Submissions from 2011
Inhibition of NF-kappaB signaling retards eosinophilic dermatitis in SHARPIN-deficient mice., Y Liang, R E. Seymour, and J P. Sundberg
Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice., R Liegel, B Chang, R Dubielzig, and D J. Sidjanin
Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse., Charlotte Lindfors, Ida A K Nilsson, Pablo M Garcia-Roves, Aamir R Zuberi, Mohsen Karimi, Leah Rae Donahue, Derry C Roopenian, Jan Mulder, Mathias Uhlén, Tomas J Ekström, Muriel T Davisson, Tomas G M Hökfelt, Martin Schalling, and Jeanette E Johansen
Memory T cells from minor histocompatibility antigen-vaccinated and virus-immune donors improve GVL and immune reconstitution., Ning Li, Catherine Matte-Martone, Hong Zheng, Weiguo Cui, Srividhya Venkatesan, Hung Sheng Tan, Jennifer McNiff, Anthony J Demetris, Derry Roopenian, Susan Kaech, and Warren D Shlomchik
Mosaic analysis with double markers reveals tumor cell of origin in glioma., C Liu, J C. Sage, M R. Miller, R G. Verhaak, S Hippenmeyer, H Vogel, O Foreman, R T. Bronson, A Nishiyama, L Luo, and H Zong
Human islet cell MORF/cMORF pretargeting in a xenogeneic murine transplant model., G Liu, S Dou, D Cheng, J Leif, M Rusckowski, P R. Streeter, L D. Shultz, D J. Hnatowich, and D L. Greiner
The neonatal FcR-mediated presentation of immune-complexed antigen is associated with endosomal and phagosomal pH and antigen stability in macrophages and dendritic cells., X Liu, L Lu, Z Yang, S Palaniyandi, R Zeng, L Y. Gao, D M. Mosser, D C. Roopenian, and X Zhu
Gene therapy rescues cone structure and function in the 3-month-old rd12 mouse: a model for midcourse RPE65 leber congenital amaurosis., Xia Li, Wensheng Li, Xufeng Dai, Fansheng Kong, Qinxiang Zheng, Xiangtian Zhou, Fan Lü, Bo Chang, Bärbel Rohrer, William W Hauswirth, Jia Qu, and Ji-jing Pang
Genetic variation of ESR1 and its co-activator PPARGC1B is synergistic in augmenting the risk of estrogen receptor-positive breast cancer., Yuqing Li, Yi Li, Sara Wedrén, Guoliang Li, Tze Howe Charn, Kartiki Vasant Desai, Carine Bonnard, Kamila Czene, Keith Humphreys, Hatef Darabi, Kristjana Einarsdóttir, Tuomas Heikkinen, Kristiina Aittomäki, Carl Blomqvist, Kee Seng Chia, Heli Nevanlinna, Per Hall, Edison T Liu, and Jianjun Liu
Transfer of IgG in the female genital tract by MHC class I-related neonatal Fc receptor (FcRn) confers protective immunity to vaginal infection., Z Li, S Palaniyandi, R Zeng, W Tuo, D C. Roopenian, and X Zhu
Defective hematopoietic stem cell and lymphoid progenitor development in the Ts65Dn mouse model of Down syndrome: potential role of oxidative stress., Laureanne Pilar E Lorenzo, Haiyan Chen, Kristen E Shatynski, Sarah Clark, Rong Yuan, David E Harrison, Paul J Yarowsky, and Mark S Williams
A neonatal Fc receptor-targeted mucosal vaccine strategy effectively induces HIV-1 antigen-specific immunity to genital infection., L Lu, S Palaniyandi, R Zeng, Y Bai, X Liu, Y Wang, C D. Pauza, D C. Roopenian, and X Zhu
Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy., C M. Lutz, S Kariya, S Patruni, M A. Osborne, D Liu, C E. Henderson, D K. Li, L Pellizzoni, J Rojas, D M. Valenzuela, A J. Murphy, M L. Winberg, and U R. Monani
An ENU-induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degeneration., D M. Maddox, W L. Hicks, D Vollrath, M M. LaVail, J K. Naggert, and P M. Nishina
An essential role for the association of CD47 to SHPS-1 in skeletal remodeling., L A. Maile, V E. DeMambro, C Wai, S Lotinun, A W. Aday, B E. Capps, W G. Beamer, C J. Rosen, and D R. Clemmons
