UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 112

Sortiert nach

Spectrum of small mutations in the dystrophin coding region

American journal of human genetics, 1995-07, Vol.57 (1), p.22-33

1995

Link zum Volltext

Verfügbarkeit prüfen

Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome

Human genetics, 2001-02, Vol.108 (2), p.109-115

2001

Link zum Volltext

Verfügbarkeit prüfen

Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletion

Neurology, 1997-02, Vol.48 (2), p.486

1997

Link zum Volltext

Verfügbarkeit prüfen

Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formation

Human molecular genetics, 1993-03, Vol.2 (3), p.311-313

1993

Link zum Volltext

Verfügbarkeit prüfen

A novel splice site mutation in a Becker muscular dystrophy patient

Journal of medical genetics, 1996-04, Vol.33 (4), p.324-327

1996

Link zum Volltext

Verfügbarkeit prüfen

A molecular protocol for diagnosing myotonic dystrophy

Clinical chemistry (Baltimore, Md.), 1995-01, Vol.41 (1), p.69

1995

Link zum Volltext

Verfügbarkeit prüfen

Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16

Human molecular genetics, 1994-07, Vol.3 (7), p.1173-1174

1994

Link zum Volltext

Verfügbarkeit prüfen

Detection of an exon 53 polymorphism in the dystrophin gene

Human genetics, 1993-10, Vol.92 (3), p.302-304

1993

Link zum Volltext

Verfügbarkeit prüfen

A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient

Nature genetics, 1993-08, Vol.4 (4), p.357-360

1993

Link zum Volltext

Verfügbarkeit prüfen

Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2

Genetics in medicine, 2002-01, Vol.4 (1), p.20-26

2002

Link zum Volltext

Verfügbarkeit prüfen

Germline mosaicism at the fragile X locus

American journal of medical genetics, 1995-01, Vol.55 (3), p.384-386

1995

Link zum Volltext

Verfügbarkeit prüfen

Heteroduplex analysis of the dystrophin gene: Application to point mutation and carrier detection

American journal of medical genetics, 1994-03, Vol.50 (1), p.68-73

1994

Link zum Volltext

Verfügbarkeit prüfen

Nonsense mutations in a Becker muscular dystrophy and an intermediate patient

Human mutation, 1996, Vol.7 (1), p.72-75

1996

Link zum Volltext

Verfügbarkeit prüfen

Exon 44 nonsense mutation in two-duchenne muscular dystrophy brothers detected by heteroduplex analysis

Human mutation, 1993, Vol.2 (3), p.192-195

1993

Link zum Volltext

Verfügbarkeit prüfen

Rapid DNA haplotyping using a multiplex heteroduplex approach: Application to duchenne muscular dystrophy carrier testing

Human mutation, 1995, Vol.5 (3), p.263-268

1995

Link zum Volltext

Verfügbarkeit prüfen

On thermodynamics of AdS black holes in M-theory

The European physical journal. C, Particles and fields, 2016-02, Vol.76 (2), p.1, Article 73

2016

Link zum Volltext

Verfügbarkeit prüfen

On heat properties of AdS black holes in higher dimensions

The journal of high energy physics, 2015-05, Vol.2015 (5), p.1, Article 149

2015

Link zum Volltext

Verfügbarkeit prüfen

The optical features of noncommutative charged 4D-AdS-Einstein–Gauss–Bonnet black hole: shadow and deflection angle

The European physical journal. C, Particles and fields, 2024-04, Vol.84 (4), p.350-15, Article 350

2024

Link zum Volltext

Verfügbarkeit prüfen

Maxwell’s equal-area law for Gauss–Bonnet–Anti-de Sitter black holes

The European physical journal. C, Particles and fields, 2015-02, Vol.75 (2), p.1-9, Article 71

2015

Link zum Volltext

Verfügbarkeit prüfen

New thieno[3,2-d]pyrimidine-based derivatives: Design, synthesis and biological evaluation as antiproliferative agents, EGFR and ARO inhibitors inducing apoptosis in breast cancer cells

Bioorganic chemistry, 2021-10, Vol.115, p.105208-105208, Article 105208

2021

Link zum Volltext

Verfügbarkeit prüfen

Measurement of radon gas concentration and effective dose in water from the Midelt region of Morocco, Using nuclear track detectors (LR-115)

E3S web of conferences, 2023-01, Vol.469, p.10

2023

Link zum Volltext

Verfügbarkeit prüfen

Optical behaviors of black holes in Starobinsky–Bel–Robinson gravity

General relativity and gravitation, 2023-10, Vol.55 (10), Article 110

2023

Link zum Volltext

Verfügbarkeit prüfen

On Thermodynamics of AdS Black Holes in Arbitrary Dimensions

Chinese physics letters, 2012, Vol.29 (10), p.100401-1-100401-3

2012

Link zum Volltext

Verfügbarkeit prüfen

Deep Networks with Stochastic Depth

Computer Vision – ECCV 2016, p.646-661

Link zum Volltext

Verfügbarkeit prüfen

Noncommutative inspired 5D charged black hole in Einstein–Gauss–Bonnet theory

European physical journal plus, 2022-12, Vol.137 (12), p.1339, Article 1339

2022

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 112

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(84)
Mit Volltextzugriff
(106)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Spectrum of small mutations in the dystrophin coding region

Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome

Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletion

Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formation

A novel splice site mutation in a Becker muscular dystrophy patient

A molecular protocol for diagnosing myotonic dystrophy

Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16

Detection of an exon 53 polymorphism in the dystrophin gene

A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient

Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2

Germline mosaicism at the fragile X locus

Heteroduplex analysis of the dystrophin gene: Application to point mutation and carrier detection

Nonsense mutations in a Becker muscular dystrophy and an intermediate patient

Exon 44 nonsense mutation in two-duchenne muscular dystrophy brothers detected by heteroduplex analysis

Rapid DNA haplotyping using a multiplex heteroduplex approach: Application to duchenne muscular dystrophy carrier testing

On thermodynamics of AdS black holes in M-theory

On heat properties of AdS black holes in higher dimensions

The optical features of noncommutative charged 4D-AdS-Einstein–Gauss–Bonnet black hole: shadow and deflection angle

Maxwell’s equal-area law for Gauss–Bonnet–Anti-de Sitter black holes

New thieno[3,2-d]pyrimidine-based derivatives: Design, synthesis and biological evaluation as antiproliferative agents, EGFR and ARO inhibitors inducing apoptosis in breast cancer cells

Measurement of radon gas concentration and effective dose in water from the Midelt region of Morocco, Using nuclear track detectors (LR-115)

Optical behaviors of black holes in Starobinsky–Bel–Robinson gravity

On Thermodynamics of AdS Black Holes in Arbitrary Dimensions

Deep Networks with Stochastic Depth

Noncommutative inspired 5D charged black hole in Einstein–Gauss–Bonnet theory

Suchergebnisse filtern