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Submissions from 2000

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Defective mesonephric cell migration is associated with abnormal testis cord development in C57BL/6J XY(Mus domesticus) mice., K H. Albrecht, B Capel, L L. Washburn, and E M. Eicher

It's a knockout!, A V. Anagnostopoulos

Gene ontology: tool for the unification of biology. The Gene Ontology Consortium., M Ashburner, C A. Ball, J A. Blake, D Botstein, A P. Davis, J T. Eppig, M A. Harris, D P. Hill, J E. Richardson, M Ringwald, and al Et

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Role of gamma interferon and interleukin-4 in host defense against the human filarial parasite Brugia malayi., S Babu, L M. Ganley, T R. Klei, L D. Shultz, and T V. Rajan

Sizing up the set of H genes in mice., D W. Bailey

Heterogeneity of Porphyromonas gingivalis strains in the induction of alveolar bone loss in mice., P J. Baker, M Dixon, R T. Evans, and D C. Roopenian

Genetic control of susceptibility to porphyromonas gingivalis-induced alveolar bone loss in mice [In Process Citation], P J. Baker, M Dixon, and D C. Roopenian

Adhesion molecule deficiencies increase Porphyromonas gingivalis-induced alveolar bone loss in mice., P J. Baker, L DuFour, M Dixon, and D C. Roopenian

Effect of ex vivo cytokine treatment on human cord blood engraftment in NOD-scid mice., K Ballen, P S. Becker, D Greiner, H Valinski, D Shearin, V Berrios, G Dooner, C C. Hsieh, J Wuu, L Shultz, J Cerny, J Leif, F M. Stewart, and P Quesenberry

Amelioration of severe hereditary spherocytosis in nonablated adult mice by marrow transplantation., J E. Barker, S Deveau, and N J. Wandersee

Insulin-like growth factor I and bone: from mouse to man., W G. Beamer, L R. Donahue, and C J. Rosen

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Spontaneous fracture (sfx): a mouse genetic model of defective peripubertal bone formation., W G. Beamer, C J. Rosen, R T. Bronson, W Gu, L R. Donahue, D J. Baylink, C C. Richardson, G C. Crawford, and J E. Barker

Distinct regulatory elements direct delta1 expression in the nervous system and paraxial mesoderm of transgenic mice [In Process Citation], J Beckers, A Caron, d e. Hrabe, S Hans, Ortega J. Campos, and A Gossler

The mouse rib-vertebrae mutation disrupts anterior-posterior somite patterning and genetically interacts with a delta1 null allele [In Process Citation], J Beckers, N Schlautmann, and A Gossler

Genealogies of mouse inbred strains., J A. Beck, S Lloyd, M Hafezparast, Pierce M. Lennon, J T. Eppig, M F. Festing, and E M. Fisher

Related function of mouse SOX3, SOX9, and SRY HMG domains assayed by male sex determination., D E. Bergstrom, M Young, K H. Albrecht, and E M. Eicher

HER-2/neu and p53 expression versus tamoxifen resistance in estrogen receptor-positive, node-positive breast cancer., D A Berry, H B Muss, A D Thor, L Dressler, Edison T. Liu, G Broadwater, D R Budman, I C Henderson, M Barcos, D Hayes, and L Norton

Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X chromosome short arm with respect to evolutionary breakpoints on the mouse X chromosome., H J. Blair, V Reed, E Gormally, J B. Wilson, J Novak, R R. McInnes, S J. Phillips, B A. Taylor, and Y Boyd

The Mouse Genome Database (MGD): expanding genetic and genomic resources for the laboratory mouse. The Mouse Genome Database Group., J A. Blake, J T. Eppig, J E. Richardson, and M T. Davisson

Post-transcriptional control and male infertility., R E. Braun

Temporal control of protein synthesis during spermatogenesis., R E. Braun

Heritable susceptibility for colitis in mice induced by IL-10 deficiency., I J. Bristol, M A. Farmer, Y Cong, X X. Zheng, T B. Strom, C O. Elson, J P. Sundberg, and E H. Leiter

How to study pathologic phenotypes of knockout mice., R T. Bronson

The adhesion signaling molecule p190 RhoGAP is required for morphogenetic processes in neural development., M R. Brouns, S F. Matheson, K Q. Hu, I Delalle, V S. Caviness, J Silver, R T. Bronson, and J Settleman

Neurotrophin expression by spinal motoneurons in adult and developing rats., C R. Buck, K L. Seburn, and T C. Cope

Mouse tumor biology database (MTB): enhancements and current status., C J. Bult, D M. Krupke, J P. Sundberg, and J T. Eppig

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Agrin isoforms with distinct amino termini: differential expression, localization, and function., R W. Burgess, W C. Skarnes, and J R. Sanes

