Submissions from 2001
Experimental design for gene expression microarrays., M K. Kerr and G A. Churchill
Statistical design and the analysis of gene expression microarray data., M K. Kerr and G A. Churchill
Targeted Disruption of the Myocilin Gene (Myoc) Suggests that Human Glaucoma-Causing Mutations Are Gain of Function., B S. Kim, O V. Savinova, M V. Reedy, J Martin, Y Lun, L Gan, R S. Smith, S I. Tomarev, S W. John, and R L. Johnson
Genetic analysis of a new mouse model for non-insulin-dependent diabetes., J H. Kim, S Sen, C S. Avery, E Simpson, P Chandler, P M. Nishina, G A. Churchill, and J K. Naggert
Maximum life spans in mice are extended by wild strain alleles., S Klebanov, C M. Astle, T H. Roderick, K Flurkey, J R. Archer, J Chen, and D E. Harrison
Maximum life spans in mice are extended by wild strain alleles., S Klebanov, C M. Astle, T H. Roderick, K Flurkey, J R. Archer, J Chen, and D E. Harrison
p35 and p39 are essential for cyclin-dependent kinase 5 function during neurodevelopment., J Ko, S Humbert, R T. Bronson, S Takahashi, A B. Kulkarni, E Li, and L H. Tsai
Mapping of rabbit chromosome 1 markers generated from a microsatellite-enriched chromosome-specific library., R Korstanje, G F. Gillissen, Bieman M. den, S A. Versteeg, Oost B AU Fox van, Lith H. van, and Zutphen L. van
Mapping of microsatellite loci and association of aorta atherosclerosis with LG VI markers in the rabbit., R Korstanje, G F. Gillissen, L P. Kodde, Bieman M. Den, A Lankhorst, Zutphen L. Van, and Lith H. Van
Desmutagenic and bio-antimutagenic activity of docosahexaenoic acid and eicosapentaenoic acid in cultured Chinese hamster V79 cells., Y Kuroda, N Shima, K Yazawa, and K Kaji
Analysis of glomerulosclerosis and atherosclerosis in lecithin cholesterol acyltransferase-deficient mice., G Lambert, N Sakai, B L. Vaisman, E B. Neufeld, B Marteyn, C C. Chan, B Paigen, E Lupia, and al et
Chromosomal organization of candidate genes involved in cholesterol gallstone formation: a murine gallstone map., F Lammert, M C. Carey, and B Paigen
Transgenic studies of pain and analgesia: mutation or background genotype?, W R. Lariviere, E J. Chesler, and J S. Mogil
The NOD mouse: a model for insulin-dependent diabetes mellitus., E H. Leiter
The NOD mouse: a model for insulin-dependent diabetes mellitus., E H. Leiter
Transgenic mice for the preparation of puromycin-resistant primary embryonic fibroblast feeder layers for embryonic stem cell selection., E R. Linnell, C P. Lerner, K A. Johnson, C A. Leach, T R. Ulrich, W C. Rafferty, and E M. Simpson
Distinct roles of nerve and muscle in postsynaptic differentiation of the neuromuscular synapse., W Lin, R W. Burgess, B Dominguez, S L. Pfaff, J R. Sanes, and K F. Lee
Tyrosine phosphorylation of Grb2 by Bcr/Abl and epidermal growth factor receptor: a novel regulatory mechanism for tyrosine kinase signaling., S Li, A D. Couvillon, B B. Brasher, and Etten R. Van
Interleukin 3 and granulocyte-macrophage colony-stimulating factor are not required for induction of chronic myeloid leukemia-like myeloproliferative disease in mice by BCR/ABL., S Li, S Gillessen, M H. Tomasson, G Dranoff, D G. Gilliland, and E t. Van
Transcriptional repression and developmental functions of the atypical vertebrate GATA protein TRPS1., T H. Malik, S A. Shoichet, P Latham, T G. Kroll, L L. Peters, and R A. Shivdasani
Unusual resistance of ALR/Lt mouse beta cells to autoimmune destruction: role for beta cell-expressed resistance determinants., C E. Mathews, R T. Graser, A Savinov, D V. Serreze, and E H. Leiter
