نتائج البحث - "Osama Refai"

1

Academic Journal

Tissue-Specific Functions of fem-2/PP2c Phosphatase and fhod-1/formin During Caenorhabditis elegans Embryonic Morphogenesis

المؤلفون: Osama Refai, Ryan B. Smit, SarahBeth Votra, David Pruyne, Paul E. Mains

المصدر: G3: Genes, Genomes, Genetics, Vol 8, Iss 7, Pp 2277-2290 (2018)

مصطلحات موضوعية: C. elegans, morphogenesis, epidermis, embryo, formin, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2160-1836

URL الوصول: https://doaj.org/article/de11945567ad4d469c8a02b30893d75d

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2

Academic Journal

Dopamine-dependent, swimming-induced paralysis arises as a consequence of loss of function mutations in the RUNX transcription factor RNT-1.

المؤلفون: Sarah B Robinson, Osama Refai, J Andrew Hardaway, Sarah Sturgeon, Tessa Popay, Daniel P Bermingham, Phyllis Freeman, Jane Wright, Randy D Blakely

المصدر: PLoS ONE, Vol 14, Iss 5, p e0216417 (2019)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/32e797a1cc844287ae6b70bf8eca487b

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3

Academic Journal

Levatorplasty’s role in rectal prolapse management for patients with wide pelvic hiatus: a cohort study

المؤلفون: Mohamed Yehia Elbarmelgi, Ali Ahmed Shafik, Shady Fathy Badee, Osama Refaie Mohamed, Mohamed Tamer

المصدر: BMC Surgery, Vol 25, Iss 1, Pp 1-10 (2025)

مصطلحات موضوعية: Rectal prolapse, Pelvic hiatus, Recurrence, Defecography, Surgery, RD1-811

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2482

URL الوصول: https://doaj.org/article/ed16a539c566400d8bfc376984e3bbda

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4

Allosteric Modulator KM822 Attenuates Behavioral Actions of Amphetamine in Caenorhabditis elegans through Interactions with the Dopamine Transporter DAT-1

المؤلفون: Osama Refai, Shaili Aggarwal, Mary Hongying Cheng, Zayna Gichi, Joseph M. Salvino, Ivet Bahar, Randy D. Blakely, Ole V. Mortensen

المصدر: Molecular Pharmacology. 101:123-131

مصطلحات موضوعية: Pharmacology, Molecular Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::503a54a0e04621d4a1534e1bef461e2a
https://doi.org/10.1124/molpharm.121.000400

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5

Tissue-Specific Functions of fem-2/PP2c Phosphatase and fhod-1/formin During Caenorhabditis elegans Embryonic Morphogenesis

المؤلفون: Ryan B. Smit, David Pruyne, Osama Refai, Paul E. Mains, SarahBeth Votra

المصدر: G3: Genes|Genomes|Genetics
G3: Genes, Genomes, Genetics, Vol 8, Iss 7, Pp 2277-2290 (2018)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0718e67dea5621322be32aa92e2cce47
http://europepmc.org/articles/PMC6027879

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6

Dopamine-dependent, swimming-induced paralysis arises as a consequence of loss of function mutations in the RUNX transcription factor RNT-1

المؤلفون: Tessa Popay, Osama Refai, Jane Wright, Sarah B. Robinson, Sarah M. Sturgeon, Daniel P. Bermingham, Randy D. Blakely, J. Andrew Hardaway, Phyllis Freeman