Clinical utility gene card for: Alström syndrome., Jan D Marshall, Pietro Maffei, Sebastian Beck, Timothy G Barrett, and Richard B Paisey
Alström syndrome: genetics and clinical overview., Jan D Marshall, Pietro Maffei, Gayle B Collin, and Jürgen K Naggert
Architecture of energy balance traits in emerging lines of the Collaborative Cross., W F. Mathes, D L. Aylor, D R. Miller, G A. Churchill, E J. Chesler, Manuel de Villena F. Pardo, D W. Threadgill, and D Pomp
MHC class I family proteins retard systemic lupus erythematosus autoimmunity and B cell lymphomagenesis., Caroline G McPhee, Thomas J Sproule, Dong-Mi Shin, Jason A Bubier, William H Schott, Martin P Steinbuck, Lia Avenesyan, Herbert C Morse, and Derry C Roopenian
Autism candidate genes via mouse phenomics., Terrence F Meehan, Christopher J Carr, Jeremy J Jay, Carol J Bult, Elissa J Chesler, and Judith A Blake
Logical development of the cell ontology., T F. Meehan, A M. Masci, A Abdulla, L G. Cowell, J A. Blake, C J. Mungall, and A D. Diehl
Sertoli cell-specific deletion of the androgen receptor compromises testicular immune privilege in mice., Jing Meng, Anne R Greenlee, Chloe J Taub, and Robert E Braun
A spontaneous mutation in Srebf2 leads to cataracts and persistent skin wounds in the lens opacity 13 (lop13) mouse., Kate M Merath, Bo Chang, Richard Dubielzig, Richard Jeannotte, and Duska J Sidjanin
Bardet-Biedl syndrome with end-stage kidney disease in a four-year-old Romanian boy: a case report., C M. Mihai, J D. Marshall, and R M. Stoicescu
Rapamycin, but not resveratrol or simvastatin, extends life span of genetically heterogeneous mice., R A. Miller, D E. Harrison, C M. Astle, J A. Baur, K Flurkey, M A. Javors, J F. Nelson, C J. Orihuela, S Pletcher, and al et
The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., T H. Min, M Kriebel, S Hou, and E M. Pera
Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy., Satomi Mitsuhashi, Hideyuki Hatakeyama, Minako Karahashi, Tomoko Koumura, Ikuya Nonaka, Yukiko K Hayashi, Satoru Noguchi, Roger B Sher, Yasuhito Nakagawa, Giovanni Manfredi, Yu-ichi Goto, Gregory A Cox, and Ichizo Nishino
A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesis., S Mitsuhashi, A Ohkuma, B Talim, K Ikeda, I Nonaka, R B. Sher, G A. Cox, H Topaloglu, and al et
Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels., William W Motley, Kevin L Seburn, Mir Hussain Nawaz, Kathy E Miers, Jun Cheng, Anthony Antonellis, Eric D Green, Kevin Talbot, Xiang-Lei Yang, Kenneth H Fischbeck, and Robert W Burgess
Cross-product extensions of the Gene Ontology., C J. Mungall, M Bada, T Z. Berardini, J Deegan, A Ireland, M A. Harris, D P. Hill, and J Lomax
Mouse resources for craniofacial research., S A. Murray
Genomic loci and candidate genes underlying inflammatory nociception., H K. Nair, H Hain, R M. Quock, V M. Philip, E J. Chesler, J K. Belknap, and W R. Lariviere
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice., K S. Nair, Aifa M. Hmani, I M. Cosma, W Bouassida, B Hakim, Z Benzina, I Soto, P Soderkvist, G R. Howell, R S. Smith, H Ayadi, and S W. John
The Protein Ontology: a structured representation of protein forms and complexes., D A. Natale, C N. Arighi, W C. Barker, J A. Blake, C J. Bult, M Caudy, H J. Drabkin, P D'Eustachio, A V. Evsikov, and al et
Regulation of NKB pathways and their roles in the control of Kiss1 neurons in the arcuate nucleus of the male mouse., V M. Navarro, M L. Gottsch, M Wu, Galiano D. Garcia, S J. Hobbs, M A. Bosch, L Pinilla, D K. Clifton, A Dearth, O K. Ronnekleiv, R E. Braun, R D. Palmiter, Sempere M. Tena, M Alreja, and R A. Steiner
