Cristina Skrypnyk

Cristina Skrypnyk

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Cristina Skrypnyk

Cristina Skrypnyk

Publications by authors named "Cristina Skrypnyk"

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Decreased expression of circulating microRNA-126 in patients with type 2 diabetic nephropathy: A potential blood-based biomarker.

Exp Ther Med 2016 Aug 26;12(2):815-822. Epub 2016 May 26.

Department of Life Sciences, Medical Biotechnology, College of Graduate Studies, Arabian Gulf University, Manama 26671, Kingdom of Bahrain.

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https://www.spandidos-publications.com/10.3892/etm.2016.3395
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http://dx.doi.org/10.3892/etm.2016.3395DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950785PMC
August 2016

Exome Sequencing and the Management of Neurometabolic Disorders.

N Engl J Med 2016 Jun 25;374(23):2246-55. Epub 2016 May 25.

From the Centre for Molecular Medicine and Therapeutics (M.T.-G., C. Shyr, X.C.Y., L.-H.Z., J.J.Y.L., B.I.D., I.G., W.W.W., C.D.K.), the Departments of Medical Genetics (M.T.-G., C. Shyr, C.J.R., X.C.Y., J.J.Y.L., L.A., J.M.F., S.L., M.M., M.I.V.A., A.M.L., W.W.W.), Pediatrics (C.J.R., G.A.H., R.S., L.-H.Z., A.P.B., B.I.D., M.B.C., M.D., T.D., J.D., A. Michoulas, D.M., J.R., K.R.S., K.S., S.E.T., John Wu, S.S.-I., C.D.K.), and Pathology and Laboratory Medicine (B.R., P.E., H.V., G.S.), the Child and Family Research Institute (M.T.-G., C. Shyr, C.J.R., G.A.H., X.C.Y., A.P.B., J.J.Y.L., B.I.D., L.A., M.B.C., M.D., J.D., J.M.F., I.G., S.L., M.M., D.M., J.R., K.R.S., K.S., S.E.T., M.I.V.A., John Wu, P.E., A.M.L., H.V., S.S.-I., G.S., W.W.W., C.D.K.), and the Division of Endocrinology, Adult Metabolic Diseases Clinic (A. Mattman, S. Sirrs), University of British Columbia, and the Divisions of Biochemical Diseases (G.A.H., R.S., B.S., S.S.-I., C.D.K.), Pediatric Neurology (M.B.C., M.D., A. Michoulas, K.S.), Pediatric Nephrology (J.D.), Pediatric Endocrinology (D.M.), and Immunology (S.E.T.) and the Division of Hematology, Oncology and Transplantation, Michael Cuccione Childhood Cancer Research Program (J.R., K.R.S., John Wu), BC Children's Hospital, Vancouver, the Department of Pathology and Laboratory Medicine, Hospital for Sick Children, University of Toronto, Toronto (J.C.), the Department of Biological and Computing Sciences, University of Alberta (R.M., D.W.), and the National Institute for Nanotechnology (D.W.), Edmonton, AB, and the Department of Biomedical Physiology and Kinesiology, Simon Fraser University, Burnaby, BC (M. Abdelsayed, P.R.) - all in Canada; the Division of Genetics, Department of Pediatrics, King Saud Bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia (M. Alfadhel); the Division of Metabolism and Children's Research Center, University Children's Hospital Zurich, Zurich (M.R.B., P.B.), and the Departmen

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http://dx.doi.org/10.1056/NEJMoa1515792DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4983272PMC
June 2016

Time-course effect of high-glucose-induced reactive oxygen species on mitochondrial biogenesis and function in human renal mesangial cells.

Cell Biol Int 2016 Jan 1;40(1):36-48. Epub 2015 Sep 1.

Department of Molecular Medicine/Al-Jawhara Centre for Molecular Medicine, Genetics and Inherited Disorders, College of Medicine and Medical Sciences, Arabian Gulf University, Salmaniya Avenue, Road 2904, Building 293, Block 329, Manama, Kingdom of Bahrain.

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http://dx.doi.org/10.1002/cbin.10520DOI Listing
January 2016

[Use of MLPA test in the detection of subtelomeric rearrangements--case report].

Rev Med Chir Soc Med Nat Iasi 2009 Apr-Jun;113(2):516-22

Facultatea de Medicină, Disciplina de Genetică Medicală, Universitatea de Medicină si Farmacie Gr.T. Popa Iaşi.

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June 2011

[MLPA technique--principles and use in practice].

Rev Med Chir Soc Med Nat Iasi 2007 Oct-Dec;111(4):1001-4

Disciplina de Genetică Medicală, Facultatea de Medicină, Universitatea de Medicină si Farmacie "Gr.T. Popa", Iaşi.

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July 2008

Failure to detect DUP25 in lymphoblastoid cells derived from patients with panic disorder and control individuals representing European and American populations.

Eur J Hum Genet 2004 Jun;12(6):505-8

Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1038/sj.ejhg.5201181DOI Listing
June 2004

Retinoblastoma, pinealoma, and mild overgrowth in a boy with a deletion of RB1 and neighbor genes on chromosome 13q14.

Am J Med Genet A 2004 Feb;124A(4):397-401

Institute of Clinical Genetics, Dresden University of Technology, Fetscherstrasse 74, D-01307 Dresden, Germany.

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http://dx.doi.org/10.1002/ajmg.a.20410DOI Listing
February 2004

Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies.

Am J Med Genet 2002 Nov;113(2):207-12

Institute of Clinical Genetics, Technical University, Dresden, Germany.

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http://dx.doi.org/10.1002/ajmg.10764DOI Listing
November 2002