A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis., S Mazeyrat, N Saut, V Grigoriev, S K. Mahadevaiah, O A. Ojarikre, A Rattigan, C Bishop, E M. Eicher, M J. Mitchell, and P S. Burgoyne
Defects in development of the kidney, heart and eye vasculature in mice homozygous for a hypomorphic Notch2 mutation., B McCright, X Gao, L Shen, J Lozier, Y Lan, M Maguire, D Herzlinger, G Weinmaster, R Jiang, and T Gridley
Requirement for the murine zinc finger protein ZFR in perigastrulation growth and survival., M J. Meagher and R E. Braun
The nude mouse skin phenotype: the role of Foxn1 in hair follicle development and cycling., L Mecklenburg, M Nakamura, J P. Sundberg, and R Paus
Distinguishing self from nonself: immunogenicity of the murine H47 locus is determined by a single amino acid substitution in an unusual peptide., L M. Mendoza, G Villaflor, P Eden, D Roopenian, and N Shastri
Insulin-like growth factor binding proteins in femoral and vertebral bone marrow stromal cells: expression and regulation by thyroid hormone and dexamethasone., M Milne, J M. Quail, C J. Rosen, and D T. Baran
Combined histologic and molecular features reveal previously unappreciated subsets of lymphoma in AKXD recombinant inbred mice., H C. Morse, C F. Qi, M Hori, Heath L. Taddesse, K Ozato, B A. Taylor, J M. Ward, N A. Jenkins, N G. Copeland, and T N. Fredrickson
Expression of Pcdh15 in the inner ear, nervous system and various epithelia of the developing embryo., C L. Murcia and R P. Woychik
Sequence interpretation. Functional annotation of mouse genome sequences., J H. Nadeau, R Balling, G Carlson, N Copeland, J Eppig, W N. Frankel, D Goldowitz, J Schimenti, and al et
Mouse models for the Wolf-Hirschhorn deletion syndrome., D Naf, L A. Wilson, R A. Bergstrom, R S. Smith, N C. Goodwin, A Verkerk, Ommen G. van, S L. Ackerman, W N. Frankel, and J C. Schimenti
Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4., J M. Newton, Barak O. Cohen, N Hagiwara, J M. Gardner, M T. Davisson, R A. King, and M H. Brilliant
Classification, clinical manifestations, and immunopathological mechanisms of the epithelial variant of paraneoplastic autoimmune multiorgan syndrome: a reappraisal of paraneoplastic pemphigus., V T. Nguyen, A Ndoye, K D. Bassler, L D. Shultz, M C. Shields, B S. Ruben, R J. Webber, M R. Pittelkow, P J. Lynch, and S A. Grando
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)., D Y. Nishimura, C C. Searby, N B. Haider, E Heon, A Iannaccone, D Bonneau, L G. Biesecker, S G. Jacobson, E M. Stone, and al et
A null mutation in inositol polyphosphate 4-phosphatase type I causes selective neuronal loss in weeble mutant mice., A Nystuen, M E. Legare, L D. Shultz, and W N. Frankel
Lutheran blood group glycoprotein and its newly characterized mouse homologue specifically bind alpha5 chain-containing human laminin with high affinity., S F. Parsons, G Lee, F A. Spring, T N. Willig, L L. Peters, J A. Gimm, M J. Tanner, N Mohandas, D J. Anstee, and J A. Chasis
Absence of germline infection in male mice following intraventricular injection of adenovirus., A H. Peters, J Drumm, C Ferrell, D A. Roth, D M. Roth, M McCaman, P L. Novak, J Friedman, R Engler, and R E. Braun
Unique design for fixed ventilated changing station., T Peterson and J Farley
Experimental and computational approaches yield a high-resolution, 1-Mb physical map of the region harboring the mouse t haplotype sterility factor, tcs1., A Planchart and J C. Schimenti
