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...

Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?

Neurology, 2007-05, Vol.68 (22), p.1883-1894

2007

Volltextzugriff (PDF)

Mutations in Emery-Dreifuss Muscular Dystrophy and their Effects on Emerin Protein Expression

Human molecular genetics, 1998-05, Vol.7 (5), p.855-864

1998

Volltextzugriff (PDF)

Les conductrices symptomatiques pour les dystrophinopathies avec biais d'inactivation du chromosome X

Revue neurologique, 2003-09, Vol.159 (8-9), p.775-780

2003

Volltextzugriff (PDF)

Identification by STS PCR Screening of a Microdeletion in Xp21.3–22.1 Associated with Non-specific Mental Retardation

Human molecular genetics, 1996-07, Vol.5 (7), p.977-979

1996

Volltextzugriff (PDF)

Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene

Neuromuscular disorders : NMD, 2004, Vol.14 (1), p.10-18

2004

Volltextzugriff (PDF)

G.P.6 02 Somatic and germinal mosaicism of an out-of-frame deletion in the dystrophin gene in an adult male patient with predominant dilated cardiomyopathy

Neuromuscular disorders : NMD, 2006-10, Vol.16 (9), p.698-698

2006

Volltextzugriff (PDF)

G.P.4.09 Looking for a third gene causing Emery-Dreifuss muscular dystrophy: Lessons and perspectives

Neuromuscular disorders : NMD, 2006-10, Vol.16 (9), p.677-678

2006

Volltextzugriff (PDF)

Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with ‘de novo’ duplication of dystrophin gene

Neuromuscular disorders : NMD, 2001-07, Vol.11 (5), p.494-498

2001

Volltextzugriff (PDF)

Early presentation of X-linked Emery–Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy

Neuromuscular disorders : NMD, 1998-04, Vol.8 (2), p.72-76

1998

Volltextzugriff (PDF)

Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias

Revue neurologique, 2003-09, Vol.159 (8-9), p.775-780

2003

Volltextzugriff (PDF)

Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy

Croatian medical journal, 2000-12, Vol.41 (4), p.389

2000

Volltextzugriff (PDF)

A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase loci

Neuromuscular disorders : NMD, 1997-12, Vol.7 (8), p.499-504

1997

Volltextzugriff (PDF)

Analysis of the emerin gene in familial and sporadic cases of emery-dreifuss muscular dystrophy

Neuromuscular disorders : NMD, 1996-03, Vol.6 (2), p.S16-S16

1996

Volltextzugriff (PDF)

Early onset X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy

Neuromuscular disorders : NMD, 1997-09, Vol.7 (6), p.444-445

1997

Volltextzugriff (PDF)

A family with severe pseudo-dominant Emery-Dreifuss muscular dystrophy due to emerin deficiency

Neuromuscular disorders : NMD, 1997-09, Vol.7 (6), p.445-445

1997

Volltextzugriff (PDF)

How Daughters Tell Their Mums to Behave

Developmental cell, 2021-01, Vol.56 (2), p.161-163

2021

Volltextzugriff (PDF)

Adherens junction treadmilling during collective migration

Nature cell biology, 2014-07, Vol.16 (7), p.639-651

2014

Volltextzugriff (PDF)

Platelet lysates promote mesenchymal stem cell expansion: A safety substitute for animal serum in cell-based therapy applications

Journal of cellular physiology, 2005-11, Vol.205 (2), p.228-236

2005

Volltextzugriff (PDF)

PTEN inhibits AMPK to control collective migration

Nature communications, 2022-08, Vol.13 (1), p.4528-4528, Article 4528

2022

Volltextzugriff (PDF)

JNK Signaling Controls Border Cell Cluster Integrity and Collective Cell Migration

Current biology, 2008-04, Vol.18 (7), p.538-544

2008

Volltextzugriff (PDF)

An actin-based viscoplastic lock ensures progressive body-axis elongation

Nature (London), 2019-09, Vol.573 (7773), p.266-270

2019

Volltextzugriff (PDF)

Connexin 30 controls astroglial polarization during postnatal brain development

Development (Cambridge), 2018-02, Vol.145 (4), p.dev155275-dev155275

2018

Volltextzugriff (PDF)

Phosphorylation Networks Regulating JNK Activity in Diverse Genetic Backgrounds

Science (American Association for the Advancement of Science), 2008-10, Vol.322 (5900), p.453-456

2008

Volltextzugriff (PDF)

Gender equality within boards: comparing quota and soft law

European journal of law and economics, 2024-04, Vol.57 (1-2), p.1-35

2024

Volltextzugriff (PDF)

French CEOs' Compensations: What is the Cost of a Mandatory Upper Limit?

CESifo economic studies, 2010-06, Vol.56 (2), p.165-191

Llense, Fabienne

2010

Volltextzugriff (PDF)

1 – 25 von 37

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(34)
Mit Volltextzugriff
(27)

Publikationsform

Artikel
(37)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?

Mutations in Emery-Dreifuss Muscular Dystrophy and their Effects on Emerin Protein Expression

Les conductrices symptomatiques pour les dystrophinopathies avec biais d'inactivation du chromosome X

Identification by STS PCR Screening of a Microdeletion in Xp21.3–22.1 Associated with Non-specific Mental Retardation

Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene

G.P.6 02 Somatic and germinal mosaicism of an out-of-frame deletion in the dystrophin gene in an adult male patient with predominant dilated cardiomyopathy

G.P.4.09 Looking for a third gene causing Emery-Dreifuss muscular dystrophy: Lessons and perspectives

Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with ‘de novo’ duplication of dystrophin gene

Early presentation of X-linked Emery–Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy

Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias

Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy

A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase loci

Analysis of the emerin gene in familial and sporadic cases of emery-dreifuss muscular dystrophy

Early onset X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy

A family with severe pseudo-dominant Emery-Dreifuss muscular dystrophy due to emerin deficiency

How Daughters Tell Their Mums to Behave

Adherens junction treadmilling during collective migration

Platelet lysates promote mesenchymal stem cell expansion: A safety substitute for animal serum in cell-based therapy applications

PTEN inhibits AMPK to control collective migration

JNK Signaling Controls Border Cell Cluster Integrity and Collective Cell Migration

An actin-based viscoplastic lock ensures progressive body-axis elongation

Connexin 30 controls astroglial polarization during postnatal brain development

Phosphorylation Networks Regulating JNK Activity in Diverse Genetic Backgrounds

Gender equality within boards: comparing quota and soft law

French CEOs' Compensations: What is the Cost of a Mandatory Upper Limit?

Suchergebnisse filtern