UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 38

Sortiert nach

Modularization of biochemical networks based on classification of Petri net t-invariants

BMC bioinformatics, 2008-02, Vol.9 (1), p.90-90, Article 90

2008

Link zum Volltext

Verfügbarkeit prüfen

β1-Adrenoceptor gene variations: a role in idiopathic dilated cardiomyopathy?

Journal of molecular medicine (Berlin, Germany), 2000-02, Vol.78 (2), p.87-93

2000

Link zum Volltext

Verfügbarkeit prüfen

Petri net modelling of gene regulation of the Duchenne muscular dystrophy

BioSystems, 2008-05, Vol.92 (2), p.189-205

2008

Link zum Volltext

Verfügbarkeit prüfen

Polymorphism in the human E-selectin gene detected by PCR-SSCP

Human genetics, 1994-10, Vol.94 (4), p.452-453

1994

Link zum Volltext

Verfügbarkeit prüfen

Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se

Journal of molecular medicine (Berlin, Germany), 2000, Vol.78 (10), p.569-574

2000

Link zum Volltext

Verfügbarkeit prüfen

Apoptotic neurodegeneration following trauma is markedly enhanced in the immature brain

Annals of neurology, 1999-06, Vol.45 (6), p.724-735

1999

Link zum Volltext

Verfügbarkeit prüfen

DMA polymorphisms in adhesion molecule genes ? a new risk factor for early atherosclerosis

Human genetics, 1996-01, Vol.97 (1)

1996

Link zum Volltext

Verfügbarkeit prüfen

DNA polymorphisms in adhesion molecule genes : a new risk factor for early atherosclerosis

Human genetics, 1996, Vol.97 (1), p.15-20

1996

Link zum Volltext

Verfügbarkeit prüfen

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients

Human molecular genetics, 1993-11, Vol.2 (11), p.1877-1881

1993

Link zum Volltext

Verfügbarkeit prüfen

Antisense oligonucleotides and short interfering RNAs silencing the cyclin-dependent kinase inhibitor p21 improve proliferation of Duchenne muscular dystrophy patients' primary skeletal myoblasts

Journal of molecular medicine (Berlin, Germany), 2005, Vol.83 (1), p.64-71

2005

Link zum Volltext

Verfügbarkeit prüfen

Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy

Human genetics, 2004, Vol.114 (2), p.149-156

2004

Link zum Volltext

Verfügbarkeit prüfen

Treatment of ataxia in isolated vitamin E deficiency caused by α-tocopherol transfer protein deficiency

The Journal of pediatrics, 1999-02, Vol.134 (2), p.240-244

1999

Link zum Volltext

Verfügbarkeit prüfen

Functional Characterization of Atherosclerosis-Associated Ser128Arg and Leu554Phe E-Selectin Mutations

Biological chemistry, 1999-06, Vol.380 (6), p.661-667

1999

Link zum Volltext

Verfügbarkeit prüfen

E-selectin polymorphism and atherosclerosis: an association study

Human molecular genetics, 1994-11, Vol.3 (11), p.1935-1937

1994

Link zum Volltext

Verfügbarkeit prüfen

Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy

Neuromuscular disorders : NMD, 2000-12, Vol.10 (8), p.572-577

2000

Link zum Volltext

Verfügbarkeit prüfen

A Cysteine 3340 Substitution in the Dystroglycan-Binding Domain of Dystrophin Associated with Duchenne Muscular Dystrophy, Mental Retardation and Absence of the ERG b-Wave

Human molecular genetics, 1996-07, Vol.5 (7), p.973-975

1996

Link zum Volltext

Verfügbarkeit prüfen

Genomic organization of the human excitatory amino acid transporter gene GLT-1

Neuroreport, 1997-02, Vol.8 (3), p.775-777

1997

Link zum Volltext

Verfügbarkeit prüfen

The glial glutamate transporter complementary DNA in patients with amyotrophic lateral sclerosis

Annals of neurology, 1996-09, Vol.40 (3), p.456-459

1996

Link zum Volltext

Verfügbarkeit prüfen

Examination of telomere lengths in muscle tissue casts doubt on replicative aging as cause of progression in duchenne muscular dystrophy

