Submissions from 2008
The Mouse Tumor Biology database., D M. Krupke, D A. Begley, J P. Sundberg, C J. Bult, and J T. Eppig
Loss of Rb1 in the gastrointestinal tract of Apc1638N mice promotes tumors of the cecum and proximal colon., M H. Kucherlapati, K Yang, K Fan, M Kuraguchi, D Sonkin, A Rosulek, M Lipkin, R T. Bronson, B J. Aronow, and R Kucherlapati
Genetic variation in Glp1r expression influences the rate of gastric emptying in mice., K G. Kumar, L O. Byerley, J Volaufova, D J. Drucker, G A. Churchill, R Li, B York, A Zuberi, and B K. Richards
T cell-specific siRNA delivery suppresses HIV-1 infection in humanized mice., P Kumar, H S. Ban, S S. Kim, H Wu, T Pearson, D L. Greiner, K Y. Lee, M Peipp, G H. Fey, N Manjunath, L D. Shultz, S K. Lee, and al et
Cardiovascular Research and the Laboratory Mouse, Ray Lambert
Developmental control of sumoylation pathway proteins in mouse male germ cells., Salle S. La, F Sun, X D. Zhang, M J. Matunis, and M A. Handel
Temporal migration of gonadotrophin-releasing hormone-1 neurones is modified in GAD67 knockout mice., J M. Lee, J Tiong, D M. Maddox, B G. Condie, and S Wray
In childhood acute lymphoblastic leukemia, blasts at different stages of immunophenotypic maturation have stem cell properties., C le Viseur, M Hotfilder, S Bomken, K Wilson, S Rottgers, A Schrauder, A Rosemann, J Irving, R W. Stam, L D. Shultz, J Harbott, H Jurgens, M Schrappe, R Pieters, and J Vormoor
Dense nuclear cataract caused by the gammaB-crystallin S11R point mutation., L Li, B Chang, C Cheng, D Chang, N L. Hawes, C H. Xia, and X Gong
Relationships of dietary fat, body composition, and bone mineral density in inbred mouse strain panels., R Li, K L. Svenson, L R. Donahue, L L. Peters, and G A. Churchill
Modeling human Philadelphia chromosome-positive leukemia in mice., S Li
Early mechanical dysfunction of the diaphragm in the muscular dystrophy with myositis (Ttnmdm) model., M A. Lopez, P S. Pardo, G A. Cox, and A M. Boriek
Access to immunology through the Gene Ontology., R C. Lovering, E B. Camon, J A. Blake, and A D. Diehl
Notch signaling regulates bile duct morphogenesis in mice., J Lozier, B McCright, and T Gridley
Mechanisms of DNA double-strand break repair in hematopoietic homeostasis and oncogenesis., S A. Maas, L B. Caddle, and KD Mills
Analysis of the QTL for sleep homeostasis in mice: Homer1a is a likely candidate., M Mackiewicz, B Paigen, N Naidoo, and A I. Pack
Whole-body vibration slows the acquisition of fat in mature female rats., G F. Maddalozzo, U T. Iwaniec, R T. Turner, C J. Rosen, and J J. Widrick
Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses., D M. Maddox, K A. Vessey, G L. Yarbrough, B M. Invergo, D R. Cantrell, S Inayat, V Balannik, W L. Hicks, N L. Hawes, S Byers, R S. Smith, R Hurd, D Howell, R G. Gregg, B Chang, J K. Naggert, J B. Troy, L H. Pinto, P M. Nishina, and M A. McCall
Full-field electroretinography and marked variability in clinical phenotype of Alstrom syndrome., E Malm, V Ponjavic, P M. Nishina, J K. Naggert, E G. Hinman, S Andreasson, J D. Marshall, and C Moller
The mitochondrial protease AFG3L2 is essential for axonal development., F Maltecca, A Aghaie, D G. Schroeder, L Cassina, B A. Taylor, S J. Phillips, M Malaguti, S Previtali, J L. Guenet, A Quattrini, G A. Cox, and G Casari