Identification of the Mhc region as an asthma susceptibility locus in recombinant congenic mice., M C. Nawijn, B J. Piavaux, P V. Jeurink, R Gras, M A. Reinders, T Stearns, S Foote, M N. Hylkema, P C. Groot, R Korstanje, and A J. Oosterhout
Evaluation of matrix effects in analysis of estrogen using liquid chromatography-tandem mass spectrometry., Hien P Nguyen, Li Li, Imam S Nethrapalli, Ningning Guo, C Dominique Toran-Allerand, David E Harrison, C Michael Astle, and Kevin A Schug
Prevention of "Humanized" diabetogenic CD8 T-cell responses in HLA-transgenic NOD mice by a multipeptide coupled-cell approach., M Niens, A E. Grier, M Marron, T W. Kay, D L. Greiner, and D V. Serreze
Long-term retinal function and structure rescue using capsid mutant AAV8 vector in the rd10 mouse, a model of recessive retinitis pigmentosa., J J. Pang, X Dai, S E. Boye, I Barone, B Lei, B Chang, R Barlow, E Strettoi, and W W. Hauswirth
A new mode of corticothalamic transmission revealed in the Gria4(-/-) model of absence epilepsy., J T. Paz, A S. Bryant, K Peng, L Fenno, O Yizhar, W N. Frankel, K Deisseroth, and J R. Huguenard
Both the variability and level of mouse allergen exposure influence the phenotype of the immune response in workers at a mouse facility., R D. Peng, B Paigen, P A. Eggleston, K A. Hagberg, M Krevans, Brosnan J. Curtin, C Benson, W G. Shreffler, and E C. Matsui
Arrayed primer extension technology simplifies mutation detection in Bardet-Biedl and Alstrom syndrome., I Pereiro, B E. Hoskins, J D. Marshall, G B. Collin, J K. Naggert, Gallego T. Pineiro, E Oitmaa, D Valverde, and P L. Beales
Genetic analysis in the Collaborative Cross breeding population., Vivek M Philip, Greta Sokoloff, Cheryl L Ackert-Bicknell, Martin Striz, Lisa Branstetter, Melissa A Beckmann, Jason S Spence, Barbara L Jackson, Leslie D Galloway, Paul Barker, Ann M Wymore, Patricia R Hunsicker, David C Durtschi, Ginger S Shaw, Sarah Shinpock, Kenneth F Manly, Darla R Miller, Kevin D Donohue, Cymbeline T Culiat, Gary A Churchill, William R Lariviere, Abraham A Palmer, Bruce F O'Hara, Brynn H Voy, and Elissa J Chesler
The nude mutant gene Foxn1 is a HOXC13 regulatory target during hair follicle and nail differentiation., C S. Potter, N D. Pruett, M J. Kern, M A. Baybo, A R. Godwin, K A. Potter, R L. Peterson, J P. Sundberg, and A Awgulewitsch
Mitotic defects lead to pervasive aneuploidy and accompany loss of RB1 activity in mouse LmnaDhe dermal fibroblasts., C H. Pratt, M Curtain, L R. Donahue, and L S. Shopland
SHARPIN is an endogenous inhibitor of beta1-integrin activation., J K. Rantala, J Pouwels, T Pellinen, S Veltel, P Laasola, E Mattila, C S. Potter, T Duffy, J P. Sundberg, and al et
Voltage sensitive phosphoinositide phosphatases of Xenopus: their tissue distribution and voltage dependence., W J. Ratzan, A V. Evsikov, Y Okamura, and L A. Jaffe
Changes in brain β-amyloid deposition and aquaporin 4 levels in response to altered agrin expression in mice., Steven M Rauch, Kathy Huen, Miles C Miller, Hira Chaudry, Melissa Lau, Joshua R Sanes, Conrad E Johanson, Edward G Stopa, and Robert W Burgess
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn., Laura G Reinholdt, Yueming Ding, Griffith J Gilbert, Griffith T Gilbert, Anne Czechanski, Jeffrey P Solzak, Randall J Roper, Mark T Johnson, Leah Rae Donahue, Cathleen Lutz, and Muriel T Davisson
