نتایج جستجو برای: 359

تعداد نتایج: 3896  

2001
Moritoshi Hirono Takashi Sugiyama Yasushi Kishimoto Ikuko Sakai Takahito Miyazawa Masahiro Kishio Hiroko Inoue Kazuki Nakao Masayuki Ikeda Shigenori Kawahara Yutaka Kirino Hidenori Horie Yoshihiro Ishikawa Tohru Yoshioka

From the ‡Department of Molecular Neurobiology, Advanced Research Institute for Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555, the ¶Department of Molecular Neurobiology, School of Human Sciences, Waseda University, 2-579-15 Mikajima, Tokorozawa-shi, Saitama 359-1192, the Laboratory of Neurobiophysics, School of Pharmaceutical Sciences, The University of To...

2013
Khurts Shilagardi Shuo Li Fengbao Luo Faiz Marikar Rui Duan Peng Jin Ji Hoon Kim Katherine Murnen Elizabeth H. Chen

clicking here. colleagues, clients, or customers by , you can order high-quality copies for your If you wish to distribute this article to others here. following the guidelines can be obtained by Permission to republish or repurpose articles or portions of articles ): April 23, 2013 www.sciencemag.org (this information is current as of The following resources related to this article are avail...

Journal: :Physiological reviews 1969
R E Smith B A Horwitz

Historical Background. ..................................................... 330 PhylogeneticDistribution .................................................. 332 AnatomyandTopology ................................................... 333 Vasculature of Brown Adipose Tissue. ...................................... 338 Microcirculation and vascularity .......................................... 338 G...

Journal: :Genetics and molecular research : GMR 2007
L E P Calliari C A Longui M N Rocha C D C Faria C Kochi M R Melo M B Melo O Monte

Adrenal hypoplasia congenita (AHC) is a rare disease that can be caused by many abnormalities, including an X-linked form. Mutations in the DAX1 gene have been assigned as the genetic cause of AHC. We describe here three siblings with AHC, clinically presented at different ages, two in the neonatal period and one oligosymptomatic during infancy. Molecular analysis was able to detect a novel mut...

Journal: :Neuromuscular disorders : NMD 2005
E Mikesová K Hühne B Rautenstrauss R Mazanec L Baránková M Vyhnálek O Horácek P Seeman

Mutations in the early growth response 2 gene (EGR2) cause demyelinating neuropathies differing in severity and age of onset. We tested 46 unrelated Czech patients with dominant or sporadic demyelinating CMT neuropathy for mutations in the EGR2 gene. One novel de-novo mutation (Arg359Gln, R359Q) was identified in heterozygous state in a patient with a typical CMT1 phenotype, progressive moderat...

Journal: :Journal of financial studies & research 2022

This paper explores the tax evasion attitudes of taxpayers in Lebanon, a multi-religious country suffering from prevalent evasion. The study surveys 359 Lebanese to determine demographic factors influencing their perception toward

Journal: :Journal of Latin American Studies 2022

Cassia Roth, A Miscarriage of Justice: Women's Reproductive Lives and the Law in Early Twentieth-Century Brazil (Stanford, CA: Stanford University Press, 2020), pp. xv + 359, £25.99, pb. - Volume 54 Issue 3

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