Search Results - "Trofimov, Dmitry"
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Distinct gene expression patterns for CD14++ and CD16++ monocytes in preeclampsia
Published in Scientific reports (14-09-2022)“…Preeclampsia (PE) is a serious gestational complication affecting the life of a mother and child. The immunophenotype and gene expression profile of isolated…”
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Vertical Transmission of SARS-CoV-2 in Second Trimester Associated with Severe Neonatal Pathology
Published in Viruses (10-03-2021)“…The effects of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection in women on the gestation course and the health of the fetus,…”
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Author Correction: Distinct gene expression patterns for CD14++ and CD16++ monocytes in preeclampsia
Published in Scientific reports (07-11-2022)Get full text
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4
Procoagulant Activity in Amniotic Fluid Is Associated with Fetal-Derived Extracellular Vesicles
Published in Current issues in molecular biology (13-06-2022)“…Procoagulant activity in amniotic fluid (AF) is positively correlated with phosphatidylserine (PS) and tissue factor (TF)-expressing(+) extracellular vesicles…”
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5
Preventive Triple Gene Therapy Reduces the Negative Consequences of Ischemia-Induced Brain Injury after Modelling Stroke in a Rat
Published in International journal of molecular sciences (18-09-2020)“…Currently, the main fundamental and clinical interest for stroke therapy is focused on developing a neuroprotective treatment of a penumbra region within the…”
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6
Gene Expression Changes and Associated Pathways Involved in the Progression of Prostate Cancer Advanced Stages
Published in Frontiers in genetics (21-01-2021)“…Prostate cancer (PC) is one of the most common cancers among men worldwide, and advanced PCs, such as locally advanced PC (LAPC) and castration-resistant PC…”
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7
Torque Teno Virus (TTV) distribution in healthy Russian population
Published in Virology journal (07-09-2009)“…Torque teno virus (TTV) is a circular, single-stranded DNA virus that chronically infects healthy individuals of all ages worldwide. There is a lot of data on…”
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CYP2C9 and VKORC1 genotyping for the quality of long-standing warfarin treatment in Russian patients
Published in The pharmacogenomics journal (01-10-2020)“…A total of 263 warfarin naive patients with indications to long-term anticoagulation were included in prospective multicenter study and randomized into…”
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Novel Approaches to Possible Targeted Therapies and Prophylaxis of Uterine Fibroids
Published in Diseases (01-11-2023)“…Uterine leiomyomas are the most common benign tumors in women of childbearing age. They may lead to problems of conception or complications during the…”
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Clinical Evaluation of Nasopharyngeal, Oropharyngeal, Nasal Swabs, and Saliva for the Detection of SARS-CoV-2 by Direct RT-PCR
Published in Diagnostics (Basel) (27-04-2022)“…Nasopharyngeal swab (NPS) and oropharyngeal swab (OPS) are the most widely used upper respiratory tract specimens for diagnosis of SARS-CoV-2 using RT-qPCR. In…”
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NETO2 Is Deregulated in Breast, Prostate, and Colorectal Cancer and Participates in Cellular Signaling
Published in Frontiers in genetics (10-12-2020)“…The gene (neuropilin and tolloid-like 2) encodes a protein that acts as an accessory subunit of kainate receptors and is predominantly expressed in the brain…”
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12
Differentially methylated CpG sites associated with the high-risk group of prostate cancer
Published in Journal of integrative bioinformatics (22-12-2020)“…Prostate cancer (PC) is one of the most common and socially significant oncological diseases among men. Bioinformatic analysis of omics data allows identifying…”
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Impact TMPRSS2-ERG Molecular Subtype on Prostate Cancer Recurrence
Published in Life (Basel, Switzerland) (21-06-2021)“…Currently, seven molecular subtypes of prostate cancer (PCa) are known, the most common of which being the subtype characterized by the presence of the…”
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Prenatal diagnosis of Prader‐Willi syndrome due to uniparental disomy with NIPS: Case report and literature review
Published in Molecular genetics & genomic medicine (01-10-2020)“…Background PWS is challenging to diagnose prenatally due to a lack of precise and well‐characterized fetal phenotypes and noninvasive markers. Here we present…”
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Familial Predisposition to Leiomyomata: Searching for Protective Genetic Factors
Published in Biomedicines (21-02-2022)“…In order to determine genetic loci associated with decreasing risk of uterine leiomyomata (UL), a genome-wide association study (GWAS) was performed. We…”
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The spleen as a possible source of serine protease inhibitors and migrating monocytes required for liver regeneration after 70% resection in mice
Published in Frontiers in cell and developmental biology (07-09-2023)“…Introduction: The role of the immune system in liver repair is fundamentally complex and most likely involves the spleen. The close connection between the two…”
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Molecular diagnosis of tuberous sclerosis complex in fetuses and infants: an institutional case series
Published in Journal of clinical pathology (01-11-2024)“…We describe the clinical and genetic characteristics of fetuses and infants diagnosed with tuberous sclerosis complex (TSC) in our centre, prenatally or…”
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Expanding phenotype of MED13-associated syndrome presenting novel de novo missense variant in a patient with multiple congenital anomalies
Published in BMC medical genomics (14-05-2024)“…Whole exome sequencing allows rapid identification of causative single nucleotide variants and short insertions/deletions in children with congenital anomalies…”
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The underestimated role of major skin commensal Malassezia furfur in the development of neonatal invasive fungal infections
Published in Heliyon (01-10-2024)“…In recent years, some new evidence on the role of Malassezia in late-onset sepsis in immunocompromised patients have been published, but there are still very…”
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Correction to: Does the uterine microbiota affect the reproductive outcomes in women with recurrent implantation failures?
Published in BMC women's health (15-05-2023)Get full text
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