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...

Differential modulation of unapposed connexin 43 hemichannel electrical conductance by protein kinase C isoforms

Pflügers Archiv, 2008-06, Vol.456 (3), p.519-527

2008

Volltextzugriff (PDF)

Novel Mechanism for Brugada Syndrome: Defective Surface Localization of an SCN5A Mutant(R1432G)

Circulation research, 2001-06, Vol.88 (12), p.e78-e83

2001

Volltextzugriff (PDF)

HERNIE DE LITTRE OMBILICALE CHEZ LADULTE: A PROPOS DUN CAS

International journal of advanced research (Indore), 2024-09, Vol.12 (9), p.386-389

2024

Volltextzugriff (PDF)

INGESTION DE CORPS ETRANGERS DANS LE MILIEU CARCERAL

International journal of advanced research (Indore), 2024-04, Vol.12 (4), p.153-157

2024

Volltextzugriff (PDF)

Hirschsprung’s Disease in Adult Revealed by an Occlusive Syndrome: A Case Report

Scholars Journal of Medical Case Reports, 2023-05, Vol.11 (5), p.904-907

2023

Volltextzugriff (PDF)

Expression and Intracellular Localization of an SCN5A Double Mutant R1232W/T1620M Implicated in Brugada Syndrome

Circulation research, 2002-01, Vol.90 (1), p.e11-e16

2002

Volltextzugriff (PDF)

Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes

FEBS letters, 2000-12, Vol.487 (2), p.224-228

2000

Volltextzugriff (PDF)

A Newly Characterized SCN5A Mutation Underlying Brugada Syndrome Unmasked by Hyperthermia

Journal of cardiovascular electrophysiology, 2003-04, Vol.14 (4), p.407-411

2003

Volltextzugriff (PDF)

Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes

Cardiovascular research, 2000-04, Vol.46 (1), p.55-65

2000

Volltextzugriff (PDF)

SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells

FEBS letters, 2000-02, Vol.467 (1), p.12-16

2000

Volltextzugriff (PDF)

Protein kinase C activation inhibits Ca sub(V)1.3 calcium channel at NH sub(2)-terminal serine 81 phosphorylation site

American journal of physiology. Heart and circulatory physiology, 2006-10, Vol.291 (4), p.H1614-H1622

2006

Volltextzugriff (PDF)

Overview of an automatic underground distribution fault location system

2009 IEEE Power & Energy Society General Meeting, 2009, p.1-5

2009

Volltextzugriff (PDF)

Primary Retroperitoneal Tumors: A Report of 08 Cases at the General Surgery Department of The Mohamed VI University Hospital in Marrakech

SAS Journal of Surgery, 2024-05, Vol.10 (5), p.537-539

2024

Volltextzugriff (PDF)

Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome

Canadian journal of cardiology, 2004-03, Vol.20 (4), p.425-430

2004

Volltextzugriff (PDF)

Atrial fibrillation: molecular biology has yet to impact management

Journal of cardiovascular electrophysiology, 2004-02, Vol.15 (2), p.224-225

2004

Volltextzugriff (PDF)

Localization and modulation of alpha sub(1D) (Cav1.3) L-type Ca channel by protein kinase A

American journal of physiology. Heart and circulatory physiology, 2005-05, Vol.288 (5), p.H2123-H2130

2005

Volltextzugriff (PDF)

Detection of Incipient Faults in Underground Medium Voltage Cables

2008 61st Annual Conference for Protective Relay Engineers, 2008, p.349-366

2008

Volltextzugriff (PDF)

The hum of all its parts : ...but thanks to incessant upgrading, system software installed in the early sixties is still faithfully humming along for the banks

Canadian banker (1983), 1993-07, Vol.100 (3), p.33

Baroudi, G

1993

Volltextzugriff (PDF)

Homozygous SCN5A Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block

Circulation research, 2001-07, Vol.89 (2), p.193-193

2001

Volltextzugriff (PDF)

Microorganisms and Characteristics of Laban

Journal of dairy science, 1976-02, Vol.59 (2), p.200-202

1976

Volltextzugriff (PDF)

A two-stage framework for fair autonomous robot deployment using virtual forces

Transportation research. Part A, Policy and practice, 2020-11, Vol.141, p.35-50

2020

Volltextzugriff (PDF)

How Do Career Aspirations Benefit Organizations? The Mediating Roles of the Proactive and Relational Aspects of Contemporary Work

Frontiers in psychology, 2018-11, Vol.9, p.2150-2150

2018

Volltextzugriff (PDF)

Early combined immunosuppression for the management of Crohn's disease (REACT): a cluster randomised controlled trial

The Lancet (British edition), 2015-11, Vol.386 (10006), p.1825-1834

2015

Volltextzugriff (PDF)

Delayed maturation and migration of excitatory neurons in the juvenile mouse paralaminar amygdala

Neuron (Cambridge, Mass.), 2024-02, Vol.112 (4), p.574-592.e10

2024

Volltextzugriff (PDF)

Amendment of soil by biochars and activated carbons to reduce chlordecone bioavailability in piglets

Chemosphere (Oxford), 2018-11, Vol.210, p.486-494

2018

Volltextzugriff (PDF)

1 – 25 von 67

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(50)
Mit Volltextzugriff
(59)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Differential modulation of unapposed connexin 43 hemichannel electrical conductance by protein kinase C isoforms

Novel Mechanism for Brugada Syndrome: Defective Surface Localization of an SCN5A Mutant(R1432G)

HERNIE DE LITTRE OMBILICALE CHEZ LADULTE: A PROPOS DUN CAS

INGESTION DE CORPS ETRANGERS DANS LE MILIEU CARCERAL

Hirschsprung’s Disease in Adult Revealed by an Occlusive Syndrome: A Case Report

Expression and Intracellular Localization of an SCN5A Double Mutant R1232W/T1620M Implicated in Brugada Syndrome

Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes

A Newly Characterized SCN5A Mutation Underlying Brugada Syndrome Unmasked by Hyperthermia

Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes

SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells

Protein kinase C activation inhibits Ca sub(V)1.3 calcium channel at NH sub(2)-terminal serine 81 phosphorylation site

Overview of an automatic underground distribution fault location system

Primary Retroperitoneal Tumors: A Report of 08 Cases at the General Surgery Department of The Mohamed VI University Hospital in Marrakech

Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome

Atrial fibrillation: molecular biology has yet to impact management

Localization and modulation of alpha sub(1D) (Cav1.3) L-type Ca channel by protein kinase A

Detection of Incipient Faults in Underground Medium Voltage Cables

The hum of all its parts : ...but thanks to incessant upgrading, system software installed in the early sixties is still faithfully humming along for the banks

Homozygous SCN5A Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block

Microorganisms and Characteristics of Laban

A two-stage framework for fair autonomous robot deployment using virtual forces

How Do Career Aspirations Benefit Organizations? The Mediating Roles of the Proactive and Relational Aspects of Contemporary Work

Early combined immunosuppression for the management of Crohn's disease (REACT): a cluster randomised controlled trial

Delayed maturation and migration of excitatory neurons in the juvenile mouse paralaminar amygdala

Amendment of soil by biochars and activated carbons to reduce chlordecone bioavailability in piglets

Suchergebnisse filtern