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...

Simultaneous mutation scanning for gross deletions, duplications and point mutations in the DMD gene

European journal of human genetics : EJHG, 2008-01, Vol.16 (1), p.53-61

2008

Volltextzugriff (PDF)

Identification and quantification of somatic mosaicism for a point mutation in a Duchenne muscular dystrophy family

Journal of medical genetics, 1999-04, Vol.36 (4), p.313-315

1999

Volltextzugriff (PDF)

A small intraexonic deletion within the dystrophin gene suggests a possible mechanism of mutagenesis

Human genetics, 1997-05, Vol.99 (5), p.658-662

1997

Volltextzugriff (PDF)

A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods

Journal of medical genetics, 1991-05, Vol.28 (5), p.304-311

1991

Volltextzugriff (PDF)

Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy

The Lancet (British edition), 1993-01, Vol.341 (8840), p.273-275

1993

Volltextzugriff (PDF)

Tripeptide-copper complex GHK-Cu (II) transiently improved healing outcome in a rat model of ACL reconstruction

Journal of orthopaedic research, 2015-07, Vol.33 (7), p.1024-1033

2015

Volltextzugriff (PDF)

Tracking cardiac engraftment and distribution of implanted bone marrow cells: Comparing intra-aortic, intravenous, and intramyocardial delivery

The Journal of thoracic and cardiovascular surgery, 2009-05, Vol.137 (5), p.1225-1233.e1

2009

Volltextzugriff (PDF)

Effect of graft tensioning on mechanical restoration in a rat model of anterior cruciate ligament reconstruction using free tendon graft

Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA, 2013-05, Vol.21 (5), p.1226-1233

2013

Volltextzugriff (PDF)

The contribution of X-linked coding variation to severe developmental disorders

Nature communications, 2021-01, Vol.12 (1), p.627-627, Article 627

2021

Volltextzugriff (PDF)

Alberta Infant Motor Scale: Reliability and Validity When Used on Preterm Infants in Taiwan

Physical therapy, 2000-02, Vol.80 (2), p.168-178

2000

Volltextzugriff (PDF)

Mutations at the mitochondrial DNA polymerase ( POLG ) locus associated with male infertility

Nature genetics, 2001-11, Vol.29 (3), p.261-262

2001

Volltextzugriff (PDF)

Association of Resistin Gene 3′-Untranslated Region +62G→A Polymorphism with Type 2 Diabetes and Hypertension in a Chinese Population

The journal of clinical endocrinology and metabolism, 2003-03, Vol.88 (3), p.1258-1263

2003

Volltextzugriff (PDF)

Comparison of Clinical Application of the Abbott HBV PCR Kit and the Versant HBV DNA 3.0 Test to Measure Serum Hepatitis B Virus DNA in Taiwanese Patients

The Kaohsiung journal of medical sciences, 2009-08, Vol.25 (8), p.413-422

2009

Volltextzugriff (PDF)

Effect of Nucleotides on Diarrhea and Immune Responses in Healthy Term Infants in Taiwan

Journal of pediatric gastroenterology and nutrition, 2003-01, Vol.36 (1), p.37-43

2003

Volltextzugriff (PDF)

Pulsatile ocular blood flow in patients with Graves' ophthalmopathy

Eye (London), 2005-02, Vol.19 (2), p.159-162

2005

Volltextzugriff (PDF)

Live/Real Time Three-Dimensional Transthoracic Echocardiographic Assessment of Left Ventricular Volumes, Ejection Fraction, and Mass Compared with Magnetic Resonance Imaging

Echocardiography (Mount Kisco, N.Y.), 2007-02, Vol.24 (2), p.166-173

2007

Volltextzugriff (PDF)

Smoking-Associated Mitochondrial DNA Mutations and Lipid Peroxidation in Human Lung Tissues

American journal of respiratory cell and molecular biology, 1998-12, Vol.19 (6), p.901-909

1998

Volltextzugriff (PDF)

Lipophilic antioxidants and iron status in ESRD patients on hemodialysis

Nephron (2015), 2000-12, Vol.86 (4), p.428-435

2000

Volltextzugriff (PDF)

Early versus late nutrition support in premature neonates with respiratory distress syndrome

Nutrition (Burbank, Los Angeles County, Calif.), 2003-03, Vol.19 (3), p.257-260

2003

Volltextzugriff (PDF)

CT angiography of intracranial aneurysms: advantages and pitfalls

European journal of radiology, 1997-07, Vol.25 (1), p.14-19

1997

Volltextzugriff (PDF)