المصدر: PLoS ONE, Vol 14, Iss 5, p e0216417 (2019)
PLoS ONE

مصطلحات موضوعية: 0301 basic medicine, Nematoda, Physiology, Dopamine, Mutant, Gene Expression, medicine.disease_cause, Biochemistry, chemistry.chemical_compound, 0302 clinical medicine, Mathematical and Statistical Techniques, Animal Cells, Loss of Function Mutation, Medicine and Health Sciences, Neurotransmitter, Neurons, Mutation, Multidisciplinary, Genetically Modified Organisms, Statistics, Eukaryota, Animal Models, Phenotype, Cell biology, Deletion Mutation, Experimental Organism Systems, Caenorhabditis Elegans, Physical Sciences, Engineering and Technology, Medicine, Cellular Types, Genetic Engineering, Research Article, Biotechnology, Signal Transduction, Science, Bioengineering, Biology, Neurotransmission, Research and Analysis Methods, 03 medical and health sciences, Model Organisms, DNA-binding proteins, medicine, Genetics, Animals, Paralysis, Gene Regulation, Statistical Methods, Caenorhabditis elegans Proteins, Transcription factor, Loss function, Swimming, Analysis of Variance, Tyrosine hydroxylase, Genetically Modified Animals, Biological Locomotion, Dopaminergic Neurons, Organisms, Biology and Life Sciences, Proteins, Cell Biology, Invertebrates, Regulatory Proteins, 030104 developmental biology, chemistry, Cellular Neuroscience, Animal Studies, Caenorhabditis, 030217 neurology & neurosurgery, Mathematics, Neuroscience, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f980a998ca46ad04eaead54e0a93f2b
https://doaj.org/article/32e797a1cc844287ae6b70bf8eca487b

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7

Abstracts of the 52nd Workshop for Pediatric Research

المؤلفون: Rhea van den Bruck, Patrick P. Weil, Thomas Ziegenhals, Philipp Schreiner, Stefan Juranek, Daniel Gödde, Silvia Vogel, Frauke Schuster, Valerie Orth, Johannes Dörner, Daniel Pembaur, Meike Röper, Stefan Störkel, Hubert Zirngibl, Stefan Wirth, Andreas C. W. Jenke, Jan Postberg, Nikolas Boy, Jana Heringer, Gisela Haege, Esther M. Glahn, Georg F. Hoffmann, Sven F. Garbade, Peter Burgard, Stefan Kölker, Cho-Ming Chao, Faady Yahya, Alena Moiseenko, Amit Shrestha, Negah Ahmadvand, Jennifer Quantius, Jochen Wilhelm, Elie El-Agha, Klaus-Peter Zimmer, Saverio Bellusci, Christian Staufner, Holger Prokisch, Stephan Seeliger, Matthias Müller, Andreas Hippe, Henrik Steinkraus, Roland Wauer, Burkhard Lachmann, Sigrun R. Hofmann, Christian M. Hedrich, Jakob Zierk, Farhad Arzideh, Rainer Haeckel, Wolfgang Rascher, Manfred Rauh, Markus Metzler, Sebastian Thieme, Joanna Bandoła, Cornelia Richter, Martin Ryser, Arshad Jamal, Michelle P. Ashton, Malte von Bonin, Matthias Kuhn, Ezio Bonifacio, Reinhard Berner, Sebastian Brenner, Johanna Hammersen, Cristina Has, Nora Naumann-Bartsch, Daniel Stachel, Dimitra Kiritsi, Stephan Söder, Mathilde Tardieu, Leena Bruckner-Tuderman, Holm Schneider, F. Bohne, D. Langer, R. Cencic, T. Eggermann, U. Zechner, J. Pelletier, F. Zepp, T. Enklaar, D. Prawitt, Martin Pech, Markus Weckmann, Femke-Anouska Heinsen, Andre Franke, Christine Happle, Anna-Maria Dittrich, Gesine Hansen, Oliver Fuchs, Erika von Mutius, Brian G. Oliver, Matthias V. Kopp, Claudia Paret, Alexandra Russo, Johanna Theruvath, Bettina Keller, Khalifa El Malki, Nadine Lehmann, Arthur Wingerter, Marie A. Neu, Gerhold-Ay Aslihan, Wolfgang Wagner, Clemens Sommer, Torsten Pietsch, Larissa Seidmann, Jörg Faber, Felix Schreiner, Merle Ackermann, Michael Michalik, Eva Rother, Andras Bilkei-Gorzo, Ildiko Racz, Laura Bindila, Beat Lutz, Jörg Dötsch, Andreas Zimmer, Joachim Woelfle, Hendrik S. Fischer, Tim L. Ullrich, Christoph Bührer, Christoph Czernik, Gerd Schmalisch, Robert Stein, Judith Hagenbuchner, Ursula Kiechl-Kohlendorfer, Petra Obexer, Michael J. Ausserlechner, Niki T. Loges, Adrien Tobias Frommer, Julia Wallmeier, Heymut Omran, Soner Öner-Sieben, Martina Gimpfl, Jan Rozman, Martin Irmler, Johannes Beckers, Martin Hrabe De Angelis, Adelbert Roscher, Eckhard Wolf, Regina Ensenauer, Karolina Nemes, Michael Frühwald, Martin Hasselblatt, Reiner Siebert, Uwe Kordes, Marcel Kool, Haicui Wang, Holly Hardy, Osama Refai, Katy E. S. Barwick, Holly H. Zimmerman, Joachim Weis, Emma L. Baple, Andrew H. Crosby, Sebahattin Cirak, C. Hellmuth, O. Uhl, M. Standl, J. Heinrich, E. Thiering, B. Koletzko, Lena Blümel, Kornelius Kerl, Daniel Picard, Michael C. Frühwald, Max C. Liebau, Guido Reifenberger, Arndt Borkhardt, Marc Remke, D. Tews, M. Wabitsch, P. Fischer-Posovszky, Mike-Andrew Westhoff, Lisa Nonnenmacher, Julia Langhans, Lukas Schneele, Nancy Trenkler, Klaus-Michael Debatin

