Search Results - "defected"

Analysis of the expression and distribution of protein O-linked mannose β1,2-N-acetylglucosaminyltransferase 1 in the normal adult mouse brain by Hanxiao Jiang, Yuxue Feng, Guiqiong He, Guiqiong He, Yuanjie Liu, Yuanjie Liu, Xiaofeng Li

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"Primum Non Nocere" Two Preventable Cases with Drug Intoxication during Newborn Period" by Rüya Çolak, Ezgi Yangın Ergon, Senem Alkan Özdemir, Ferit Kulalı, Meral Yıldız, Oğuzhan Kalkanlı, Tülin Gökmen Yıldırım, Şebnem Çalkavur

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Histological Assessment of the Effects of Derma + Flex®, versus Black Silk Suture on Oral Mucosal Primary Wound Healing in Rabbits by Mohamed Saad Aziz, Ziad H. Deleme, Ahmed Salih Khudhur

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Determination of DMFT Index in Patients with End Stage Renal Disease Being Treated by Hemodialysis in Ali Asghar Medical Center by H - Khademi, A Mohamadi

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Abnormal nociception and opiate sensitivity of STOP null mice exhibiting elevated levels of the endogenous alkaloid morphine by Aunis Dominique, Van Dorsselaer Alain, Bianchi Enrica, Delalande François, Stuber Denise, Deloulme Jean-Christophe, Schweitzer Annie, Kemmel Véronique, Laux Alexis, Muller Arnaud H, Charlet Alexandre, Andrieux Annie, Poisbeau Pierrick, Goumon Yannick

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A regulated NMD mouse model supports NMD inhibition as a viable therapeutic option to treat genetic diseases by Josh Echols, Amna Siddiqui, Yanying Dai, Viktoria Havasi, Richard Sun, Aneta Kaczmarczyk, Kim M. Keeling

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Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disorders by Shingo Koyama, Hidenori Sato, Manabu Wada, Toru Kawanami, Mitsuru Emi, Takeo Kato

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Computer-guided implant placement associated with computer-aided bone regeneration in the treatment of atrophied partially edentulous alveolar ridges: A proof-of-concept study by Pier Paolo Poli, Anand Kumar Muktadar, Francisley Ávila Souza, Carlo Maiorana, Mario Beretta

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Loss of GATA4 C-Terminus by p.S335X Mutation Modulates Coronary Artery Vascular Smooth Muscle Cell Phenotype by Ting-Yan Yu, Xin-Xin Chen, Qing-Wen Liu, Fang-Fang Ma, Hong-Lang Huang, Lei Zhou, Wei Zhang

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Identification of potential metabolic biomarkers of polycystic ovary syndrome in follicular fluid by SWATH mass spectrometry by Zhengao Sun, Hsun-Ming Chang, Aijuan Wang, Jingyan Song, Xingxing Zhang, Jiayin Guo, Peter C. K. Leung, Fang Lian

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Right Atrial Mechanics in Children with Pulmonary Arterial Hypertension Associated with Congenital Heart Disease by Gamze Vuran, Timur Meşe, Murat Muhtar Yılmazer, Engin Gerçeker, Cüneyt Zihni

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Asian/White differences in the relationship of maternal age to low birth weight: Analysis of the PRAMS Survey, 2004-2011 by Sangmi Kim

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تحولات مفهوم الإنسان في فلسفة الحداثة وفلسفة ما بعد الحداثة من مأزق إنسان التأليه إلى مأزق إنسان التشويه... by مصطفى كيحل

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The regulatory roles of Smad2/3 protein and SMURF2 gene expression in granulosa cells of germinal vesicle and metaphase II oocytes in polycystic ovarian syndrome: A case-control st... by Marzieh Ghorbani, Marzieh Sanoee Farimani, Iraj Khodadadi, Sina Mohagheghi, Iraj Amiri, Heidar Tayebinia

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Arap1 loss causes retinal pigment epithelium phagocytic dysfunction and subsequent photoreceptor death by Andy Shao, Antonio Jacobo Lopez, JiaJia Chen, Addy Tham, Seanne Javier, Alejandra Quiroz, Sonia Frick, Edward M. Levine, K. C. Kent Lloyd, Brian C. Leonard, Christopher J. Murphy, Thomas M. Glaser, Ala Moshiri

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Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report by Youssef El Kadiri, Ilham Ratbi, Fatima Zahra Laarabi, Yamna Kriouile, Abdelaziz Sefiani, Jaber Lyahyai

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Imaging in children with ataxia-telangiectasia-The radiologist's approach by Katarzyna Jończyk-Potoczna, Jakub Potoczny, Aleksandra Szczawińska-Popłonyk

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Efficacy and Safety of Fluoride in Children: A Narrative Review by Pegah Nasiri, Ali Malekzadeh Shafaroudi, Nadia Elyassi Gorgi, Milad Arab-Nozari, Azam Nahvi

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A Novel de Novo Mutation in the CD40 Ligand Gene in a Patient With a Mild X-Linked Hyper-IgM Phenotype Initially Diagnosed as CVID: New Aspects of Old Diseases by Tábata T. França, Luiz F. B. Leite, Tiago A. Maximo, Christiane G. Lambert, Nuria B. Zurro, Wilma C. N. Forte, Antonio Condino-Neto

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Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success by Emine Çamtosun, Ayşehan Akıncı, Leman Kayaş, Nurdan Çiftçi, İbrahim Tekedereli

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