검색어 : 통합검색[Gibson Lindsay C.]
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81
- A search for glueballs and a study of doouble pomeron exchange at the CERN intersecting storage rings
- The Axial Field Spectrometer Collaboration; Å kesson, T.; Albrow, M.G.; Almehed, S.; Batley, R.; Benary, O.; Boggild, H.; Botner, O.; Breuker, H.; Burkert, V.; Carosi, R.; Carter, A.A.; Carter, J.R.; Cecil, P.C.; Chung, S.U.; Cleland, W.E.; Cockerill, D.; Dagan, S.; Dahl-Jensen, E.; Dahl-Jensen, I.; Dam, P.; Damgaard, G.; Evans, W.M.; Fabjan, C.W.; Frandsen, P.; Frankel, S.; Frati, W.; Gibson, M.D.; Goerlach, U.; Goodrick, M.J.; Hansen, K.H.; Hedberg, V.; Hiddleston, J.W.; Hilke, H.J.; Jarlskog, G.; Killian, T.; Kroeger, R.; Kulka, K.; Lans, J.v.d.; Lindsay, J.; Lissauer, D.; Lorstad, B.; Ludlam, T.; Markou, A.; McCubbin, N.A.; Mjornmark, U.; Moller, R.; Molzon, W.; Nielsen, B.S.; Nilsson, A.; Olsen, L.H.; Oren, Y.; Pritchard, T.W.; Rosselet, L.; Rosso, E.; Rudge, A.; Stumer, I.; Sullivan, M.; Thompson, J.A.; Thorstenson, G.; Vella, E.; Weygand, D.; Williamson, J.G.; Willis, W.J.; Winik, M.; Witzeling, W.; Woody, C.; ; (Nuclear physics, B, v.264, 1986, pp.154-184)
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82
- The evaporative cooling system for the ATLAS inner detector
- Attree, D; Anderson, B; Anderssen, E C; Akhnazarov, V; Apsimon, R J; Barclay, P; Batchelor, L E; Bates, R L; Battistin, M; Bendotti, J; Berry, S; Bitadze, A; Bizzel, J P; Bonneau, P; Bosteels, M; Butterworth, J M; Butterworth, S; Carter, A A; Carter, J R; Catinaccio, A; Corbaz, F; Danielsson, H O; Danilevich, E; Dixon, N; Dixon, S D; Doherty, F; Dorholt, O; Doubrava, M; Egorov, K; Einsweiler, K; Falou, A C; Feraudet, P; Ferrari, P; Fowler, K; Fraser, J T; French, R S; Galuska, M; Gannaway, F; Gariano, G; Gibson, M D; Gilchriese, M; Giugni, D; Godlewski, J; Gousakov, I; Gorski, B; Hallewell, G D; Hartman, N; Hawkings, R J; Haywood, S J; Hessey, N P; Ilyashenko, I; Infante, S; Jackson, J N; Jones, T J; Kaplon, J; Katunin, S; Lindsay, S; Luisa, L; Massol, N; McEwan, F; McMahon, S J; Menot, C; Mistry, J; Morris, J; Muskett, D M; Nagai, K; Nichols, A; Nicholson, R; Nickerson, R B; Nielsen, S L; Nordahl, P E; Olcese, M; ; University College London, Department of Physics and Astronomy, Gower Street, London, WC1E 6BT, United Kingdom; University College London, Department of Physics and Astronomy, Gower Street, London, WC1E 6BT, United Kingdom; Lawrence Berkeley National Laboratory and University of California, Physics Division, MS50B-6227, 1 Cyclotron Road, Berkeley, CA 94720, United States of America; TRIUMF, 4004 Wesbrook Mall, Vancouver, B.C. V6T 2A3, Canada; Rutherford Appleton Laboratory, Science and Technology Facilities Council, Harwell Science and Innovation Campus, Didcot OX11 0QX, United Kingdom; Rutherford Appleton Laboratory, Science and Technology Facilities Council, Harwell Science and Innovation Campus, Didcot OX11 0QX, United Kingdom; Rutherford Appleton Laboratory, Science and Technology Facilities Council, Harwell Science and Innovation Campus, Didcot OX11 0QX, United Kingdom; University of Glasgow, Department of Physics and Astronomy, Glasgow G12 8QQ, United Kingdom; CERN, CH -; (Journal of instrumentation an IOP and SISSA journal, v.3, 2008, pp.P07003-P07003)
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83
- Correction to: De novo and inherited <i>TCF20</i> pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome
