Plenary Presentations *
Oral Presentations *
Poster Presentations:
Complex Genetics and Disease
Modifiers *
Developmental Genetics *
Functional Genomics *
Gene Discovery *
Genetic Manipulations to
Alter Gene Function *
Mouse Models: Human Disease and Pharmacogenetics *
Sequence Annotation and Comparative Analysis
of Genomes *
Attendees *
Sponsors
* Table
of Contents
* Photographs * Awards
Oral Presentations
THE MOSAIC STRUCTURE OF VARIATION IN THE MOUSE
GENOME
K Lindblad-Toh, Wade
C, Zody MC, Kirby A, Kulbolkas EJ,
Lander ES , Daly MJ
MOUSE GENOME ENCYCLOPEDIA
Y Hayashizaki
COMPARATIVE SEQUENCE ANALYSIS OF 3.6 MB OF
THE MOUSE AND HUMAN MAJOR HISTOCOMPATIBILITY COMPLEX (MHC)
A. Kumánovics,
Takada T, Jones EP, Fischer Lindahl K
MOUSE GENOME SEQUENCE ANALYSIS AND INTEGRATION
WITH THE HUMAN GENOME
DM Church,
Agarwala R, Frankel WN, Schriml L, Maglott D,
Schuler G and the NCBI Annotation Team
COMPARATIVE AND COLLABORATIVE BIOINFORMATICS
REQUIRED TO STUDY GENE NETWORKS THAT CREATE PHENOTYPES
J Snoddy,
Baker E Wang H-N, Peng X, Kirov S
Leuze M, Galloway L,
Schmoyer D, Baes F,
Jackson B, Jones B,
the Tennessee Mouse Genome Consortium and the Integrative Neuroscience Initiative on Alcoholism-Stress
Program Project.
MRC UK MOUSE SEQUENCING PROGRAMME – DETAILED
ANALYSIS OF THE DEL(1 SVEA36H REGION ON MOUSE CHROMOSOME 13
JM Hancock,
Mallon AM, Weekes J, Hancock JM, Denny P,
Ashurst J, Wilming L,
Peyrefiwte S, Botcherby MRM, Gautier P, Hummerich H,
Cross S, van Heyningen V,
Edgar R, Leaves N,
Greystrong J, Greenham L, Jones S,
Maggott K, Manjunath S,
Russell E, Strachan G,
Strivens M, North P,
Boal E, Cobley V,
Hunter G, Kimberley G,
Cave-Berry L, Mathews L, Simms S,
Gregory S, Evans R,
Hubbard T, Durbin R,
Cadman M, McKeone R,
Southwell A, Sellick C,
Iravani M, White S,
Little P, Jackson I,
Rogers J, Campbell RD &
Brown SDM
MAPPING BIOLOGY TO THE MOUSE GENOME
C Bult, Eppig
J, Ringwald M, Blake J, Richardson J,
Kadin J, Mouse Genome Informatics Curation
and Software Teams
SEQUENCING AND TARGETED ANALYSIS OF MOUSE
CHROMOSOMES 2, 4, 11 & X
S.G. Gregory, Barrett
I, Sims S, Williams S, Plumb R,
Mathews L, McLay K, Grafham D, Hunt A,
Jones M, Wilming L, Ashurst J, Beck S,
Rogers J
PATHBASE: A MOUSE PATHOLOGY DATABASE AND REFERENCE
SOURCE FOR IMAGES OF MUTANT MOUSE HISTOPATHOLOGY
PN Schofield,
Bard A, Rozell B, Goessner W, Delvenne P,
Sariola H, Ellender M,
Ward A
STRUCTURAL ANALYSES OF MAMMALIAN GENOME WITH
BAC ENDS
S Zhao, Shetty
J, Shatsman S, Geer K, Shewarzblin A,
and TIGR BAC End Team
Rat Genome
Database: A comparative genomics platform for rat, mouse And human
PJ Tonellato,
Twigger S, Eppig J, Lu J, Shimoyama M,
Pasko D, Bromberg S,
Ginster J, Chen CF,
Nigam R, Gopinathrao G,
Ramachandran H, Kwitek-Black A, Maglott D, Schuler G,
Stahl F, Levan G,
Jacob H
Lps2, A NOVEL AND CRUCIAL COMPONENT OF THE
LPS SIGNALING PATHWAY, IDENTIFIED BY GERMLINE SATURATION MUTAGENESIS
WITH ENU.
