UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 45

Sortiert nach

Three-Year Follow-Up after Intrauterine mTOR Inhibitor Administration for Fetus with TSC-Associated Rhabdomyoma

International journal of molecular sciences, 2023-08, Vol.24 (16), p.12886

2023

Volltextzugriff (PDF)

Investigating the genetic characteristics of the Csangos, a traditionally Hungarian speaking ethnic group residing in Romania

Journal of human genetics, 2020-12, Vol.65 (12), p.1093-1103

2020

Volltextzugriff (PDF)

Molecular genetic investigation of hereditary breast and ovarian cancer patients in the Southern Transdanubian region: widening the mutation spectrum and searching for new pathogenic variants using next-generation methods

Pathology oncology research, 2024-08, Vol.30, p.1611813

2024

Volltextzugriff (PDF)

Xp11.2 Duplication in Females: Unique Features of a Rare Copy Number Variation

Frontiers in genetics, 2021-04, Vol.12, p.635458-635458

2021

Volltextzugriff (PDF)

GCKR gene functional variants in type 2 diabetes and metabolic syndrome: do the rare variants associate with increased carotid intima-media thickness?

Cardiovascular diabetology, 2010-11, Vol.9 (1), p.79-79

2010

Volltextzugriff (PDF)

Apolipoprotein A5 gene C56G variant confers risk for the development of large-vessel associated ischemic stroke

Journal of neurology, 2008-05, Vol.255 (5), p.649-654

2008

Volltextzugriff (PDF)

Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation

Current medicinal chemistry, 2008-06, Vol.15 (13), p.1257

2008

Volltextzugriff (PDF)

Functional Variants of Glucokinase Regulatory Protein and Apolipoprotein A5 Genes in Ischemic Stroke

Journal of molecular neuroscience, 2010-05, Vol.41 (1), p.121-128

2010

Volltextzugriff (PDF)

Common functional variants of APOA5 and GCKR accumulate gradually in association with triglyceride increase in metabolic syndrome patients

Molecular biology reports, 2012-02, Vol.39 (2), p.1949-1955

2012

Volltextzugriff (PDF)

Apolipoprotein A5 gene promoter region T-1131C polymorphism associates with elevated circulating triglyceride levels and confers susceptibility for development of ischemic stroke

Journal of molecular neuroscience, 2006-01, Vol.29 (2), p.177-184

2006

Volltextzugriff (PDF)

Apolipoprotein A5 T-1131C variant confers risk for metabolic syndrome

Pathology oncology research, 2007-01, Vol.13 (3), p.243-247

2007

Volltextzugriff (PDF)

Triglyceride Level-Influencing Functional Variants of the ANGPTL3, CILP2, and TRIB1 Loci in Ischemic Stroke

Neuromolecular medicine, 2011-09, Vol.13 (3), p.179-186

2011

Volltextzugriff (PDF)

H Protein of Bacteriophage 16-3 and RkpM Protein of Sinorhizobium meliloti 41 Are Involved in Phage Adsorption

Journal of Bacteriology, 2004-03, Vol.186 (6), p.1591-1597

2004

Volltextzugriff (PDF)

Stepwise Positive Association Between APOA5 Minor Allele Frequencies and Increasing Plasma Triglyceride Quartiles in Random Patients with Hypertriglyceridemia of Unclarified Origin

Pathology oncology research, 2011-03, Vol.17 (1), p.39-44

2011

Volltextzugriff (PDF)

Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases

JIMD reports, 2013, Vol.9, p.105-111

2013

Volltextzugriff (PDF)

Gene testing in Treacher Collins syndrome

Orvosi hetilap, 2020-12, Vol.161 (52), p.2201

2020

Volltextzugriff (PDF)

Genetic Variability and Haplotype Profile of MDR1 (ABCB1) in Roma and Hungarian Population Samples with a Review of the Literature

Drug metabolism and pharmacokinetics, 2011-01, Vol.26 (2), p.206-215

2011

Volltextzugriff (PDF)

Three periods of one and a half decade of ischemic stroke susceptibility gene research: lessons we have learned

Genome medicine, 2010-09, Vol.2 (9), p.64-64

2010

Volltextzugriff (PDF)

