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Publikováno v:
ResearcherID
Physical Review Letters, 2012, 109(17), 171802
Digital.CSIC. Repositorio Institucional del CSIC
instname
Physical Review Letters, 2012, 109(17), 171802
Digital.CSIC. Repositorio Institucional del CSIC
instname
We report a measurement of the bottom-strange meson mixing phase βs using the time evolution of Bs0→J/ψ(→μ+μ-)ϕ(→K+K-) decays in which the quark-flavor content of the bottom-strange meson is identified at production. This measurement uses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7273ab69635924907fed0959031acfb8
http://hdl.handle.net/11567/970578
http://hdl.handle.net/11567/970578
Publikováno v:
Neurology India; Jul2008, Vol. 56 Issue 3, p314-324, 11p
Akademický článek
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Autor:
Vishnu N; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Venkatesan M; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Madaris TR; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Venkateswaran MK; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Stanley K; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Ramachandran K; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Chidambaram A; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Madesh AK; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Yang W; Institute for Regenerative Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA., Nair J; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Narkunan M; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Muthukumar T; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Karanam V; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Joseph LC; Department of Medicine, College of Physicians and Surgeons of Columbia University, 650 W 168 Street, New York, NY 10032, USA., Le A; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Osidele A; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Aslam MI; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA., Morrow JP; Department of Medicine, College of Physicians and Surgeons of Columbia University, 650 W 168 Street, New York, NY 10032, USA., Malicdan MC; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA; NIH Undiagnosed Diseases Program, Office of the Clinical Director, National Human Genome Research Institute, and the Common Fund, National Institutes of Health, Bethesda, MD 20892, USA., Stathopulos PB; Department of Physiology and Pharmacology, Western University, London, ON N6A 5C1, Canada., Madesh M; Department of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Center for Mitochondrial Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA. Electronic address: muniswamy@uthscsa.edu.
Publikováno v:
Molecular cell [Mol Cell] 2024 Apr 04; Vol. 84 (7), pp. 1321-1337.e11. Date of Electronic Publication: 2024 Mar 20.
Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability.
Autor:
Dutta D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030., Kanca O; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030., Shridharan RV; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030., Marcogliese PC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030., Steger B; NIH Undiagnosed Diseases Program, National Human Genome Research Institute, NIH, Bethesda, MD 20892., Morimoto M; NIH Undiagnosed Diseases Program, National Human Genome Research Institute, NIH, Bethesda, MD 20892., Frost FG; NIH Undiagnosed Diseases Program, National Human Genome Research Institute, NIH, Bethesda, MD 20892., Macnamara E; NIH Undiagnosed Diseases Program, National Human Genome Research Institute, NIH, Bethesda, MD 20892., Wangler MF; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030., Yamamoto S; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030., Jenny A; Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, New York, NY 10461.; Department of Genetics, Albert Einstein College of Medicine, New York, NY 10461., Adams D; NIH Undiagnosed Diseases Program, National Human Genome Research Institute, NIH, Bethesda, MD 20892., Malicdan MC; NIH Undiagnosed Diseases Program, National Human Genome Research Institute, NIH, Bethesda, MD 20892., Bellen HJ; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2024 Feb 27; Vol. 121 (9), pp. e2322582121. Date of Electronic Publication: 2024 Feb 21.
Autor:
Mattijssen S; Section on Molecular and Cell Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD 20892, USA., Kerkhofs K; Section on Molecular and Cell Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD 20892, USA., Stephen J; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA., Yang A; RNA Biology Laboratory, National Cancer Institute, Frederick, MD, 21702 USA., Han CG; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA., Tadafumi Y; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA., Iben JR; Molecular Genetics Core, NICHD, NIH, Bethesda, MD 20892, USA., Mishra S; Section on Molecular and Cell Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD 20892, USA., Sakhawala RM; Section on Molecular and Cell Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD 20892, USA., Ranjan A; Section on Molecular and Cell Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD 20892, USA., Gowda M; Department of Obstetrics & Gynaecology, Jawaharlal Institute of Post-Graduate Medical Education and Research, Puducherry, India., Gahl WA; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.; NIH Undiagnosed Diseases Program, NIH, Bethesda, MD 20892, USA., Gu S; RNA Biology Laboratory, National Cancer Institute, Frederick, MD, 21702 USA., Malicdan MC; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.; NIH Undiagnosed Diseases Program, NIH, Bethesda, MD 20892, USA., Maraia RJ; Section on Molecular and Cell Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD 20892, USA.
Publikováno v:
BioRxiv : the preprint server for biology [bioRxiv] 2024 Feb 05. Date of Electronic Publication: 2024 Feb 05.
Autor:
Forsyth R; Department of Pediatrics and McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Parisi MA; Intellectual & Developmental Disabilities Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA., Altintas B; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA., Malicdan MC; National Institutes of Health Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Maryland, USA., Vilboux T; Inova Functional Laboratory, Inova Health System, Fairfax, Virginia, USA.; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Knoll J; Division of Genetics and Genomics, Harvard Medical School, Boston, Massachusetts, USA., Brooks BP; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA., Zein WM; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA., Gahl WA; National Institutes of Health Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Maryland, USA.; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Toro C; Undiagnosed Disease Network, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Gunay-Aygun M; Department of Pediatrics and McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical genetics [Am J Med Genet C Semin Med Genet] 2022 Mar; Vol. 190 (1), pp. 121-130. Date of Electronic Publication: 2022 Mar 21.
