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Semen Cryopreservation to Expand Male Fertility in Cancer Patients: Intracase Evaluation of Semen Quality.
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- Journal of Personalized Medicine, 2023, v. 13, n. 12, p. 1654, doi. 10.3390/jpm13121654
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- Article
Deletion of the Spata3 Gene Induces Sperm Alterations and In Vitro Hypofertility in Mice.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 4, p. 1959, doi. 10.3390/ijms22041959
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- Article
Genetic Variants of ANGPT1 , CD39 , FGF2 and MMP9 Linked to Clinical Outcome of Bevacizumab Plus Chemotherapy for Metastatic Colorectal Cancer.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 3, p. 1381, doi. 10.3390/ijms22031381
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- Article
COVID-19 and Individual Genetic Susceptibility/Receptivity: Role of ACE1/ACE2 Genes, Immunity, Inflammation and Coagulation. Might the Double X-Chromosome in Females Be Protective against SARS-CoV-2 Compared to the Single X-Chromosome in Males?
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- International Journal of Molecular Sciences, 2020, v. 21, n. 10, p. 3474, doi. 10.3390/ijms21103474
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- Article
Sex/Gender-Specific Imbalance in CVD: Could Physical Activity Help to Improve Clinical Outcome Targeting CVD Molecular Mechanisms in Women?
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- International Journal of Molecular Sciences, 2020, v. 21, n. 4, p. 1477, doi. 10.3390/ijms21041477
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- Article
"Bridging the Gap" Everything that Could Have Been Avoided If We Had Applied Gender Medicine, Pharmacogenetics and Personalized Medicine in the Gender-Omics and Sex-Omics Era.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 1, p. 296, doi. 10.3390/ijms21010296
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- Article
Changes in Adipose Tissue Distribution and Association between Uric Acid and Bone Health during Menopause Transition.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 24, p. 6321, doi. 10.3390/ijms20246321
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- Article
F13A1 Gene Variant (V34L) and Residual Circulating FXIIIA Levels Predict Short- and Long-Term Mortality in Acute Myocardial Infarction after Coronary Angioplasty.
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- International Journal of Molecular Sciences, 2018, v. 19, n. 9, p. 2766, doi. 10.3390/ijms19092766
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- Article
Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes.
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- International Journal of Molecular Sciences, 2015, v. 16, n. 10, p. 23463, doi. 10.3390/ijms161023463
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- Article
Effect of Factor XIII-A G185T Polymorphism on Visual Prognosis after Photodynamic Therapy for Neovascular Macular Degeneration.
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- International Journal of Molecular Sciences, 2015, v. 16, n. 8, p. 19796, doi. 10.3390/ijms160819796
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- Article
Genetic Association and Altered Gene Expression of Mir-155 in Multiple Sclerosis Patients.
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- International Journal of Molecular Sciences, 2011, v. 12, n. 12, p. 8695, doi. 10.3390/ijms12128695
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- Article
LINE-1 global DNA methylation, iron homeostasis genes, sex and age in sudden sensorineural hearing loss (SSNHL).
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00562-9
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- Article
Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls.
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- European Journal of Epidemiology, 2013, v. 28, n. 8, p. 621, doi. 10.1007/s10654-013-9825-8
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- Article
Investigation of in vitro cytotoxicity of the redox state of ionic iron in neuroblastoma cells.
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- Journal of Neurosciences in Rural Practice, 2012, v. 3, n. 3, p. 301, doi. 10.4103/0976-3147.102611
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- Article
Reference materials (RMs) for analysis of the human factor II (prothrombin) gene G20210A mutation.
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- Clinical Chemistry & Laboratory Medicine, 2005, v. 43, n. 8, p. 862, doi. 10.1515/CCLM.2005.145
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- Article
Review: Interplay of Iron Metallobiology, Metalloproteinases, and FXIII, and Role of Their Gene Variants in Venous Leg Ulcer.
