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Results 1 - 20 of 590  for Central Connecticut State University

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Gain of 1q is associated with inferior event‐free and overall survival in patients with favorable histology Wilms tumor: A report from the Children's Oncology Group

Gratias, Eric J. ; Jennings, Lawrence J. ; Anderson, James R. ; Dome, Jeffrey S. ; Grundy, Paul ; Perlman, Elizabeth J.

Cancer, 01 November 2013, Vol.119(21), pp.3887-3894 [Peer Reviewed Journal]

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2
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Identification of a novel recurrent 1q42.2‐1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas

Fieuw, Annelies ; Kumps, Candy ; Schramm, Alexander ; Pattyn, Filip ; Menten, Björn ; Antonacci, Francesca ; Sudmant, Peter ; Schulte, Johannes H. ; Van Roy, N ; Vergult, Sarah ; Buckley, Patrick G. ; De Paepe, A ; Noguera, Rosa ; Versteeg, Rogier ; Stallings, Raymond ; Eggert, Angelika ; Vandesompele, Jo ; De Preter, K ; Speleman, Frank

International Journal of Cancer, 01 June 2012, Vol.130(11), pp.2599-2606 [Peer Reviewed Journal]

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3
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Occupational Exposure to Benzene and Chromosomal Structural Aberrations in the Sperm of Chinese Men

Marchetti, Francesco ; Eskenazi, Brenda ; Weldon, Rosana H ; Li, Guilan ; Zhang, Luoping ; Rappaport, Stephen M ; Schmid, Thomas E ; Xing, Caihong ; Kurtovich, Elaine ; Wyrobek, Andrew J

Environmental Health Perspectives, 2012, Vol.120(2), p.229-234 [Peer Reviewed Journal]

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4
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Nine year old boy with chromosome 1q23.3‐q25.1 deletion

Lam, Felicia ; Morris, Colleen

American Journal of Medical Genetics Part A, November 2016, Vol.170(11), pp.3013-3017 [Peer Reviewed Journal]

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5
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Global analysis of chromosome 1 genes among patients with lung adenocarcinoma, squamous carcinoma, large-cell carcinoma, small-cell carcinoma, or non-cancer

Zhang, Yong ; Wang, Haiyun ; Wang, Jian ; Bao, Lianming ; Wang, Lingyan ; Huo, Jiayuan ; Wang, Xiangdong

Cancer and Metastasis Reviews, 2015, Vol.34(2), pp.249-264 [Peer Reviewed Journal]

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6
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Sequence analysis of chromosome 1 revealed different selection patterns between Chinese wild mice and laboratory strains

Xu, Fuyi ; Hu, Shixian ; Chao, Tianzhu ; Wang, Maochun ; Li, Kai ; Zhou, Yuxun ; Xu, Hongyan ; Xiao, Junhua

Molecular Genetics and Genomics, 2017, Vol.292(5), pp.1111-1121 [Peer Reviewed Journal]

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De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature

Perrone, M.D ; Rocca, M.S ; Bruno, I ; Faletra, F ; Pecile, V ; Gasparini, P

European Journal of Medical Genetics, February 2012, Vol.55(2), pp.117-119 [Peer Reviewed Journal]

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8
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The distal partial trisomy 1q syndrome and dystonic tremor

Oyama, Genko ; Rodriguez, Ramon L ; Fernandez, Hubert H ; Jacobson, Charles E ; Ong, Tiara L ; Hwynn, Nelson ; Malaty, Irene A ; Okun, Michael S

Parkinsonism and Related Disorders, 2011, Vol.17(2), pp.128-129 [Peer Reviewed Journal]

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9
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Congenic Mouse Strains Enable Discrimination of Genetic Determinants Contributing to Fear and Fear Memory

Wilson, Yvette ; Brodnicki, Thomas ; Lawrence, Andrew ; Murphy, Mark

Behavior Genetics, 2011, Vol.41(2), pp.278-287 [Peer Reviewed Journal]

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10
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Mapping of leptin and its syntenic genes to chicken chromosome 1p

Seroussi, Eyal ; Pitel, Frederique ; Leroux, Sophie ; Morisson, Mireille ; Bornelöv, Susanne ; Miyara, Shoval ; Yosefi, Sara ; Cogburn, Larry A. ; Burt, David W. ; Andersson, Leif ; Friedman-Einat, Miriam ;Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för medicinsk biokemi och mikrobiologi

BMC Genetics, 2017, Vol. 18 [Peer Reviewed Journal]

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Familial Duplication/Deletion of 1q42.13q43 as Meiotic Consequence of an Intrachromosomal Insertion in Chromosome 1