Deficiency of PPARbeta/delta in the epidermis results in defective cutaneous permeability barrier homeostasis and increased inflammation., M Q. Man, G D. Barish, M Schmuth, D Crumrine, Y Barak, S Chang, Y Jiang, R M. Evans, P M. Elias, and K R. Feingold
The orphan G protein-coupled receptor, Gpr161, encodes the vacuolated lens locus and controls neurulation and lens development., P G. Matteson, J Desai, R Korstanje, G Lazar, T E. Borsuk, J Rollins, S Kadambi, J Joseph, T Rahman, J Wink, R Benayed, B Paigen, and J H. Millonig
Genetic mapping of vocalization to a series of increasing acute footshocks using B6.A consomic and B6.D2 congenic mouse strains., D B. Matthews, E J. Chesler, M N. Cook, J Cockroft, V M. Philip, and D Goldowitz
Genetic ablation of alphav integrins in epithelial cells of the eyelid skin and conjunctiva leads to squamous cell carcinoma., J H. McCarty, M Barry, D Crowley, R T. Bronson, Hulbert A. Lacy, and R O. Hynes
[Alstrom syndrome: clinical and genetic features, and a diagnostic guide to foresee complications.], J Mendioroz, E Bermejo, J D. Marshall, J K. Naggert, G B. Collin, and Frias M. Martinez
The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered Hoxc gene expression in the ears., S E. Mentzer, J P. Sundberg, A Awgulewitsch, H H. Chao, D A. Carpenter, W D. Zhang, E M. Rinchik, and Y You
Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies., T Miki, T A. Zwingman, M Wakamori, C M. Lutz, S A. Cook, D A. Hosford, K Herrup, C F. Fletcher, Y Mori, W N. Frankel, and V A. Letts
mTORC1 promotes survival through translational control of Mcl-1., J R. Mills, Y Hippo, F Robert, S M. Chen, A Malina, C J. Lin, U Trojahn, H G. Wendel, A Charest, R T. Bronson, S C. Kogan, R Nadon, D E. Housman, S W. Lowe, and J Pelletier
Somatic inactivation of the PHD2 prolyl hydroxylase causes polycythemia and congestive heart failure., Y A. Minamishima, J Moslehi, N Bardeesy, D Cullen, R T. Bronson, and W G. Kaelin
Conditioned media from mouse osteosarcoma cells promote MC3T3-E1 cell proliferation using JAKs and PI3-K/Akt signal crosstalk., K Mori, F Blanchard, C Charrier, S Battaglia, K Ando, L Duplomb, L D. Shultz, F Redini, and D Heymann
Overexpression of innate immune response genes in a model of recessive polycystic kidney disease., M Mrug, J Zhou, Y Woo, X Cui, A J. Szalai, J Novak, G A. Churchill, and Woodford L. Guay
Selective delivery of beta cell antigen to dendritic cells in vivo leads to deletion and tolerance of autoreactive CD8+ T cells in NOD mice., A Mukhopadhaya, T Hanafusa, I Jarchum, Y G. Chen, Y Iwai, D V. Serreze, R M. Steinman, K V. Tarbell, and T P. DiLorenzo
Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in mice., Y Nakano, Guess C. Longo, D E. Bergstrom, W M. Nauseef, S M. Jones, and B Banfi
Analysis of gene expression in a developmental context emphasizes distinct biological leitmotifs in human cancers., K Naxerova, C J. Bult, A Peaston, K Fancher, B B. Knowles, S Kasif, and I S. Kohane
Patients with acute myeloid leukemia and RAS mutations benefit most from postremission high-dose cytarabine: a Cancer and Leukemia Group B study., Andreas Neubauer, Kati Maharry, Krzysztof Mrózek, Christian Thiede, Guido Marcucci, Peter Paschka, Robert J Mayer, Richard A Larson, Edison Liu, and Clara D Bloomfield