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- International Journal of Lower Extremity Wounds, 2010, v. 9, n. 4, p. 166, doi. 10.1177/1534734610384653
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- Article
Traditional Herbal Remedies with a Multifunctional Therapeutic Approach as an Implication in COVID-19 Associated Co-Infections.
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- Coatings (2079-6412), 2020, v. 10, n. 8, p. 761, doi. 10.3390/coatings10080761
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- Article
C6orf10 Low-Frequency and Rare Variants in Italian Multiple Sclerosis Patients.
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- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00573
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- Article
Genetic Predictors of Response to Photodynamic Therapy.
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- Molecular Diagnosis & Therapy, 2011, v. 15, n. 4, p. 195, doi. 10.1007/BF03256411
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- Article
Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation.
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- Antioxidants, 2019, v. 8, n. 8, p. 287, doi. 10.3390/antiox8080287
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- Article
Nanobiomaterials for vascular biology and wound management: A review.
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- Veins & Lymphatics, 2018, v. 7, n. 2, p. 34, doi. 10.4081/vl.2018.7196
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- Article
Factor XIII V34L polymorphism modulates the risk of chronic venous leg ulcer progression and extension.
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- Wound Repair & Regeneration, 2004, v. 12, n. 5, p. 512, doi. 10.1111/j.1067-1927.2004.012503.x
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- Article
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis.
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- Human Molecular Genetics, 2014, v. 23, n. 25, p. 6746, doi. 10.1093/hmg/ddu392
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- Article
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis.
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- Human Molecular Genetics, 2012, v. 21, n. 25, p. 1, doi. 10.1093/hmg/ddu392
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- Article
Redox metals homeostasis in multiple sclerosis and amyotrophic lateral sclerosis: a review.
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- Cell Death & Disease, 2018, v. 9, n. 3, p. 1, doi. 10.1038/s41419-018-0379-2
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- Article
The Active Metabolite of Warfarin (3'-Hydroxywarfarin) and Correlation with INR, Warfarin and Drug Weekly Dosage in Patients under Oral Anticoagulant Therapy: A Pharmacogenetics Study.
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- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0162084
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- Article
DHFR 19-bp insertion/deletion polymorphism and MTHFR C677T in adult acute lymphoblastic leukaemia: Is the risk reduction due to intracellular folate unbalancing?
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- American Journal of Hematology, 2009, v. 84, n. 8, p. 526, doi. 10.1002/ajh.21451
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- Article
A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): A risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases.
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- American Journal of Hematology, 2001, v. 67, n. 3, p. 183, doi. 10.1002/ajh.1104
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- Article
Factor XIII Contrasts the Effects of Metalloproteinases in Human Dermal Fibroblast Cultured Cells.
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- Vascular & Endovascular Surgery, 2004, v. 38, n. 5, p. 431, doi. 10.1177/153857440403800506
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- Article
circRNAs as Epigenetic Regulators of Integrity in Blood–Brain Barrier Architecture: Mechanisms and Therapeutic Strategies in Multiple Sclerosis.
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- Cells (2073-4409), 2024, v. 13, n. 16, p. 1316, doi. 10.3390/cells13161316
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- Article
Micropatterned Neurovascular Interface to Mimic the Blood–Brain Barrier's Neurophysiology and Micromechanical Function: A BBB-on-CHIP Model.
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- Cells (2073-4409), 2022, v. 11, n. 18, p. N.PAG, doi. 10.3390/cells11182801
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- Article
Sustainable Agriculture through Multidisciplinary Seed Nanopriming: Prospects of Opportunities and Challenges.
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- Cells (2073-4409), 2021, v. 10, n. 9, p. 2428, doi. 10.3390/cells10092428
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- Article
Host genetics impact on SARS-CoV-2 vaccine-induced immunoglobulin levels and dynamics: The role of TP53, ABO, APOE, ACE2, HLA-A, and CRP genes.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.1028081
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- Article
Genetic Architecture of the 3D-Fibrin Meshwork in Pregnancy Maintenance.