Pediatric research, 1997-08, Vol.42 (2), p.226-231

1997

Link zum Volltext

Verfügbarkeit prüfen

Muskeldystrophien

Monogen bedingte Erbkrankheiten 1, p.3-30

Link zum Volltext

Verfügbarkeit prüfen

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis

Cell, 1987-01, Vol.48 (2), p.351-357

1987

Link zum Volltext

Verfügbarkeit prüfen

Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se

Journal of molecular medicine (Berlin, Germany), 2000-01, Vol.78 (10), p.569-574

2000

Link zum Volltext

Verfügbarkeit prüfen

A small in-frame deletion within the protease domain of muscle-specific calpain, p94 causes early-onset limb-girdle muscular dystrophy 2A

Human mutation, 1998, Vol.11 (S1), p.S298-S300

1998

Link zum Volltext

Verfügbarkeit prüfen

beta sub(1)-Adrenoceptor gene variations: a role in idiopathic dilated cardiomyopathy?

Journal of molecular medicine (Berlin, Germany), 2000-02, Vol.78 (2), p.87-93

2000

Link zum Volltext

Verfügbarkeit prüfen

Four new polymorphisms in the human dystrophin gene from an Argentinian population

Muscle & nerve, 1997-11, Vol.20 (11), p.1451-1453

1997

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 38

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(37)
Mit Volltextzugriff
(38)

Publikationsform

Artikel
(37)
Buchkapitel
(1)

Sprache

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(27)
Science & Technology
(27)
Humans
(25)
Biological And Medical Sciences
(21)
Medical Sciences
(18)
Neurology
(14)
Genetics & Heredity
(13)
Male
(12)
Base Sequence
(11)
Diseases Of Striated Muscles. Neuromuscular Diseases
(10)
Adult
(8)
Animals
(8)
Muscular Dystrophies - Genetics
(8)
Biochemistry & Molecular Biology
(7)
Child
(7)
Female
(7)
Genes
(7)
Polymerase Chain Reaction
(7)
Molecular Sequence Data
(6)
Mutation
(6)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Modularization of biochemical networks based on classification of Petri net t-invariants

β1-Adrenoceptor gene variations: a role in idiopathic dilated cardiomyopathy?

Petri net modelling of gene regulation of the Duchenne muscular dystrophy

Polymorphism in the human E-selectin gene detected by PCR-SSCP

Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se

Apoptotic neurodegeneration following trauma is markedly enhanced in the immature brain

DMA polymorphisms in adhesion molecule genes ? a new risk factor for early atherosclerosis

DNA polymorphisms in adhesion molecule genes : a new risk factor for early atherosclerosis

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients

Antisense oligonucleotides and short interfering RNAs silencing the cyclin-dependent kinase inhibitor p21 improve proliferation of Duchenne muscular dystrophy patients' primary skeletal myoblasts

Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy

Treatment of ataxia in isolated vitamin E deficiency caused by α-tocopherol transfer protein deficiency

Functional Characterization of Atherosclerosis-Associated Ser128Arg and Leu554Phe E-Selectin Mutations

E-selectin polymorphism and atherosclerosis: an association study

Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy

A Cysteine 3340 Substitution in the Dystroglycan-Binding Domain of Dystrophin Associated with Duchenne Muscular Dystrophy, Mental Retardation and Absence of the ERG b-Wave

Genomic organization of the human excitatory amino acid transporter gene GLT-1

The glial glutamate transporter complementary DNA in patients with amyotrophic lateral sclerosis

Examination of telomere lengths in muscle tissue casts doubt on replicative aging as cause of progression in duchenne muscular dystrophy

Muskeldystrophien

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis

Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se

A small in-frame deletion within the protease domain of muscle-specific calpain, p94 causes early-onset limb-girdle muscular dystrophy 2A

beta sub(1)-Adrenoceptor gene variations: a role in idiopathic dilated cardiomyopathy?

Four new polymorphisms in the human dystrophin gene from an Argentinian population

Suchergebnisse filtern