Submissions from 2003
Effects of pressure overload on extracellular matrix expression in the heart of the atrial natriuretic peptide-null mouse., D Wang, S Oparil, J A. Feng, P Li, G Perry, L B. Chen, M Dai, S W. John, and Y F. Chen
Using advanced intercross lines for high-resolution mapping of HDL cholesterol quantitative trait loci., X Wang, Roy I. Le, E Nicodeme, R Li, R Wagner, C Petros, G A. Churchill, S Harris, A Darvasi, J Kirilovsky, P L. Roubertoux, and B Paigen
Mice with targeted mutation of peroxiredoxin 6 develop normally but are susceptible to oxidative stress., X Wang, S A. Phelan, Semb K. Forsman, E F. Taylor, C Petros, A Brown, C P. Lerner, and B Paigen
Toward the genetics of mammalian reproduction: induction and mapping of gametogenesis mutants in mice., J O. Ward, L G. Reinholdt, S A. Hartford, L A. Wilson, R J. Munroe, K J. Schimenti, B J. Libby, M O'Brien, J K. Pendola, J Eppig, and J C. Schimenti
Loss of myosin VI reduces secretion and the size of the Golgi in fibroblasts from Snell's waltzer mice., C L. Warner, A Stewart, J P. Luzio, K P. Steel, R T. Libby, Jones J. Kendrick, and F Buss
Acoustic startle and prepulse inhibition in 40 inbred strains of mice., J F. Willott, L Tanner, J O'Steen, K R. Johnson, M A. Bogue, and L Gagnon
The heritability of antinociception II: pharmacogenetic mediation of three over-the-counter analgesics in mice., S G. Wilson, C D. Bryant, W R. Lariviere, M S. Olsen, B E. Giles, E J. Chesler, and J S. Mogil
The heritability of antinociception: common pharmacogenetic mediation of five neurochemically distinct analgesics., S G. Wilson, S B. Smith, E J. Chesler, K A. Melton, J J. Haas, B Mitton, K Strasburg, L Hubert, Zas S. Rodriguez, and J S. Mogil
The Development of a Highly Informative Mouse Simple Sequence Length Polymorphism (SSLP) Marker Set and Construction of a Mouse Family Tree Using Parsimony Analysis., P D. Witmer, K F. Doheny, M K. Adams, C D. Boehm, J S. Dizon, J L. Goldstein, T M. Templeton, A M. Wheaton, P N. Dong, E W. Pugh, R L. Nussbaum, K Hunter, J A. Kelmenson, L B. Rowe, and M J. Brownstein
FXR and ABCG5/ABCG8 as determinants of cholesterol gallstone formation from quantitative trait locus mapping in mice., H Wittenburg, M A. Lyons, R Li, G A. Churchill, M C. Carey, and B Paigen
Mapping cholesterol gallstone susceptibility (Lith) genes in inbred mice., H Wittenburg, M A. Lyons, B Paigen, and M C. Carey
Complete nucleotide sequence of the chloroplast genome from a leptosporangiate fern, Adiantum capillus-veneris L., P G. Wolf, C A. Rowe, R B. Sinclair, and M Hasebe
p190RhoGAP can act to inhibit PDGF-induced gliomas in mice: a putative tumor suppressor encoded on human chromosome 19q13.3., R M. Wolf, N Draghi, X Liang, C Dai, L Uhrbom, C Eklof, B Westermark, E C. Holland, and M D. Resh
Telomere dysfunction and Atm deficiency compromises organ homeostasis and accelerates ageing., K K. Wong, R S. Maser, R M. Bachoo, J Menon, D R. Carrasco, Y Gu, F W. Alt, and R A. DePinho
MAANOVA: A software package for the analysis of spotted cDNA microarray experiments., H Wu, M K. Kerr, X Q. Cui, and G A. Churchill
Zygote arrest 1 (Zar1) is a novel maternal-effect gene critical for the oocyte-to-embryo transition., X Wu, M M. Viveiros, J J. Eppig, Y Bai, S L. Fitzpatrick, and M M. Matzuk
The H4(b) Minor Histocompatibility Antigen Is Caused by a Combination of Genetically Determined and Posttranslational Modifications., R Yadav, Y Yoshimura, A Boesteanu, G J. Christianson, W U. Ajayi, R Shashidharamurthy, A K. Stanic, D C. Roopenian, and S Joyce