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- Italian Journal of Anatomy & Embryology / Archivio Italiano di Anatomia Ed Embriologia, 2023, p. 58
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- Article
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster.
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- British Journal of Haematology, 2003, v. 121, n. 4, p. 632, doi. 10.1046/j.1365-2141.2003.04339.x
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- Article
TRAIL, OPG, and TWEAK in kidney disease: biomarkers or therapeutic targets?
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- Clinical Science, 2019, v. 133, n. 10, p. 1145, doi. 10.1042/CS20181116
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- Article
Perspective on Quantitative Structure–Toxicity Relationship (QSTR) Models to Predict Hepatic Biotransformation of Xenobiotics.
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- Livers, 2023, v. 3, n. 3, p. 448, doi. 10.3390/livers3030032
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- Article
Impact of methylenetetrahydrofolate reductase C677T polymorphism on the efficacy of photodynamic therapy in patients with neovascular age-related macular degeneration.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-38919-7
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- Article
Inherited genetic predispositions in F13A1 and F13B genes predict abdominal adhesion formation: identification of gender prognostic indicators.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35185-x
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- Article
Gene Dosage of F5 c.3481C>T Stop-Codon (p.R1161Ter) Switches the Clinical Phenotype from Severe Thrombosis to Recurrent Haemorrhage: Novel Hypotheses for Readthrough Strategy.
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- Genes, 2024, v. 15, n. 4, p. 432, doi. 10.3390/genes15040432
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- Article
Cis -Segregation of c.1171C>T Stop Codon (p.R391*) in SERPINC1 Gene and c.1691G>A Transition (p.R506Q) in F5 Gene and Selected GWAS Multilocus Approach in Inherited Thrombophilia.
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- Genes, 2021, v. 13, n. 6, p. 934, doi. 10.3390/genes12060934
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- Article
Genetics and Epigenetics of One-Carbon Metabolism Pathway in Autism Spectrum Disorder: A Sex-Specific Brain Epigenome?
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- Genes, 2021, v. 12, n. 5, p. 782, doi. 10.3390/genes12050782
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- Article
KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy.
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- Genes, 2021, v. 12, n. 3, p. 408, doi. 10.3390/genes12030408
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- Article
Genetic Hypothesis and Pharmacogenetics Side of Renin-Angiotensin-System in COVID-19.
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- Genes, 2020, v. 11, n. 9, p. 1044, doi. 10.3390/genes11091044
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- Article
Maternal Haplotypes in DHFR Promoter and MTHFR Gene in Tuning Childhood Acute Lymphoblastic Leukemia Onset-Latency: Genetic/Epigenetic Mother/Child Dyad Study (GEMCDS).
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- Genes, 2019, v. 10, n. 9, p. 634, doi. 10.3390/genes10090634
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- Article
miRNAs Epigenetic Tuning of Wall Remodeling in the Early Phase after Myocardial Infarction: A Novel Epidrug Approach.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 17, p. 13268, doi. 10.3390/ijms241713268
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- Article
Investigating Genetic Diversity and Population Structure in Rice Breeding from Association Mapping of 116 Accessions Using 64 Polymorphic SSR Markers.
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- Crops (2673-7655), 2024, v. 4, n. 2, p. 180, doi. 10.3390/crops4020014
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- Article
Temporal and Genotype-Driven Variation of Factor VII Levels in Patients With Acute Myocardial Infarction.
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- Clinical & Applied Thrombosis/Hemostasis, 2009, v. 15, n. 1, p. 119, doi. 10.1177/1076029607308875
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- Article
Different Anticoagulant Response to Activated Protein C (APC test) and to Agkistrodon Contortix Venom (ACV test) in a Family with FV-R506Q Substitution.
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- Clinical & Applied Thrombosis/Hemostasis, 1997, v. 3, n. 3, p. 168
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- Article
Sudden Sensorineural Hearing Loss and Polymorphisms in Iron Homeostasis Genes: New Insights from a Case-Control Study.
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- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/834736
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- Article