A quantitative assay for crossover and noncrossover molecular events at individual recombination hotspots in both male and female gametes., S H. Ng, E Parvanov, P M. Petkov, and K Paigen
Anesthetic considerations for in vivo imaging studies., Nicholson A, Klaunberg B
The chromosome 11 region from strain 129 provides protection from sex reversal in XYPOS mice., G Nikolova, J S. Sinsheimer, E M. Eicher, and E Vilain
Beyond positional cloning of single gene mutations: use of mouse models to examine allelic variance and to identify genetic modifiers., Patsy M. Nishina and Juergen K. Naggert
SIRT1 redistribution on chromatin promotes genomic stability but alters gene expression during aging., P Oberdoerffer, S Michan, M McVay, R Mostoslavsky, J Vann, S K. Park, A Hartlerode, J Stegmuller, A Hafner, P Loerch, S M. Wright, K D. Mills, A Bonni, B A. Yankner, R Scully, T A. Prolla, F W. Alt, and D A. Sinclair
Conserving, distributing and managing genetically modified mouse lines by sperm cryopreservation., G C. Ostermeier, M V. Wiles, J S. Farley, and R A. Taft
The recombinational anatomy of a mouse chromosome., K Paigen, J P. Szatkiewicz, K Sawyer, N Leahy, E D. Parvanov, S H. Ng, J H. Graber, K W. Broman, and P M. Petkov
AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation., J J. Pang, S L. Boye, A Kumar, A Dinculescu, W Deng, J Li, Q Li, A Rani, T C. Foster, B Chang, N L. Hawes, J H. Boatright, and W W. Hauswirth
A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination., B L. Patton, B Wang, Y S. Tarumi, K L. Seburn, and R W. Burgess
Human adult testis-derived pluripotent stem cells: revealing plasticity from the germline., C J. Payne and R E. Braun
Creation of "humanized" mice to study human immunity., T Pearson, D L. Greiner, and L D. Shultz
Humanized SCID mouse models for biomedical research., T Pearson, D L. Greiner, and L D. Shultz
Humanized SCID mouse models for biomedical research., T Pearson, D L. Greiner, and L D. Shultz
A new immunodeficient hyperglycaemic mouse model based on the Ins2Akita mutation for analyses of human islet and beta stem and progenitor cell function., T Pearson, L D. Shultz, J Lief, L Burzenski, B Gott, T Chase, O Foreman, A A. Rossini, R Bottino, M Trucco, and D L. Greiner
Non-obese diabetic-recombination activating gene-1 (NOD-Rag1 null) interleukin (IL)-2 receptor common gamma chain (IL2r gamma null) null mice: a radioresistant model for human lymphohaematopoietic engraftment., T Pearson, L D. Shultz, D Miller, M King, J Laning, W Fodor, A Cuthbert, L Burzenski, B Gott, B Lyons, O Foreman, A A. Rossini, and D L. Greiner
Genome Reshuffling for Advanced Intercross Permutation (GRAIP): simulation and permutation for advanced intercross population analysis., J L. Peirce, K W. Broman, L Lu, E J. Chesler, G Zhou, D C. Airey, A E. Birmingham, and R W. Williams
A critical assessment of Mus musculus gene function prediction using integrated genomic evidence., Castillo L. Pena, M Tasan, C Grant, Z Barutcuoglu, D P. Hill, Farley D. Warde, C Grouios, D Ray, J A. Blake, and al et
Progressive morphological and functional defects in retinas from alpha1 integrin-null mice., Y W. Peng, M Zallocchi, D T. Meehan, D Delimont, B Chang, N Hawes, W Wang, and D Cosgrove