Localization of hair shaft protein VSIG8 in the hair follicle, nail unit, and oral cavity., R H. Rice, M A. Phillips, and J P. Sundberg
Mouse mutants and phenotypes: accessing information for the study of mammalian gene function., M Ringwald and J T. Eppig
The IKMC web portal: a central point of entry to data and resources from the International Knockout Mouse Consortium., M Ringwald, V Iyer, J C. Mason, K R. Stone, H D. Tadepally, J A. Kadin, C J. Bult, J T. Eppig, and al et
Targeting of a T cell agonist peptide to lysosomes by DNA vaccination induces tolerance in the nonobese diabetic mouse., E I. Rivas, J P. Driver, N Garabatos, M Presa, C Mora, F Rodriguez, D V. Serreze, and T Stratmann
Coronary artery disease from isolated non-H2-determined incompatibilities in transplanted mouse hearts., P S. Russell, C M. Chase, J C. Madsen, T Hirohashi, L D. Cornell, T J. Sproule, R B. Colvin, and D C. Roopenian
Targeted disruption of the CCR5 gene in human hematopoietic stem cells stimulated by peptide nucleic acids., Erica B Schleifman, Ranjit Bindra, Jean Leif, Jacob del Campo, Faye A Rogers, Pradeep Uchil, Olaf Kutsch, Leonard D Shultz, Priti Kumar, Dale L Greiner, and Peter M Glazer
New approaches to the representation and analysis of phenotype knowledge in human diseases and their animal models., Paul N Schofield, John P Sundberg, Robert Hoehndorf, and Georgios V Gkoutos
Pathology of the laboratory mouse: an International Workshop on Challenges for High Throughput Phenotyping., P N. Schofield, P Dubus, L Klein, M Moore, C McKerlie, J M. Ward, and J P. Sundberg
Loss of intra-islet CD20 expression may complicate efficacy of B-cell-directed type 1 diabetes therapies., D V. Serreze, H D. Chapman, M Niens, R Dunn, M R. Kehry, J P. Driver, M Haller, C Wasserfall, and M A. Atkinson
Rhabdomyosarcomas in aging A/J mice., R B. Sher, G A. Cox, K D. Mills, and J P. Sundberg
Humanized mice as a preclinical tool for infectious disease and biomedical research., L D. Shultz, M A. Brehm, S Bavari, and D L. Greiner
Genetic analysis of mouse strains with variable serum sodium concentrations identifies the Nalcn sodium channel as a novel player in osmoregulation., A P. Sinke, C Caputo, S W. Tsaih, R Yuan, D Ren, P M. Deen, and R Korstanje
Altered testicular gene expression patterns in mice lacking the polyubiquitin gene Ubb., Shamim A Sinnar, Christopher L Small, Ryan M Evanoff, Laura G Reinholdt, Michael D Griswold, Ron R Kopito, and Kwon-Yul Ryu
GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma., Karin E Smedby, Jia Nee Foo, Christine F Skibola, Hatef Darabi, Lucia Conde, Henrik Hjalgrim, Vikrant Kumar, Ellen T Chang, Nathaniel Rothman, James R Cerhan, Angela R Brooks-Wilson, Emil Rehnberg, Ishak D Irwan, Lars P Ryder, Peter N Brown, Paige M Bracci, Luz Agana, Jacques Riby, Wendy Cozen, Scott Davis, Patricia Hartge, Lindsay M Morton, Richard K Severson, Sophia S Wang, Susan L Slager, Zachary S Fredericksen, Anne J Novak, Neil E Kay, Thomas M Habermann, Bruce Armstrong, Anne Kricker, Sam Milliken, Mark P Purdue, Claire M Vajdic, Peter Boyle, Qing Lan, Shelia H Zahm, Yawei Zhang, Tongzhang Zheng, Stephen Leach, John J Spinelli, Martyn T Smith, Stephen J Chanock, Leonid Padyukov, Lars Alfredsson, Lars Klareskog, Bengt Glimelius, Mads Melbye, Edison T Liu, Hans-Olov Adami, Keith Humphreys, and Jianjun Liu
Context-dependent function of "GATA switch" sites in vivo., Jonathan W Snow, Jennifer J. Trowbridge, Kirby D Johnson, Tohru Fujiwara, Nikla E Emambokus, Jeffrey A Grass, Stuart H Orkin, and Emery H Bresnick
