Human Genetics & Embryology

World Congress on Human Genetics

November 07- 08, 2016 Barcelona, Spain

Scientific Tracks Abstracts

• Comparative system genetics view of endometriosis and uterine leiomyoma

  Vladislav S Baranov

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• Molecular features of serrated colorectal polyps

  Andrew Ruszkiewicz

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• Genetic deafness: From molecular level to patient care

  Xuezhong Liu

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• Bioinformatics investigation of SNP distributions among human populations

  Alexei Fedorov

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• Nutritional genetics in diabetes and obesity management

  Michael Philip Nova

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• Identification of causal variants in North Indian families with ocular disorders

  Mousumi Mutsuddi and Shashank Gupta

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• SLCO1B1 gene polymorphisms pattern among Croatian Roma

  Tatjana Skaric-Juric, Zeljka Tomas, Matea Zajc Petranovic, Nina Smolej Narancic, Nada Bozina, Branka Janicijevic and Marijana Pericic Salihovic

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• Foldback intercoil DNA: What it means to life science

  Byung-Dong Kim

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• A maternity case with human remains from a XIII-XIV century burial at Uceda, Guadalajara, Central Spain

  C Gomes, S Palomo-Diez, E Dorado-Fernandez, E Ruiz-Mediavilla, C Magana-Loarte, I Ramirez-Gonzalez, A M Lopez-Parra, C Baeza-Richer, J Gibaja and E Arroyo-Pardo

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• Epigenetic changes induced by pregnancy complications may initiate latter development of cardiovascular and cerebrovascular diseases in the mother

  Ilona Hromadnikova, Katerina Kotlabova, Lucie Hympanova and Ladislav Krofta

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• Role of TSGA10 gene in angiogenesis and tumor metastasis: What is the link?

  Kamran Mansouri, Ali Mostafie, Davood Rezazadeh, Mohsen and Mohammad Hossein Modarressi

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• Nano-silver suture as a new application for healing of periodontal flaps: In vitro histopathological, double blind study

  Majid Zakeri

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• Generation of improved human cerebral organoids from single copy DYRK1A knockout induced pluripotent stem cells in trisomy 21: Hypothetical solutions for neurodevelopmental models and therapeutic alternatives in Down syn

  E Sacide Caglayan

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• Association of genetic variations of genes that play a role in vitamin D metabolism with susceptibility to tuberculosis in Kazakhstan

  Chee Kai Chan

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• Where human speed limit goes for short and long term running? A multifactor analysis through energetic metabolic pathways, genetic variations into ethnics and statistical approaches

  Frenkel Guisado Bourzac

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• Genotype-related vascular phenotype in dementia: Impact on the pharmacogenetic outcome

  Ramon Cacabelos

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• Cardiovascular and cerebrovascular disease associated microRNAs are dysregulated in placental tissues affected with preeclampsia and intrauterine growth restriction

  Ilona Hromadnikova, Katerina Kotlabova, Lucie Hympanova and Ladislav Krofta

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• Comprehensive pedigree analyses of metabolism-related diseases for the evaluation of genetic predisposition to obesity: Gender and aging are critical factors

  E Sacide Caglayan and Lale S Akan

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• Legal and ethical milestones of Random Human Nature Principle

  Seyed Mohammad Azin

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• Mutation p.Y572C in androgen receptor gene is associated with Sertoli cell only phenotype in a patient with complete androgen insensitivity

  Ihtisham Bukhari, Guangyuan Li, Liu Wang, Xiaohua Jiang, Furhan Iqbal, Yuanwei Zhang, Zhang Huan, Howard J Cooke, Dexin Yu and Qinghua Shi

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