Telomere dysfunction promotes genome instability and metastatic potential in a K-ras p53 mouse model of lung cancer., S A. Perera, R S. Maser, H Xia, K McNamara, A Protopopov, L Chen, A F. Hezel, C F. Kim, R T. Bronson, D H. Castrillon, L Chin, N Bardeesy, R A. Depinho, and K K. Wong
Genetic influence on immune phenotype revealed strain-specific variations in peripheral blood lineages., S B. Petkova, R Yuan, S W. Tsaih, W Schott, D C. Roopenian, and B Paigen
The dual bromodomain and WD repeat-containing mouse protein BRWD1 is required for normal spermiogenesis and the oocyte-embryo transition., D L. Philipps, K Wigglesworth, S A. Hartford, F Sun, S Pattabiraman, K Schimenti, M Handel, J J. Eppig, and J C. Schimenti
Mitochondrial oxidative phosphorylation and energetic status are reflected by morphology of mitochondrial network in INS-1E and HEP-G2 cells viewed by 4Pi microscopy., Hlavata L. Plecita, M Lessard, J Santorova, J Bewersdorf, and P Jezek
Evidence for Hox-specified positional identities in adult vasculature., N D. Pruett, R P. Visconti, D F. Jacobs, D Scholz, T McQuinn, J P. Sundberg, and A Awgulewitsch
Dependence of antibody-mediated presentation of antigen on FcRn., S W. Qiao, K Kobayashi, F E. Johansen, L M. Sollid, J T. Andersen, E Milford, D C. Roopenian, W I. Lencer, and R S. Blumberg
Light optical precision measurements of the active and inactive Prader-Willi syndrome imprinted regions in human cell nuclei., J Rauch, T A. Knoch, I Solovei, K Teller, S Stein, K Buiting, B Horsthemke, J Langowski, T Cremer, M Hausmann, and C Cremer
Utility of antiPax5 in the diagnosis of lymphoproliferative disorders and neoplasia in mice., J E. Rehg and J P. Sundberg
Bone marrow expressing a diabetes resistance MHC class II allele: diabetes deviation by chronic immune stimulation., P Reifsnyder, W Schott, D Pomerleau, M D. Lessard, B W. Soper, and E H. Leiter
Plexin-A2 and its ligand, Sema6A, control nucleus-centrosome coupling in migrating granule cells., J Renaud, G Kerjan, I Sumita, Y Zagar, V Georget, D Kim, C Fouquet, K Suda, M Sanbo, F Suto, S L. Ackerman, K J. Mitchell, H Fujisawa, and A Chedotal
High-precision structural analysis of subnuclear complexes in fixed and live cells via spatially modulated illumination (SMI) microscopy., J Reymann, D Baddeley, M Gunkel, P Lemmer, W Stadter, T Jegou, K Rippe, C Cremer, and U Birk
Impaired embryonic haematopoiesis yet normal arterial development in the absence of the Notch ligand Jagged1., Moreno A. Robert, J Guiu, Herguido C. Ruiz, M E. Lopez, Esteve J. Ingles, L Riera, A Tipping, T Enver, E Dzierzak, T Gridley, L Espinosa, and A Bigas
Targeted deletion of alpha-adducin results in absent beta- and gamma-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice., R F. Robledo, S L. Ciciotte, B Gwynn, K E. Sahr, D M. Gilligan, N Mohandas, and L L. Peters
Notch2 is required for maintaining sustentacular cell function in the adult mouse main olfactory epithelium., S Rodriguez, H M. Sickles, C Deleonardis, A Alcaraz, T Gridley, and D M. Lin
Regulation of Alstrom syndrome gene expression during adipogenesis and its relationship with fat cell insulin sensitivity., S Romano, G Milan, C Veronese, G B. Collin, J D. Marshall, C Centobene, F Favaretto, Pra C. Dal, A Scarda, S Leandri, J K. Naggert, P Maffei, and R Vettor