- Vetrini, Francesco; McKee, Shane; Rosenfeld, Jill A.; Suri, Mohnish; Lewis, Andrea M.; Nugent, Kimberly Margaret; Roeder, Elizabeth; Littlejohn, Rebecca O.; Holder, Sue; Zhu, Wenmiao; Alaimo, Joseph T.; Graham, Brett; Harris, Jill M.; Gibson, James B.; Pastore, Matthew; McBride, Kim L.; Komara, Makanko; Al-Gazali, Lihadh; Al Shamsi, Aisha; Fanning, Elizabeth A.; Wierenga, Klaas J.; Scott, Daryl A.; Ben-Neriah, Ziva; Meiner, Vardiella; Cassuto, Hanoch; Elpeleg, Orly; Lloyd Holder Jr, J.; Burrage, Lindsay C.; Seaver, Laurie H.; Van Maldergem, Lionel; Mahida, Sonal; Soul, Janet S.; Marlatt, Margaret; Matyakhina, Ludmila; Vogt, Julie; Gold, June-Anne; Park, Soo-Mi; Varghese, Vinod; Lampe, Anne K.; Kumar, Ajith; Lees, Melissa; Holder-Espinasse, Muriel; McConnell, Vivienne; Bernhard, Birgitta; Blair, Ed; Harrison, Victoria; Muzny, Donna M.; Gibbs, Richard A.; Elsea, Sarah H.; Posey, Jennifer E.; Bi, Weimin; Lalani, Seema; Xia, Fan; Yang, Y; Baylor Genetics, Houston, TX 77021 USA; Northern Ireland Regional Genetics Service, Belfast City Hospital, Belfast, UK; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Nottingham Genetics Service, Nottingham City Hospital, Nottingham, UK; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; North West Thames Regional Genetics Service, 759 Northwick Park Hospital, London, UK; Baylor Genetics, Houston, TX 77021 USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Dell C; (Genome medicine, v.11, 2019, pp.16)
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84
- De novo and inherited <i>TCF20</i> pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome
- Vetrini, Francesco; McKee, Shane; Rosenfeld, Jill A.; Suri, Mohnish; Lewis, Andrea M.; Nugent, Kimberly Margaret; Roeder, Elizabeth; Littlejohn, Rebecca O.; Holder, Sue; Zhu, Wenmiao; Alaimo, Joseph T.; Graham, Brett; Harris, Jill M.; Gibson, James B.; Pastore, Matthew; McBride, Kim L.; Komara, Makanko; Al-Gazali, Lihadh; Al Shamsi, Aisha; Fanning, Elizabeth A.; Wierenga, Klaas J.; Scott, Daryl A.; Ben-Neriah, Ziva; Meiner, Vardiella; Cassuto, Hanoch; Elpeleg, Orly; Holder Jr, J. Lloyd; Burrage, Lindsay C.; Seaver, Laurie H.; Van Maldergem, Lionel; Mahida, Sonal; Soul, Janet S.; Marlatt, Margaret; Matyakhina, Ludmila; Vogt, Julie; Gold, June-Anne; Park, Soo-Mi; Varghese, Vinod; Lampe, Anne K.; Kumar, Ajith; Lees, Melissa; Holder-Espinasse, Muriel; McConnell, Vivienne; Bernhard, Birgitta; Blair, Ed; Harrison, Victoria; Muzny, Donna M.; Gibbs, Richard A.; Elsea, Sarah H.; Posey, Jennifer E.; Bi, Weimin; Lalani, Seema; Xia, Fan; Yang, Y; Baylor Genetics, Houston, TX 77021 USA; Northern Ireland Regional Genetics Service, Belfast City Hospital, Belfast, UK; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Nottingham Genetics Service, Nottingham City Hospital, Nottingham, UK; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; North West Thames Regional Genetics Service, 759 Northwick Park Hospital, London, UK; Baylor Genetics, Houston, TX 77021 USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030 USA; Dell C; (Genome medicine, v.11, 2019, pp.12)
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85
- MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis
