Submissions from 2003
Customized molecular phenotyping by quantitative gene expression and pattern recognition analysis., S Akilesh, D J. Shaffer, and D Roopenian
Sry Expression Level and Protein Isoform Differences Play a Role in Abnormal Testis Development in C57BL/6J Mice Carrying Certain Sry Alleles., K H. Albrecht, M Young, L L. Washburn, and E M. Eicher
Dlx transcription factors regulate differentiation of dopaminergic neurons of the ventral thalamus., G L. Andrews, K Yun, J L. Rubenstein, and G S. Mastick
Connecting sequence and biology in the laboratory mouse., R M. Baldarelli, D P. Hill, J A. Blake, D Bradt, S Cousins, K S. Frazer, S Ramachandran, D Reed, M Ringwald, B L. King, L J. Maltais, L M. McKenzie, J T. Eppig, J E. Richardson, J A. Kadin, and C J. Bult
Retroposon compensatory mechanism hypothesis not supported: Zfa knockout mice are fertile., K G. Banks, K A. Johnson, C P. Lerner, C L. Mahaffey, R T. Bronson, and E M. Simpson
Donor cell replacement in mice transplanted in utero is limited by immune-independent mechanisms., J E. Barker, A J. Schuldt, M D. Lessard, C D. Jude, C A. Vogler, and B W. Soper
Donor cell expansion is delayed following nonablative in utero transplantation to treat murine mucopolysaccharidosis type VII., J E. Barker, A J. Schuldt, M L. Lessard, C D. Jude, C A. Vogler, and B W. Soper
In collaboration: the Jackson Laboratory Craniofacial Resource., J D. Bauschatz, M M. Curtain, M T. Davisson, P W. Lane, and L R. Donahue
Overlapping deletions spanning the proximal two-thirds of the mouse t complex., D E. Bergstrom, R A. Bergstrom, R J. Munroe, B K. Lee, V L. Browning, Y You, E M. Eicher, and J C. Schimenti
Normoblastosis, a murine model for ankyrin-deficient hemolytic anemia, is caused by a hypomorphic mutation in the erythroid ankyrin gene Ank1., C S. Birkenmeier, E J. Gifford, and J E. Barker
The effects of parathyroid hormone and alendronate alone or in combination in postmenopausal osteoporosis., D M. Black, S L. Greenspan, K E. Ensrud, L Palermo, J A. McGowan, T F. Lang, P Garnero, M L. Bouxsein, J P. Bilezikian, and C J. Rosen
Mouse and rat genome informatics., J A. Blake, J Eppig, and C J. Bult
MGD: the Mouse Genome Database., J A. Blake, J E. Richardson, C J. Bult, J A. Kadin, and J T. Eppig
Mouse Phenome Project: understanding human biology through mouse genetics and genomics., M Bogue
Love at first site., L Bonetta and M T. Davisson
Manipulation of stem cell proliferation and lineage commitment: visualisation of label-retaining cells in wholemounts of mouse epidermis., K M. Braun, C Niemann, U B. Jensen, J P. Sundberg, Vargas V. Silva, and F M. Watt
Genetic modulation of tau phosphorylation in the mouse., J Brich, F S. Shie, B W. Howell, R Li, K Tus, E K. Wakeland, L W. Jin, M Mumby, G Churchill, J Herz, and J A. Cooper
Peroxisome proliferator-activated receptor-gamma-deficient heterozygous mice develop an exacerbated neural antigen-induced Th1 response and experimental allergic encephalomyelitis., J J. Bright, C Natarajan, G Muthian, Y Barak, and R M. Evans
TCF and Groucho-related genes influence pituitary growth and development., M L. Brinkmeier, M A. Potok, K B. Cha, T Gridley, S Stifani, J Meeldijk, H Clevers, and S A. Camper
R/qtl: QTL mapping in experimental crosses., K W. Broman, H Wu, S Sen, and G A. Churchill
Osteoporosis., S A. Brown and C J. Rosen
A band 3-based macrocomplex of integral and peripheral proteins in the RBC membrane., L J. Bruce, R Beckmann, M L. Ribeiro, L L. Peters, J A. Chasis, J Delaunay, N Mohandas, D J. Anstee, and M J. Tanner
