022-11, Vol.10

2022

Volltextzugriff (PDF)

Observing high-k magnons with Mie-resonance-enhanced Brillouin light scattering

Communications physics, 2023-05, Vol.6 (1), p.94-10, Article 94

2023

Volltextzugriff (PDF)

Characterization of Pathogenic Variants Associated with Hereditary Thrombocytopenias in Families from the Czech Republic

Blood, 2019-11, Vol.134 (Supplement_1), p.2343-2343

2019

Volltextzugriff (PDF)

A novel thrombocytopenia-4-causing CYCS gene variant decreases caspase activity: Three-generation study

British journal of haematology, 2024-08

2024

Volltextzugriff (PDF)

C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies

International journal of hematology, 2018-12, Vol.108 (6), p.652-657

2018

Volltextzugriff (PDF)

Impact of thrombocytopenia-associated c.-118C>T and c.-140C>G ANKRD26 5’UTR variants in three-generational pedigree

Platelets (Edinburgh), 2024-12, Vol.35 (1), p.2388103

2024

Volltextzugriff (PDF)

A GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome

International journal of molecular sciences, 2022-01, Vol.23 (2), p.885

2022

Volltextzugriff (PDF)

A novel germline mutation of the SFTPA1 gene in familial interstitial pneumonia

Human genome variation, 2019-03, Vol.6 (1), p.12-12, Article 12

2019

Volltextzugriff (PDF)

Extensive, 3.8 Mb-Sized Deletion of 22q12 in a Patient with Bilateral Schwannoma, Intellectual Disability, Sensorineural Hearing Loss, and Epilepsy

Molecular syndromology, 2023-10, Vol.14 (5), p.439-448

2023

Volltextzugriff (PDF)

A novel germline mutation in GP1BA gene N-terminal domain in monoallelic Bernard-Soulier syndrome

Platelets (Edinburgh), 2018-12, Vol.29 (8), p.827-833

2018

Volltextzugriff (PDF)

Life-history of the parthenogenetic oonopid spider, Triaeris stenaspis (Araneae: Oonopidae)

European journal of entomology, 2009-01, Vol.106 (2), p.217-223

2009

Volltextzugriff (PDF)

Ex-vivo 3D cellular models of pancreatic ductal adenocarcinoma: from embryonic development to precision oncology

Pancreas, 2024-07

2024

Volltextzugriff (PDF)

Genetic diagnostics of familial hematopoietic disorders

Klinická onkologie, 2023-10, Vol.36 (Suppl 1)

2023

Volltextzugriff (PDF)

Measuring spatially resolved phase of nanoscale spin waves

2023 IEEE International Magnetic Conference - Short Papers (INTERMAG Short Papers), 2023, p.1-2

2023

Volltextzugriff (PDF)

A novel germline mutation in GP1BA gene N-terminal domain in monoallelic Bernard-Soulier syndrome

Platelets, 2018, Vol.29 (8), p.827-833

2018

Volltextzugriff (PDF)

1 – 16 von 16

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(14)
Mit Volltextzugriff
(11)

Publikationsform

Sprache

Englisch
(16)

Erscheinungsjahr

n.n

Thema

Science & Technology
(9)
Life Sciences & Biomedicine
(8)
Inherited Thrombocytopenia
(4)
Female
(3)
Gp1ba
(3)
Hematology
(3)
Humans
(3)
Araneae
(2)
Autosomal Dominant Variant
(2)
Bernard-Soulier Syndrome - Genetics
(2)
Dna Mutational Analysis
(2)
Genes
(2)
Genetic Predisposition To Disease
(2)
Genetics & Heredity
(2)
Male
(2)
Monoallelic Bernard-Soulier Syndrome
(2)
Mutation
(2)
Pedigree
(2)
Physical Sciences
(2)
Platelet Count
(2)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Improving Performance Estimation for FPGA-Based Accelerators for Convolutional Neural Networks

Two lines of defense in the pupas of ichneumonid wasp parasitoids associated with spider hosts

Observing high-k magnons with Mie-resonance-enhanced Brillouin light scattering

Characterization of Pathogenic Variants Associated with Hereditary Thrombocytopenias in Families from the Czech Republic

A novel thrombocytopenia-4-causing CYCS gene variant decreases caspase activity: Three-generation study

C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies

Impact of thrombocytopenia-associated c.-118C>T and c.-140C>G ANKRD26 5’UTR variants in three-generational pedigree

A GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome

A novel germline mutation of the SFTPA1 gene in familial interstitial pneumonia

Extensive, 3.8 Mb-Sized Deletion of 22q12 in a Patient with Bilateral Schwannoma, Intellectual Disability, Sensorineural Hearing Loss, and Epilepsy

A novel germline mutation in GP1BA gene N-terminal domain in monoallelic Bernard-Soulier syndrome

Life-history of the parthenogenetic oonopid spider, Triaeris stenaspis (Araneae: Oonopidae)

Ex-vivo 3D cellular models of pancreatic ductal adenocarcinoma: from embryonic development to precision oncology

Genetic diagnostics of familial hematopoietic disorders

Measuring spatially resolved phase of nanoscale spin waves

A novel germline mutation in GP1BA gene N-terminal domain in monoallelic Bernard-Soulier syndrome

Suchergebnisse filtern