UB Paderborn / Katalog / Suche / in CDI

The association between TIPARP gene polymorphisms rs2665390 and ovarian cancer susceptibility

Gynecologic oncology reports, 2023-06, Vol.47, p.101175-101175, Article 101175

2023

Link zum Volltext

Verfügbarkeit prüfen

Mitochondrial genomes from modern horses reveal the major haplogroups that underwent domestication

Proceedings of the National Academy of Sciences - PNAS, 2012-02, Vol.109 (7), p.2449-2454

2012

Link zum Volltext

Verfügbarkeit prüfen

Association of ABCB1 and SLC22A16 Gene Polymorphisms with Incidence of Doxorubicin-Induced Febrile Neutropenia: A Survey of Iranian Breast Cancer Patients

PloS one, 2016-12, Vol.11 (12), p.e0168519-e0168519

2016

Link zum Volltext

Verfügbarkeit prüfen

Analysis of the HEXA, HEXB, ARSA, and SMPD1 Genes in 68 Iranian Patients

Journal of molecular neuroscience, 2022-03, Vol.72 (3), p.555-564

2022

Link zum Volltext

Verfügbarkeit prüfen

Ancient migratory events in the Middle East: new clues from the Y-chromosome variation of modern Iranians

PloS one, 2012-07, Vol.7 (7), p.e41252-e41252

2012

Link zum Volltext

Verfügbarkeit prüfen

Evaluation of FTO rs9939609 and MC4R rs17782313 Polymorphisms as Prognostic Biomarkers of Obesity: A Population-Based Cross-Sectional Study

Oman medical journal, 2019-01, Vol.34 (1), p.56-62

2019

Link zum Volltext

Verfügbarkeit prüfen

The Study of rs693 and rs515135 in APOB in People with Familial Hypercholestrolemia

Cell journal (Yakhteh), 2019-04, Vol.21 (1), p.86-91

2019

Link zum Volltext

Verfügbarkeit prüfen

Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patients

PloS one, 2014-04, Vol.9 (4), p.e94069-e94069

2014

Link zum Volltext

Verfügbarkeit prüfen

Investigation of FGF21 mRNA levels and relative mitochondrial DNA copy number levels and their relation in nonalcoholic fatty liver disease: a case-control study

Frontiers in molecular biosciences, 2023-06, Vol.10, p.1203019-1203019

2023

Link zum Volltext

Verfügbarkeit prüfen

Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations

Hereditas, 2022-01, Vol.159 (1), p.8-8, Article 8

2022

Link zum Volltext

Verfügbarkeit prüfen

The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian men

Genes & Genomics, 2023, 45(4), , pp.519-529

2023

Link zum Volltext

Verfügbarkeit prüfen

Two novel tyrosinase (TYR) gene mutations with pathogenic impact on oculocutaneous albinism type 1 (OCA1)

PloS one, 2014-09, Vol.9 (9), p.e106656-e106656

2014

Link zum Volltext

Verfügbarkeit prüfen

Following the Trace of HVS II Mitochondrial Region Within the Nine Iranian Ethnic Groups Based on Genetic Population Analysis

Biochemical genetics, 2022-06, Vol.60 (3), p.987-1006

2022

Link zum Volltext

Verfügbarkeit prüfen

The effect of CHRNA3 rs1051730 C>T and ABCB1 rs3842 A>G polymorphisms on non-small cell lung cancer and nicotine dependence in Iranian population

Heliyon, 2021-09, Vol.7 (9), p.e07867-e07867, Article e07867

2021

Link zum Volltext

Verfügbarkeit prüfen

Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972 and rs9657904 Polymorphisms with Multiple Sclerosis in Iranian Population

Oman medical journal, 2020-07, Vol.35 (4), p.1-9

2020

Link zum Volltext

Verfügbarkeit prüfen

Zataria multiflora Boiss. Essential Oil Induce Apoptosis in Two Human Colon Cancer Cell Lines (HCT116 & SW48)

Iranian journal of public health, 2020-04, Vol.49 (4), p.753-762

2020

Link zum Volltext

Verfügbarkeit prüfen

The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD Child

Iranian journal of allergy, asthma, and immunology, 2023-02, Vol.22 (1), p.119

2023

Link zum Volltext

Verfügbarkeit prüfen

Association of Single Nucleotide Polymorphisms in the VDR and CYP27B1 Genes with Risk of Developing Vitamin D3 Deficiency

Journal of pure & applied microbiology : an international research journal of microbiology, 2021-03, Vol.15 (1), p.201-211