Autor:
Han ST; Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, United States of America. Electronic address: ted.han@nih.gov., Kim AC; Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, United States of America., Garcia K; Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, United States of America., Schimmenti LA; Department of Clinical Genomics, Ophthalmology, Otorhinolaryngology, and Biochemistry and Molecular Biology, Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55902, United States of America., Macnamara E; Undiagnosed Diseases Program, Office of the Director, National Institutes of Health, Bethesda, MD 20892, United States of America., Network UD; Undiagnosed Diseases Network, Common Fund, Office of the Director, NIH, Bethesda, MD 20892, United States of America., Gahl WA; Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, United States of America; Undiagnosed Diseases Program, Office of the Director, National Institutes of Health, Bethesda, MD 20892, United States of America., Malicdan MC; Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, United States of America; Undiagnosed Diseases Program, Office of the Director, National Institutes of Health, Bethesda, MD 20892, United States of America., Tifft CJ; Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, United States of America; Undiagnosed Diseases Program, Office of the Director, National Institutes of Health, Bethesda, MD 20892, United States of America.
Publikováno v:
Molecular genetics and metabolism [Mol Genet Metab] 2022 Mar; Vol. 135 (3), pp. 221-229. Date of Electronic Publication: 2022 Feb 01.
Autor:
Carrillo N; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.; Therapeutics for Rare and Neglected Diseases, National Institutes of Health, Bethesda, MD, USA., Malicdan MC; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA., Leoyklang P; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA., Shrader JA; Department of Rehabilitation Medicine, NIH Clinical Center, National Institutes of Health, Bethesda, MD, USA., Joe G; Department of Rehabilitation Medicine, NIH Clinical Center, National Institutes of Health, Bethesda, MD, USA., Slota C; Therapeutics for Rare and Neglected Diseases, National Institutes of Health, Bethesda, MD, USA., Perreault J; Therapeutics for Rare and Neglected Diseases, National Institutes of Health, Bethesda, MD, USA., Heiss JD; National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA., Class B; Therapeutics for Rare and Neglected Diseases, National Institutes of Health, Bethesda, MD, USA., Liu CY; Radiology and Imaging Sciences, NIH Clinical Center, National Institutes of Health, Bethesda, MD, USA., Bradley K; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA., Jodarski C; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA., Ciccone C; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA., Driscoll C; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA., Parks R; Department of Rehabilitation Medicine, NIH Clinical Center, National Institutes of Health, Bethesda, MD, USA., Van Wart S; Enhanced Pharmacodynamics LLC, Buffalo, NY, USA., Bayman L; Clinical Trials Statistical and Data Management Center, University of Iowa, Iowa City, IA, USA., Coffey CS; Clinical Trials Statistical and Data Management Center, University of Iowa, Iowa City, IA, USA., Quintana M; Berry Consultants LLC, Austin, TX, USA., Berry SM; Berry Consultants LLC, Austin, TX, USA., Huizing M; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA., Gahl WA; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA. gahlw@mail.nih.gov.
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Nov; Vol. 23 (11), pp. 2067-2075. Date of Electronic Publication: 2021 Jul 13.
Autor:
Boulin T; Institut NeuroMyoGène, Univ Lyon, Université Claude Bernard Lyon 1, CNRS UMR 5310, INSERM U1217, Lyon 69008, France., Itani O; C. elegans Model Organism Screening Center, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA., El Mouridi S; Institut NeuroMyoGène, Univ Lyon, Université Claude Bernard Lyon 1, CNRS UMR 5310, INSERM U1217, Lyon 69008, France., Leclercq-Blondel A; Institut NeuroMyoGène, Univ Lyon, Université Claude Bernard Lyon 1, CNRS UMR 5310, INSERM U1217, Lyon 69008, France., Gendrel M; Institut NeuroMyoGène, Univ Lyon, Université Claude Bernard Lyon 1, CNRS UMR 5310, INSERM U1217, Lyon 69008, France; Institut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, Université Paris Sciences et Lettres Research University, Paris 75005, France., Macnamara E; Undiagnosed Diseases Program Translational Laboratory, NHGRI, National Institutes of Health, Bethesda, MD 20892, USA., Soldatos A; Undiagnosed Diseases Program Translational Laboratory, NHGRI, National Institutes of Health, Bethesda, MD 20892, USA., Murphy JL; Undiagnosed Diseases Program Translational Laboratory, NHGRI, National Institutes of Health, Bethesda, MD 20892, USA., Gorman MP; Department of Neurology, Neuroimmunology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA., Lindsey A; C. elegans Model Organism Screening Center, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA., Shimada S; Undiagnosed Diseases Program Translational Laboratory, NHGRI, National Institutes of Health, Bethesda, MD 20892, USA., Turner D; C. elegans Model Organism Screening Center, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA., Silverman GA; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA., Baldridge D; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA., Malicdan MC; Undiagnosed Diseases Program Translational Laboratory, NHGRI, National Institutes of Health, Bethesda, MD 20892, USA., Schedl T; C. elegans Model Organism Screening Center, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA; Department of Genetics, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA., Pak SC; C. elegans Model Organism Screening Center, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO 63110, USA. Electronic address: stephen.pak@wustl.edu.
Publikováno v:
Molecular genetics and metabolism [Mol Genet Metab] 2021 Sep-Oct; Vol. 134 (1-2), pp. 195-202. Date of Electronic Publication: 2021 Aug 09.