المصدر: Mol. Cell. Pediatr. 4, 1:5 (2017)

مصطلحات موضوعية: 0303 health sciences, medicine.medical_specialty, business.industry, Pediatric research, MEDLINE, Pharmaceutical Science, medicine.disease, 03 medical and health sciences, 0302 clinical medicine, 030228 respiratory system, Complementary and alternative medicine, Medicine, Pharmacology (medical), business, Intensive care medicine, 030304 developmental biology, Primary ciliary dyskinesia

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c381432a607bacb099fbfd71c2ff806
https://doi.org/10.1186/s40348-017-0071-0

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8

Extension of theCaenorhabditis elegansPharyngeal M1 Neuron Axon Is Regulated by Multiple Mechanisms

المؤلفون: Patricia D. A. Rohs, Paul E Mains, Jeb Gaudet, Osama Refai

المصدر: G3: Genes|Genomes|Genetics

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::149c88991821c4f1bb60649396443f4a
https://doi.org/10.1534/g3.113.008466

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9

Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization

مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Mutation, Missense, Presynaptic Terminals, Medizin, macromolecular substances, Biology, Gene mutation, Neuromuscular junction, Frameshift mutation, Animals, Genetically Modified, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, medicine, Animals, Humans, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Myasthenic Syndromes, Congenital, Genetics, Symporters, Homozygote, Brain, Infant, Membrane Transport Proteins, Transporter, Original Articles, Congenital myasthenic syndrome, medicine.disease, Axons, Pedigree, Choline transporter, Protein Transport, HEK293 Cells, 030104 developmental biology, medicine.anatomical_structure, Endocrinology, nervous system, Neurodevelopmental Disorders, Child, Preschool, Cholinergic, Female, Neurology (clinical), Atrophy, 030217 neurology & neurosurgery, Acetylcholine, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bbd8088b5fbc5456351f3bc402e6385
https://www.ncbi.nlm.nih.gov/pubmed/29088354

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10

Recessively-acting choline transporter mutations associated with severe congenital myasthenia disrupt transporter surface trafficking in vitro and in vivo

المؤلفون: Jane Wright, Andrew H. Crosby, Osama Refai, Randy D. Blakely, Mark Russell, Omar A. Abdul-Rahman, Joachim Weis, Emma L. Baple, S. Salter, Holly H. Zimmerman, Thomas Sejersen, John K. Chilton, Holly Hardy, Haicui Wang, Ulrike Schara, Sebahattin Cirak

المصدر: Neuromuscular Disorders. 27:S220-S221

مصطلحات موضوعية: Choline transporter, Neurology, In vivo, Pediatrics, Perinatology and Child Health, Medizin, Transporter, Neurology (clinical), Pharmacology, Biology, Congenital myasthenia, Genetics (clinical), In vitro

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86c6ae8fab45cabc98493ad8b2c37732
https://doi.org/10.1016/j.nmd.2017.06.454

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11

De novo 12;17 translocation upstream of SOX9 resulting in 46,XX testicular disorder of sex development

المؤلفون: Lori Terry, Harry Ostrer, Alexander Pearlman, Tamison Jewett, Andrew Friedman, Osama Refai, Mary Ann Perle

المصدر: American journal of medical genetics. Part A. (2)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8715da1460c45621e9c9a592374ef02
https://pubmed.ncbi.nlm.nih.gov/20082466

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