- Mak, Christopher C Y; Doherty, Dan; Lin, Angela E; Vegas, Nancy; Cho, Megan T; Viot, Gé raldine; Dimartino, Clé mantine; Weisfeld-Adams, James D; Lessel, Davor; Joss, Shelagh; Li, Chumei; Gonzaga-Jauregui, Claudia; Zarate, Yuri A; Ehmke, Nadja; Horn, Denise; Troyer, Caitlin; Kant, Sarina G; Lee, Youngha; Ishak, Gisele E; Leung, Gordon; Barone Pritchard, Amanda; Yang, Sandra; Bend, Eric G; Filippini, Francesca; Roadhouse, Chelsea; Lebrun, Nicolas; Mehaffey, Michele G; Martin, Pierre-Marie; Apple, Benjamin; Millan, Francisca; Puk, Oliver; Hoffer, Mariette J V; Henderson, Lindsay B; McGowan, Ruth; Wentzensen, Ingrid M; Pei, Steven; Zahir, Farah R; Yu, Mullin; Gibson, William T; Seman, Ann; Steeves, Marcie; Murrell, Jill R; Luettgen, Sabine; Francisco, Elizabeth; Strom, Tim M; Amlie-Wolf, Louise; Kaindl, Angela M; Wilson, William G; Halbach, Sara; Basel-Salmon, Lina; Lev-El, Noa; Denecke, Jonas; Vissers, Lisenka E L M; Radtke; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China; Department of Pediatrics, University of Washington, Seattle, WA, USA; Medical Genetics, MassGeneral Hospital for Children, Boston, MA, USA; Laboratory of Embryology and Genetics of Human Malformation, Institut National de la Santé et de la Recherche Mé dicale (INSERM) UMR 1163, Institut Imagine, Paris, France; GeneDx, Gaithersburg, MD, USA; Gyné cologie Obsté trique, Hô pital Cochin, Hô pitaux Universitaires Paris Centre (HUPC), Assistance Publique Hô pitaux de Paris (AP-HP), Paris, France; Laboratory of Embryology and Genetics of Human Malformation, Institut National de la Santé et de la Recherche Mé dicale (INSERM) UMR 1163, Institut Imagine, Paris, France; Section of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado-Denver School of Medicine; (Brain : a journal of neurology, v.143, 2020, pp.55-68)
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86
- Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
- Cirulli, Elizabeth T.; Lasseigne, Brittany N.; Petrovski, Slavé ; Sapp, Peter C.; Dion, Patrick A.; Leblond, Claire S.; Couthouis, Julien; Lu, Yi-Fan; Wang, Quanli; Krueger, Brian J.; Ren, Zhong; Keebler, Jonathan; Han, Yujun; Levy, Shawn E.; Boone, Braden E.; Wimbish, Jack R.; Waite, Lindsay L.; Jones, Angela L.; Carulli, John P.; Day-Williams, Aaron G.; Staropoli, John F.; Xin, Winnie W.; Chesi, Alessandra; Raphael, Alya R.; McKenna-Yasek, Diane; Cady, Janet; Vianney de Jong, J. M. B.; Kenna, Kevin P.; Smith, Bradley N.; Topp, Simon; Miller, Jack; Gkazi, Athina; Al-Chalabi, Ammar; van den Berg, Leonard H.; Veldink, Jan; Silani, Vincenzo; Ticozzi, Nicola; Shaw, Christopher E.; Baloh, Robert H.; Appel, Stanley; Simpson, Ericka; Lagier-Tourenne, Clotilde; Pulst, Stefan M.; Gibson, Summer; Trojanowski, John Q.; Elman, Lauren; McCluskey, Leo; Grossman, Murray; Shneider, Neil A.; Chung, Wendy K.; Ravits, John M.; Glass, Jonathan D.; Center for Applied Genomics and Precision Medicine, Duke University School of Medicine, Durham, NC 27708, USA.; HudsonAlpha Institute for Biotechnology, Huntsville, AL 35806, USA.; Institute for Genomic Medicine, Columbia University, New York, NY 10032, USA.; Department of Neurology, University of Massachusetts Medical School, Worcester, MA 01655, USA.; Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec H3A 2B4, Canada.; Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec H3A 2B4, Canada.; Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.; Institute for Genomic Medicine, Columbia University, New York, NY 10032, USA.; Institute for Genomic Medicine, Columbia University, New York, NY 10032, USA.; Institute for Genomic Medicine, Columbia University, New York, NY 10032, USA.; Institute for Genomic Medicine, Columbia Universi; (Science, v.347, 2015, pp.1436-1441)
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87