From mouse to man: redefining the role of insulin-like growth factor-I in the acquisition of bone mass., S Yakar and C J. Rosen
Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low electroconvulsive threshold., Y Yang, B J. Beyer, J F. Otto, T P. O'Brien, V A. Letts, H S. White, and W N. Frankel
Patterning of the lateral ganglionic eminence by the Gsh1 and Gsh2 homeobox genes regulates striatal and olfactory bulb histogenesis and the growth of axons through the basal ganglia., K Yun, S Garel, S Fischman, and J L. Rubenstein
Paracrine overexpression of IGFBP-4 in osteoblasts of transgenic mice decreases bone turnover and causes global growth retardation., M Zhang, M C. Faugere, H Malluche, C J. Rosen, S D. Chernausek, and T L. Clemens
Loss of the Tg737 protein results in skeletal patterning defects., Q Zhang, N S. Murcia, L R. Chittenden, W G. Richards, E J. Michaud, R P. Woychik, and B K. Yoder
Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6., Q Zhang, B Zhao, W Li, N Oiso, E K. Novak, M E. Rusiniak, R Gautam, R W. Elliott, E M. Eicher, P Liang, T N. O'Sullivan, N A. Jenkins, and al et
Bombesin/gastrin-releasing peptide receptor: a potential target for antibody-mediated therapy of small cell lung cancer., J Zhou, J Chen, M Mokotoff, R Zhong, L D. Shultz, and E D. Ball
Integrating computationally assembled mouse transcript sequences with the Mouse Genome Informatics (MGI) database., Y Zhu, B L. King, B Parvizi, B P. Brunk, C J. Stoeckert, J Quackenbush, J Richardson, and C J. Bult
E2F3 loss has opposing effects on different pRB-deficient tumors, resulting in suppression of pituitary tumors but metastasis of medullary thyroid carcinomas., U Ziebold, E Y. Lee, R T. Bronson, and J A. Lees
Proapoptotic BID is required for myeloid homeostasis and tumor suppression., S S. Zinkel, C C. Ong, D O. Ferguson, H Iwasaki, K Akashi, R T. Bronson, J L. Kutok, F W. Alt, and S J. Korsmeyer
Submissions from 2002
Novel vertebrate genes and putative regulatory elements identified at kidney disease and NR2E1/fierce loci., B S. Abrahams, G M. Mak, M L. Berry, D L. Palmquist, J R. Saionz, A Tay, Y H. Tan, S Brenner, E M. Simpson, and B Venkatesh
Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene., W Ahmad, M S. Ratterree, A A. Panteleyev, V M. Aita, J P. Sundberg, and A M. Christiano
A compendium of mouse knockouts with inner ear defects., A V. Anagnostopoulos
It's a knockout! Male infertility and neuropathology., A V. Anagnostopoulos
Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice., M G. Anderson, R S. Smith, N L. Hawes, A Zabaleta, B Chang, J L. Wiggs, and S W. John
T cell knockout mice have diminished alveolar bone loss after oral infection with Porphyromonas gingivalis., P J. Baker, L Howe, J Garneau, and D C. Roopenian
Genetic susceptibility to chronic periodontal disease., P J. Baker and D C. Roopenian
The underlying principles of scientific publication., C A. Ball, G Sherlock, H Parkinson, Sera P. Rocca, H C. Causton, T Gaasterland, F Holstege, M Ringwald, P Spellman, C J. Stoeckert, A Brazma, and J Quackenbush
Standards for microarray data., C A. Ball, G Sherlock, H Parkinson, Sera P. Rocca, D Cavalieri, P Hingamp, M Ringwald, P Spellman, J E. Stewart, R Taylor, A Brazma, and J Quackenbush
Effects of peroxisome proliferator-activated receptor delta on placentation, adiposity, and colorectal cancer., Y Barak, D Liao, W He, E S. Ong, M C. Nelson, J M. Olefsky, R Boland, and R M. Evans
Elizabeth S. Russell, May 1, 1913 - May 28, 2001., J E. Barker and W K. Silvers
Genetics and bone using the mouse understand man., W G. Beamer, L R. Donahue, and C J. Rosen