Silipigni, Rosamaria ; Monfrini, Edoardo ; Baccarin, Marco ; Giangiobbe, Sara ; Lalatta, Faustina ; Guerneri, Silvana ; Bedeschi, Maria Francesca

Cytogenetic and Genome Research, January 2018, Vol.153(2), pp.73-80 [Peer Reviewed Journal]

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12
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A novel locus on chromosome 1 underlies the evolution of a melanic plumage polymorphism in a wild songbird

Bourgeois, Yann X. C ; Delahaie, Boris ; Gautier, Mathieu ; Lhuillier, Emeline ; Malé, Pierre-Jean G ; Bertrand, Joris A. M ; Cornuault, Josselin ; Wakamatsu, Kazumasa ; Bouchez, Olivier ; Mould, Claire ; Bruxaux, Jade ; Holota, Hélène ; Milá, Borja ; Thébaud, Christophe

Royal Society Open Science, 2017, Vol.4(2) [Peer Reviewed Journal]

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13
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BMD regulation on mouse distal chromosome 1, candidate genes, and response to ovariectomy or dietary fat

Beamer, Wesley G ; Shultz, Kathryn L ; Coombs, Harold F ; Demambro, Victoria E ; Reinholdt, Laura G ; Ackert‐Bicknell, Cheryl L ; Canalis, Ernesto ; Rosen, Clifford J ; Donahue, Leah Rae

Journal of Bone and Mineral Research, January 2011, Vol.26(1), pp.88-99 [Peer Reviewed Journal]

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14
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Supernumerary Isochromosome 1, idic(1)(p12), Leading to Tetrasomy 1q in Burkitt Lymphoma

Roug, A.S ; Wendtland, P ; Bendix, K ; Kjeldsen, E

Cytogenetic and Genome Research, December 2013, Vol.142(1), pp.7-13 [Peer Reviewed Journal]

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15
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Different segregation patterns in five carriers due to a pericentric inversion of chromosome 1

Luo, Yuqin ; Xu, Chenming ; Sun, Yixi ; Wang, Liya ; Chen, Songchang ; Jin, Fan

Systems Biology in Reproductive Medicine, 01 December 2014, Vol.60(6), pp.367-372 [Peer Reviewed Journal]

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16
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Pathogenetic role of an autoimmune susceptibility locus derived from MRL/MpJ strain chromosome 1 in chronic pancreas inflammation

Okada, Y ; Nakamura, T ; Ichii, O ; Otsuka, S ; Kon, Y

Lupus, October 2014, Vol.23(11), pp.1112-1123 [Peer Reviewed Journal]

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17
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Failure to Confirm Allelic Association Between Markers at the CAPON Gene Locus and Schizophrenia in a British Sample

Puri, Vinay ; Mcquillin, Andrew ; Thirumalai, Srinivasa ; Lawrence, Jacob ; Krasucki, Robert ; Choudhury, Khalid ; Datta, Susmita ; Kerwin, Simon ; Quested, Digby ; Bass, Nicholas ; Pimm, Jonathan ; Lamb, Graham ; Moorey, Helen ; Kandasami, Gomathinayagam ; Badacsonyi, Allison ; Kelly, Katie ; Morgan, Jenny ; Punukollu, Bhaskar ; Nadeem, Haitham ; Curtis, David

Biological Psychiatry, 2006, Vol.59(2), pp.195-197 [Peer Reviewed Journal]

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18
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Association of complement receptor 1 gene polymorphisms with cognitive function

Zijlstra, L. E ; Jukema, J. W ; Mooijaart, S. P ; De Vries, M. A ; Stott, D. J ; Castro Cabezas, M ; Trompet, S

Physiological Genomics, 2018, Vol.50(2), p.102-103 [Peer Reviewed Journal]

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19
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Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes

Marletta Cristina ; Valli Roberto ; Pressato Barbara ; Mare Lydia ; Montalbano Giuseppe ; Menna Giuseppe ; Loffredo Giuseppe ; Bernardo Maria ; Vinti Luciana ; Ferrari Simona ; Di Cesare-Merlone Alessandra ; Zecca Marco ; Lo Curto Francesco ; Locatelli Franco ; Pasquali Francesco ; Maserati Emanuela

Molecular Cytogenetics, 01 October 2012, Vol.5(1), p.39 [Peer Reviewed Journal]

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20
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LncRNA FAL1 is a negative prognostic biomarker and exhibits pro‐oncogenic function in osteosarcoma

Wang, Yanlong ; Zhao, Zhenyu ; Zhang, Shenqi ; Li, Zhaopeng ; Li, Dawei ; Yang, Sen ; Zhang, Hai ; Zeng, Xiangyu ; Liu, Jianyu

Journal of Cellular Biochemistry, October 2018, Vol.119(10), pp.8481-8489 [Peer Reviewed Journal]

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