Rezultati - Mohammad Othman
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Probiotics for preventing preterm labour od Mohammad Othman, Žarko Alfirević, James P Neilson
Izdano 2007Revisão -
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A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration od Atsuhiro Kanda, Wei Chen, Mohammad Othman, Kari Branham, Matthew Brooks, Ritu Khanna, Shirley He, Robert Lyons, Gonçalo R. Abecasis, Anand Swaroop
Izdano 2007Artigo -
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Bacterial feeding, Leishmania infection and distinct infection routes induce differential defensin expression in Lutzomyia longipalpis od Erich Loza Telleria, Maurício Roberto Viana Sant’Anna, Mohammad Othman Alkurbi, André Nóbrega Pitaluga, Rod J. Dillon, Yara Maria Traub-Csekö
Izdano 2013Artigo -
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Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively od Debra A. Thompson, Christina L. McHenry, Yun Li, Julia E. Richards, Mohammad Othman, E. Schwinger, Douglas Vollrath, Samuel G. Jacobson, Andreas Gal
Izdano 2002Artigo -
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CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration od Mingyao Li, Pelin Atmaca-Sönmez, Mohammad Othman, Kari Branham, Ritu Khanna, Michael S. Wade, Yun Li, Liming Liang, Sepideh Zareparsi, Anand Swaroop, Gonçalo R. Abecasis
Izdano 2006Artigo -
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Intramuscular Cobinamide Sulfite in a Rabbit Model of Sub-Lethal Cyanide Toxicity od Brenner, Matthew, Kim, Jae G., Mahon, Sari B., Lee, Jangwoen, Kreuter, Kelly A., Blackledge, William, Mukai, David, Patterson, Steve, Mohammad, Othman, Sharma, Vijay S., Boss, Gerry R.
Izdano 2010Text -
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Comparison of cobinamide to hydroxocobalamin in reversing cyanide physiologic effects in rabbits using diffuse optical spectroscopy monitoring od Brenner, Matthew, Mahon, Sari B., Lee, Jangwoen, Kim, Jae, Mukai, David, Goodman, Seth, Kreuter, Kelly A., Ahdout, Rebecca, Mohammad, Othman, Sharma, Vijay S., Blackledge, William, Boss, Gerry R.
Izdano 2010Text -
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Mesenchymal Stem Cells Loaded with p5, Derived from CDK5 Activator p35, Inhibit Calcium-Induced CDK5 Activation in Endothelial Cells od Fang, Wen-Hui, Kumar, Shant, McDowell, Garry, Smith, David, Krupinski, Jurek, Olah, Peter, Al-Baradie, Raid Saleem, Al-Rukban, Mohammad Othman, Petcu, Eugene Bogdan, Slevin, Mark
Izdano 2016Text -
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Inner Retinal Abnormalities in X-linked Retinitis Pigmentosa with<i>RPGR</i>Mutations od Tomas S. Alemán, Artur V. Cideciyan, Alexander Sumaroka, Sharon Schwartz, Alejandro J. Román, Elizabeth A. M. Windsor, Janet D. Steinberg, Kari Branham, Mohammad Othman, Anand Swaroop, Samuel G. Jacobson
Izdano 2007Artigo -
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Autosomal Dominant Nanophthalmos (NNO1) with High Hyperopia and Angle-Closure Glaucoma Maps to Chromosome 11 od Mohammad Othman, Scot A. Sullivan, Gregory L. Skuta, David Cockrell, Heather M. Stringham, Catherine A. Downs, Alison Fornés, Andrew B. Mick, Michael Boehnke, Douglas Vollrath, Julia E. Richards
Izdano 1998Artigo -
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Rd9 Is a Naturally Occurring Mouse Model of a Common Form of Retinitis Pigmentosa Caused by Mutations in RPGR-ORF15 od Debra A. Thompson, Naheed W. Khan, Mohammad Othman, Bo Chang, Lin Jia, G. Grahek, Zhijian Wu, Suja Hiriyanna, Jacob Nellissery, Tiansen Li, Hemant Khanna, Peter Colosi, Anand Swaroop, John R. Heckenlively
Izdano 2012Artigo -
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X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa od Abigail T. Fahim, Lori S. Sullivan, Sara J. Bowne, Kaylie Webb-Jones, Dianna K. Wheaton, Naheed W. Khan, John R. Heckenlively, Thiran Jayasundera, Kari Branham, Chris Andrews, Mohammad Othman, Athanasios J. Karoukis, David G. Birch, Stephen P. Daiger
Izdano 2019Artigo -
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Premature Truncation of a Novel Protein, RD3, Exhibiting Subnuclear Localization Is Associated with Retinal Degeneration od James S. Friedman, Bo Chang, Chitra Kannabiran, Christina Chakarova, Hardeep Singh, Subhadra Jalali, Norman L. Hawes, Kari Branham, Mohammad Othman, Elena V. Filippova, Debra A. Thompson, Andrew R. Webster, Sten Andréasson, Samuel G. Jacobson, Shomi S. Bhattacharya, John R. Heckenlively, Anand Swaroop
Izdano 2006Artigo
Iskalna orodja:
Sorodne teme
Biology
Genetics
Medicine
Gene
Ophthalmology
Internal medicine
Macular degeneration
Genotype
Retinal
Retinal degeneration
Retinitis pigmentosa
Disease
Single-nucleotide polymorphism
Allele
Confidence interval
Genetic association
Genome-wide association study
Pathology
Phenotype
Biochemistry
Childbirth
Immunology
Locus (genetics)
Mutation
Neuroscience
Obstetrics
Odds ratio
Pregnancy
Randomized controlled trial
Antibody