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No association between MDR1 ( ABCB1) 2677G>T and 3435C>T polymorphism and sporadic colorectal cancer among Bulgarian patients.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2008, v. 134, n. 3, p. 317, doi. 10.1007/s00432-007-0279-9
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- Publication type:
- Article
Increased C-MYC copy numbers on the background of CDKN2A loss is associated with improved survival in nodular melanoma.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2007, v. 133, n. 2, p. 117, doi. 10.1007/s00432-006-0150-4
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- Publication type:
- Article
Tissue microarray analysis of EGFR and HER2 oncogene copy number alterations in squamous cell carcinoma of the larynx.
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- Journal of Cancer Research & Clinical Oncology, 2005, v. 131, n. 3, p. 199, doi. 10.1007/s00432-004-0627-y
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- Publication type:
- Article
HPV Prevalence and Type Distribution in Women With Normal or Abnormal Pap Smear in Bulgaria.
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- Journal of Medical Virology, 2014, v. 86, n. 11, p. 1905, doi. 10.1002/jmv.24020
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- Publication type:
- Article
Susceptibility to Neurodegenerative Disorders: Insights from Paleogenomic Data.
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- Human Biology, 2021, v. 93, n. 4, p. 289, doi. 10.1353/hub.2021.a917652
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- Publication type:
- Article
MicroRNA Profiling in Patients with Upper Tract Urothelial Carcinoma Associated with Balkan Endemic Nephropathy.
- Published in:
- BioMed Research International, 2016, v. 2016, p. 1, doi. 10.1155/2016/7450461
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- Publication type:
- Article
Case–control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population.
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- Journal of Human Genetics, 2009, v. 54, n. 2, p. 98, doi. 10.1038/jhg.2008.14
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- Publication type:
- Article
Novel Hypomorphic Mutation in FANCD2 Gene Observed in a Fetus with Multiple Congenital Anomalies.
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- Case Reports in Obstetrics & Gynecology, 2016, p. 1, doi. 10.1155/2016/1462818
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- Publication type:
- Article
Association of CyclinD1 Copy Number Changes with Histological Type in Ovarian Tumors.
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- Acta Oncologica, 2004, v. 43, n. 7, p. 675, doi. 10.1080/02841860410018548
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- Publication type:
- Article
High-throughput tissue microarray analysis of 11q13 gene amplification (CCND1, FGF3, FGF4, EMS1) in urinary bladder cancer.
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- Journal of Pathology, 2003, v. 201, n. 4, p. 603, doi. 10.1002/path.1481
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- Publication type:
- Article
NEW GENERATION GENOMIC PLATFORMS IN INVESTIGATION OF COMPLEX DISEASES AND BEN.
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- Contributions / Prilozi (1857-9345), 2014, v. 35, n. 1, p. 25
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- Publication type:
- Article
METHYLATION ANALYSIS ON WHOLE GENOME LEVEL. WHAT DID WE LEARN FROM BEN STUDIES?
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- Contributions / Prilozi (1857-9345), 2014, v. 35, n. 1, p. 17
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- Publication type:
- Article
Y-Chromosome Diversity in Modern Bulgarians: New Clues about Their Ancestry.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0056779
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- Publication type:
- Article
Genetic Structure of Europeans: A View from the North-East.
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- PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005472
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- Publication type:
- Article
Bulgarians vs the other European populations: a mitochondrial DNA perspective.
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- International Journal of Legal Medicine, 2012, v. 126, n. 4, p. 497, doi. 10.1007/s00414-011-0589-y
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- Publication type:
- Article
High-Throughput Tissue Microarray Analysis of erbB-2 Gene Amplification in Urinary Bladder Cancer.
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- Urologia Internationalis, 2003, v. 71, n. 4, p. 408, doi. 10.1159/000074095
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- Publication type:
- Article
Effect of Environmental Exposure to PAHs on Somatic Chromosomes.
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- Turkish Journal of Medical Sciences, 2005, v. 35, n. 3, p. 143
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- Publication type:
- Article
Ancient mitochondrial DNA pathogenic variants putatively associated with mitochondrial disease.
- Published in:
- PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0233666
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- Publication type:
- Article
Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping.
- Published in:
- BMC Psychiatry, 2008, v. 8, p. 1, doi. 10.1186/1471-244X-8-11
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- Publication type:
- Article
Propelling Healthcare with Advanced Therapy Medicinal Products: A Policy Discussion.
- Published in:
- Biomedicine Hub, 2020, v. 5, n. 3, p. 1, doi. 10.1159/000511678
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- Publication type:
- Article
Next-generation sequencing of BRCA1 and BRCA2 in breast cancer patients and control subjects.
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- Molecular & Clinical Oncology, 2014, v. 2, n. 3, p. 435, doi. 10.3892/mco.2014.251
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- Publication type:
- Article
Clinical impact of copy number variation changes in bladder cancer samples.
- Published in:
- Experimental & Therapeutic Medicine, 2021, v. 22, n. 2, p. N.PAG, doi. 10.3892/etm.2021.10333
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- Publication type:
- Article
High-throughput tissue microarray analysis of CMYC amplificationin urinary bladder cancer.
- Published in:
- International Journal of Cancer, 2005, v. 117, n. 6, p. 952, doi. 10.1002/ijc.21253
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- Publication type:
- Article
BENEFITS AND CHALLENGES IN CONDUCTING LONG-TERM GROWTH HORMONE THERAPY IN PATIENTS WITH PRADER-WILLI SYNDROME.