Electronic tools to manage gene expression data., Begley DA, Ringwald M
A ubiquitous and conserved signal for RNA localization in chordates., J N. Betley, M C. Frith, J H. Graber, S Choo, and J O. Deshler
Members of the synaptobrevin/vesicle-associated membrane protein (VAMP) family in Drosophila are functionally interchangeable in vivo for neurotransmitter release and cell viability., S Bhattacharya, B A. Stewart, B A. Niemeyer, R W. Burgess, B D. McCabe, P Lin, G Boulianne, C J. O'Kane, and T L. Schwarz
Insulin-like growth factor I is required for the anabolic actions of parathyroid hormone on mouse bone., D D. Bikle, T Sakata, C Leary, H Elalieh, D Ginzinger, C J. Rosen, W Beamer, S Majumdar, and B P. Halloran
The Gene Ontology (GO) project: structured vocabularies for molecular biology and their application to genome and expression analysis., J A. Blake and M A. Harris
The Mouse Genome Database (MGD): the model organism database for the laboratory mouse., J A. Blake, J E. Richardson, C J. Bult, J A. Kadin, and J T. Eppig
International Workshop on Lessons from Animal Models for Human Type 1 Diabetes: analyzing target autoantigens of humoral immunity in nonobese diabetic mice., E Bonifacio, M Atkinson, G Eisenbarth, D Serreze, T W. Kay, Chan E. Lee, and B Singh
Musculoskeletal effects of the recombinant human IGF-I/IGF binding protein-3 complex in osteoporotic patients with proximal femoral fracture: a double-blind, placebo-controlled pilot study., S Boonen, C Rosen, R Bouillon, A Sommer, M McKay, D Rosen, S Adams, P Broos, J Lenaerts, J Raus, D Vanderschueren, and P Geusens
Cholesterol gallstone formation in overweight mice establishes that obesity per se is not linked directly to cholelithiasis risk., G Bouchard, D Johnson, T Carver, B Paigen, and M C. Carey
Generation of a new congenic mouse strain to test the relationships among serum insulin-like growth factor I, bone mineral density, and skeletal morphology in vivo., M L. Bouxsein, C J. Rosen, C H. Turner, C L. Ackert, K L. Shultz, L R. Donahue, G Churchill, M L. Adamo, D R. Powell, R T. Turner, R Muller, and W G. Beamer
Crossover interference in the mouse., K W. Broman, L B. Rowe, G A. Churchill, and K Paigen
A haplolethal locus uncovered by deletions in the mouse T complex., V L. Browning, R A. Bergstrom, S Daigle, and J C. Schimenti
Mapping sites responsible for interactions of agrin with neurons., R W. Burgess, D K. Dickman, L Nunez, D J. Glass, and J R. Sanes
Gene array profiling and immunomodulation studies define a cell-mediated immune response underlying the pathogenesis of alopecia areata in a mouse model and humans., J M. Carroll, K J. McElwee, K i. E, M C. Byrne, and J P. Sundberg
Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome., E A. Carver, K F. Oram, and T Gridley
Epithelial-mesenchymal transitions and cancer, Ethan A. Carver and Thomas Gridley
Cutting edge: the minor histocompatibility antigen H60 peptide interacts with both H-2Kb and NKG2D., A Cerwenka, C A. O'Callaghan, J A. Hamerman, R Yadav, W Ajayi, D C. Roopenian, S Joyce, and L L. Lanier
Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7., T H. Chae, K M. Allen, M T. Davisson, H O. Sweet, and C A. Walsh
Retinal degeneration mutants in the mouse., B Chang, N L. Hawes, R E. Hurd, M T. Davisson, S Nusinowitz, and J R. Heckenlively
A Gja8 (Cx50) point mutation causes an alteration of alpha3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice., B Chang, X Wang, N L. Hawes, R Ojakian, M T. Davisson, W K. Lo, and X Gong
