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Heparan Sulfate Proteoglycans and Human Breast Cancer Epithelial Cell Tumorigenicity.
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- Journal of Cellular Biochemistry, 2014, v. 115, n. 5, p. 967, doi. 10.1002/jcb.24746
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- Article
High-resolution loss of heterozygosity screening implicates PTPRJ as a potential tumor suppressor gene that affects susceptibility to non-hodgkin's lymphoma.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 5, p. 467, doi. 10.1002/gcc.22044
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- Article
Integrative genomic profiling reveals conserved genetic mechanisms for tumorigenesis in common entities of non-Hodgkin's lymphoma.
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- Genes, Chromosomes & Cancer, 2011, v. 50, n. 5, p. 313, doi. 10.1002/gcc.20856
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- Article
Authors response to: Critique of "Chromosome 17 and inducible nitric oxide synthase gene in human essential hypertension" by Rutherford et al. in Human Genetics published on-line September 2001.
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- Human Genetics, 2002, v. 110, n. 1, p. 100, doi. 10.1007/s00439-001-0658-2
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- Article
Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension.
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- Human Genetics, 2001, v. 109, n. 4, p. 408, doi. 10.1007/s004390100565
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- Article
Familial typical migraine: significant linkage and localization of a gene to Xq24–28.
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- Human Genetics, 2000, v. 107, n. 1, p. 18, doi. 10.1007/s004390050004
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- Article
Improving the strategy to identify historical military remains: a literature review and Y-STR meta-analysis.
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- Forensic Sciences Research, 2024, v. 9, n. 1, p. 1, doi. 10.1093/fsr/owad050
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- Article
A Potential Epigenetic Marker Mediating Serum Folate and Vitamin B<sub> 12 </sub> Levels Contributes to the Risk of Ischemic Stroke.
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- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/167976
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- Article
The Influence of OLR1 and PCSK9 Gene Polymorphisms on Ischemic Stroke: Evidence from a Meta-Analysis.
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- Scientific Reports, 2015, p. 18224, doi. 10.1038/srep18224
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- Article
Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants.
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- Cells (2073-4409), 2020, v. 9, n. 11, p. 2368, doi. 10.3390/cells9112368
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- Article
Differential gene expression in breast cancer cell lines and stroma-tumor differences in microdissected breast cancer biopsies revealed by display array analysis.
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- International Journal of Cancer, 2002, v. 100, n. 2, p. 172, doi. 10.1002/ijc.10451
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- Article
Association of estrogen receptor and glucocorticoid receptor gene polymorphisms with sporadic breast cancer.
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- International Journal of Cancer, 2001, v. 95, n. 4, p. 271, doi. 10.1002/1097-0215(20010720)95:4<271::AID-IJC1046>3.0.CO;2-D
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- Publication type:
- Article
Association of a vitamin D receptor polymorphism with sporadic breast cancer development.
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- International Journal of Cancer, 1999, v. 83, n. 6, p. 723, doi. 10.1002/(SICI)1097-0215(19991210)83:6<723::AID-IJC4>3.0.CO;2-3
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- Article
Cardiomyopathy Classification: Ongoing Debate in the Genomics Era.
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- Biotechnology Research International, 2012, p. 1, doi. 10.1155/2012/796926
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- Publication type:
- Article
Global reported impacts of COVID‐19 on lymphoma patients and the emerging clinical management approaches in response to the ongoing pandemic.
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- European Journal of Haematology, 2023, v. 110, n. 5, p. 457, doi. 10.1111/ejh.13926
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- Article
Critical evaluation of linear regression models for cell-subtype specific methylation signal from mixed blood cell DNA.
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- PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0208915
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- Article
Current Status of Pharmacogenomics Testing for Anti-Tumor Drug Therapies.
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- Molecular Diagnosis & Therapy, 2009, v. 13, n. 2, p. 65, doi. 10.1007/BF03256316
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- Publication type:
- Article
Genetic polymorphisms in DPF3 associated with risk of breast cancer and lymph node metastases.
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- Journal of Carcinogenesis, 2005, v. 4, n. 1, p. 1, doi. 10.1186/1477-3163-4-13
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- Publication type:
- Article
In silico analyses reveal common cellular pathways affected by loss of heterozygosity (LOH) events in the lymphomagenesis of Non-Hodgkin's lymphoma (NHL).
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- BMC Genomics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2164-15-390
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- Article
Principal Component and Linkage Analysis of Cardiovascular Risk Traits in the Norfolk Isolate.
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- Human Heredity, 2009, v. 68, n. 1, p. 55, doi. 10.1159/000210449
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- Article
Phenotypical Characterisation of the Isolated Norfolk Island Population Focusing on Epidemiological Indicators of Cardiovascular Disease.
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- Human Heredity, 2005, v. 60, n. 4, p. 211, doi. 10.1159/000090545
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- Publication type:
- Article
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3654, doi. 10.1093/hmg/ddt215
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- Article
Heparan Sulfate Proteoglycans as Drivers of Neural Progenitors Derived From Human Mesenchymal Stem Cells.
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- Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00134
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- Article
Genetics of Migraine: Insights into the Molecular Basis of Migraine Disorders.
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- Headache: The Journal of Head & Face Pain, 2017, v. 57, n. 4, p. 537, doi. 10.1111/head.13053
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- Article
Effects of Dietary Folate Intake on Migraine Disability and Frequency.