Nuclear positioning, higher-order folding, and gene expression of Mmu15 sequences are refractory to chromosomal translocation., K J. Snow, S M. Wright, Y Woo, L C. Titus, K D. Mills, and L S. Shopland
Combined genomic and phenotype screening reveals secretory factor SPINK1 as an invasion and survival factor associated with patient prognosis in breast cancer., Wendy Weijia Soon, Lance David Miller, Michael A Black, Cyril Dalmasso, Xiu Bin Chan, Brendan Pang, Chee Wee Ong, Manuel Salto-Tellez, Kartiki V Desai, and Edison T Liu
Germline stem cells., Allan Spradling, Margaret T Fuller, Robert E Braun, and Shosei Yoshida
Micro axial tomography: a miniaturized, versatile stage device to overcome resolution anisotropy in fluorescence light microscopy., Florian Staier, Heinz Eipel, Petr Matula, Alexei V Evsikov, Michal Kozubek, Christoph Cremer, and Michael Hausmann
An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations., M Stum, H M. McLaughlin, E L. Kleinbrink, K E. Miers, S L. Ackerman, K L. Seburn, A Antonellis, and R W. Burgess
The mouse as a model for understanding chronic diseases of aging: the histopathologic basis of aging in inbred mice., John P. Sundberg, Annerose Berndt, Beth A. Sundberg, Kathleen A. Silva, Victoria Kennedy, Roderick T. Bronson, Rong Yuan, Beverly J. Paigen, David E E. Harrison, and Paul N. Schofield
Hypothesis testing: CTLA4 co-stimulatory pathways critical in the pathogenesis of human and mouse alopecia areata., John P Sundberg, Kevin J McElwee, Joseph M Carroll, and Lloyd E King
Association between hair-induced oronasal inflammation and ulcerative dermatitis in C57BL/6 mice., John P Sundberg, Björn Rozell, and Helen Everts
Primary follicular dystrophy with scarring dermatitis in C57BL/6 mouse substrains resembles central centrifugal cicatricial alopecia in humans., J P. Sundberg, D Taylor, G Lorch, J Miller, K A. Silva, B A. Sundberg, D Roopenian, L Sperling, D Ong, L E. King, and H Everts
A mutation in Mtap2 is associated with arrest of mammalian spermatocytes before the first meiotic division., Fengyun Sun and Mary Ann Handel
Mammalian target of rapamycin up-regulation of pyruvate kinase isoenzyme type M2 is critical for aerobic glycolysis and tumor growth., Q Sun, X Chen, J Ma, H Peng, F Wang, X Zha, Y Wang, Y Jing, H Yang, R Chen, L Chang, Y Zhang, J Goto, H Onda, T Chen, M R. Wang, Y Lu, H You, D Kwiatkowski, and H Zhang
The collaborative cross: a recombinant inbred mouse population for the systems genetic era., D W. Threadgill, D R. Miller, G A. Churchill, and Villena F. de
A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice., S Tokuda, C L. Mahaffey, B Monks, C R. Faulkner, M J. Birnbaum, S C. Danzer, and W N. Frankel
Anti-inflammatory and immunomodulatory effects of bortezomib in various in vivo models., David Tung, Peter H Cheung, Pali Kaur, Oded Foreman, Anoop Kavirayani, Heather S Hain, and Saurabh Saha
Notch2 governs the rate of generation of mouse long- and short-term repopulating stem cells., Finney B. Varnum, L M. Halasz, M Sun, T Gridley, F Radtke, and I D. Bernstein
Stochastic variation of transcript abundance in C57BL/6J mice., P T. Vedell, K L. Svenson, and G A. Churchill
Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma., K N. Veth, J R. Willer, R F. Collery, M P. Gray, G B. Willer, D S. Wagner, M C. Mullins, A J. Udvadia, R S. Smith, S W. John, R G. Gregg, and B A. Link
Etiology of a genetically complex seizure disorder in Celf4 mutant mice., J L Wagnon, C L Mahaffey, W Sun, Y Yang, H-T Chao, and W N Frankel