Genetic evidence that relative synaptic efficacy biases the outcome of synaptic competition., M Buffelli, R W. Burgess, G Feng, C G. Lobe, J W. Lichtman, and J R. Sanes
Mice and more., C J. Bult
Hidden projection properties of some nonregular fractional factorial designs and their applications., D A. Bulutoglu and C S. Cheng
Roles of NPM2 in chromatin and nucleolar organization in oocytes and embryos., K H. Burns, M M. Viveiros, Y Ren, P Wang, F J. DeMayo, D E. Frail, J J. Eppig, and M M. Matzuk
Continuous infusion of endostatin inhibits differentiation, mobilization, and clonogenic potential of endothelial cell progenitors., M Capillo, P Mancuso, A Gobbi, S Monestiroli, G Pruneri, C Dell'Agnola, G Martinelli, L Shultz, and F Bertolini
A rare complex DNA rearrangement in the murine Steel gene results in exon duplication and a lethal phenotype., S Chandra, R Kapur, N Chuzhanova, V Summey, D Prentice, J Barker, D N. Cooper, and D A. Williams
Overlapping deletions define novel embryonic lethal loci in the mouse t complex., H H. Chao, S E. Mentzer, J C. Schimenti, and Y You
The major histocompatibility complex-related Fc receptor for IgG (FcRn) binds albumin and prolongs its lifespan., C Chaudhury, S Mehnaz, J M. Robinson, W L. Hayton, D K. Pearl, D C. Roopenian, and C L. Anderson
PPARdelta is a very low-density lipoprotein sensor in macrophages., A Chawla, C H. Lee, Y Barak, W He, J Rosenfeld, D Liao, J Han, H Kang, and R M. Evans
Hematopoietic senescence is postponed and hematopoietic stem cell function is enhanced by dietary restriction., J Chen, C M. Astle, and D E. Harrison
Genotype-dependence of gabapentin and pregabalin sensitivity: the pharmacogenetic mediation of analgesia is specific to the type of pain being inhibited., E J. Chesler, J Ritchie, A Kokayeff, W R. Lariviere, S G. Wilson, and J S. Mogil
Genetic correlates of gene expression in recombinant inbred strains: a relational model system to explore neurobehavioral phenotypes., E J. Chesler, J Wang, L Lu, Y Qu, K F. Manly, and R W. Williams
The aging auditory system: anatomic and physiologic changes and implications for rehabilitation., T H. Chisolm, J F. Willott, and J J. Lister
Effect of age on susceptibility to azoxymethane-induced colonic aberrant crypt foci formation in C57BL/6JNIA mice., H Chung, D Wu, R Gay, S N. Han, B Goldin, R Bronson, J Mason, D E. Smith, and S N. Meydani
Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)., S L. Ciciotte, B Gwynn, K Moriyama, M Huizing, W A. Gahl, J S. Bonifacino, and L L. Peters
Statistical tests for differential expression in cDNA microarray experiments., X Cui and G A. Churchill
Transformations for cDNA microarray data., Xiangqin Cui, M Kathleen Kerr, and Gary Churchill
Ribosomal protein S19 expression during erythroid differentiation., Costa L. Da, G Narla, T N. Willig, L L. Peters, M Parra, J Fixler, G Tchernia, and N Mohandas
Astrocyte differentiation states and glioma formation., C Dai and E C. Holland
Jonah and his friends at The Jackson Laboratory, Karen Davis and Bob Gottlieb
Safety issues in cell-based intervention trials., L Dawson, House A. Bateman, Agnew D. Mueller, H Bok, D W. Brock, A Chakravarti, M Greene, P A. King, S J. O'Brien, D H. Sachs, K E. Schill, A Siegel, D Solter, S M. Suter, C M. Verfaillie, and L B. Walters
