UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 44

Sortiert nach

Electrochemical mixed aptamer-antibody sandwich assay for mucin protein 16 detection through hybridization chain reaction amplification

Analytical and bioanalytical chemistry, 2020-10, Vol.412 (26), p.7169-7178

2020

Link zum Volltext

Verfügbarkeit prüfen

Comparison of HLA-B27 subtypes between Chinese patients with ankylosing spondylitis and non-ankylosing spondylitis carriers

Journal of international medical research, 2019-07, Vol.47 (7), p.3171-3178

2019

Link zum Volltext

Verfügbarkeit prüfen

Mono-2-ethylhexyl phthalate drives progression of PINK1-parkin-mediated mitophagy via increasing mitochondrial ROS to exacerbate cytotoxicity

Redox biology, 2021-01, Vol.38, p.101776, Article 101776

2021

Link zum Volltext

Verfügbarkeit prüfen

Mitochondrial Diabetes Is Associated with the ND4 G11696A Mutation

Biomolecules (Basel, Switzerland), 2023-05, Vol.13 (6), p.907

2023

Link zum Volltext

Verfügbarkeit prüfen

Mitochondrial tRNAGln 4394C>T Mutation May Contribute to the Clinical Expression of 1555A>G-Induced Deafness

Genes, 2022-10, Vol.13 (10), p.1794

2022

Link zum Volltext

Verfügbarkeit prüfen

The Gut Microbiota in Women Suffering from Gestational Diabetes Mellitus with the Failure of Glycemic Control by Lifestyle Modification

Journal of Diabetes Research, 2019, Vol.2019, p.6081248-12

2019

Link zum Volltext

Verfügbarkeit prüfen

Reevaluating Adiponectin's impact on obesity hypertension: a Chinese case-control study

BMC cardiovascular disorders, 2024-04, Vol.24 (1), p.208-208, Article 208

2024

Link zum Volltext

Verfügbarkeit prüfen

Role of Mitochondrial DNA Mutations in Hearing Loss

Biochemical genetics, 2013-08, Vol.51 (7-8), p.588-602

2013

Link zum Volltext

Verfügbarkeit prüfen

General anesthetic agents induce neurotoxicity through astrocytes

Neural regeneration research, 2024-06, Vol.19 (6), p.1299-1307

2024

Link zum Volltext

Verfügbarkeit prüfen

Mitochondrial DNA mutations and essential hypertension (Review)

International journal of molecular medicine, 2013-10, Vol.32 (4), p.768-774

2013

Link zum Volltext

Verfügbarkeit prüfen

Clinical Implications of Increased Nogo-B Levels in Patients With Acute Coronary Syndromes and Stable Angina Pectoris

International Heart Journal, 2015, Vol.56(3), pp.341-344

2015

Link zum Volltext

Verfügbarkeit prüfen

Role of Stromal Cell-Derived Factor-1 in Patients With Non-ST Elevation Acute Coronary Syndrome

International Heart Journal, 2014, Vol.55(3), pp.219-227

2014

Link zum Volltext

Verfügbarkeit prüfen

Mitochondria-targeted antioxidant therapy for an animal model of PCOS-IR

International journal of molecular medicine, 2019-01, Vol.43 (1), p.316-324

2019

Link zum Volltext

Verfügbarkeit prüfen

The Association Between Mitochondrial tRN[A.sup.Glu] Variants and Hearing Loss: A Case-Control Study

Pharmacogenomics and personalized medicine, 2024-03, Vol.17, p.77

2024

Link zum Volltext

Verfügbarkeit prüfen

The Association Between Mitochondrial tRNA Glu Variants and Hearing Loss: A Case-Control Study

Pharmacogenomics and personalized medicine, 2024, Vol.17, p.77

2024

Link zum Volltext

Verfügbarkeit prüfen

Electrochemical determination of the activity of DNA methyltransferase based on the methyl binding domain protein and a customized modular detector

Mikrochimica acta (1966), 2019-04, Vol.186 (4), p.229-229, Article 229

2019

Link zum Volltext

Verfügbarkeit prüfen

Late onset of type 2 diabetes is associated with mitochondrial tRNATrp A5514G and tRNASer(AGY) C12237T mutations

Journal of clinical laboratory analysis, 2022-01, Vol.36 (1), p.e24102-n/a

2022

Link zum Volltext

Verfügbarkeit prüfen

Late onset of type 2 diabetes is associated with mitochondrial tRNA Trp A5514G and tRNA Ser(AGY) C12237T mutations

Journal of clinical laboratory analysis, 2022-01, Vol.36 (1), p.e24102

2022

Link zum Volltext

Verfügbarkeit prüfen

Mitochondrial Diabetes Is Associated with the IND4/I G11696A Mutation

Biomolecules (Basel, Switzerland), 2023-05, Vol.13 (6)

2023

Link zum Volltext

Verfügbarkeit prüfen

Mitochondrial tRNA[sup.Gln] 4394CT Mutation May Contribute to the Clinical Expression of 1555AG-Induced Deafness