Spatial quantitative analysis of fluorescently labeled nuclear structures: problems, methods, pitfalls., O Ronneberger, D Baddeley, F Scheipl, P J. Verveer, H Burkhardt, C Cremer, L Fahrmeir, T Cremer, and B Joffe
Bone remodeling, energy metabolism, and the molecular clock., C J. Rosen
Sugar and bone: a not-so sweet story., C J. Rosen
The mouse polyubiquitin gene Ubb is essential for meiotic progression., K Y. Ryu, S A. Sinnar, L G. Reinholdt, S Vaccari, S Hall, M A. Garcia, T S. Zaitseva, D M. Bouley, K Boekelheide, M A. Handel, M Conti, and R R. Kopito
Cre recombinase activity specific to postnatal, premeiotic male germ cells in transgenic mice., Ngatchou P. Sadate, C J. Payne, A T. Dearth, and R E. Braun
Human BLyS facilitates engraftment of human PBL derived B cells in immunodeficient mice., M R. Schmidt, M C. Appel, L J. Giassi, D L. Greiner, L D. Shultz, and R T. Woodland
Through regulation of TCR expression levels, an Idd7 region gene(s) interactively contributes to the impaired thymic deletion of autoreactive diabetogenic CD8+ T cells in nonobese diabetic mice., D V. Serreze, Rossi C. Choisy, A E. Grier, T M. Holl, H D. Chapman, J R. Gahagan, M A. Osborne, W Zhang, B L. King, A Brown, D Roopenian, and M P. Marron
NOTCH is part of the transcriptional network regulating cell growth and survival in mouse plasmacytomas., D M. Shin, D J. Shaffer, H Wang, D C. Roopenian, and H C. Morse
Seeing the world through a new set of glasses: emerging technologies for the study of cell nuclei and chromosomes., L Shopland and J Bewersdorf
Long-term engraftment and expansion of tumor-derived memory T cells following the implantation of non-disrupted pieces of human lung tumor into NOD-scid IL2Rgamma(null) mice., Abelson M. Simpson, G F. Sonnenberg, H Takita, S J. Yokota, T F. Conway, R J. Kelleher, L D. Shultz, M Barcos, and R B. Bankert
Monitoring of anesthesia., Smith JC, Danneman PJ
Muscle development is disrupted in zebrafish embryos deficient for fibronectin., C J. Snow, M T. Peterson, A Khalil, and C A. Henry
Nordihydroguaiaretic acid and aspirin increase lifespan of genetically heterogeneous male mice., R Strong, R A. Miller, C M. Astle, R A. Floyd, K Flurkey, K L. Hensley, M A. Javors, C Leeuwenburgh, J F. Nelson, and E Ongini
Applying gene expression, proteomics and single-nucleotide polymorphism analysis for complex trait gene identification., I M. Stylianou, J P. Affourtit, K R. Shockley, R Y. Wilpan, F A. Abdi, S Bhardwaj, J Rollins, G A. Churchill, and B Paigen
Differences in DBA/1J and DBA/2J reveal lipid QTL genes., I M. Stylianou, S R. Langley, K Walsh, Y Chen, C Revenu, and B Paigen
Integrating mouse anatomy and pathology ontologies into a phenotyping database: tools for data capture and training., J P. Sundberg, B A. Sundberg, and P Schofield
Regulation of the meiotic prophase I to metaphase I transition in mouse spermatocytes., F Sun and M A. Handel
The C3H/HeJ mouse and DEBR rat models for alopecia areata: review of preclinical drug screening approaches and results., J Sun, K A. Silva, K J. McElwee, L E. King, and J P. Sundberg