Apolipoprotein A5 Gene IVS3+G476A Allelic Variant Confers Susceptibility for Development of Ischemic Stroke

Circulation Journal, 2008, Vol.72(7), pp.1065-1070

2008

Volltextzugriff (PDF)

Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation

Pathology oncology research, 2005-01, Vol.11 (2), p.82-86

2005

Volltextzugriff (PDF)

Apolipoprotein A5 IVS3+476A Allelic Variant Associates With Increased Trigliceride Levels and Confers Risk for Development of Metabolic Syndrome in Hungarians

Circulation Journal, 2008, Vol.72(1), pp.40-43

2008

Volltextzugriff (PDF)

Genetics of ischemic stroke: where are we now?

Orvosi hetilap, 2011-03, Vol.152 (12), p.455

2011

Volltextzugriff (PDF)

Significance of thiopurine s-methyltransferase gene test in a clinical case

Orvosi hetilap, 2012-02, Vol.153 (5), p.191

2012

Volltextzugriff (PDF)

Genetic Variability and Haplotype Profile of MDR1 (ABCB1) in Roma and Hungarian Population Samples with a Review of the Literature

DRUG METABOLISM AND PHARMACOKINETICS, 2011, Vol.26 (2), p.206-215

2011

Volltextzugriff (PDF)

TUBB4B gene mutation in Leber phenotype of congenital amaurosis syndrome associated with early-onset deafness

European journal of medical genetics, 2022-04, Vol.65 (4), p.104471-104471, Article 104471

2022

Volltextzugriff (PDF)

1 – 25 von 45

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(42)
Mit Volltextzugriff
(38)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Three-Year Follow-Up after Intrauterine mTOR Inhibitor Administration for Fetus with TSC-Associated Rhabdomyoma

Investigating the genetic characteristics of the Csangos, a traditionally Hungarian speaking ethnic group residing in Romania

Molecular genetic investigation of hereditary breast and ovarian cancer patients in the Southern Transdanubian region: widening the mutation spectrum and searching for new pathogenic variants using next-generation methods

Xp11.2 Duplication in Females: Unique Features of a Rare Copy Number Variation

GCKR gene functional variants in type 2 diabetes and metabolic syndrome: do the rare variants associate with increased carotid intima-media thickness?

Apolipoprotein A5 gene C56G variant confers risk for the development of large-vessel associated ischemic stroke

Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation

Functional Variants of Glucokinase Regulatory Protein and Apolipoprotein A5 Genes in Ischemic Stroke

Common functional variants of APOA5 and GCKR accumulate gradually in association with triglyceride increase in metabolic syndrome patients

Apolipoprotein A5 gene promoter region T-1131C polymorphism associates with elevated circulating triglyceride levels and confers susceptibility for development of ischemic stroke

Apolipoprotein A5 T-1131C variant confers risk for metabolic syndrome

Triglyceride Level-Influencing Functional Variants of the ANGPTL3, CILP2, and TRIB1 Loci in Ischemic Stroke

H Protein of Bacteriophage 16-3 and RkpM Protein of Sinorhizobium meliloti 41 Are Involved in Phage Adsorption

Stepwise Positive Association Between APOA5 Minor Allele Frequencies and Increasing Plasma Triglyceride Quartiles in Random Patients with Hypertriglyceridemia of Unclarified Origin

Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases

Gene testing in Treacher Collins syndrome

Genetic Variability and Haplotype Profile of MDR1 (ABCB1) in Roma and Hungarian Population Samples with a Review of the Literature

Three periods of one and a half decade of ischemic stroke susceptibility gene research: lessons we have learned

Apolipoprotein A5 Gene IVS3+G476A Allelic Variant Confers Susceptibility for Development of Ischemic Stroke

Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation

Apolipoprotein A5 IVS3+476A Allelic Variant Associates With Increased Trigliceride Levels and Confers Risk for Development of Metabolic Syndrome in Hungarians

Genetics of ischemic stroke: where are we now?

Significance of thiopurine s-methyltransferase gene test in a clinical case

Genetic Variability and Haplotype Profile of MDR1 (ABCB1) in Roma and Hungarian Population Samples with a Review of the Literature

TUBB4B gene mutation in Leber phenotype of congenital amaurosis syndrome associated with early-onset deafness

Suchergebnisse filtern