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...

Multiplex ligation-dependent probe amplification using a completely synthetic probe set

BioTechniques, 2004-09, Vol.37 (3), p.399-405

2004

Volltextzugriff (PDF)

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)

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)

DNA-damaging reagents induce apoptosis through reactive oxygen species-dependent Fas aggregation

Oncogene, 2003-11, Vol.22 (50), p.8168-8177

2003

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)

Infant exposure to polychlorinated dibenzo- p-dioxins, dibenzofurans and biphenyls (PCDD/Fs, PCBs)––correlation between prenatal and postnatal exposure

Chemosphere (Oxford), 2004-03, Vol.54 (10), p.1459-1473

2004

Volltextzugriff (PDF)

Endocrine disruptor, dioxin (TCDD)-induced mitochondrial dysfunction and apoptosis in human trophoblast-like JAR cells

Molecular human reproduction, 2010-05, Vol.16 (5), p.361-372

2010

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)

Multiple rearrangements of mitochondrial DNA in unfertilized human oocytes

Fertility and sterility, 2002-05, Vol.77 (5), p.1012-1017

2002

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)

Osmotic sucrose enhancement of single-cell embryogenesis and transformation efficiency in Oncidium

Plant cell, tissue and organ culture, 2005-05, Vol.81 (2), p.183-192

2005

Volltextzugriff (PDF)

Biomarkers of DNA damage in patients with end‐stage renal disease: mitochondrial DNA mutation in hair follicles

Nephrology, dialysis, transplantation, 2001-03, Vol.16 (3), p.561-565

2001

Volltextzugriff (PDF)

Nuchal translucence incorporated into a one-stage multifactorial screening model for Down syndrome prediction at second-trimester pregnancy

Ultrasound in medicine & biology, 2003-12, Vol.29 (12), p.1667-1674

2003

Volltextzugriff (PDF)

Apoptotic Signal of Fas Is Not Mediated by Ceramide

Blood, 1998-04, Vol.91 (8), p.2658-2663

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)

Phenytoin-mediated oxidative stress in serum of female epileptics: A possible pathogenesis in the fetal hydantoin syndrome

Human & experimental toxicology, 1997-03, Vol.16 (3), p.177-181

1997

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)

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)

1 – 25 von 28

Suche als RSS-Feed

Aktive Filter

ThemaBiological And Medical Sciences

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(27)
Mit Volltextzugriff
(25)

Publikationsform

Artikel
(28)

Sprache

Englisch
(28)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(28)
Science & Technology
(28)
Humans
(23)
Medical Sciences
(19)
Male
(16)
Female
(15)
Adult
(10)
Fundamental And Applied Biological Sciences. Psychology
(10)
Aged
(7)
Middle Aged
(7)
Genetics & Heredity
(6)
Dna, Mitochondrial - Genetics
(5)
Infant, Newborn
(5)
Molecular And Cellular Biology
(5)
Mutation
(5)
Diseases Of Striated Muscles. Neuromuscular Diseases
(4)
Neurology
(4)
Polymerase Chain Reaction
(4)
Analysis Of Variance
(3)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Multiplex ligation-dependent probe amplification using a completely synthetic probe set

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

Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy

DNA-damaging reagents induce apoptosis through reactive oxygen species-dependent Fas aggregation

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

Infant exposure to polychlorinated dibenzo- p-dioxins, dibenzofurans and biphenyls (PCDD/Fs, PCBs)––correlation between prenatal and postnatal exposure

Endocrine disruptor, dioxin (TCDD)-induced mitochondrial dysfunction and apoptosis in human trophoblast-like JAR cells

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

Multiple rearrangements of mitochondrial DNA in unfertilized human oocytes

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

Pulsatile ocular blood flow in patients with Graves' ophthalmopathy

Osmotic sucrose enhancement of single-cell embryogenesis and transformation efficiency in Oncidium

Biomarkers of DNA damage in patients with end‐stage renal disease: mitochondrial DNA mutation in hair follicles

Nuchal translucence incorporated into a one-stage multifactorial screening model for Down syndrome prediction at second-trimester pregnancy

Apoptotic Signal of Fas Is Not Mediated by Ceramide

Lipophilic antioxidants and iron status in ESRD patients on hemodialysis

Phenytoin-mediated oxidative stress in serum of female epileptics: A possible pathogenesis in the fetal hydantoin syndrome

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

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

Aktive Filter

Suchergebnisse filtern