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis., L R. Donahue, B Chang, S Mohan, N Miyakoshi, J E. Wergedal, D J. Baylink, N L. Hawes, C J. Rosen, Bailey P. Ward, Q Y. Zheng, R T. Bronson, K R. Johnson, and M T. Davisson
High-resolution genetic map of X-linked juvenile-type granulosa cell tumor susceptibility genes in mouse., A M. Dorward, K L. Shultz, Bicknell C. Ackert, E M. Eicher, and W G. Beamer
An investigation of the predictors of bone mineral density and response to therapy with alendronate in osteoporotic men., W M. Drake, D L. Kendler, C J. Rosen, and E S. Orwoll
The ichq mutant mouse, a model for the human skin disorder harlequin ichthyosis: mapping, keratinocyte culture, and consideration of candidate genes involved in epidermal growth regulation., M Dunnwald, A R. Zuberi, K Stephens, R Le, J P. Sundberg, P Fleckman, and B A. Dale
Comment on " 'Stemness': transcriptional profiling of embryonic and adult stem cells" and "a stem cell molecular signature"., A V. Evsikov and D Solter
Public stem cell banks: considerations of justice in stem cell research and therapy., R R. Faden, L Dawson, House A. Bateman, D M. Agnew, H Bok, D W. Brock, A Chakravarti, X J. Gao, M Greene, J A. Hansen, P A. King, S J. O'Brien, A Siegel, D Solter, S M. Suter, C M. Verfaillie, L B. Walters, and J D. Gearhart
Glycerol regulates stratum corneum hydration in sebaceous gland deficient (asebia) mice., J W. Fluhr, Qiang M. Mao, B E. Brown, P W. Wertz, D Crumrine, J P. Sundberg, K R. Feingold, and P M. Elias
Development of an enhanced GFP-based dual-color reporter to facilitate genetic screens for the recovery of mutations in mice., A C. Frank, K A. Meyers, I C. Welsh, and T P. O'Brien
Fas-deficient C3.MRL-Tnfrsf6(lpr) mice and Fas ligand-deficient C3H/HeJ-Tnfsf6(gld) mice are relatively resistant to the induction of alopecia areata by grafting of alopecia areata-affected skin from C3H/HeJ mice., Paul P. Freyschmidt, K J. McElwee, V Botchkarev, S Kissling, E Wenzel, J P. Sundberg, R Happle, and R Hoffmann
CDS annotation in full-length cDNA sequence., M Furuno, T Kasukawa, R Saito, J Adachi, H Suzuki, R Baldarelli, Y Hayashizaki, and Y Okazaki
Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions., K Gardiner, A Fortna, L Bechtel, and M T. Davisson
Epigenesis versus preformation during mammalian development. Introduction., R L. Gardner, M A. Surani, and D Solter
Cyclin E ablation in the mouse., Y Geng, Q Yu, E Sicinska, M Das, J E. Schneider, S Bhattacharya, W M. Rideout, R T. Bronson, H Gardner, and P Sicinski
Variations in yeast 3'-processing cis-elements correlate with transcript stability., J H. Graber
Genetic models in applied physiology: selected contribution: effects of spaceflight on immunity in the C57BL/6 mouse. II. Activation, cytokines, erythrocytes, and platelets., D S. Gridley, G A. Nelson, L L. Peters, P J. Kostenuik, T A. Bateman, S Morony, L S. Stodieck, D L. Lacey, S J. Simske, and M J. Pecaut
Notch signaling and inherited disease syndromes., T Gridley
Synopsis: XVIIth Testis Workshop, "Functional Genomics of Male Reproduction"., M A. Handel and M P. Hardy
An immunodominant minor histocompatibility alloantigen that initiates corneal allograft rejection., Z Haskova, T J. Sproule, D C. Roopenian, and A B. Ksander
Distinct osteoclast precursors in the bone marrow and extramedullary organs characterized by responsiveness to Toll-like receptor ligands and TNF-alpha., S Hayashi, T Yamada, M Tsuneto, T Yamane, M Takahashi, L D. Shultz, and H Yamazaki