- Published in:
- Genetika (0534-0012), 2020, v. 52, n. 1, p. 149, doi. 10.2298/GENSR2001149A
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- Publication type:
- Article
STK11 GENE MUTATIONS AMONG PATIENTS WITH SPORADIC BREAST CANCER.
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- Genetika (0534-0012), 2017, v. 49, n. 2, p. 399, doi. 10.2298/GENSR1702399A
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- Publication type:
- Article
Comparative <sup>I</sup>H NMR Metabolomic Urinalysis of People Diagnosed with Balkan Endemic Nephropathy, and Healthy Subjects, in Romania and Bulgaria: A Pilot Study.
- Published in:
- Toxins, 2011, v. 3, n. 7, p. 815, doi. 10.3390/toxins3070815
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- Publication type:
- Article
Significance of molecular-cytogenetic aberrations for the achievement of first remission in de novo acute myeloid leukemia.
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- Turkish Journal of Hematology, 2008, v. 25, n. 4, p. 190
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- Publication type:
- Article
EGFR and hTERT Expression as a Diagnostic Approach for Non-small Cell Lung Cancer in High Risk Groups.
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- Biomarkers in Cancer, 2010, n. 2, p. 57
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- Publication type:
- Article
Etiology of Balkan Endemic Nephropathy and Associated Urothelial Cancer.
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- American Journal of Nephrology, 2006, v. 26, n. 1, p. 1, doi. 10.1159/000090705
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- Publication type:
- Article
Spatio-temporal dynamics of pathogenic variants associated with monogenic disorders reconstructed with ancient DNA.
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- PLoS ONE, 2022, v. 17, n. 6, p. 1, doi. 10.1371/journal.pone.0269628
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- Publication type:
- Article
NEW PROSPECTS IN MEDICAL RESEARCH IN BULGARIA -- CONSORTIUM FOR STRUCTURAL GENOMICS AND IN SILICO DRUG DESIGN.
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- Advances in Bulgarian Science, 2007, v. 2, p. 40
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- Publication type:
- Article
Introduction of the QF-PCR analysis for the purposes of prenatal diagnosis in Bulgaria-estimation of applicability of 6 STR markers on chromosomes 21 and 18.
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- Prenatal Diagnosis, 2004, v. 24, n. 3, p. 202, doi. 10.1002/pd.820
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- Publication type:
- Article
Philadelphia-positive case negative for JAK2 V617F mutation with hyperdiploidic karyotype: A case report.
- Published in:
- Molecular & Clinical Oncology, 2019, v. 11, n. 6, p. 607, doi. 10.3892/mco.2019.1933
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- Publication type:
- Article
Ancient human mitochondrial genomes from Bronze Age Bulgaria: new insights into the genetic history of Thracians.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-41945-0
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- Publication type:
- Article
Rare Pathogenic Variants in Pooled Whole-Exome Sequencing Data Suggest Hyperammonemia as a Possible Cause of Dementia Not Classified as Alzheimer's Disease or Frontotemporal Dementia.
- Published in:
- Genes, 2024, v. 15, n. 6, p. 753, doi. 10.3390/genes15060753
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- Publication type:
- Article
Pathogenic Variants Associated with Rare Monogenic Diseases Established in Ancient Neanderthal and Denisovan Genome-Wide Data.
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- Genes, 2023, v. 14, n. 3, p. 727, doi. 10.3390/genes14030727
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- Publication type:
- Article
Phenotypic variability and neuropsychological findings associated with C9orf72 repeat expansions in a Bulgarian dementia cohort.
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- PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0208383
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- Publication type:
- Article
Influence of detection of pretreatment cytogenetic abnormalities on first complete remission and survival in adult acute lymphoblastic leukemia.
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- Turkish Journal of Hematology, 2011, v. 28, n. 3, p. 176, doi. 10.5152/tjh.2011.51
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- Publication type:
- Article
Tissue Microarray Analysis of C-MYC Oncogene Copy Number Changes in Larynx Carcinoma.
- Published in:
- ORL, 2005, v. 67, n. 2, p. 92, doi. 10.1159/000084995
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- Publication type:
- Article
Genetic Differences between Five European Populations.
- Published in:
- Human Heredity, 2010, v. 70, n. 2, p. 141, doi. 10.1159/000313854
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- Publication type:
- Article
A de novo microdeletion 2p24.3-25.1 identified in a girl with global development delay.
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- BioDiscovery, 2017, p. 1, doi. 10.7750/BioDiscovery.2015.18.1
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- Publication type:
- Article
Reply from the Authors.
- Published in:
- 2004
- By:
- Publication type:
- Letter
Urinary neopterin concentrations in patients with Balkan endemic nephropathy (BEN).
- Published in:
- Kidney International, 2003, v. 64, n. 5, p. 1817, doi. 10.1046/j.1523-1755.2003.00280.x
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- Publication type:
- Article
Spontaneous and induced chromosome aberrations in Balkan endemic nephropathy.
- Published in:
- Kidney International Supplement, 1991, n. 34, p. S-97, doi. 10.1111/1523-1755.ep15012280
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- Publication type:
- Article
Whole genome methylation array analysis reveals new aspects in Balkan endemic nephropathy etiology.
- Published in:
- BMC Nephrology, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2369-14-225
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- Publication type:
- Article
Whole genome methylation array analysis reveals new aspects in Balkan endemic nephropathy etiology.
- Published in:
- 2013
- By:
- Publication type:
- journal article