UB Paderborn / Katalog / Suche / in CDI

1 – 20 von 20

Sortiert nach

In Vivo Imaging of oskar mRNA Transport Reveals the Mechanism of Posterior Localization

Cell, 2008-09, Vol.134 (5), p.843-853

2008

Volltextzugriff (PDF)

bicoid mRNA localises to the Drosophila oocyte anterior by random Dynein-mediated transport and anchoring

eLife, 2016-10, Vol.5

2016

Volltextzugriff (PDF)

The search for new antigenic targets in myasthenia gravis

Annals of the New York Academy of Sciences, 2012-12, Vol.1275 (1), p.123-128

2012

Volltextzugriff (PDF)

Clinical features of the myasthenic syndrome arising from mutations in GMPPB

Journal of neurology, neurosurgery and psychiatry, 2016-08, Vol.87 (8), p.802-809

2016

Volltextzugriff (PDF)

Late presentations of congenital myasthenic syndromes: How many do we miss?

Muscle & nerve, 2016-10, Vol.54 (4), p.721-727

2016

Volltextzugriff (PDF)

Collagen Q – A potential target for autoantibodies in myasthenia gravis

Journal of the neurological sciences, 2015-01, Vol.348 (1), p.241-244

2015

Volltextzugriff (PDF)

Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies

Brain (London, England : 1878), 2015-09, Vol.138 (Pt 9), p.2493-2504

2015

Volltextzugriff (PDF)

Congenital myasthenic syndromes due to mutations in ALG2 and ALG14

Brain (London, England : 1878), 2013-03, Vol.136 (Pt 3), p.944-956

2013

Volltextzugriff (PDF)

Analysis of the expression patterns, subcellular localisations and interaction partners of Drosophila proteins using a pigP protein trap library

Development (Cambridge), 2014-10, Vol.141 (20), p.3994-4005

2014

Volltextzugriff (PDF)

The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome

Human molecular genetics, 2012-09, Vol.21 (17), p.3765-3775

2012

Volltextzugriff (PDF)

Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndrome

Annals of the New York Academy of Sciences, 2012-12, Vol.1275 (1), p.29-35

2012

Volltextzugriff (PDF)

Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular Aggregates

American journal of human genetics, 2012-07, Vol.91 (1), p.193-201

2012

Volltextzugriff (PDF)

Late presentations of congenital myasthenic syndromes: How many do we miss?: Late Presentations of CMS

Muscle & nerve, 2016-10, Vol.54 (4), p.721-727

2016

Volltextzugriff (PDF)

Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1

Neuromuscular disorders : NMD, 2013-06, Vol.23 (6), p.469-472

2013

Volltextzugriff (PDF)

Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1

Journal of neurology, neurosurgery and psychiatry, 2013-10, Vol.84 (10), p.1119-1125

2013

Volltextzugriff (PDF)

LIMB GIRDLE SYNDROMES: MYASTHENIA OR MYOPATHY

Journal of neurology, neurosurgery and psychiatry, 2016-12, Vol.87 (12), p.e1-e1

2016

Volltextzugriff (PDF)

Using the mRNA-MS2/MS2CP-FP system to study mRNA transport during Drosophila oogenesis

Methods in molecular biology (Clifton, N.J.), 2011, Vol.714, p.265

2011

Volltextzugriff (PDF)

FLIPing heterokaryons to analyze nucleo-cytoplasmic shuttling of yeast proteins

RNA (Cambridge), 2006-05, Vol.12 (5), p.921-930

2006

Volltextzugriff (PDF)

Mechanisms of mrna localisation during drosophila oogenesis

Belaya, Katsiaryna

2008

Volltextzugriff (PDF)

1 – 20 von 20

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(18)
Mit Volltextzugriff
(18)

Publikationsform

Artikel
(19)
Dissertationen
(1)

Sprache

Englisch
(20)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(17)
Science & Technology
(17)
Humans
(12)
Female
(11)
Male
(9)
Myasthenic Syndromes, Congenital - Genetics
(9)
Mutation
(8)
Animals
(7)
Clinical Neurology
(7)
Neurosciences & Neurology
(7)
Adolescent
(6)
Adult
(6)
Congenital Myasthenic Syndrome
(6)
Glycosylation
(6)
Biochemistry & Molecular Biology
(5)
Middle Aged
(5)
Neurology
(5)
Neurosciences
(5)
Young Adult
(5)
Cell Biology
(4)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

In Vivo Imaging of oskar mRNA Transport Reveals the Mechanism of Posterior Localization

bicoid mRNA localises to the Drosophila oocyte anterior by random Dynein-mediated transport and anchoring

Structures of DPAGT1 Explain Glycosylation Disease Mechanisms and Advance TB Antibiotic Design

The search for new antigenic targets in myasthenia gravis

Clinical features of the myasthenic syndrome arising from mutations in GMPPB

Late presentations of congenital myasthenic syndromes: How many do we miss?

Collagen Q – A potential target for autoantibodies in myasthenia gravis

Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies

Congenital myasthenic syndromes due to mutations in ALG2 and ALG14

Analysis of the expression patterns, subcellular localisations and interaction partners of Drosophila proteins using a pigP protein trap library

The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome

Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndrome

Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular Aggregates

Late presentations of congenital myasthenic syndromes: How many do we miss?: Late Presentations of CMS

Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1

Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1

LIMB GIRDLE SYNDROMES: MYASTHENIA OR MYOPATHY

Using the mRNA-MS2/MS2CP-FP system to study mRNA transport during Drosophila oogenesis

FLIPing heterokaryons to analyze nucleo-cytoplasmic shuttling of yeast proteins

Mechanisms of mrna localisation during drosophila oogenesis

Suchergebnisse filtern