Pathogenesis of cholesterol gallstone disease: role of the liver., M C. Carey and B Paigen

Mice mutant for Egfr and Shp2 have defective cardiac semilunar valvulogenesis., B Chen, R T. Bronson, L D. Klaman, T G. Hampton, J F. Wang, P J. Green, T Magnuson, P S. Douglas, J P. Morgan, and B G. Neel

Characterization of a hematopoietic stem cell with engraftment advantage, J Chen, C M. Astle, and D E. Harrison

Genetic regulation of primitive hematopoietic stem cell senescence., J Chen, C M. Astle, and D E. Harrison

Primitive hematopoietic stem cell function in vivo is uniquely high in the CXB-12 mouse strain., J Chen, C M. Astle, Sieburg C. Muller, and D E. Harrison

Toward the yeastification of mouse genetics: chemical mutagenesis of embryonic stem cells., Y Chen, J Schimenti, and T Magnuson

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Genotype-based screen for ENU-induced mutations in mouse embryonic stem cells., Y Chen, D Yee, K Dains, A Chatterjee, J Cavalcoli, E Schneider, J Om, R P. Woychik, and T Magnuson

The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals., R Chrast, H S. Scott, M P. Papasavvas, C Rossier, E S. Antonarakis, C Barras, M T. Davisson, C Schmidt, X Estivill, M Dierssen, M Pritchard, and S E. Antonarakis

Persistent hyperplastic tunica vasculosa lentis and persistent hyperplastic primary vitreous in transgenic line TgN3261Rpw., C M. Colitz, D E. Malarkey, R P. Woychik, and J E. Wilkinson

Disruption of Eph/ephrin signaling affects migration and proliferation in the adult subventricular zone, J C. Conover, F Doetsch, Verdugo J. Garcia, N W. Gale, G D. Yancopoulos, and Buylla A. Alvarez

Genetically defined risk of salt sensitivity in an intercross of Brown Norway and Dahl S rats., A W. Cowley, M Stoll, A S. Greene, M L. Kaldunski, P J. Tonellato, N J. Schork, P Dumas, and H J. Jacob

The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development [In Process Citation], G A. Cox, C L. Mahaffey, A Nystuen, V A. Letts, and W N. Frankel

Cryopreservation of murine spermatozoa., J K. Critser and L E. Mobraaten

A sequence-specific RNA binding complex expressed in murine germ cells contains MSY2 and MSY4., H G. Davies, F Giorgini, M A. Fajardo, and R E. Braun

Grey intense: a new mouse mutation affecting pigmentation., M T. Davisson, K R. Johnson, R T. Bronson, Bailey P. Ward, S A. Cook, B S. Harris, and L R. Donahue

Repositories of mouse mutations and inbred, congenic, and recombinant inbred strains., M T. Davisson and J J. Sharp

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Male contraception: views to the 21st century, Bethesda, MD, USA, 9-10 September 1999., L V. DePaolo, B T. Hinton, and R E. Braun

Expression of Cre recombinase in mouse oocytes: a means to study maternal effect genes., Vries W. de, L T. Binns, K S. Fancher, J Dean, R Moore, R Kemler, and B B. Knowles

Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitro., G J. Dooner, J E. Barker, P G. Gallagher, M E. Debatis, A H. Brown, B G. Forget, and P S. Becker

Quantitative trait locus mapping of genes regulating pulmonary PKC activity and PKC-alpha content., Nield L. Dwyer, B Paigen, S E. Porter, and A M. Malkinson

The C3H/HeJBir mouse model: a high susceptibility phenotype for colitis., C O. Elson, Y Cong, and J Sundberg

Development of mouse and rat oocytes in chimeric reaggregated ovaries after interspecific exchange of somatic and germ cell components [In Process Citation], J J. Eppig and K Wigglesworth

Metaphase I arrest and spontaneous parthenogenetic activation of strain LTXBO oocytes: chimeric reaggregated ovaries establish primary lesion in oocytes., J J. Eppig, K Wigglesworth, and Y Hirao

Algorithms for mutant sorting: the need for phenotype vocabularies., J T. Eppig

Electronic tools for accessing the mouse genome., J T. Eppig

The mouse genome database: a resource for today and tomorrow., J T. Eppig, J A. Blake, M T. Davisson, J A. Kadin, and J E. Richardson

Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data [In Process Citation], D Fallin and N J. Schork

Branchial cysts in laboratory mice [In Process Citation], M P. France, J P. Sundberg, and G Martinic

Mouse mutagenesis is 'in'. Sharing experience and resources in large-scale functional genomics: mutagenesis of the mouse genome, Georgia Genetics Symposium II, Athens, Georgia, 6-9 September 2000., W N. Frankel

