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Surgery for Obesity and Related Diseases : Official Journal of the American Society for Bariatric Surgery|April 1, 2022
Measures of glucose homeostasis during and after duodenal exclusion using a duodenal-jejunal bypass liner in a normoglycemic, nonobese canine modelRebecca L Paszkiewicz, Miguel A Burch, Isaac Asare Bediako, et al.
Gastroenterology|December 8, 2010
Liver X receptor signaling is a determinant of stellate cell activation and susceptibility to fibrotic liver diseaseSimon W Beaven, Kevin Wroblewski, Jiaohong Wang, et al.
Oncology Reports|June 26, 2008
Novel complex t(V;9;22) rearrangements in three cases with chronic myeloid leukemia and a rare translocation in a case with classical Philadelphia chromosomeHasmik Mkrtchyan, Seda Ghazaryan, Gayane Avetisyan, et al.
Plos One|March 17, 2010
Early embryonic chromosome instability results in stable mosaic pattern in human tissuesHasmik Mkrtchyan, Madeleine Gross, Sophie Hinreiner, et al.
Molecular Cytogenetics|December 18, 2013
First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae)Fan Xiaobo, Krit Pinthong, Hasmik Mkrtchyan, et al.
International Journal of Molecular Medicine|July 30, 2009
Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogeneticsMarina Manvelyan, Philipp Kempf, Anja Weise, et al.
Molecular Cytogenetics|May 13, 2008
Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?Vladimir Trifonov, Simon Fluri, Franz Binkert, et al.
Cancer Genetics and Cytogenetics|February 2, 2010
Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemiaHasmik Mkrtchyan, Daniela Ribeiro Garcia Ney, Eliane Soares de Ventura, et al.
European Journal of Medical Genetics|April 21, 2009
Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndromeAnna D Polityko, Olga M Khurs, Anna I Kulpanovich, et al.
Cancer Genetics and Cytogenetics|August 12, 2009
A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21Amanda Faria de Figueiredo, Hasmik Mkrtchyan, Thomas Liehr, et al.
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