Fine mapping of Ath6, a quantitative trait locus for atherosclerosis in mice., M K. Purcell, J L. Mu, D C. Higgins, R Elango, H Whitmore, S Harris, and B Paigen
The impact of reduced frequency of cage changes on the health of mice housed in ventilated cages., Whitaker C. Reeb, B Paigen, W G. Beamer, R T. Bronson, G A. Churchill, I B. Schweitzer, and D D. Myers
The Mouse Gene Expression Database (GXD)., M Ringwald, J T. Eppig, D A. Begley, J P. Corradi, I J. McCright, T F. Hayamizu, D P. Hill, J A. Kadin, and J E. Richardson
Molecular and functional mapping of the piebald deletion complex on mouse chromosome 14., J J. Roix, Greenberg A. Hagge, D M. Bissonnette, S Rodick, L B. Russell, and T P. O'Brien
Defining the genetics of osteoporosis: using the mouse to understand man., C J. Rosen, W G. Beamer, and L R. Donahue
Clinical review 123: Anabolic therapy for osteoporosis., C J. Rosen and J P. Bilezikian
Emerging anabolic treatments for osteoporosis., C J. Rosen and P J. Rackoff
Relatively normal human lymphopoiesis but rapid turnover of newly formed B cells in transplanted nonobese diabetic/SCID mice., M I. Rossi, K L. Medina, K Garrett, G Kolar, P C. Comp, L D. Shultz, J D. Capra, P Wilson, A Schipul, and P W. Kincade
Cardiac conduction abnormalities in a mouse model of Lyme borreliosis., S Saba, B A. VanderBrink, G Perides, L J. Glickstein, M S. Link, M K. Homoud, R T. Bronson, M Estes, and P J. Wang
Intraocular pressure in genetically distinct mice: an update and strain survey., O V. Savinova, F Sugiyama, J E. Martin, S I. Tomarev, B J. Paigen, R S. Smith, and S W. John
Monoallelic gene expression in mice: who? When? How? Why?, J Schimenti
Genome partitioning and whole-genome analysis., N J. Schork
The future of genetic case-control studies., N J. Schork, D Fallin, B Thiel, X Xu, U Broeckel, H J. Jacob, and D Cohen
Use of coisogenic host blastocysts for efficient establishment of germline chimeras with C57BL/6J ES cell lines., Gossler K. Schuster, A W. Lee, C P. Lerner, H J. Parker, V W. Dyer, V E. Scott, A Gossler, and J C. Conover
A statistical framework for quantitative trait mapping., S Sen and G A. Churchill
Th1 to Th2 cytokine shifts in nonobese diabetic mice: sometimes an outcome, rather than the cause, of diabetes resistance elicited by immunostimulation., D V. Serreze, H D. Chapman, C M. Post, E A. Johnson, Pinzon W. Suarez, and A Rabinovitch
Autoreactive diabetogenic T-cells in NOD mice can efficiently expand from a greatly reduced precursor pool., D V. Serreze, E A. Johnson, H D. Chapman, R T. Graser, M P. Marron, T P. DiLorenzo, P Silveira, Y Yoshimura, S G. Nathenson, and S Joyce
Genes and cellular requirements for autoimmune diabetes susceptibility in nonobese diabetic mice., D V. Serreze and E H. Leiter
Genetically engineered mice. Husbandry and resources., J J. Sharp, C C. Linder, and L E. Mobraaten
Genome-wide epistatic interaction analysis reveals complex genetic determinants of circadian behavior in mice., K Shimomura, Zeddies S. Low, D P. King, T D. Steeves, A Whiteley, J Kushla, P D. Zemenides, A Lin, M H. Vitaterna, G A. Churchill, and J S. Takahashi
The mouse anterior chamber angle and trabecular meshwork develop without cell death., R S. Smith, A Zabaleta, O V. Savinova, and S W. John