Treatment with an anti-CD44v10-specific antibody inhibits the onset of alopecia areata in C3H/HeJ mice [In Process Citation], Paul P. Freyschmidt, S Seiter, M Zoller, A Konig, A Ziegler, J P. Sundberg, R Happle, and R Hoffmann

Hypoglycaemia, liver necrosis and perinatal death in mice lacking all isoforms of phosphoinositide 3-kinase p85 alpha., D A. Fruman, Jarvis F. Mauvais, D A. Pollard, C M. Yballe, D Brazil, R T. Bronson, C R. Kahn, and L C. Cantley

Mouse FcgammaRI: identification and functional characterization of five new alleles., A L. Gavin, E H. Leiter, and P M. Hogarth

Granule cells and cerebellar boundaries: analysis of Unc5h3 mutant chimeras., D Goldowitz, K M. Hamre, S A. Przyborski, and S L. Ackerman

A novel mechanism of resistance to mouse mammary tumor virus infection., T V. Golovkina

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Identification of a CD8 T cell that can independently mediate autoimmune diabetes development in the complete absence of CD4 T cell helper functions., R T. Graser, T P. DiLorenzo, F Wang, G J. Christianson, H D. Chapman, D C. Roopenian, S G. Nathenson, and D V. Serreze

Bisphosphonates: safety and efficacy in the treatment and prevention of osteoporosis., S L. Greenspan, S T. Harris, H Bone, P D. Miller, E S. Orwoll, N B. Watts, and C J. Rosen

Quantitative trait loci modulate renal cystic disease severity in the mouse bpk model [In Process Citation], Woodford L. Guay, C J. Wright, G Walz, and G A. Churchill

Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism., B Gwynn, S L. Ciciotte, S J. Hunter, L L. Washburn, R S. Smith, S G. Andersen, R T. Swank, E C. Dell'Angelica, J S. Bonifacino, E M. Eicher, and L L. Peters

Genomic, transcriptional and mutational analysis of the mouse microphthalmia locus [In Process Citation], J H. Hallsson, J Favor, C Hodgkinson, T Glaser, M L. Lamoreux, R Magnusdottir, G J. Gunnarsson, H O. Sweet, N G. Copeland, N A. Jenkins, and E Steingrimsson

NZB mice exhibit a primary T cell defect in fetal thymic organ culture., Y Hashimoto, K Dorshkind, Rodriguez E. Montecino, N Taguchi, L Shultz, and M E. Gershwin

GFP-tagged expression and immunohistochemical studies to determine the subcellular localization of the tubby gene family members [In Process Citation], W He, S Ikeda, R T. Bronson, G Yan, P M. Nishina, M A. North, and J K. Naggert

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Combined activation of Ras and Akt in neural progenitors induces glioblastoma formation in mice., E C. Holland, J Celestino, C Dai, L Schaefer, R E. Sawaya, and G N. Fuller

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Astrocytes give rise to oligodendrogliomas and astrocytomas after gene transfer of polyoma virus middle T antigen in vivo., E C. Holland, Y Li, J Celestino, C Dai, L Schaefer, R A. Sawaya, and G N. Fuller

Genetics of mouse mammary tumor virus-induced mammary tumors: linkage of tumor induction to the gag gene., L M. Hook, Y Agafonova, S R. Ross, S J. Turner, and T V. Golovkina

Effects of the non-pseudoautosomal region of the Y-chromosome on behavior in female offspring of two congenic strains of mice., B J. Hoplight, L Mobraaten, G F. Sherman, L A. Hyde, S Harding, and V H. Denenberg

Vascular effects following homozygous disruption of p47(phox) : An essential component of NADPH oxidase., E Hsich, B H. Segal, P J. Pagano, F E. Rey, B Paigen, J Deleonardis, R F. Hoyt, S M. Holland, and T Finkel

E2F4 is essential for normal erythrocyte maturation and neonatal viability., P O. Humbert, C Rogers, S Ganiatsas, R L. Landsberg, J M. Trimarchi, S Dandapani, C Brugnara, S Erdman, M Schrenzel, R T. Bronson, and J A. Lees

Mouse chromosome 15., K Huppi, B Spear, D Siwarski, and V Letts

Modulation of transforming growth factor beta1 gene expression in the mammary gland by insulin-like growth factor I and octreotide., H Huynh, W Beamer, M Pollak, and T W. Chan

Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene., S Ikeda, N Shiva, A Ikeda, R S. Smith, S Nusinowitz, G Yan, T R. Lin, S Chu, J R. Heckenlively, M A. North, J K. Naggert, P M. Nishina, and M P. Duyao

