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Prevalence and distribution of Borrelia burgdorferi sensu lato genotypes among ixodid ticks in three regions of Ukraine

Regulatory mechanisms in biosystems, 2023-07, Vol.14 (3), p.511-515

2023

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Non-collagenous extracellular matrix protein dermatopontin may play a role as another component of transforming growth factor-β signaling pathway in colon carcinogenesis

Iranian journal of basic medical sciences, 2021-04, Vol.24 (4), p.444-450

2021

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Overview of Next‐Generation Sequencing Technologies

Current protocols in molecular biology (Print), 2018-04, Vol.122 (1), p.e59-n/a

2018

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Identification of a novel homozygous mutation in the DDR2 gene from a patient with spondylo-meta-epiphyseal dysplasia by whole exome sequencing

Iranian journal of basic medical sciences, 2021-02, Vol.24 (2), p.191-195

2021

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Trigeminal Autonomic Cephalalgias Manifested As The Only Initial Symptom Of Ehlers-Danlos Syndrome Type IV

Journal of pain research, 2019-01, Vol.12, p.3215-3220

2019

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Identification of the novel HLA‐DQB102:85 and HLA‐DRB101:01:30 alleles in Russian individuals

HLA, 2017-08, Vol.90 (2), p.135-136

2017

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Designing of sequencing assay assisted by capillary electrophoresis based on DNA folding analysis: An application to the VCAM1 gene

Electrophoresis, 2012-04, Vol.33 (7), p.1215-1219

2012

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DNA Sequencing Analysis Software for Sanger Data- Sets: Comparisons of Basic features Useful for Mutational Studies

Current trends in biotechnology and pharmacy, 2014-01, Vol.8 (1), p.11-17

2014

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First Report of Novel PTEN variant in breast cancer from Pakistan: A predictive variable of diagnostic importance

The FASEB journal, 2021-05, Vol.35 (S1), p.n/a, Article fasebj.2021.35.S1.05516

2021

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Two Different MLC1 Variants Compounded with a Common Variant S93L in Japanese Patients of Megalencephalic Leukoencephalopathy with Subcortical Cysts

Tokyo Women's Medical University Journal, 2020/12/25, Vol.4, pp.94-97

2020

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Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & Immunology

Journal of allergy and clinical immunology, 2020-01, Vol.145 (1), p.46-69

2020

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Constitutional variants in POT1, TERF2IP, and ACD genes in patients with melanoma in the Polish population

European journal of cancer prevention, 2020-11, Vol.29 (6), p.511-519

2020

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Guidelines for Sanger sequencing and molecular assay monitoring

Journal of veterinary diagnostic investigation, 2020-11, Vol.32 (6), p.767-775

2020

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Optimization of a DNA extraction method using Subepidermis from Austrocylindropuntia and Opuntia-Opuntioideae

Revista de Investigación, Desarrollo e Innovación (En línea), 2022-08, Vol.12 (2), p.305-314

2022

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A Sensitive Assay Enriched with Blue/White Screening to Empower Sequencing Analysis for G > A Hotspot Mutation in Codon 13 of KRAS Gene

Journal of nanoscience and nanotechnology, 2017-12, Vol.17 (12), p.9176-9181

2017

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PHYLOGENETIC ANALYSIS OF TWELVE BULGARIAN SEQUENCES BASED ON PARTIAL OPEN READING FRAME 2 GENOME FRAGMENT OF HEPATITIS E VIRUS

Problems of infectious and parasitic diseases, 2024-05, Vol.52 (1), p.5-12

2024

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Phylogenetic position of Nigerian species of Curcuma longa (Zingiberaceae) in the Current Infrageneric Classification

Fountain Journal of Natural and Applied Sciences (FUJNAS), 2024-03, Vol.13 (1)

2024

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Molecular Characterization of Acute Bee Paralysis Virus (ABPV) and Black Queen Cell Virus (BQCV) in Honeybees (Apis mellifera L. (Hymenoptera: Apidae)) from the Campinas Region

Sociobiology (Chico, CA), 2024-06, Vol.71 (2), p.e10306

2024

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Human Immunodeficiency Virus Drug Resistance: 2018 Recommendations of the International Antiviral Society-USA Panel

Clinical infectious diseases, 2019-01, Vol.68 (2), p.177-187

2019

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REEP4 variant analysis in blepharospasm and other neurological disorders