N-WASP deficiency reveals distinct pathways for cell surface projections and microbial actin-based motility., S B. Snapper, F Takeshima, I Anton, C H. Liu, S M. Thomas, D Nguyen, D Dudley, H Fraser, D Purich, Ilasaca M. Lopez, C Klein, L Davidson, R Bronson, R C. Mulligan, F Southwick, R Geha, M B. Goldberg, F S. Rosen, J H. Hartwig, and F W. Alt
Phenotypic variations of orpk mutation and chromosomal localization of modifiers influencing kidney phenotype., C Sommardahl, M Cottrell, J E. Wilkinson, R P. Woychik, and D K. Johnson
Nonablative neonatal marrow transplantation attenuates functional and physical defects of beta-glucuronidase deficiency., B W. Soper, M D. Lessard, C A. Vogler, B Levy, W G. Beamer, W S. Sly, and J E. Barker
Interleukin-4 receptor-Stat6 signaling in murine infections with a tissue-dwelling nematode parasite., L Spencer, L Shultz, and T V. Rajan
Naturally variant autosomal and sex-linked loci determine the severity of iron overload in beta 2-microglobulin-deficient mice., T J. Sproule, E C. Jazwinska, R S. Britton, B R. Bacon, R E. Fleming, W S. Sly, and D C. Roopenian
Oxidative stress in aging in the C57B16/J mouse cochlea., H Staecker, Q Y. Zheng, and de water Van
Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein-methyltransferase superfamily., Perkins G. Steele, W Fang, X H. Yang, Gele M. Van, T Carling, J Gu, I M. Buyse, J A. Fletcher, J Liu, R Bronson, R B. Chadwick, la Chapelle de, X Zhang, F Speleman, and S Huang
A genomic-systems biology map for cardiovascular function., M Stoll, A W. Cowley, P J. Tonellato, A S. Greene, M L. Kaldunski, R J. Roman, P Dumas, N J. Schork, Z Wang, and H J. Jacob
Concordance of murine quantitative trait loci for salt-induced hypertension with rat and human loci., F Sugiyama, G A. Churchill, D C. Higgins, C Johns, K P. Makaritsis, H Gavras, and B Paigen
Mouse models of blood pressure regulation and hypertension., F Sugiyama, K i. Yagami, and B Paigen
Morphology of hair in normal and mutant laboratory mice., J P. Sundberg and L E. King
Animal models for male pattern (androgenetic) alopecia., J P. Sundberg, L E. King, and C Bascom
Comparison of permeating and nonpermeating cryoprotectants for mouse sperm cryopreservation., J M. Sztein, K Noble, J S. Farley, and L E. Mobraaten
Increased Expression of mXBP-1 (TREB-5) in Thymic B Cells in New Zealand Mice., N Taguchi, A Ansari, T Hsu, Y Hashimoto, K Dorshkind, L Shultz, M Naiki, and M E. Gershwin
B Cells are Selectively Associated with Thymic Cortical but not Medullary Pathology in NZB Mice., N Taguchi, Y Hashimoto, T Hsu, A A. Ansari, L Shultz, K Dorshkind, S Ikehara, M Naiki, and M E. Gershwin
Motoneuron survival is enhanced in the absence of neuromuscular junction formation in embryos., J Terrado, R W. Burgess, T DeChiara, G Yancopoulos, J R. Sanes, and A C. Kato
A glutamic acid decarboxylase 65-specific Th2 cell clone immunoregulates autoimmune diabetes in nonobese diabetic mice., R Tisch, B Wang, M A. Atkinson, D V. Serreze, and R Friedline
Antigen-specific mediated suppression of beta cell autoimmunity by plasmid DNA vaccination., R Tisch, B Wang, D J. Weaver, B Liu, T Bui, J Arthos, and D V. Serreze
Induction of myeloproliferative disease in mice by tyrosine kinase fusion oncogenes does not require granulocyte-macrophage colony-stimulating factor or interleukin-3., M H. Tomasson, I R. Williams, S Li, J Kutok, D Cain, S Gillessen, G Dranoff, E t. Van, and D G. Gilliland
A new spectrin, beta IV, has a major truncated isoform that associates with promyelocytic leukemia protein nuclear bodies and the nuclear matrix., W T. Tse, J Tang, O Jin, C Korsgren, K M. John, A L. Kung, B Gwynn, L L. Peters, and S E. Lux