Oocyte regulation of metabolic cooperativity between mouse cumulus cells and oocytes: BMP15 and GDF9 control cholesterol biosynthesis in cumulus cells., Y Q. Su, K Sugiura, K Wigglesworth, M J. O'Brien, J P. Affourtit, S A. Pangas, M M. Matzuk, and J J. Eppig
Candidate genes for obesity revealed from a C57BL/6J x 129S1/SvImJ intercross., Z Su, R Korstanje, S W. Tsaih, and B Paigen
Candidate genes for plasma triglyceride, FFA, and glucose revealed from an intercross between inbred mouse strains NZB/B1NJ and NZW/LacJ., Z Su, S W. Tsaih, J Szatkiewicz, Y Shen, and B Paigen
A new mouse mutant for the LDL receptor identified using ENU mutagenesis., K L. Svenson, N Ahituv, R S. Durgin, H Savage, P A. Magnani, O Foreman, B Paigen, and L L. Peters
An imputed genotype resource for the laboratory mouse., J P. Szatkiewicz, G L. Beane, Y Ding, L Hutchins, Manuel de Pardo, and G A. Churchill
Virtues and limitations of the preimplantation mouse embryo as a model system., R A. Taft
An en masse phenotype and function prediction system for Mus musculus., M Tasan, W Tian, D P. Hill, F D. Gibbons, J A. Blake, and F P. Roth
Promoting coherent minimum reporting guidelines for biological and biomedical investigations: the MIBBI project., Chris F Taylor, Dawn Field, Susanna-Assunta Sansone, Jan Aerts, Rolf Apweiler, Michael Ashburner, Catherine A Ball, Pierre-Alain Binz, Molly Bogue, Tim Booth, Alvis Brazma, Ryan R Brinkman, Adam Michael Clark, Eric W Deutsch, Oliver Fiehn, Jennifer Fostel, Peter Ghazal, Frank Gibson, Tanya Gray, Graeme Grimes, John M Hancock, Nigel W Hardy, Henning Hermjakob, Randall K Julian, Matthew Kane, Carsten Kettner, Christopher Kinsinger, Eugene Kolker, Martin Kuiper, Nicolas Le Novère, Jim Leebens-Mack, Suzanna E Lewis, Phillip Lord, Ann-Marie Mallon, Nishanth Marthandan, Hiroshi Masuya, Ruth McNally, Alexander Mehrle, Norman Morrison, Sandra Orchard, John Quackenbush, James M Reecy, Donald G Robertson, Philippe Rocca-Serra, Henry Rodriguez, Heiko Rosenfelder, Javier Santoyo-Lopez, Richard H Scheuermann, Daniel Schober, Barry Smith, Jason Snape, Christian J Stoeckert, Keith Tipton, Peter Sterk, Andreas Untergasser, Jo Vandesompele, and Stefan Wiemann
The NLR gene family: a standard nomenclature., J P. Ting, R C. Lovering, E S. Alnemri, J Bertin, J M. Boss, A Godzik, J A. Harton, J P. Hugot, N Inohara, A Mackenzie, L J. Maltais, G Nunez, Y Ogura, J C. Reed, and V Steimle
Notch2 is required for the proliferation of cardiac neural crest-derived smooth muscle cells., P Varadkar, M Kraman, D Despres, G Ma, J Lozier, and B McCright
Targeted deletion reveals essential and overlapping functions of the miR-17 through 92 family of miRNA clusters., A Ventura, A G. Young, M M. Winslow, L Lintault, A Meissner, S J. Erkeland, J Newman, R T. Bronson, D Crowley, J R. Stone, R Jaenisch, P A. Sharp, and T Jacks
Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome., S V. Voronov, S G. Frere, S Giovedi, E A. Pollina, C Borel, H Zhang, C Schmidt, E C. Akeson, M R. Wenk, L Cimasoni, O Arancio, M T. Davisson, S E. Antonarakis, K Gardiner, Camilli P. De, and Paolo G. Di
Differential effects of Usp14 and Uch-L1 on the ubiquitin proteasome system and synaptic activity., B J. Walters, S L. Campbell, P C. Chen, A P. Taylor, D G. Schroeder, L E. Dobrunz, Tsakonas K. Artavanis, H L. Ploegh, J A. Wilson, G A. Cox, and S M. Wilson