Search Results - "Mkrtchyan, Hasmik"
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First Molecular Cytogenetic High Resolution Characterization of the NIH 3T3 Cell Line by Murine Multicolor Banding
Published in The journal of histochemistry and cytochemistry (01-04-2013)“…Since being established in 1963, the murine fibroblast cell line NIH 3T3 has been used in thousands of studies. NIH 3T3 immortalized spontaneously and became…”
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2
Toll-like receptor 4 mediates synergism between alcohol and HCV in hepatic oncogenesis involving stem cell marker Nanog
Published in Proceedings of the National Academy of Sciences - PNAS (03-02-2009)“…Alcohol synergistically enhances the progression of liver disease and the risk for liver cancer caused by hepatitis C virus (HCV). However, the molecular…”
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3
Exenatide Treatment Alone Improves β-Cell Function in a Canine Model of Pre-Diabetes
Published in PloS one (11-07-2016)“…Exenatide's effects on glucose metabolism have been studied extensively in diabetes but not in pre-diabetes. We examined the chronic effects of exenatide alone…”
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4
Psychometric and Logometric Properties of the Armenian Version of Augmentative and Alternative Communication Assessment Questionnaire: Assessing Reliability and Validity
Published in Journal of psycholinguistic research (01-02-2022)“…The study describes the development of the AAC-Arm questionnaire and its initial psychometric and logometric testing for reliability and validity. Psychometric…”
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5
Can behavioral interventions increase physical activity in youth with cerebral palsy? A scoping review
Published in Health Problems of Civilization (01-01-2021)“…The primary goal of adaptive physical and special education is to increase the participation of individuals with special motor needs in educational and social…”
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Rare neurological diseases in children: current paradigm of communicational interventions and inclusion
Published in Psiholìngvìstika (03-10-2018)“…The goal of the presented work is to identify the optimum strategy for the enhancement of communication in patients with rare neurological disorders based on…”
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Effectiveness and Determinant Variables of Augmentative and Alternative Communication Interventions in Cerebral Palsy Patients with Communication Deficit: a Systematic Review
Published in CoDAS (São Paulo) (2021)“…Assess the effectiveness of augmentative and alternative communication (AAC) interventions in patients with CP and to reveal determinant variables of main…”
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Preliminary Assessment of the Need and Awareness of Augmentative and Alternative Communication Systems in Armenia
Published in Iranian journal of public health (01-01-2019)“…No Abstract###…”
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9
Correlations of back muscle electromyography and gait analysis data as a basis for exercise prescription in patients with lumbar disc herniation
Published in Physiotherapy quarterly (2021)“…Introduction The principles and practice of physical rehabilitation in patients with lumbar disc herniation still remain controversial. The objective of the…”
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10
Early embryonic chromosome instability results in stable mosaic pattern in human tissues
Published in PloS one (09-03-2010)“…The discovery of copy number variations (CNV) in the human genome opened new perspectives on the study of the genetic causes of inherited disorders and the…”
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EFFECT OF A METHOD FOR DEVELOPING COMMUNICATION SKILLS ON PHYSICAL ACTIVITY IN CHILDREN WITH INTELLECTUAL DISABILITIES
Published in Health Problems of Civilization (01-07-2022)Get full text
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Simile as an Indispensable Element of Expressiveness
Published in Armenian Folia Anglistika (15-04-2015)“…Every piece of fiction is a piece of poetic accessory. Poetic language is conditioned by the unification of incompatible notions, implicitness and covertness…”
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Paradoxes in O. Wilde’s “The Picture of Dorian Gray”
Published in Armenian Folia Anglistika (15-10-2013)“…One of the underlying functions of any piece of literary work is its aesthetic impact on the reader. The Picture of Dorian Gray by O. Wilde has completely…”
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14
The Human Genome Puzzle - the Role of Copy Number Variation in Somatic Mosaicism
Published in Current genomics (01-09-2010)“…The discovery of copy number variations (CNV) in the human genome opened new perspectives in the study of the genetic causes of inherited disorders and the…”
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15
Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis
Published in International journal of hematology (01-02-2011)“…Classical Burkitt lymphoma/leukemia (BL/L) presenting L3 morphology is found in 1% of childhood ALL. Recently, it has been described that secondary…”
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Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report
Published in Molecular cytogenetics (09-11-2009)“…The well-known typical fusion gene BCR/ABL can be observed in connection with a complex translocation event in only 2-10% of cases with chronic myeloid…”
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A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3
Published in Molecular cytogenetics (16-03-2010)“…The so-called Philadelphia (Ph) chromosome is present in almost all cases with chronic myeloid leukemia (CML). Around 5-10% of these patients show complex…”
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Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?
Published in Molecular cytogenetics (15-04-2008)“…Small supernumerary marker chromosomes (sSMC) are present ~2.6 x 106 human worldwide. sSMC are a heterogeneous group of derivative chromosomes concerning their…”
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Extra Copies of der(21)t(12;21) plus Deletion of ETV6 Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome
Published in Case reports in genetics (01-01-2012)“…Acute lymphoblastic leukemia (ALL), CD10+ B-cell precursor, represents the most frequent type of childhood ALL from 3 to 6 years of age. The t(12;21)(p13;q22)…”
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"Second hit" models of alcoholic liver disease
Published in Seminars in liver disease (01-05-2009)“…Alcoholic liver disease (ALD) is a lifestyle disease with its pathogenesis and individual predisposition governed by gene-environment interactions. Based on…”
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