UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 42

Sortiert nach

Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy

Nature genetics, 2012-04, Vol.44 (4), p.450-455

2012

Volltextzugriff (PDF)

PP2A Inhibitor PME-1 Drives Kinase Inhibitor Resistance in Glioma Cells

Cancer research (Chicago, Ill.), 2016-12, Vol.76 (23), p.7001-7011

2016

Volltextzugriff (PDF)

Distinct Muscle Biopsy Findings in Genetically Defined Adult-Onset Motor Neuron Disorders

PloS one, 2016-03, Vol.11 (3), p.e0151376-e0151376

2016

Volltextzugriff (PDF)

Atypical phenotypes in titinopathies explained by second titin mutations

Annals of neurology, 2014-02, Vol.75 (2), p.230-240

2014

Volltextzugriff (PDF)

Mutations in the N-terminal Actin-Binding Domain of Filamin C Cause a Distal Myopathy

American journal of human genetics, 2011-06, Vol.88 (6), p.729-740

2011

Volltextzugriff (PDF)

Characterization of a novel cell line established from a patient with Herceptin-resistant breast cancer

Molecular cancer therapeutics, 2004-12, Vol.3 (12), p.1585-1592

2004

Volltextzugriff (PDF)

Diagnostically important muscle pathology in DNAJB6 mutated LGMD1D

Acta neuropathologica communications, 2016-02, Vol.4 (10), p.9-9, Article 9

2016

Volltextzugriff (PDF)

Gene expression profiling in tibial muscular dystrophy reveals unfolded protein response and altered autophagy

PloS one, 2014-03, Vol.9 (3), p.e90819-e90819

2014

Volltextzugriff (PDF)

PME-1 Protects Extracellular Signal-Regulated Kinase Pathway Activity from Protein Phosphatase 2A―Mediated Inactivation in Human Malignant Glioma

Cancer research (Chicago, Ill.), 2009-04, Vol.69 (7), p.2870-2877

2009

Volltextzugriff (PDF)

Level of Civic Knowledge and Attitude as Antidotes of Civic Engagement among Secondary School Students in Oyo State, Nigeria

International journal of education and literacy studies, 2019-10, Vol.7 (4), p.124

2019

Volltextzugriff (PDF)

Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish family

Neuromuscular disorders : NMD, 2011-08, Vol.21 (8), p.551-555

2011

Volltextzugriff (PDF)

Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibers

Acta neuropathologica, 2010-04, Vol.119 (4), p.495-500

2010

Volltextzugriff (PDF)

Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2

Acta neuropathologica, 2010-04, Vol.119 (4), p.465-479

2010

Volltextzugriff (PDF)

Cytoplasmic LRIG2 expression is associated with poor oligodendroglioma patient survival

Neuropathology, 2009-06, Vol.29 (3), p.242-247

2009

Volltextzugriff (PDF)

A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patient

Journal of neurology, 2011-06, Vol.258 (6), p.1157-1163

2011

Volltextzugriff (PDF)

New immunohistochemical method for improved myotonia and chloride channel mutation diagnostics

Neurology, 2012-11, Vol.79 (22), p.2194

2012

Volltextzugriff (PDF)

Perinuclear leucine-rich repeats and immunoglobulin-like domain proteins (LRIG1-3) as prognostic indicators in astrocytic tumors

Acta neuropathologica, 2006-03, Vol.111 (3), p.238-246

2006

Volltextzugriff (PDF)

Socio-economic laxity on university students : implication for social values and sexual morality

Journal of Education Research and Rural Community Development, 2019-12, Vol.1 (2), p.38-50

2019

Volltextzugriff (PDF)

Lamin A/C Mutation Affecting Primarily the Right Side of the Heart

Cardiogenetics, 2013-04, Vol.3 (1), p.e1-e1

2013

Volltextzugriff (PDF)

Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations

Brain (London, England : 1878), 2010-05, Vol.133 (5), p.1451-1459

2010

Volltextzugriff (PDF)

Differential Isoform Expression and Selective Muscle Involvement in Muscular Dystrophies

The American journal of pathology, 2015-10, Vol.185 (10), p.2833-2842

2015

Volltextzugriff (PDF)

Mutant (CCTG)n Expansion Causes Abnormal Expression of Zinc Finger Protein 9 (ZNF9) in Myotonic Dystrophy Type 2

The American journal of pathology, 2010-12, Vol.177 (6), p.3025-3036

2010

Volltextzugriff (PDF)

Abnormal splicing of NEDD4 in myotonic dystrophy type 2: possible link to statin adverse reactions

The American journal of pathology, 2014-08, Vol.184 (8), p.2322-2332

2014

Volltextzugriff (PDF)

Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations

European journal of human genetics : EJHG, 2014-06, Vol.22 (6), p.801-808

2014

Volltextzugriff (PDF)

Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2

Journal of neurology, 2012-10, Vol.259 (10), p.2090-2099

2012

Volltextzugriff (PDF)

1 – 25 von 42

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(36)
Mit Volltextzugriff
(40)

Publikationsform

Sprache

Englisch
(42)
Japanisch
(14)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy

PP2A Inhibitor PME-1 Drives Kinase Inhibitor Resistance in Glioma Cells

Distinct Muscle Biopsy Findings in Genetically Defined Adult-Onset Motor Neuron Disorders

Atypical phenotypes in titinopathies explained by second titin mutations

Mutations in the N-terminal Actin-Binding Domain of Filamin C Cause a Distal Myopathy

Characterization of a novel cell line established from a patient with Herceptin-resistant breast cancer

Diagnostically important muscle pathology in DNAJB6 mutated LGMD1D

Gene expression profiling in tibial muscular dystrophy reveals unfolded protein response and altered autophagy

PME-1 Protects Extracellular Signal-Regulated Kinase Pathway Activity from Protein Phosphatase 2A―Mediated Inactivation in Human Malignant Glioma

Level of Civic Knowledge and Attitude as Antidotes of Civic Engagement among Secondary School Students in Oyo State, Nigeria

Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish family

Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibers

Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2

Cytoplasmic LRIG2 expression is associated with poor oligodendroglioma patient survival

A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patient

New immunohistochemical method for improved myotonia and chloride channel mutation diagnostics

Perinuclear leucine-rich repeats and immunoglobulin-like domain proteins (LRIG1-3) as prognostic indicators in astrocytic tumors

Socio-economic laxity on university students : implication for social values and sexual morality

Lamin A/C Mutation Affecting Primarily the Right Side of the Heart

Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations

Differential Isoform Expression and Selective Muscle Involvement in Muscular Dystrophies

Mutant (CCTG)n Expansion Causes Abnormal Expression of Zinc Finger Protein 9 (ZNF9) in Myotonic Dystrophy Type 2

Abnormal splicing of NEDD4 in myotonic dystrophy type 2: possible link to statin adverse reactions

Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations

Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2

Suchergebnisse filtern