Search Results - "Muscular Dystrophy"

Prevention of Tracheo-Innominate Artery Fistula Formation as a Complication of Tracheostomy: Two Case Reports by Byungsun Yoo, Bongjin Lee, June Dong Park, Seong Keun Kwon, Jae Gun Kwak

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CRISPR/Cas9-Mediated Genome Editing Corrects Dystrophin Mutation in Skeletal Muscle Stem Cells in a Mouse Model of Muscle Dystrophy by Pei Zhu, Furen Wu, Jeffrey Mosenson, Hongmei Zhang, Tong-Chuan He, Wen-Shu Wu

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Full-length Dysferlin Transfer by the Hyperactive Sleeping Beauty Transposase Restores Dysferlin-deficient Muscle by Helena Escobar, Verena Schöwel, Simone Spuler, Andreas Marg, Zsuzsanna Izsvák

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Whole Transcriptome Analysis (RNA Sequencing) of Peripheral Blood Mononuclear Cells of Vitiligo Patients by E. Reimann, K. Kingo, M. Karelson, P. Reemann, E. Vasar, H. Silm, S. Kõks

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Prenatal diagnosis of de novo DMD duplication by multiplex ligation-dependent probe amplification (MLPA) after noninvasive prenatal screening (NIPS) at 11 gestational weeks by Soo Hyun Kim, So Yeon Hong, Min Jin Lee, Kyung Min Kang, Ji Eun Park, Sung Han Shim, Dong Hyun Cha

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Extreme Maternal Metabolic Acidosis Leading to Fetal Distress and Emergency Caesarean Section by Nicolas Cecere, Corinne Hubinont, Arnauld Kabulu Kadingi, Marie-Françoise Vincent, Peter Van den Bergh, Anna Onnela, Philippe Hantson

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Prenatal diagnosis in Islamic countries: A narrative review in 2013 by Mehrnoush Kosaryan, Khadijeh Rabiei

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Targeted Myostatin Gene Editing in Multiple Mammalian Species Directed by a Single Pair of TALE Nucleases by Li Xu, Piming Zhao, Andrew Mariano, Renzhi Han

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Lamin A/C truncation in dilated cardiomyopathy with conduction disease by Huber Jill M, Culley Mary R, MacLeod Heather M, McNally Elizabeth M

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Prime editing optimized RTT permits the correction of the c.8713C>T mutation in DMD gene by Cedric Happi Mbakam, Joel Rousseau, Yaoyao Lu, Anne Bigot, Kamel Mamchaoui, Vincent Mouly, Jacques P. Tremblay

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Dysferlinopathy: Spectrum of pathological changes in skeletal muscle tissue by N Gayathri, R Alefia, A Nalini, T C Yasha, M Anita, Vani Santosh, S K Shankar

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Antisense Oligonucleotide Therapy for the Nervous System: From Bench to Bedside with Emphasis on Pediatric Neurology by Man Amanat, Christina L. Nemeth, Amena Smith Fine, Doris G. Leung, Ali Fatemi

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Proteomic profiling of the interface between the stomach wall and the pancreas in dystrophinopathy by Paul Dowling, Stephen Gargan, Margit Zweyer, Hemmen Sabir, Michael Henry, Paula Meleady, Dieter Swandulla, Kay Ohlendieck

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Muscle Mass as a Biomarker for Health Status and Function in Pediatric Individuals with Neuromuscular Disabilities: A Systematic Review by Isabella R. Ferrara, Cristina L. Sadowsky

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Prenatal diagnosis in Islamic countries: A narrative review in 2013 by Mehrnoush Kosaryan, Khadijeh Rabiei

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Manejo de longo prazo em crianças com transtornos neuromusculares Long-term management of children with neuromuscular disorders by Eugen-Matthias Strehle

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Long-term Exon Skipping Studies With 2'-O-Methyl Phosphorothioate Antisense Oligonucleotides in Dystrophic Mouse Models by Christa L Tanganyika-de Winter, Hans Heemskerk, Tatyana G Karnaoukh, Maaike van Putten, Sjef J de Kimpe, Judith van Deutekom, Annemieke Aartsma-Rus

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Targeting TGF-β Signaling by Antisense Oligonucleotide-mediated Knockdown of TGF-β Type I Receptor by Dwi U Kemaladewi, Svitlana Pasteuning, Joke W van der Meulen, Sandra H van Heiningen, Gert-Jan van Ommen, Peter ten Dijke, Annemieke Aartsma-Rus, Peter AC 't Hoen, Willem M Hoogaars

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Oxidised Albumin Levels in Plasma and Skeletal Muscle as Biomarkers of Disease Progression and Treatment Efficacy in Dystrophic <i>mdx</i> Mice by Jessica R. Terrill, Angelo Patrick R. Bautista, Irene Tsioutsias, Miranda D. Grounds, Peter G. Arthur

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Beneficial Role of Exercise in the Modulation of <em>mdx </em>Muscle Plastic Remodeling and Oxidative Stress by Monica Frinchi, Giuseppe Morici, Giuseppa Mudó, Maria R. Bonsignore, Valentina Di Liberto

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