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...

Specificity of ε and non-ε isoforms of arabidopsis 14-3-3 proteins towards the H+-ATPase and other targets

PloS one, 2014-03, Vol.9 (6), p.e90764

2014

Volltextzugriff (PDF)

The Italian registry for patients with Prader-Willi syndrome

Orphanet journal of rare diseases, 2023-02, Vol.18 (1), p.28-28, Article 28

2023

Volltextzugriff (PDF)

Understanding the role of the Q338H MUTYH variant in oxidative damage repair

Nucleic acids research, 2013-04, Vol.41 (7), p.4093-4103

2013

Volltextzugriff (PDF)

Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes

Human molecular genetics, 2008-07, Vol.17 (13), p.2018-2029

2008

Volltextzugriff (PDF)

Counteracting Effects Operating on Src Homology 2 Domain-containing Protein-tyrosine Phosphatase 2 (SHP2) Function Drive Selection of the Recurrent Y62D and Y63C Substitutions in Noonan Syndrome

The Journal of biological chemistry, 2012-08, Vol.287 (32), p.27066-27077

2012

Volltextzugriff (PDF)

Retinoblastoma-independent antiproliferative activity of novel intracellular antibodies against the E7 oncoprotein in HPV 16-positive cells

BMC cancer, 2011-01, Vol.11 (1), p.17-17, Article 17

2011

Volltextzugriff (PDF)

Prion protein paralog doppel protein interacts with alpha-2-macroglobulin: a plausible mechanism for doppel-mediated neurodegeneration

PloS one, 2009-06, Vol.4 (6), p.e5968-e5968

2009

Volltextzugriff (PDF)

The Occurrence of 275 Rare Diseases and 47 Rare Disease Groups in Italy. Results from the National Registry of Rare Diseases

International journal of environmental research and public health, 2018-07, Vol.15 (7), p.1470

2018

Volltextzugriff (PDF)

Correction: Prion Protein Paralog Doppel Protein Interacts with Alpha-2-Macroglobulin: A Plausible Mechanism for Doppel-Mediated Neurodegeneration

PloS one, 2009-08, Vol.4 (8)

2009

Volltextzugriff (PDF)

Registries or non-pharmacological observational studies? An operational attempt to draw the line and to provide some suggestions for the ethical evaluation of rare disease registries (Supplementary Materials)

Annali dell'Istituto superiore di sanità, 2024-01, Vol.60 (1), p.29

2024

Volltextzugriff (PDF)

Recommendations for Improving the Quality of Rare Disease Registries

International journal of environmental research and public health, 2018-08, Vol.15 (8), p.1644

2018

Volltextzugriff (PDF)

Gaucher disease due to saposin C deficiency is an inherited lysosomal disease caused by rapidly degraded mutant proteins

Human molecular genetics, 2014-11, Vol.23 (21), p.5814-5826

2014

Volltextzugriff (PDF)

The RD-Connect Registry & Biobank Finder: a tool for sharing aggregated data and metadata among rare disease researchers

European journal of human genetics : EJHG, 2018-05, Vol.26 (5), p.631-643

2018

Volltextzugriff (PDF)

Identification of key regions and genes important in the pathogenesis of sezary syndrome by combining genomic and expression microarrays

Cancer research (Chicago, Ill.), 2009-11, Vol.69 (21), p.8438-8446

2009

Volltextzugriff (PDF)

Specificity of [epsilon] and Non-[epsilon] Isoforms of Arabidopsis 14-3-3 Proteins Towards the H.sup.+-ATPase and Other Targets

PloS one, 2014-03, Vol.9 (3), p.e90764

2014

Volltextzugriff (PDF)

The Italian National Rare Diseases Registry: a model of comparison and integration with Hospital Discharge Data

Journal of public health (Oxford, England), 2019-03, Vol.41 (1), p.46-54

2019

Volltextzugriff (PDF)

The Italian project for surveillance prevention and health care planning of congenital anomalies including Zika virus

European journal of medical genetics, 2018-09, Vol.61 (9), p.572-572

2018

Volltextzugriff (PDF)

The Interaction with HMG20a/b Proteins Suggests a Potential Role for β-Dystrobrevin in Neuronal Differentiation

The Journal of biological chemistry, 2010-08, Vol.285 (32), p.24740-24750

2010

Volltextzugriff (PDF)

Functional analysis of MUTYH mutated proteins associated with familial adenomatous polyposis

DNA repair, 2010-06, Vol.9 (6), p.700-707

2010

Volltextzugriff (PDF)

Phosphorylation on threonine 11 of [beta]-dystrobrevin alters its interaction with kinesin heavy chain

The FEBS journal, 2012-11, Vol.279 (22), p.4131

2012

Volltextzugriff (PDF)

Phosphorylation on threonine 11 of β‐dystrobrevin alters its interaction with kinesin heavy chain