A reduced peripheral blood CD4(+) lymphocyte proportion is a consistent ageing phenotype., J Chen, K Flurkey, and D E. Harrison
Quantitative trait loci regulating relative lymphocyte proportions in mouse peripheral blood., J Chen and D E. Harrison
Identification and ranking of genetic and laboratory environment factors influencing a behavioral trait, thermal nociception, via computational analysis of a large data archive., E J. Chesler, S G. Wilson, W R. Lariviere, Zas S. Rodriguez, and J S. Mogil
Influences of laboratory environment on behavior., E J. Chesler, S G. Wilson, W R. Lariviere, Zas S. Rodriguez, and J S. Mogil
Real-time T-cell profiling identifies H60 as a major minor histocompatibility antigen in murine graft-versus-host disease., E Y. Choi, G J. Christianson, Y Yoshimura, N Jung, T J. Sproule, S Malarkannan, S Joyce, and D C. Roopenian
Immunodominance of H60 is caused by an abnormally high precursor T cell pool directed against its unique minor histocompatibility antigen peptide., E Y. Choi, G J. Christianson, Y Yoshimura, T J. Sproule, N Jung, S Joyce, and D C. Roopenian
T Cell Developmental Defects in 'Viable Motheaten' Mice Deficient in SHP-1 Protein-Tyrosine Phosphatase. Developmental Defects are Corrected in vitro in the Presence of Normal Hematopoietic-Origin Stromal Cells and in vivo by Exogenous IL-7., S W. Christianson, D L. Greiner, D Deluca, J Leif, N E. Phillips, S M. Hayes, S Hayashi, M J. Joliat, B L. Lyons, and L D. Shultz
What is the 'true' function of skin?, C M. Chuong, B J. Nickoloff, P M. Elias, L A. Goldsmith, E Macher, P A. Maderson, J P. Sundberg, H Tagami, P M. Plonka, Pederson K. Thestrup, B A. Bernard, J M. Schroder, and al et
Fundamentals of experimental design for cDNA microarrays., G A. Churchill
Development of mice expressing a single D-type cyclin., M A. Ciemerych, A M. Kenney, E Sicinska, I Kalaszczynska, R T. Bronson, D H. Rowitch, H Gardner, and P Sicinski
Mutant mouse models reveal the relative roles of E2F1 and E2F3 in vivo., J E. Cloud, C Rogers, T L. Reza, U Ziebold, J R. Stone, M H. Picard, A M. Caron, R T. Bronson, and J A. Lees
Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alstrom syndrome., G B. Collin, J D. Marshall, A Ikeda, W V. So, Eggitt I. Russell, P Maffei, S Beck, C F. Boerkoel, N Sicolo, M Martin, P M. Nishina, and J K. Naggert
The subventricular zone: new molecular and cellular developments., J C. Conover and R L. Allen
Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth., S L. Cotman, V Vrbanac, L A. Lebel, R L. Lee, K A. Johnson, L R. Donahue, A M. Teed, K Antonellis, R T. Bronson, T J. Lerner, and M E. MacDonald
Meta-analyses of therapies for postmenopausal osteoporosis. IX: Summary of meta-analyses of therapies for postmenopausal osteoporosis., A Cranney, G Guyatt, L Griffith, G Wells, P Tugwell, and C Rosen
A murine model of CML blast crisis induced by cooperation between BCR/ABL and NUP98/HOXA9., A B. Dash, I R. Williams, J L. Kutok, M H. Tomasson, E Anastasiadou, K Lindahl, S Li, E t. Van, J Borrow, D Housman, B Druker, and D G. Gilliland
Reduced growth of human sarcoma xenografts in hosts homozygous for the lit mutation., K Deitel, D Dantzer, P Ferguson, M Pollak, W Beamer, I Andrulis, and R Bell
In vitro and in vivo hematopoietic potential of human stem cells residing in muscle tissue., C Dell'Agnola, C Rabascio, P Mancuso, M Capillo, G Pruneri, A Gobbi, S Minucci, S Ronzoni, S Volorio, L Calabrese, N Tradati, G Martinelli, L Shultz, and F Bertolini