Mouse model of subretinal neovascularization with choroidal anastomosis., J R. Heckenlively, N L. Hawes, M Friedlander, S Nusinowitz, R Hurd, M Davisson, and B Chang
Muscle-specific Pparg deletion causes insulin resistance., A L. Hevener, W He, Y Barak, J Le, G Bandyopadhyay, P Olson, J Wilkes, R M. Evans, and J Olefsky
Adipose-specific peroxisome proliferator-activated receptor gamma knockout causes insulin resistance in fat and liver but not in muscle., W He, Y Barak, A Hevener, P Olson, D Liao, J Le, M Nelson, E Ong, J M. Olefsky, and R M. Evans
Intrinsic requirement for zinc finger transcription factor Gfi-1 in neutrophil differentiation., H Hock, M J. Hamblen, H M. Rooke, D Traver, R T. Bronson, S Cameron, and S H. Orkin
Mouse genetics as a tool for elucidating molecular pathways involved in hearing loss., A Ikeda, J K. Naggert, and P M. Nishina
Aberrant actin cytoskeleton leads to accelerated proliferation of corneal epithelial cells in mice deficient for destrin (actin depolymerizing factor)., S Ikeda, L A. Cunningham, D Boggess, C D. Hobson, J P. Sundberg, J K. Naggert, R S. Smith, and P M. Nishina
Towards understanding the function of the tubby gene family in the retina., S Ikeda, A Ikeda, J K. Naggert, and P M. Nishina
Delayed occurrence of fatal neoplastic diseases in ames dwarf mice: correlation to extended longevity., Y Ikeno, R T. Bronson, G B. Hubbard, S Lee, and A Bartke
Temporal expression of cell cycle-related proteins during spermatogenesis: establishing a timeline for onset of the meiotic divisions., A Inselman, S Eaker, and M A. Handel
Mouse parvovirus: survival of the fittest., R O. Jacoby and A L. Smith
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene., K R. Johnson, L H. Gagnon, L S. Webb, L L. Peters, N L. Hawes, B Chang, and Q Y. Zheng
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5., K R. Johnson, P W. Lane, S A. Cook, B S. Harris, Bailey P. Ward, R T. Bronson, B L. Lyons, L D. Shultz, and M T. Davisson
Subversion of the innate immune system by a retrovirus., B A. Jude, Y Pobezinskaya, J Bishop, S Parke, R M. Medzhitov, A V. Chervonsky, and T V. Golovkina
Sustained hepatic expression of FoxM1B in transgenic mice has minimal effects on hepatocellular carcinoma development but increases cell proliferation rates in preneoplastic and early neoplastic lesions., O A. Kalinina, S A. Kalinin, E W. Polack, I Mikaelian, S Panda, R H. Costa, and G R. Adami
Development and evaluation of an automated annotation pipeline and cDNA annotation system., T Kasukawa, M Furuno, I Nikaido, H Bono, D A. Hume, C Bult, D P. Hill, R Baldarelli, J Gough, A Kanapin, H Matsuda, L M. Schriml, Y Hayashizaki, and J Quackenbush
G protein-coupled receptor genes in the FANTOM2 database., Y Kawasawa, L M. McKenzie, D P. Hill, H Bono, and M Yanagisawa
Appearance of human plasma cells following differentiation of human B cells in NOD/SCID mouse spleen., K Kikuchi, Z X. Lian, X S. He, A A. Ansari, M Ishibashi, H Miyakawa, L D. Shultz, S Ikehara, and M E. Gershwin
New leptin receptor mutations in mice: Lepr(db-rtnd), Lepr(db-dmpg) and Lepr(db-rlpy)., J H. Kim, P N. Taylor, D Young, S Y. Karst, P M. Nishina, and J K. Naggert
Graft-versus-host disease can be separated from graft-versus-lymphoma effects by control of lymphocyte trafficking with FTY720., Y M. Kim, T Sachs, W Asavaroengchai, R Bronson, and M Sykes
Oxidative stress, cell cycle, and neurodegeneration., J A. Klein and S L. Ackerman
