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Cell Death & Disease|January 11, 2014
PSTPIP2 dysregulation contributes to aberrant terminal differentiation in GATA-1-deficient megakaryocytes by activating LYNL Liu, Q Wen, R Gong, et al.European Journal of Human Genetics : EJHG|November 27, 2008
Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing lossSandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Christine Eng, et al.Reproduction (Cambridge, England)|October 28, 2020
Blastomere removal affects homeostatic control leading to obesity in male miceMagdalena Kotlarska, Dawid Winiarczyk, Wiesława Florek, et al.American Journal of Medical Genetics. Part A|July 15, 2005
Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array-based comparative genomic hybridization in a patient with mental retardation and dysmorphic featuresKwei Shuai Hwang, Margaret A Pearson, Pawel Stankiewicz, et al.BMC Biology|September 24, 2014
Human endogenous retroviral elements promote genome instability via non-allelic homologous recombinationIan M Campbell, Tomasz Gambin, Piotr Dittwald, et al.Journal of Contemporary Brachytherapy|March 2, 2022
Pre-operative high-dose-rate brachytherapy in early-stage cervical cancer: long-term single-center resultsSylwia Kellas-Ślęczka, Piotr Wojcieszek, Marta Szlag, et al.Journal of Clinical Medicine|July 27, 2024
Gender Differences in Survival after Coronary Artery Bypass Grafting-13-Year Results from KROK RegistryGrzegorz Hirnle, Adrian Stankiewicz, Maciej Mitrosz, et al.Journal of Applied Genetics|May 15, 2007
Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patientsJoanna Pietrzak, Kristin Mrasek, Ewa Obersztyn, et al.Journal of Environmental Radioactivity|December 20, 2020
A novel specialized tissue culture incubator designed and engineered for radiobiology experiments in a sub-natural background radiation research environmentJake Pirkkanen, Taylor Laframboise, Peter Liimatainen, et al.American Journal of Human Genetics|February 24, 2005
Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasiaGopalrao V N Velagaleti, Gabriel A Bien-Willner, Jill K Northup, et al.Pageof 185