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Gene expression patterns of CRYM and SIGLEC10 in Alzheimer's disease: potential early diagnostic indicators.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-023-09113-w
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- Publication type:
- Article
Neurotrophin growth factors and their receptors as promising blood biomarkers for Alzheimer's Disease: a gene expression analysis study.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-023-08959-4
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- Publication type:
- Article
Neurotrophin growth factors and their receptors as promising blood biomarkers for Alzheimer’s Disease: a gene expression analysis study.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-023-08959-4
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- Publication type:
- Article
Gene expression patterns of CRYM and SIGLEC10 in Alzheimer's disease: potential early diagnostic indicators.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-023-09113-w
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- Publication type:
- Article
Expression analysis of inhibitory B7 family members in Alzheimer's disease.
- Published in:
- Metabolic Brain Disease, 2023, v. 38, n. 8, p. 2563, doi. 10.1007/s11011-023-01274-8
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- Publication type:
- Article
Complete Loss of Myelin protein zero (MPZ) in a patient with a late onset Charcot-Marie-Tooth (CMT).
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- Metabolic Brain Disease, 2023, v. 38, n. 6, p. 1963, doi. 10.1007/s11011-023-01201-x
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- Publication type:
- Article
Assessing the expression of two post-transcriptional BDNF regulators, TTP and miR-16 in the peripheral blood of patients with Schizophrenia.
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- BMC Psychiatry, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12888-022-04442-9
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- Publication type:
- Article
Analysis of ROQUIN, Tristetraprolin (TTP), and BDNF/miR-16/TTP regulatory axis in late onset Alzheimer's disease.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.933019
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- Publication type:
- Article
Downregulation of miR-185 is a common pathogenic event in 22q11.2 deletion syndrome-related and idiopathic schizophrenia.
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- Metabolic Brain Disease, 2022, v. 37, n. 4, p. 1175, doi. 10.1007/s11011-022-00918-5
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- Publication type:
- Article
Expression Analysis of Ermin and Listerin E3 Ubiquitin Protein Ligase 1 Genes in the Periphery of Patients with Schizophrenia.
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- Journal of Molecular Neuroscience, 2022, v. 72, n. 2, p. 246, doi. 10.1007/s12031-021-01928-1
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- Publication type:
- Article
Long Non-Coding RNAs, Novel Offenders or Guardians in Multiple Sclerosis: A Scoping Review.
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- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.774002
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- Publication type:
- Article
STRs: Ancient Architectures of the Genome beyond the Sequence.
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- Journal of Molecular Neuroscience, 2021, v. 71, n. 12, p. 2441, doi. 10.1007/s12031-021-01850-6
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- Publication type:
- Article
DOCK8-related Immunodeficiency Syndrome (DIDS): Report of Novel Mutations in Iranian Patients.
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- Journal of Molecular Neuroscience, 2021, v. 71, n. 12, p. 2456, doi. 10.1007/s12031-021-01843-5
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- Publication type:
- Article
Expression Analysis of Ermin and Listerin E3 Ubiquitin Protein Ligase 1 Genes in Autistic Patients.
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- Frontiers in Molecular Neuroscience, 2021, v. 14, p. 1, doi. 10.3389/fnmol.2021.701977
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- Publication type:
- Article
Report of Two Turner affected patients with dicentric X chromosome.
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- Research in Medicine: Journal of Research in Medical Sciences, 2021, v. 45, n. 2, p. 92
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- Publication type:
- Article
New insight into clinical heterogeneity and inheritance diversity of FBLN5-related cutis laxa.
- Published in:
- 2021
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- Publication type:
- journal article
GAA gene mutation detection following clinical evaluation and enzyme activity analysis in Azeri Turkish patients with Pompe disease.
- Published in:
- Metabolic Brain Disease, 2020, v. 35, n. 7, p. 1127, doi. 10.1007/s11011-020-00586-3
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- Publication type:
- Article
Genetic discoveries and advances in late‐onset Alzheimer's disease.
- Published in:
- Journal of Cellular Physiology, 2019, v. 234, n. 10, p. 16873, doi. 10.1002/jcp.28372
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- Publication type:
- Article
Integrative analysis of OIP5‐AS1/HUR1 to discover new potential biomarkers and therapeutic targets in multiple sclerosis.
- Published in:
- Journal of Cellular Physiology, 2019, v. 234, n. 10, p. 17351, doi. 10.1002/jcp.28355
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- Publication type:
- Article
Down-regulation of ERMN expression in relapsing remitting multiple sclerosis.
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- Metabolic Brain Disease, 2019, v. 34, n. 5, p. 1261, doi. 10.1007/s11011-019-00429-w
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- Publication type:
- Article
The Neuronal Ceroid Lipofuscinoses-Linked Loss of Function CLN5 and CLN8 Variants Disrupt Normal Lysosomal Function.
- Published in:
- NeuroMolecular Medicine, 2019, v. 21, n. 2, p. 160, doi. 10.1007/s12017-019-08529-7
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- Publication type:
- Article
A Novel Regulatory Function of Long Non-coding RNAs at Different Levels of Gene Expression in Multiple Sclerosis.
- Published in:
- Journal of Molecular Neuroscience, 2019, v. 67, n. 3, p. 434, doi. 10.1007/s12031-018-1248-2
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- Publication type:
- Article
Association Study of ANRIL Genetic Variants and Multiple Sclerosis.