Genes, 2022-10, Vol.13 (10)

2022

Link zum Volltext

Verfügbarkeit prüfen

Myricetin inhibits NLRP3 inflammasome activation via reduction of ROS-dependent ubiquitination of ASC and promotion of ROS-independent NLRP3 ubiquitination

Toxicology and applied pharmacology, 2019-02, Vol.365, p.19-29

2019

Link zum Volltext

Verfügbarkeit prüfen

Colorable role of interleukin (IL)-6 in obesity hypertension: A hint from a Chinese adult case-control study

Cytokine (Philadelphia, Pa.), 2023-08, Vol.168, p.156226-156226, Article 156226

2023

Link zum Volltext

Verfügbarkeit prüfen

The Association Between Mitochondrial tRNAGlu Variants and Hearing Loss: A Case-Control Study

Pharmacogenomics and personalized medicine, 2024-03, Vol.17, p.77-89

2024

Link zum Volltext

Verfügbarkeit prüfen

Neutrophil CD64 index as a good biomarker for early diagnosis of bacterial infection in pregnant women during the flu season

Influenza and other respiratory viruses, 2023-08, Vol.17 (8), p.e13191-n/a

2023

Link zum Volltext

Verfügbarkeit prüfen

Point mutation in mitochondrial tRNA gene is associated with polycystic ovary syndrome and insulin resistance

Molecular medicine reports, 2016-04, Vol.13 (4), p.3169-3172

2016

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 44

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(38)
Mit Volltextzugriff
(43)

Publikationsform

Artikel
(44)

Sprache

Englisch
(44)
Japanisch
(2)

Erscheinungsjahr

n.n

Thema

Science & Technology
(31)
Life Sciences & Biomedicine
(25)
Humans
(17)
Female
(12)
Mutation
(10)
Male
(9)
Dna, Mitochondrial - Genetics
(8)
Adult
(7)
Biochemistry & Molecular Biology
(7)
Mitochondria
(7)
Mitochondrial Dna
(7)
Deafness
(6)
Medicine, Research & Experimental
(6)
Research & Experimental Medicine
(6)
Transfer Rna
(6)
Asian Continental Ancestry Group - Genetics
(5)
Base Sequence
(5)
Hypertension
(5)
Aged
(4)
Animals
(4)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Electrochemical mixed aptamer-antibody sandwich assay for mucin protein 16 detection through hybridization chain reaction amplification

Comparison of HLA-B27 subtypes between Chinese patients with ankylosing spondylitis and non-ankylosing spondylitis carriers

Mono-2-ethylhexyl phthalate drives progression of PINK1-parkin-mediated mitophagy via increasing mitochondrial ROS to exacerbate cytotoxicity

Mitochondrial Diabetes Is Associated with the ND4 G11696A Mutation

Mitochondrial tRNAGln 4394C>T Mutation May Contribute to the Clinical Expression of 1555A>G-Induced Deafness

The Gut Microbiota in Women Suffering from Gestational Diabetes Mellitus with the Failure of Glycemic Control by Lifestyle Modification

Reevaluating Adiponectin's impact on obesity hypertension: a Chinese case-control study

Role of Mitochondrial DNA Mutations in Hearing Loss

General anesthetic agents induce neurotoxicity through astrocytes

Mitochondrial DNA mutations and essential hypertension (Review)

Clinical Implications of Increased Nogo-B Levels in Patients With Acute Coronary Syndromes and Stable Angina Pectoris

Role of Stromal Cell-Derived Factor-1 in Patients With Non-ST Elevation Acute Coronary Syndrome

Mitochondria-targeted antioxidant therapy for an animal model of PCOS-IR

The Association Between Mitochondrial tRN[A.sup.Glu] Variants and Hearing Loss: A Case-Control Study

The Association Between Mitochondrial tRNA Glu Variants and Hearing Loss: A Case-Control Study

Electrochemical determination of the activity of DNA methyltransferase based on the methyl binding domain protein and a customized modular detector

Late onset of type 2 diabetes is associated with mitochondrial tRNATrp A5514G and tRNASer(AGY) C12237T mutations

Late onset of type 2 diabetes is associated with mitochondrial tRNA Trp A5514G and tRNA Ser(AGY) C12237T mutations

Mitochondrial Diabetes Is Associated with the IND4/I G11696A Mutation

Mitochondrial tRNA[sup.Gln] 4394CT Mutation May Contribute to the Clinical Expression of 1555AG-Induced Deafness

Myricetin inhibits NLRP3 inflammasome activation via reduction of ROS-dependent ubiquitination of ASC and promotion of ROS-independent NLRP3 ubiquitination

Colorable role of interleukin (IL)-6 in obesity hypertension: A hint from a Chinese adult case-control study

The Association Between Mitochondrial tRNAGlu Variants and Hearing Loss: A Case-Control Study

Neutrophil CD64 index as a good biomarker for early diagnosis of bacterial infection in pregnant women during the flu season

Point mutation in mitochondrial tRNA gene is associated with polycystic ovary syndrome and insulin resistance

Suchergebnisse filtern