During the early prediabetic period in NOD mice, the pathogenic CD8(+) T-cell population comprises multiple antigenic specificities., T P. DiLorenzo, S M. Lieberman, T Takaki, S Honda, H D. Chapman, P Santamaria, D V. Serreze, and S G. Nathenson
The mammalian oocyte orchestrates the rate of ovarian follicular development., J J. Eppig, K Wigglesworth, and F L. Pendola
Corralling conditional mutations: A unified resource for mouse phenotypes., J T. Eppig, J A. Blake, D L. Burkart, C W. Goldsmith, C M. Lutz, and C L. Smith
Neuronal loss and brain atrophy in mice lacking cathepsins B and L., U Felbor, B Kessler, W Mothes, H H. Goebel, H L. Ploegh, R T. Bronson, and B R. Olsen
Purkinje cell degeneration (pcd) phenotypes caused by mutations in the axotomy-induced gene, Nna1., Gonzalez A. Fernandez, Spada A. La, J Treadaway, J C. Higdon, B S. Harris, R L. Sidman, J I. Morgan, and J Zuo
The netrin 1 receptors Unc5h3 and Dcc are necessary at multiple choice points for the guidance of corticospinal tract axons., J H. Finger, R T. Bronson, B Harris, K Johnson, S A. Przyborski, and S L. Ackerman
The Snell dwarf mutation Pit1(dw) can increase life span in mice., K Flurkey, J Papaconstantinou, and D E. Harrison
Interleukin-10-deficient mice are less susceptible to the induction of alopecia areata., Paul P. Freyschmidt, K J. McElwee, R Happle, S Kissling, E Wenzel, J P. Sundberg, M Zoller, and R Hoffmann
MYC expression promotes the proliferation of neural progenitor cells in culture and in vivo., D Fults, C Pedone, C Dai, and E C. Holland
Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse., H Gao, R M. Boustany, J A. Espinola, K A. Antonellis, T Gillis, X Qin, S Liu, L R. Donahue, R T. Bronson, and al et
Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis., K Gardiner, D Slavov, L Bechtel, and M Davisson
The early topography of thalamocortical projections is shifted in Ebf1 and Dlx1/2 mutant mice., S Garel, K Yun, R Grosschedl, and J L. Rubenstein
The Muscular Dystrophy with Myositis (mdm) Mouse Mutation Disrupts a Skeletal Muscle-Specific Domain of Titin., S M. Garvey, C Rajan, A P. Lerner, W N. Frankel, and G A. Cox
Translational repression by MSY4 inhibits spermatid differentiation in mice., F Giorgini, H G. Davies, and R E. Braun
APC-dependent suppression of colon carcinogenesis by PPARgamma., G D. Girnun, W M. Smith, S Drori, P Sarraf, E Mueller, C Eng, P Nambiar, D W. Rosenberg, R T. Bronson, W Edelmann, R Kucherlapati, F J. Gonzalez, and B M. Spiegelman
The family of toxin-related ecto-ADP-ribosyltransferases in humans and the mouse., G Glowacki, R Braren, K Firner, M Nissen, M Kuhl, P Reche, F Bazan, Cvrlje M. Cetkovic, E Leiter, F Haag, and Nolte F. Koch
Effects of oral dehydroepiandrosterone on bone density in young women with anorexia nervosa: a randomized trial., C M. Gordon, E Grace, S J. Emans, H A. Feldman, E Goodman, K A. Becker, C J. Rosen, C M. Gundberg, and M S. LeBoff
Anterior segment dysgenesis and the developmental glaucomas are complex traits., D B. Gould and S W. John
Stabilization of beta-catenin induces lesions reminiscent of prostatic intraepithelial neoplasia, but terminal squamous transdifferentiation of other secretory epithelia., F Gounari, S Signoretti, R Bronson, L Klein, W R. Sellers, J Kum, A Siermann, M M. Taketo, B o. von, and K Khazaie
Probabilistic prediction of Saccharomyces cerevisiae mRNA 3'-processing sites., J H. Graber, G D. McAllister, and T F. Smith
Construction of a BAC contig for a 3 cM biologically significant region of mouse chromosome 1., W K. Gu, X M. Li, B Edderkaoui, D D. Strong, K H. Lau, W G. Beamer, L R. Donahue, S Mohan, and D J. Baylink