The FEBS journal, 2012-11, Vol.279 (22), p.4131-4144

2012

Volltextzugriff (PDF)

The Interaction with HMG20a/b Proteins Suggests a Potential Role for b-Dystrobrevin in Neuronal Differentiation

The Journal of biological chemistry, 2010-08, Vol.285 (32), p.24740-24750

2010

Volltextzugriff (PDF)

Association of Dystrobrevin and Regulatory Subunit of Protein Kinase A: A New Role for Dystrobrevin as a Scaffold for Signaling Proteins

Journal of molecular biology, 2007-08, Vol.371 (5), p.1174-1187

2007

Volltextzugriff (PDF)

Concerted mutation of Phe residues belonging to the β‐dystroglycan ectodomain strongly inhibits the interaction with α‐dystroglycan in vitro

The FEBS journal, 2006-11, Vol.273 (21), p.4929-4943

2006

Volltextzugriff (PDF)

Combined High Resolution Genomic and Expression Profiles Microarray Analysis in Sezary Syndrome

Blood, 2009-11, Vol.114 (22), p.3238-3238

2009

Volltextzugriff (PDF)

1 – 25 von 33

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(33)
Mit Volltextzugriff
(32)

Publikationsform

Artikel
(33)

Sprache

Englisch
(33)
Japanisch
(3)

Erscheinungsjahr

n.n

Thema

Science & Technology
(22)
Life Sciences & Biomedicine
(20)
Humans
(14)
Biochemistry & Molecular Biology
(11)
Surface Plasmon Resonance
(8)
Animals
(7)
Mutation
(7)
Amino Acid Sequence
(6)
Molecular Sequence Data
(6)
Protein Binding
(6)
Rare Diseases
(6)
Genetics & Heredity
(5)
Kinetics
(5)
Protein Structure, Tertiary
(5)
Proteins
(5)
Dystrobrevin
(4)
Mice
(4)
Models, Molecular
(4)
Patients
(4)
Public, Environmental & Occupational Health
(4)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Specificity of ε and non-ε isoforms of arabidopsis 14-3-3 proteins towards the H+-ATPase and other targets

The Italian registry for patients with Prader-Willi syndrome

Understanding the role of the Q338H MUTYH variant in oxidative damage repair

Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes

Counteracting Effects Operating on Src Homology 2 Domain-containing Protein-tyrosine Phosphatase 2 (SHP2) Function Drive Selection of the Recurrent Y62D and Y63C Substitutions in Noonan Syndrome

Retinoblastoma-independent antiproliferative activity of novel intracellular antibodies against the E7 oncoprotein in HPV 16-positive cells

Prion protein paralog doppel protein interacts with alpha-2-macroglobulin: a plausible mechanism for doppel-mediated neurodegeneration

The Occurrence of 275 Rare Diseases and 47 Rare Disease Groups in Italy. Results from the National Registry of Rare Diseases

Correction: Prion Protein Paralog Doppel Protein Interacts with Alpha-2-Macroglobulin: A Plausible Mechanism for Doppel-Mediated Neurodegeneration

Registries or non-pharmacological observational studies? An operational attempt to draw the line and to provide some suggestions for the ethical evaluation of rare disease registries (Supplementary Materials)

Recommendations for Improving the Quality of Rare Disease Registries

Gaucher disease due to saposin C deficiency is an inherited lysosomal disease caused by rapidly degraded mutant proteins

The RD-Connect Registry & Biobank Finder: a tool for sharing aggregated data and metadata among rare disease researchers

Identification of key regions and genes important in the pathogenesis of sezary syndrome by combining genomic and expression microarrays

Specificity of [epsilon] and Non-[epsilon] Isoforms of Arabidopsis 14-3-3 Proteins Towards the H.sup.+-ATPase and Other Targets

The Italian National Rare Diseases Registry: a model of comparison and integration with Hospital Discharge Data

The Italian project for surveillance prevention and health care planning of congenital anomalies including Zika virus

The Interaction with HMG20a/b Proteins Suggests a Potential Role for β-Dystrobrevin in Neuronal Differentiation

Functional analysis of MUTYH mutated proteins associated with familial adenomatous polyposis

Phosphorylation on threonine 11 of [beta]-dystrobrevin alters its interaction with kinesin heavy chain

Phosphorylation on threonine 11 of β‐dystrobrevin alters its interaction with kinesin heavy chain

The Interaction with HMG20a/b Proteins Suggests a Potential Role for b-Dystrobrevin in Neuronal Differentiation

Association of Dystrobrevin and Regulatory Subunit of Protein Kinase A: A New Role for Dystrobrevin as a Scaffold for Signaling Proteins

Concerted mutation of Phe residues belonging to the β‐dystroglycan ectodomain strongly inhibits the interaction with α‐dystroglycan in vitro

Combined High Resolution Genomic and Expression Profiles Microarray Analysis in Sezary Syndrome

Suchergebnisse filtern