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- Headache: The Journal of Head & Face Pain, 2015, v. 55, n. 2, p. 301, doi. 10.1111/head.12490
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- Article
Association Study of MTHFD1 Coding Polymorphisms R134 K and R653 Q With Migraine Susceptibility.
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- Headache: The Journal of Head & Face Pain, 2014, v. 54, n. 9, p. 1506, doi. 10.1111/head.12428
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- Publication type:
- Article
Investigation of Brain-Derived Neurotrophic Factor ( BDNF) Gene Variants in Migraine.
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- Headache: The Journal of Head & Face Pain, 2014, v. 54, n. 7, p. 1184, doi. 10.1111/head.12351
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- Article
Genetic Analysis of GRIA2 and GRIA4 Genes in Migraine.
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- Headache: The Journal of Head & Face Pain, 2014, v. 54, n. 2, p. 303, doi. 10.1111/head.12234
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- Publication type:
- Article
Association of a GRIA3 Gene Polymorphism With Migraine in an Australian Case-Control Cohort.
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- Headache: The Journal of Head & Face Pain, 2013, v. 53, n. 8, p. 1245, doi. 10.1111/head.12151
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- Article
The Role of the MTHFR Gene in Migraine.
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- Headache: The Journal of Head & Face Pain, 2012, v. 52, n. 3, p. 515, doi. 10.1111/j.1526-4610.2012.02106.x
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- Article
A causal role for TRESK loss of function in migraine mechanisms.
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- 2019
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- Publication type:
- journal article
Associations between Cerebrovascular Function and the Expression of Genes Related to Endothelial Function in Hormonal Migraine.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 3, p. 1694, doi. 10.3390/ijms25031694
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- Article
Can Genetic Markers Predict the Sporadic Form of Alzheimer's Disease? An Updated Review on Genetic Peripheral Markers.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 17, p. 13480, doi. 10.3390/ijms241713480
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- Article
Syndecan-1 Facilitates the Human Mesenchymal Stem Cell Osteo-Adipogenic Balance.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 11, p. 3884, doi. 10.3390/ijms21113884
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- Publication type:
- Article
Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity.
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- International Journal of Molecular Sciences, 2018, v. 19, n. 10, p. 3113, doi. 10.3390/ijms19103113
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- Publication type:
- Article
BDNF Variants May Modulate Long-Term Visual Memory Performance in a Healthy Cohort.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 3, p. 655, doi. 10.3390/ijms18030655
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- Article
Investigation of hormone receptor genes in migraine.
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- Neurogenetics, 2005, v. 6, n. 1, p. 17, doi. 10.1007/s10048-004-0205-0
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- Publication type:
- Article
The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups.
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- Neurogenetics, 2004, v. 5, n. 2, p. 129, doi. 10.1007/s10048-004-0181-4
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- Publication type:
- Article
Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes.
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- Molecular Neurobiology, 2023, v. 60, n. 6, p. 3034, doi. 10.1007/s12035-023-03255-5
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- Article
Investigating a Genetic Link Between Alzheimer's Disease and CADASIL-Related Cerebral Small Vessel Disease.
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- Molecular Neurobiology, 2022, v. 59, n. 12, p. 7293, doi. 10.1007/s12035-022-03039-3
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- Publication type:
- Article
Cytogenetic alterations in nonmelanoma skin cancer: A review.
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- Genes, Chromosomes & Cancer, 2005, v. 43, n. 3, p. 239, doi. 10.1002/gcc.20183
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- Publication type:
- Article
The <italic>NRP1</italic> migraine risk variant shows evidence of association with menstrual migraine.
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- Journal of Headache & Pain, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s10194-018-0857-z
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- Publication type:
- Article
Case-control study of ADARB1 and ADARB2 gene variants in migraine.
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- Journal of Headache & Pain, 2015, v. 16, p. 1, doi. 10.1186/s10194-015-0511-y
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- Publication type:
- Article
Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine.
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- Journal of Headache & Pain, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1129-2377-15-62
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- Publication type:
- Article
Exome Sequencing Diagnoses X-Linked Moesin-Associated Immunodeficiency in a Primary Immunodeficiency Case.
- Published in:
- Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.00420
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- Publication type:
- Article
SCANNING THE GENOME FOR ESSENTIAL HYPERTENSION LOCI.
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- Clinical & Experimental Pharmacology & Physiology, 1998, v. 25, p. S72, doi. 10.1111/j.1440-1681.1998.tb02305.x
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- Article
A LOCUS ON THE LONG ARM OF CHROMOSOME 1 AS A POSSIBLE CAUSE OF ESSENTIAL HYPERTENSION.
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- Clinical & Experimental Pharmacology & Physiology, 1991, v. 18, n. 5, p. 363, doi. 10.1111/j.1440-1681.1991.tb01464.x
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- Article
Methods for extracting genomic DNA from whole blood samples: current perspectives.
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- Journal of Biorepository Science for Applied Medicine, 2014, v. 2, p. 1
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- Publication type:
- Article
Evaluating the suitability of current mitochondrial DNA interpretation guidelines for multigenerational whole mitochondrial genome comparisons.
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- Journal of Forensic Sciences, 2022, v. 67, n. 5, p. 1766, doi. 10.1111/1556-4029.15097
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- Publication type:
- Article
Identification of Polymorphisms in EAAT1 Glutamate Transporter Gene SLC1A3 Associated with Reduced Migraine Risk.
- Published in:
- Genes, 2024, v. 15, n. 6, p. 797, doi. 10.3390/genes15060797
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- Publication type:
- Article