- Properties of jets in high-E T events produced inpp collisions at <br><tex> <tex>$$ </tex> sqrt s<tex>$$ </tex></tex><br> =63 GeV
- Å kesson, T.; Albrow, M. G.; Almehed, S.; Batley, R.; Benary, O.; Bøggild, H.; Botner, O.; Breuker, H.; Brody, H.; Burkert, V.; Callen, B.; Carosi, R.; Carter, A. A.; Carter, J. R.; Cecil, P.; Choi, Y.; Cleland, W. E.; Cockerill, D.; Dagan, S.; Dahl-Jensen, E.; Dahl-Jensen, I.; Dam, P.; Damgaard, G.; Eidelman, S.; Evans, W. M.; Fabjan, C. W.; Frandsen, P.; Frankel, S.; Frati, W.; Gibson, M.; Goerlach, U.; Gordon, H.; Hansen, K. H.; Hedberg, V.; Hiddleston, J.; Hilke, H. J.; Hooper, J.; Jarlskog, G.; Jeffreys, P.; Jensen, T.; Kalinovsky, A.; Kesseler, G.; Killian, T.; Kroeger, R.; Kulka, K.; Lans, J. v. d.; Lindsay, J.; Lissauer, D.; Lö rstad, B.; Ludlam, T.; Markou, A.; McCubbin, N. A.; Mjö rnmark, U.; Møller, R.; Molzon, W.; Nielsen, B. S.; Nilsson, A.; Olsen, L. H.; Oren, Y.; Rosselet, L.; Rosso, E.; Rudge, A.; Schindler, R.; Specht, H.; Stumer, I.; Sullivan, M.; Thompson, J.; Thorstenson, G.; Vella,; ; (Zeitschrift für Physik. C, Particles and fields, v.25, 1984, pp.13-20)
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88
- Chemotherapy Induces Bcl-2 Cleavage in Lymphoid Leukemic Cell Lines
- Fortney, James E.; Hall, Brett M.; Bartrug, Lindsay; Gibson, Laura F.; Department of Pediatrics, P.O. Box 9214, Robert C. Byrd Health Sciences Center, West Virginia University, Morgantown, WV 26506, USA; Department of Microbiology, Immunology, and Cell Biology, Robert C. Byrd Health Sciences Center, West Virginia University, Morgantown, WV, USA; Mary Babb Randolph Cancer Center Blood and Marrow Transplantation Program, Robert C. Byrd Health Sciences Center, West Virginia University, Morgantown, WV, USA; (Leukemia & lymphoma, v.43, 2002, pp.2171-2178)
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89
- Hepatitis B or C virus infection and risk of non-Hodgkin lymphoma among solid organ transplant recipients
- Morton, Lindsay M.; Gibson, Todd M.; Clarke, Christina A.; Lynch, Charles F.; Weisenburger, Dennis D.; Engels, Eric A.; ; (Haematologica, v.99, 2014, pp.70-73)
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90
- Eccentric exercise markedly increases c-Jun NH<sub>2</sub>-terminal kinase activity in human skeletal muscle
- Boppart, Marni D.; Aronson, Doron; Gibson, Lindsay; Roubenoff, Ronenn; Abad, Leslie W.; Bean, Jonathan; Goodyear, Laurie J.; Fielding, Roger A.; Research Division, Joslin Diabetes Center, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, and; Research Division, Joslin Diabetes Center, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, and; Research Division, Joslin Diabetes Center, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, and; Nutrition, Exercise Physiology, and Sarcopenia Laboratory, Jean Mayer United States Department of Agriculture Human Nutrition Research Center on Aging, Tufts University, and; Nutrition, Exercise Physiology, and Sarcopenia Laboratory, Jean Mayer United States Department of Agriculture Human Nutrition Research Center on Aging, Tufts University, and; Department of Physical Medicine and Rehabilitation, Spaulding Rehabilitation Hospital, Harvard Medical School, Boston, Massachusetts 02111; Research Division, Joslin Diabetes Center, Department of Medicine, Brigham and Women's Hospital and Harvard Medical S; (Journal of applied physiology, v.87, 1999, pp.1668-1673)
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