Adenylate cyclase 1 promotes strengthening and experience-dependent plasticity of whisker relay synapses in the thalamus., Hao Wang, Hong Liu, Daniel R Storm, and Zhong-wei Zhang
Elimination of redundant synaptic inputs in the absence of synaptic strengthening., Hao Wang, Hong Liu, and Zhong-wei Zhang
Mechanisms of antigen presentation to T cells in murine graft-versus-host disease: cross-presentation and the appearance of cross-presentation., Xiaojian Wang, Hongmei Li, Catherine Matte-Martone, Weiguo Cui, Ning Li, Hung Sheng Tan, Derry C. Roopenian, and Warren D Shlomchik
Combining FISH with localisation microscopy: Super-resolution imaging of nuclear genome nanostructures., Y Weiland, P Lemmer, and C Cremer
HLA-A2-matched peripheral blood mononuclear cells from type 1 diabetic patients, but not nondiabetic donors, transfer insulitis to NOD-scid/gammac(null)/HLA-A2 transgenic mice concurrent with the expansion of islet-specific CD8+ T cells., Larry F. Whitfield, E F. Young, G Talmage, E Fudge, A Azam, S Patel, J Largay, W Byrd, J Buse, A S. Calikoglu, L D. Shultz, and J A. Frelinger
NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development., J Won, de Evsikova Marin, R S. Smith, W L. Hicks, M M. Edwards, Guess C. Longo, T Li, J K. Naggert, and P M. Nishina
Mouse model resources for vision research., J Won, L Y. Shi, W Hicks, J Wang, R Hurd, J K. Naggert, B Chang, and P M. Nishina
Comparative proteomics reveals deficiency of SLC9A1 (sodium/hydrogen exchanger NHE1) in beta-adducin null red cells., J M. Wooden, G L. Finney, E Rynes, M J. Maccoss, A J. Lambert, R F. Robledo, L L. Peters, and D M. Gilligan
Subspecific origin and haplotype diversity in the laboratory mouse., H Yang, J R. Wang, J P. Didion, R J. Buus, A H. Yu, P Tucker, P Boursot, L McMillan, G A. Churchill, and al et
Low-level expression of let-7a in gastric cancer and its involvement in tumorigenesis by targeting RAB40C., Q Yang, Z Jie, H Cao, A R. Greenlee, C Yang, F Zou, and Y Jiang
Lack of protein 4.1G causes altered expression and localization of the cell adhesion molecule nectin-like 4 in testis and can cause male infertility., Shaomin Yang, Haibo Weng, Lixiang Chen, Xinhua Guo, Marilyn Parra, John Conboy, Gargi Debnath, Amy J Lambert, Luanne L Peters, Anthony J Baines, Narla Mohandas, and Xiuli An
Efficient mucosal vaccination mediated by the neonatal Fc receptor., L Ye, R Zeng, Y Bai, D C. Roopenian, and X Zhu
Mice as a mammalian model for research on the genetics of aging., R Yuan, L L. Peters, and B Paigen
Self-assembled monolayer-assisted silicon nanowire biosensor for detection of protein-DNA interactions in nuclear extracts from breast cancer cell., Guo-Jun Zhang, Min Joon Huang, Jun'An Jason Ang, Edison T Liu, and Kartiki Vasant Desai
Estradiol promotes and maintains cumulus cell expression of natriuretic peptide receptor 2 (NPR2) and meiotic arrest in mouse oocytes in vitro., M Zhang, Y Q. Su, K Sugiura, K Wigglesworth, G Xia, and J J. Eppig
Insulin-like growth factor-1 increases bone calcium accumulation only during rapid growth in female rats., Qinmin Zhang, Meryl E Wastney, Clifford J Rosen, Wesley G Beamer, and Connie M Weaver
A deficiency of ceramide biosynthesis causes cerebellar purkinje cell neurodegeneration and lipofuscin accumulation., L Zhao, S D. Spassieva, T J. Jucius, L D. Shultz, H E. Shick, W B. Macklin, Y A. Hannun, L M. Obeid, and S L. Ackerman
The role of miR-506 in transformed 16HBE cells induced by anti-benzo[a]pyrene-trans-7,8-dihydrodiol-9,10-epoxide., Y Zhao, H Liu, Y Li, J Wu, A R. Greenlee, C Yang, and Y Jiang