Dystonia, 2024-01, Vol.3

2024

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Long-read sequencing: An effective method for genetic analysis of CYP21A2 variation in congenital adrenal hyperplasia

Clinica chimica acta, 2023-07, Vol.547, p.117419-117419, Article 117419

2023

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Two Different MLC1 Variants Compounded with a Common Variant S93L in Japanese Patients of Megalencephalic Leukoencephalopathy with Subcortical Cysts

Tokyo Women's Medical University Journal, 2020, pp.2020007

2020

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Genetic features of patients with MPS type IIIB: Description of five pathogenic gene variations

Gene, 2024-06, Vol.913, p.148354-148354, Article 148354

2024

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Distribution pattern of UGT1A6 and UGT2B7 gene polymorphism and its impact on the pharmacokinetics of valproic acid and carbamazepine: Prospective genetic association study conducted in Pakistani patients with epilepsy

Gene, 2024-01, Vol.892, p.147886-147886, Article 147886

2024

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Whole Exome Sequencing as an Effective Molecular Diagnosis Tool for Craniofacial Fibrous Dysplasia with Ocular Complications

Current eye research, 2024-09, Vol.49 (9), p.996-1003

2024

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Prevalence and distribution of Borrelia burgdorferi sensu lato genotypes among ixodid ticks in three regions of Ukraine

Non-collagenous extracellular matrix protein dermatopontin may play a role as another component of transforming growth factor-β signaling pathway in colon carcinogenesis

Overview of Next‐Generation Sequencing Technologies

Identification of a novel homozygous mutation in the DDR2 gene from a patient with spondylo-meta-epiphyseal dysplasia by whole exome sequencing

Trigeminal Autonomic Cephalalgias Manifested As The Only Initial Symptom Of Ehlers-Danlos Syndrome Type IV

Identification of the novel HLA‐DQB102:85 and HLA‐DRB101:01:30 alleles in Russian individuals

Designing of sequencing assay assisted by capillary electrophoresis based on DNA folding analysis: An application to the VCAM1 gene

DNA Sequencing Analysis Software for Sanger Data- Sets: Comparisons of Basic features Useful for Mutational Studies

First Report of Novel PTEN variant in breast cancer from Pakistan: A predictive variable of diagnostic importance

Two Different MLC1 Variants Compounded with a Common Variant S93L in Japanese Patients of Megalencephalic Leukoencephalopathy with Subcortical Cysts

Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & Immunology

Constitutional variants in POT1, TERF2IP, and ACD genes in patients with melanoma in the Polish population

Guidelines for Sanger sequencing and molecular assay monitoring

Optimization of a DNA extraction method using Subepidermis from Austrocylindropuntia and Opuntia-Opuntioideae

A Sensitive Assay Enriched with Blue/White Screening to Empower Sequencing Analysis for G > A Hotspot Mutation in Codon 13 of KRAS Gene

PHYLOGENETIC ANALYSIS OF TWELVE BULGARIAN SEQUENCES BASED ON PARTIAL OPEN READING FRAME 2 GENOME FRAGMENT OF HEPATITIS E VIRUS

Phylogenetic position of Nigerian species of Curcuma longa (Zingiberaceae) in the Current Infrageneric Classification

Molecular Characterization of Acute Bee Paralysis Virus (ABPV) and Black Queen Cell Virus (BQCV) in Honeybees (Apis mellifera L. (Hymenoptera: Apidae)) from the Campinas Region

Human Immunodeficiency Virus Drug Resistance: 2018 Recommendations of the International Antiviral Society-USA Panel

REEP4 variant analysis in blepharospasm and other neurological disorders

Long-read sequencing: An effective method for genetic analysis of CYP21A2 variation in congenital adrenal hyperplasia

Two Different MLC1 Variants Compounded with a Common Variant S93L in Japanese Patients of Megalencephalic Leukoencephalopathy with Subcortical Cysts

Genetic features of patients with MPS type IIIB: Description of five pathogenic gene variations

Distribution pattern of UGT1A6 and UGT2B7 gene polymorphism and its impact on the pharmacokinetics of valproic acid and carbamazepine: Prospective genetic association study conducted in Pakistani patients with epilepsy

Whole Exome Sequencing as an Effective Molecular Diagnosis Tool for Craniofacial Fibrous Dysplasia with Ocular Complications

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