Phenotypic characterization of Lith genes that determine susceptibility to cholesterol cholelithiasis in inbred mice: soluble pronucleating proteins in gallbladder and hepatic biles., Erpecum K. van, D Q. Wang, F Lammert, B Paigen, A K. Groen, and M C. Carey
Evidence that protein kinase C (PKC) participates in the meiosis I to meiosis II transition in mouse oocytes., M M. Viveiros, Y Hirao, and J J. Eppig
Murine mucopolysaccharidosis VIL: impact of therapies on the phenotype, clinical course, and pathology in a model of a lysosomal storage disease., C Vogler, J Barker, M S. Sands, B Levy, N Galvin, and W S. Sly
A novel model of murine mucopolysaccharidosis type VII due to an intracisternal a particle element transposition into the beta-glucuronidase gene: clinical and pathologic findings., C Vogler, B Levy, N Galvin, M S. Sands, E H. Birkenmeier, W S. Sly, and J Barker
Apoptosis in ultrasound-produced threshold lesions in the rabbit brain., N Vykhodtseva, N McDannold, H Martin, R T. Bronson, and K Hynynen
Reduced incidence of thrombosis in mice with hereditary spherocytosis following neonatal treatment with normal hematopoietic cells., N J. Wandersee, J C. Lee, S A. Deveau, and J E. Barker
Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis., N J. Wandersee, A N. Roesch, N R. Hamblen, Moes J. de, derValk M. van, R T. Bronson, J A. Gimm, N Mohandas, P Demant, and J E. Barker
Characterization of Corn1 mice: Alteration of epithelial and stromal cell gene expression., I Wang, C W. Kao, C Liu, S Saika, P M. Nishina, J P. Sundberg, R S. Smith, and W W. Kao
Role of protein synthesis in the development of a transcriptionally permissive state in one-cell stage mouse embryos., Q Wang, Y G. Chung, W N. deVries, M Struwe, and K E. Latham
C57BL/6J-T-Associated Sex Reversal in Mice Is Caused by Reduced Expression of a Mus domesticus Sry Allele., L L. Washburn, K H. Albrecht, and E M. Eicher
Gsh2 and Pax6 play complementary roles in dorsoventral patterning of the mammalian telencephalon., K Yun, S Potter, and J L. Rubenstein
Scd3--a novel gene of the stearoyl-CoA desaturase family with restricted expression in skin., Y Zheng, S M. Prouty, A Harmon, J P. Sundberg, K S. Stenn, and S Parimoo
A highly conserved sequence essential for translational repression of the protamine 1 messenger rna in murine spermatids., J Zhong, A H. Peters, K Kafer, and R E. Braun
Cytotoxicity of anti-cd64-ricin a chain immunotoxin against human acute myeloid leukemia cells in vitro and in scid mice., R K. Zhong, de Winkel van, T Thepen, L D. Schultz, and E D. Ball
Submissions from 2000
A sequence-specific RNA binding complex expressed in murine germ cells contains MSY2 and MSY4.
Minor Histocompatibility Antigens: From the Laboratory to the Clinic.
In vivo kinetics of murine hemopoietic stem cells., J L. Abkowitz, D Golinelli, D E. Harrison, and P Guttorp
Analysing mouse chromosomal rearrangements with G-banded chromosomes., E C. Akeson and M T. Davisson
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse., N B. Akhmedov, N I. Piriev, B Chang, A L. Rapoport, N L. Hawes, P M. Nishina, S Nusinowitz, J R. Heckenlively, T H. Roderick, C A. Kozak, M Danciger, M T. Davisson, and D B. Farber
Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer., K N. Alagramam, Reeves J. Zahorsky, C G. Wright, K S. Pawlowski, L C. Erway, L Stubbs, and R P. Woychik