Smoking-associated mitochondrial DNA mutations in human hair follicles

Environmental and molecular mutagenesis, 1997, Vol.30 (1), p.47-55

1997

Volltextzugriff (PDF)

Laparoscopic finding and imaging of the iatrogenic duodenal intramural hematoma

Hepato-gastroenterology, 1997-01, Vol.44 (13), p.139

1997

Volltextzugriff (PDF)

Serum trace elements, glutathione, copper/zinc superoxide dismutase, and lipid peroxidation in epileptic patients with phenytoin or carbamazepine monotherapy

Clinical neuropharmacology, 1998, Vol.21 (1), p.62-64

1998

Volltextzugriff (PDF)

Age-related 4,977 bp deletion in human lung mitochondrial DNA

American journal of respiratory and critical care medicine, 1996-10, Vol.154 (4 Pt 1), p.1141-1145

1996

Volltextzugriff (PDF)

Performance characteristics of two real-time PCR assays for quantification of hepatitis B virus DNA

Scandinavian journal of infectious diseases, 2009, Vol.41 (8), p.614-618

2009

Volltextzugriff (PDF)

1 – 25 von 26

Suche als RSS-Feed

Aktive Filter

ThemaMale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(25)
Mit Volltextzugriff
(22)

Publikationsform

Artikel
(26)

Sprache

Englisch
(26)
Japanisch
(3)

Erscheinungsjahr

n.n

Thema

Science & Technology
(26)
Life Sciences & Biomedicine
(25)
Humans
(23)
Female
(18)
Biological And Medical Sciences
(16)
Medical Sciences
(15)
Adult
(12)
Aged
(10)
Middle Aged
(10)
Genetics & Heredity
(6)
Infant, Newborn
(6)
Mutation
(5)
Polymerase Chain Reaction
(5)
Animals
(4)
Diseases Of Striated Muscles. Neuromuscular Diseases
(4)
Dna, Mitochondrial - Genetics
(4)
Males
(4)
Muscular Dystrophies - Genetics
(4)
Neurology
(4)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Simultaneous mutation scanning for gross deletions, duplications and point mutations in the DMD gene

Identification and quantification of somatic mosaicism for a point mutation in a Duchenne muscular dystrophy family

A small intraexonic deletion within the dystrophin gene suggests a possible mechanism of mutagenesis

A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods

Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy

Tripeptide-copper complex GHK-Cu (II) transiently improved healing outcome in a rat model of ACL reconstruction

Tracking cardiac engraftment and distribution of implanted bone marrow cells: Comparing intra-aortic, intravenous, and intramyocardial delivery

Effect of graft tensioning on mechanical restoration in a rat model of anterior cruciate ligament reconstruction using free tendon graft

The contribution of X-linked coding variation to severe developmental disorders

Alberta Infant Motor Scale: Reliability and Validity When Used on Preterm Infants in Taiwan

Mutations at the mitochondrial DNA polymerase ( POLG ) locus associated with male infertility

Association of Resistin Gene 3′-Untranslated Region +62G→A Polymorphism with Type 2 Diabetes and Hypertension in a Chinese Population

Comparison of Clinical Application of the Abbott HBV PCR Kit and the Versant HBV DNA 3.0 Test to Measure Serum Hepatitis B Virus DNA in Taiwanese Patients

Effect of Nucleotides on Diarrhea and Immune Responses in Healthy Term Infants in Taiwan

Pulsatile ocular blood flow in patients with Graves' ophthalmopathy

Live/Real Time Three-Dimensional Transthoracic Echocardiographic Assessment of Left Ventricular Volumes, Ejection Fraction, and Mass Compared with Magnetic Resonance Imaging

Smoking-Associated Mitochondrial DNA Mutations and Lipid Peroxidation in Human Lung Tissues

Lipophilic antioxidants and iron status in ESRD patients on hemodialysis

Early versus late nutrition support in premature neonates with respiratory distress syndrome

CT angiography of intracranial aneurysms: advantages and pitfalls

Smoking-associated mitochondrial DNA mutations in human hair follicles

Laparoscopic finding and imaging of the iatrogenic duodenal intramural hematoma

Serum trace elements, glutathione, copper/zinc superoxide dismutase, and lipid peroxidation in epileptic patients with phenytoin or carbamazepine monotherapy

Age-related 4,977 bp deletion in human lung mitochondrial DNA

Performance characteristics of two real-time PCR assays for quantification of hepatitis B virus DNA

Aktive Filter

Suchergebnisse filtern