Desmoglein 4 in hair follicle differentiation and epidermal adhesion. Evidence from inherited hypotrichosis and acquired pemphigus vulgaris., A Kljuic, H Bazzi, J P. Sundberg, Mir A. Martinez, R O'Shaughnessy, M G. Mahoney, M Levy, X Montagutelli, W Ahmad, V M. Aita, S Fischer, T C. Gilliam, C A. Jahoda, R J. Morris, A A. Panteleyev, V T. Nguyen, and al et
Molecular control of the oocyte to embryo transition., B B. Knowles, A V. Evsikov, Vries W. de, A E. Peaston, and D Solter
Molecular control of the oocyte to embryo transition., B B. Knowles, A V. Evsikov, V r. de, A E. Peaston, and D Solter
Dp1 is required for extra-embryonic development., M J. Kohn, R T. Bronson, E Harlow, N J. Dyson, and L Yamasaki
Genetic effects for femoral biomechanics, structure, and density in C57BL/6J and C3H/HeJ inbred mouse strains., D L. Koller, J Schriefer, Q Sun, K L. Shultz, L R. Donahue, C J. Rosen, T Foroud, W G. Beamer, and C H. Turner
Mapping of rabbit microsatellite markers using chromosome-specific libraries., R Korstanje, G F. Gillissen, S A. Versteeg, Oost B. van, A A. Bosma, Gaillard C. Rogel, Zutphen L. van, and Lith H. van
Flow cytometric and immunoblot assays for cell surface ADP-ribosylation using a monoclonal antibody specific for ethenoadenosine., C Krebs, W Koestner, M Nissen, V Welge, I Parusel, F Malavasi, E H. Leiter, R M. Santella, F Haag, and Nolte F. Koch
Notch signaling regulates left-right asymmetry determination by inducing Nodal expression., L T. Krebs, N Iwai, S Nonaka, I C. Welsh, Y Lan, R Jiang, Y Saijoh, T P. O'Brien, H Hamada, and T Gridley
Characterization of Notch3-deficient mice: Normal embryonic development and absence of genetic interactions with a Notch1 mutation., L T. Krebs, Y Xue, C R. Norton, J P. Sundberg, P Beatus, U Lendahl, A Joutel, and T Gridley
Autoimmunity as the consequence of a spontaneous mutation in Rasgrp1., K Layer, G Lin, A Nencioni, W Hu, A Schmucker, A N. Antov, X Li, S Takamatsu, T Chevassut, N A. Dower, S L. Stang, D Beier, J Buhlmann, R T. Bronson, K B. Elkon, J C. Stone, Parijs L. Van, and B Lim
Novel secreted isoform of adhesion molecule ICAM-4: potential regulator of membrane-associated ICAM-4 interactions., G Lee, F A. Spring, S F. Parsons, T J. Mankelow, L L. Peters, M J. Koury, N Mohandas, D J. Anstee, and J A. Chasis
Novel anterior segment phenotypes resulting from forkhead gene alterations: evidence for cross-species conservation of function., O J. Lehmann, S Tuft, G Brice, R Smith, A Blixt, R Bell, B Johansson, T Jordan, R A. Hitchings, P T. Khaw, S W. John, and P Carlsson
Phenotypic heterogeneity in the stargazin allelic series., V A. Letts, M G. Kang, C L. Mahaffey, B Beyer, H Tenbrink, K P. Campbell, and W N. Frankel
Positional cloning and characterization of Mei1, a vertebrate-specific gene required for normal meiotic chromosome synapsis in mice., B J. Libby, L G. Reinholdt, and J C. Schimenti
Modification of ocular defects in mouse developmental glaucoma models by tyrosinase., R T. Libby, R S. Smith, O V. Savinova, A Zabaleta, J E. Martin, F J. Gonzalez, and S W. John
Identification of the beta cell antigen targeted by a prevalent population of pathogenic CD8+ T cells in autoimmune diabetes., S M. Lieberman, A M. Evans, B Han, T Takaki, Y Vinnitskaya, J A. Caldwell, D V. Serreze, J Shabanowitz, D F. Hunt, S G. Nathenson, P Santamaria, and T P. DiLorenzo
Mouse nomenclature and maintenance of genetically engineered mice., C C. Linder
Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome., D P. Liu, C Schmidt, T Billings, and M T. Davisson