Zoekresultaten - "Human Genetics"

Genetic polymorphism and forensic application of 23 autosomal STR loci in the Han population of Panjin City, Liaoning Province, Northeastern China door Hongbo Wang, Cairui Xin, Xinyao Meng, Shihan Xing, Baotong Guo, Yuhan Chen, Bao-jie Wang, Jun Yao

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Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases. door Jean Gaschignard, Audrey Virginia Grant, Nguyen Van Thuc, Marianna Orlova, Aurélie Cobat, Nguyen Thu Huong, Nguyen Ngoc Ba, Vu Hong Thai, Laurent Abel, Erwin Schurr, Alexandre Alcaïs

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A RATional choice for translational research? door Tim Aitman, Paraminder Dhillon, Aron M. Geurts

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Genetic investigation and phylogenetic analysis of three Chinese ethnic groups using 16 X chromosome STR loci door Ruiyang Tao, Jingyi Zhang, Ruocheng Xia, Zihao Yang, Shouyu Wang, Xiaochun Zhang, Qi Yang, Suhua Zhang, Chengtao Li

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Multiomic technologies for analyses of inborn errors of immunity: from snapshot of the average cell to dynamic temporal picture at single-cell resolution door Yusuke Kawashima, Ryuta Nishikomori, Osamu Ohara

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Chapter 8 Conclusion the governance of UNESCO's Bioethics Programme door Langlois, Adèle

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Chapter 3 Global governance A conceptual framework for analysing bioethics at UNESCO door Langlois, Adèle

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Chapter 1 Introduction the governance of UNESCO's Bioethics Programme door Langlois, Adèle

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Chapter Abbreviations the governance of UNESCO's Bioethics Programme door Langlois, Adèle

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Chapter 4 Deliberating bioethics UNESCO’s standard-setting activities door Langlois, Adèle

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Chapter References the governance of UNESCO's Bioethics Programme door Langlois, Adèle

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Chapter Acknowledgements the governance of UNESCO's Bioethics Programme door Langlois, Adèle

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Chapter Interviews the governance of UNESCO's Bioethics Programme door Langlois, Adèle

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Chapter 5 Implementing bioethics UNESCO's efforts to realize and enforce the declarations door Langlois, Adèle

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Chapter Foreword the governance of UNESCO's Bioethics Programme door Langlois, Adèle

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Novel protocol for multiple-dose oral administration of the L-type Ca2+ channel blocker isradipine in mice: A dose-finding pharmacokinetic study door Tamara Theiner, Nadine J. Ortner, Herbert Oberacher, Gospava Stojanovic, Petronel Tuluc, Jörg Striessnig

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The relationship between ACTN3 R577X gene polymorphism and physical performance in amateur soccer players and sedentary individuals door Fatma E. Koku, Süleyman O. Karamızrak, Aynur S. Çiftçi, Hasan Taşlıdere, Burak Durmaz, Özgür Çoğulu

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Mutation analysis of 21 autosomal short tandem repeats in Han population from Hunan, China door Wei Xu, Yuequn Wang, Dandan Zhang, Daixin Wang, Liang Zhou, Xiangli Ye, Chaogeng Zhu, Yongzhong Shi

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Profile of pridopidine and its potential in the treatment of Huntington disease: the evidence to date door Squitieri F, de Yebenes JG

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Case Report: Developmental Delay and Acute Neuropsychiatric Episodes Associated With a de novo Mutation in the CAMK2B Gene (c.328G>A p.Glu110Lys) door Bonnie K. Dwyer, Danielle C. M. Veenma, Danielle C. M. Veenma, Kiki Chang, Howard Schulman, Howard Schulman, Geeske M. Van Woerden, Geeske M. Van Woerden, Geeske M. Van Woerden

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