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29 articles for “Chromosome”
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Role of Ayurveda in Prevention of Congenital Disorder
Abstract: Introduction: Congenital disorder or birth defect is a condition existing at or before birth regardless of cause. Birth defects vary widely in cause and symptoms. About 20–30% of all infant deaths are due to genetic disorders. Birth defects may result due to genetic or environmental factors. This includes errors of morphogenesis, infection, epigenetic modifications on a parental germline or a chromosomal abnormality. The outcome of the disorder will depend on …
Published in Journal of AYUSH: Ayurveda, Yoga, Unani, Siddha and Homeopathy · Vol. 10, Issue 3, 2021 · pp. 33–39 Read article
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In silico Prediction of Two New Conformations of Aβ42 Peptide and Possible Mechanism of Their Aggregation
Abstract: Alzheimer’s disease is one of the most studied neurodegenerative diseases. The cause for most cases of this disease is unknown. However, there are many hypotheses regarding the progression of this disease. One of the hypotheses is the amyloid hypothesis. Amyloid precursor protein present on chromosome 21 is cleaved by β and γ sectretases. The cleaved fragments of this protein, nearly 36–43 residues long aggregates and are deposited as plaque in …
Published in Research and Reviews : Journal of Computational Biology · Vol. 8, Issue 1, 2019 · pp. 1–7 Read article
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To Find the Genes in the Arabidopsis thaliana at NCBI
Abstract: *Author for CorrespondenceNavni BajpaiE-mail: Navni.bajpai@gmail.com 1,2M.sc Biotechnology, Department of Bioscience, Institute of Management Studies, Ghaziabad U.P., India Received Date: January 28, 2022Accepted Date: March 02, 2022Published Date: March 12, 2022 Citation: Navni Bajpai, Sanjeev Singh. To Find the Genes in the Arabidopsis thaliana at NCBI. Research & Reviews: Journal of Computational Biology. 2021; 10(2): 16–19p.The SET domain is a conserved amino acid motif that is present in chromosomal proteins and …
Published in Research and Reviews : Journal of Computational Biology · Vol. 10, Issue 2, 2021 · pp. 16–19 Read article
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Genetic Testing: An Intervention of Biotechnology for Healthy Motherhood
Abstract: The journey from a woman to a mother had been one of the sweetest of its kind. Having a child with a chronic illness has a major impact on the family as a whole, especially mothers. Mothers of a child with chronic disease experience difficulties in dealing with feelings which may subsequently lead to a dysfunctional family. Usually parenting stress is more on mothers caused by having their more affectionate …
Published in Research and Reviews: A Journal of Health Professions · Vol. 8, Issue 3, 2018 · pp. 87s–90s Read article
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Unilateral Ventriculomegaly or Congenital Unilateral Ventricular Dilatation
Abstract: The lateral ventricles may be larger than normal in one side or both sides. Usually it is 10 mm or less in normal foetus during routine antenatal ultrasonogram at the level of atrium. Atrium is the larger central area in lateral ventricle where the three horns anterior, posterior and inferior horns meet together. The present case is having unilateral dilated right ventricle in the mid trimester which is followed upto …
Published in Research and Reviews: A Journal of Health Professions · Vol. 3, Issue 2, 2013 · pp. 16–19 Read article
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Management of Duchenne Muscular Dystrophy by Ayurvedic Principles: A Case Study
Abstract: Duchenne muscular dystrophy is the most common and severe form of childhood muscular dystrophy, with an incidence of 1 case in 3500 male births. It is an X linked recessive disorder due to the absence or alteration of the dystrophin protein, encoded by the DMD gene on chromosome Xp21. Corticosteroids are the only medications that have shown to alter the course of DMD but are associated with their side effects …
Published in Research and Reviews : A Journal of Medical Science and Technology · Vol. 9, Issue 1, 2020 · pp. 1–5 Read article
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Plexiform Neurofibromatosis: Our Experience at Rural Setup with Review of Literature
Abstract: Neurofibromatosis 1 (NF1), also known as von Recklinghausen disease, is an autosomal-dominant condition caused by mutations of the NF1 gene, which is located at chromosome 17. The average life expectancy of patients with NF1 is probably reduced by 10–15 years, and malignancy is the most common cause of death [1]. We present a case of 28 year old female with NF-1 who presented to our OPD with a huge painless …
Published in Research and Reviews : Journal of Surgery · Vol. 5, Issue 2, 2016 · pp. 21–23 Read article
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Carbon Nanoparticles: Occupational Exposure and Genotoxic Effects
Abstract: The field of nanotechnology is revolutionizing today’s era by being the fastest emerging field. Though nanotechnology is the boon to the society, the potential toxicity of these nanoparticles should not be ignored as they can affect anyone from microbes to humans. The main focus of this paper is the toxicity of nanoparticles because people working in these areas, prone to nanoparticles are at high risk due to its toxic property. …
Published in Research and Reviews: A Journal of Toxicology · Vol. 5, Issue 1, 2015 · pp. 9–26 Read article
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The Quiet Intruder: An Insidious Presentation of Primary Plasma Cell Leukemia and a Literature Review on Current Treatment Strategies
Abstract: Introduction: Primary plasma cell leukemia (pPCL) is a rare and aggressive plasma cell dyscrasia, defined by ≥5% circulating plasma cells, with poor prognosis and rapid progression. Case Presentation: A 66-year-old African–American female with no prior medical history presented with one week of fatigue, dehydration, and polydipsia. Laboratory evaluation revealed leukocytosis, severe thrombocytopenia, acute kidney injury (creatinine 4.03 mg/dL), and hypercalcemia (13.0 mg/dL) with suppressed PTH. Imaging showed intra-abdominal lymphadenopathy without …
Published in Research and Reviews: Journal of Oncology and Hematology · Vol. 15, Issue 2, 2026 · pp. 1–5 Read article