A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice., K R. Johnson, Q Y. Zheng, and L C. Erway

Notch signalling is required for cyclic expression of the hairy-like gene HES1 in the presomitic mesoderm., C Jouve, I Palmeirim, D Henrique, J Beckers, A Gossler, Horowicz D. Ish, and O Pourquie

Comparison of recombinant growth differentiation factor-9 and oocyte regulation of KIT ligand messenger ribonucleic acid expression in mouse ovarian follicles., I M. Joyce, A T. Clark, F L. Pendola, and J J. Eppig

Metalloprotease-mediated shedding of enzymatically active mouse ecto-ADP-ribosyltransferase ART2.2 upon T cell activation [In Process Citation], S Kahl, M Nissen, R Girisch, T Duffy, E H. Leiter, F Haag, and Nolte F. Koch

Analysis of variance for gene expression microarray data., M K. Kerr, M Martin, and G A. Churchill

Development of spontaneous arthritis in beta2-microglobulin-deficient mice without expression of HLA-B27: association with deficiency of endogenous major histocompatibility complex class I expression [In Process Citation], D J. Kingsbury, J P. Mear, D P. Witte, J D. Taurog, D C. Roopenian, and R A. Colbert

Heritability of life span in mice and its implication for direct and indirect selection for longevity., S Klebanov, K Flurkey, T H. Roderick, J R. Archer, M C. Astle, J Chen, and D E. Harrison

beta2 microglobulin-deficient (B2m(null)) NOD/SCID mice are excellent recipients for studying human stem cell function., O Kollet, A Peled, T Byk, Hur H. Ben, D Greiner, L Shultz, and T Lapidot

Large-scale cDNA analysis reveals phased gene expression patterns during preimplantation mouse development [In Process Citation], M S. Ko, J R. Kitchen, X T. Wang, X H. Wang, T Sun, M J. Grahovac, G E. DePalma, R Sharara, L B. Rowe, J Eppig, and al Et

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Notch signaling is essential for vascular morphogenesis in mice., L T Krebs, Y Xue, C R Norton, J R Shutter, M Maguire, J P Sundberg, D Gallahan, V Closson, J Kitajewski, R Callahan, G H Smith, K L Stark, and T Gridley

Gene dose-dependent control of hematopoiesis and hematologic tumor suppression by CBP., A L. Kung, V I. Rebel, R T. Bronson, L E. Ch'ng, C A. Sieff, D M. Livingston, and T P. Yao

TNF-alpha induces osteoclastogenesis by direct stimulation of macrophages exposed to permissive levels of RANK ligand., J Lam, S Takeshita, J E. Barker, O Kanagawa, F P. Ross, and S L. Teitelbaum

Peaks and troughs in linkage mapping for the rheumatic diseases [editorial], J S. Lanchbury and N J. Schork

A major effect QTL determined by multiple genes in epileptic EL mice [In Process Citation], M E. Legare, F S. Bartlett, and W N. Frankel

Multiple seizure susceptibility genes on chromosome 7 in SWXL-4 congenic mouse strains., M E. Legare and W N. Frankel

The insulin gene VNTR is associated with fasting insulin levels and development of juvenile obesity., Stunff C. Le, D Fallin, N J. Schork, and P Bougneres

A common promoter variant of the leptin gene is associated with changes in the relationship between serum leptin and fat mass in obese girls., Stunff C. Le, Bihan C. Le, N J. Schork, and P Bougneres

A new spontaneous mouse mutation in the kcne1 gene [In Process Citation], V A. Letts, A Valenzuela, C Dunbar, Q Y. Zheng, K R. Johnson, and W N. Frankel

Hereditary spherocytosis in zebrafish riesling illustrates evolution of erythroid beta-spectrin structure, and function in red cell morphogenesis and membrane stability., E C. Liao, B H. Paw, L L. Peters, A Zapata, S J. Pratt, C P. Do, G Lieschke, and L I. Zon

Gastric hyperplasia in mice lacking the putative Cdc42 effector IQGAP1., S Li, Q Wang, A Chakladar, R T. Bronson, and A Bernards

Effects of physiological versus pharmacological beta-carotene supplementation on cell proliferation and histopathological changes in the lungs of cigarette smoke-exposed ferrets., C Liu, X D. Wang, R T. Bronson, D E. Smith, N I. Krinsky, and R M. Russell

Linkage mapping in populations with karyotypic rearrangements., K D. Livingstone, G Churchill, and M K. Jahn

Mutations in the WRN gene in mice accelerate mortality in a p53-null background., D B. Lombard, C Beard, B Johnson, R A. Marciniak, J Dausman, R Bronson, J E. Buhlmann, R Lipman, R Curry, A Sharpe, R Jaenisch, and L Guarente