2021

Link zum Volltext

Verfügbarkeit prüfen

Prevalence of the CYP2C192 (681 G>A), 3 (636 G>A) and 17 (‑806 C>T) alleles among an Iranian population of different ethnicities

Molecular medicine reports, 2018-01, Vol.17 (3), p.4195-4202

2018

Link zum Volltext

Verfügbarkeit prüfen

Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration

TheScientificWorld, 2012-01, Vol.2012, p.635183-7

2012

Link zum Volltext

Verfügbarkeit prüfen

Confirmation of Hyperimmunoglobulin E Syndrome in Two Patients with an Ocular Problem: Detection of Two New DOCK8 Mutations

Iranian journal of allergy, asthma, and immunology, 2022-06, Vol.21 (3), p.355

2022

Link zum Volltext

Verfügbarkeit prüfen

Mitochondrial Polymorphisms, in The D-Loop Area, Are Associated with Brain Tumors

Cell journal (Yakhteh), 2019-10, Vol.21 (3), p.350-356

2019

Link zum Volltext

Verfügbarkeit prüfen

Investigating the Variation of TREC/KREC in Combined Immunodeficiencies

Iranian journal of allergy, asthma, and immunology, 2021-08, Vol.20 (4), p.402

2021

Link zum Volltext

Verfügbarkeit prüfen

Mitochondrial Variants in Pompe Disease: A Comparison between Classic and Non-Classic Forms

Cell journal (Yakhteh), 2018-10, Vol.20 (3), p.333-339

2018

Link zum Volltext

Verfügbarkeit prüfen

Evaluation of 'FTO rs9939609' and 'MC4R rs17782313' polymorphisms as prognostic biomarkers of obesity: A populationbased cross-sectional study

Oman medical journal, 2019-01, Vol.34 (1), p.56-62

2019

Link zum Volltext

Verfügbarkeit prüfen

Menü

Weitere Dienste

Einstellungen

The association between TIPARP gene polymorphisms rs2665390 and ovarian cancer susceptibility

Mitochondrial genomes from modern horses reveal the major haplogroups that underwent domestication

Association of ABCB1 and SLC22A16 Gene Polymorphisms with Incidence of Doxorubicin-Induced Febrile Neutropenia: A Survey of Iranian Breast Cancer Patients

Analysis of the HEXA, HEXB, ARSA, and SMPD1 Genes in 68 Iranian Patients

Ancient migratory events in the Middle East: new clues from the Y-chromosome variation of modern Iranians

Evaluation of FTO rs9939609 and MC4R rs17782313 Polymorphisms as Prognostic Biomarkers of Obesity: A Population-Based Cross-Sectional Study

The Study of rs693 and rs515135 in APOB in People with Familial Hypercholestrolemia

Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patients

Investigation of FGF21 mRNA levels and relative mitochondrial DNA copy number levels and their relation in nonalcoholic fatty liver disease: a case-control study

Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations

The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian men

Two novel tyrosinase (TYR) gene mutations with pathogenic impact on oculocutaneous albinism type 1 (OCA1)

Following the Trace of HVS II Mitochondrial Region Within the Nine Iranian Ethnic Groups Based on Genetic Population Analysis

The effect of CHRNA3 rs1051730 C>T and ABCB1 rs3842 A>G polymorphisms on non-small cell lung cancer and nicotine dependence in Iranian population

Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972 and rs9657904 Polymorphisms with Multiple Sclerosis in Iranian Population

Zataria multiflora Boiss. Essential Oil Induce Apoptosis in Two Human Colon Cancer Cell Lines (HCT116 & SW48)

The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD Child

Association of Single Nucleotide Polymorphisms in the VDR and CYP27B1 Genes with Risk of Developing Vitamin D3 Deficiency

Prevalence of the CYP2C192 (681 G>A), 3 (636 G>A) and 17 (‑806 C>T) alleles among an Iranian population of different ethnicities

Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration

Confirmation of Hyperimmunoglobulin E Syndrome in Two Patients with an Ocular Problem: Detection of Two New DOCK8 Mutations

Mitochondrial Polymorphisms, in The D-Loop Area, Are Associated with Brain Tumors

Investigating the Variation of TREC/KREC in Combined Immunodeficiencies

Mitochondrial Variants in Pompe Disease: A Comparison between Classic and Non-Classic Forms

Evaluation of 'FTO rs9939609' and 'MC4R rs17782313' polymorphisms as prognostic biomarkers of obesity: A populationbased cross-sectional study

Suchergebnisse filtern