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- Journal of Molecular Neuroscience, 2018, v. 65, n. 1, p. 54, doi. 10.1007/s12031-018-1069-3
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- Publication type:
- Article
First Case Report of Costello Syndrome in the Azeri Turkish Population.
- Published in:
- 2017
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- Publication type:
- Case Study
Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes.
- Published in:
- Metabolic Brain Disease, 2017, v. 32, n. 5, p. 1685, doi. 10.1007/s11011-017-0048-7
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- Publication type:
- Article
Expression Study and Clinical Correlations of MYC and CCAT2 in Breast Cancer Patients.
- Published in:
- 2017
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- Publication type:
- journal article
Ras-like without CAAX 2 (RIT2): a susceptibility gene for autism spectrum disorder.
- Published in:
- Metabolic Brain Disease, 2017, v. 32, n. 3, p. 751, doi. 10.1007/s11011-017-9969-4
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- Publication type:
- Article
The Importance of VEGF-KDR Signaling Pathway Genes should Not Be Ignored When the Risk of Developing Multiple Sclerosis is Taken into Consideration.
- Published in:
- Journal of Molecular Neuroscience, 2017, v. 62, n. 1, p. 73, doi. 10.1007/s12031-017-0912-2
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- Publication type:
- Article
Genetic Factors Affecting Late-Onset Alzheimer's Disease Susceptibility.
- Published in:
- NeuroMolecular Medicine, 2016, v. 18, n. 1, p. 37, doi. 10.1007/s12017-015-8376-4
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- Publication type:
- Article
DNA METHYLATION ASSESSMENT AS A PROGNOSTIC FACTOR IN INVASIVE BREAST CANCER USING METHYLATION-SPECIFIC MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION.
- Published in:
- EXCLI Journal, 2016, v. 15, n. ., p. 11, doi. 10.17179/excli2015-485
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- Publication type:
- Article
Association of CLU and TLR2 gene polymorphisms with late-onset Alzheimer disease in a northwestern Iranian population.
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- Turkish Journal of Medical Sciences, 2015, v. 45, n. 5, p. 1082, doi. 10.3906/sag-1406-64
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- Publication type:
- Article
DNA REPAIR GENE XRCC3 241MET VARIANT AND BREAST CANCER SUSCEPTIBILITY OF AZERI POPULATIONIN IRANIAN.
- Published in:
- Genetika (0534-0012), 2015, v. 47, n. 2, p. 733, doi. 10.2298/GENSR1502733G
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- Publication type:
- Article
A STUDY ON ASSOCIATION OF POLYMORPHISMS IN Calpain10 AND TCF7L2 GENES WITH TYPE 2 DIABETES MELLITUS.
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- Genetika (0534-0012), 2015, v. 47, n. 1, p. 161, doi. 10.2298/GENSR1501161R
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- Publication type:
- Article
Genetic Evidence for the Involvement of Variants at APOE, BIN1, CR1, and PICALM Loci in Risk of Late-Onset Alzheimer's Disease and Evaluation for Interactions with APOE Genotypes.
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- Journal of Molecular Neuroscience, 2014, v. 54, n. 4, p. 780, doi. 10.1007/s12031-014-0377-5
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- Publication type:
- Article
ESTROGEN RECEPTOR ALPHA GENE POLYMORPHISMS IN PATIENTS WITH LATE ONSET ALZHEIMER'S DISEASE.
- Published in:
- Genetika (0534-0012), 2014, v. 46, n. 2, p. 437, doi. 10.2298/GENSR1402437S
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- Publication type:
- Article
MUTATION SCREENING OF FAMILIAL MEDITERRANEAN FEVER IN THE AZERI TURKISH POPULATION: GENOTYPE--PHENOTYPE CORRELATION AND THE CLINICAL PROFILE VARIABILITY.
- Published in:
- Genetika (0534-0012), 2014, v. 46, n. 2, p. 611, doi. 10.2298/GENSR1402611G
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- Publication type:
- Article
Polymorphism of the cytochrome P-450 1A1 (A2455G) in women with breast cancer in Eastern Azerbaijan, Iran.
- Published in:
- Iranian Journal of Basic Medical Sciences, 2014, v. 17, n. 3, p. 227
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- Publication type:
- Article
Association of CALHM1 gene polymorphism with late-onset Alzheimer disease.
- Published in:
- Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 50, doi. 10.1097/01.MXE.0000430777.29752.3a
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- Publication type:
- Article
INVESTIGATION OF FIVE POLYMORPHIC DNA MARKERS ASSOCIATED WITH LATE ONSET ALZHEIMER DISEASE.
- Published in:
- Genetika (0534-0012), 2013, v. 45, n. 2, p. 503, doi. 10.2298/GENSR1302503G
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- Publication type:
- Article
Genetic association of TNF-alpha-308 G/A and -863 C/A polymorphisms with late onset Alzheimer's disease in Azeri Turk population of Iran.
- Published in:
- 2011
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- Publication type:
- Journal Article
Genetic association of TNF-α-308 G/A and -863 C/A polymorphisms with late onset Alzheimer's disease in Azeri Turk population of Iran.
- Published in:
- Journal of Research in Medical Sciences, 2011, v. 16, n. 8, p. 1006
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- Publication type:
- Article