K Hoebe, Du
X, Goode J, Tabeta K, Mann J, Beutler B
Institutions:
The Scripps Research Institute
MUTATIONS IN THE BICAUDAL C GENE ON CHROMOSOME
10 CAUSE SEVERE POLYCYSTIC KIDNEY DISEASE IN THE MOUSE
EC Bryda,
Price SJ, Cogswell C, Hou X, , Flaherty L
Institutions:
Joan C. Edwards School of Medicine, Marshall University, Wadsworth
Center, University of Alabama at Birmingham
THE QUAKINGVIABLE MUTANT IS PARKIN-DEFICIENT
D Lorenzetti,
Vogel H, Noveroske J, Justice M
A CANDIDATE GENE FOR THE NEURONAL SODIUM
CHANNEL MODIFIER, SCNM1
DA Buchner, de
Haan G, Kearney JA, Adamska M, Meisler MH
LARGE SCALE GENE FUNCTION AND DRUG DISCOVERY
IN THE POST-GENOME ERA
A Sands, Zambrowicz
B
A NOVEL TRANSGENIC LINE OF MICE EXHIBITING
AUTOSOMAL RECESSIVE MALE-SPECIFIC LETHALITY AND NAFLD
A Buchberg, Sollars
V, McEntee B, Engiles J, Rothstein J
MICE HEMIZYGOUS FOR ENU-INDUCED MUTATIONS
AT THE FIT1 LOCUS HAVE DNA SEQUENCE AND STRUCTURAL ALTERATIONS
IN PICALM, A GENE FOR A CLATHRIN-ASSEMBLY PROTEIN
M Klebig,
Potter M, 1, Johnson E, 1, Hill M, Kerley M,
Rainwater L, 1, Rinchik EM
DEAFNESS AND PIGMENTATION DEFECTS IN VARITINT-WADDLER
(Va) MICE CAUSED BY MUTATIONS IN Mcoln3, A NEW MEMBER OF THE MUCOLIPIN
GENE FAMILY
K. Noben-Trauth, Di
Palma F, Belyantseva I, Kim H, Kachar B
A MUTATION IN THE EVI1 LOCUS PREDISPOSES TO
LATE ONSET OTITIS MEDIA WITH EFFUSION (OME) IN THE MOUSE DEAFNESS
MODEL Junbo.
NJ Parkinson, Tsai
H-T, Brooker D, MacKenzie F,
Hardisty R, Clements S,
Glenister P, Brown S
POSITIONAL CLONING OF THE FLAVIVIRUS RESISTANCE
GENE (FLV)
A Perelygin, Scherbik
S, Stockman B, Li Y , Brinton M
Institutions:
Georgia State University
CREATING NEW MOUSE MODELS OF CARDIOVASCULAR
DISEASE USING RANDOM MUTAGENESIS
S.L. Adamson, Kelsey
L, Voronina I, Milenkovic Z, Whiteley J, Vukobradovic I,
and others in the Centre for Modelling Human Disease.
DEVELOPMENTAL GENETICS OF MOUSE CHROMOSOME
2
R. Conlon, Qian
Z, Sa X, LePage DF
IDENTIFICATION, MAPPING AND CLONING OF NEW
TYPE 2 DIABETES MODELS FROM ENU MUTAGENESIS
RD Cox,
Toye A, Bentley E, Goldsworthy M, Moir L, Mijat V,
Hugill A, Hough T,
Mansell S, Abdul-Hussein S, Gray
I, Hunter J,
Brown SDM
USING ENU TO CREATE MOUSE MODELS OF HUMAN
EYE DISEASE
SH Cross,
Thaung C, Morgan J, West K, McKie L,
Clark BJ, Brown SDM,
Jackson IJ
MOUSE MODELS FOR BEHAVIOURAL DISORDERS: ENU
SCREEN FOR REST:ACTIVITY MUTATIONS IN MICE
M Bucan, David Kapfhamer, 1, Gillian Leach,
1, Yi Sun, Sigrid C. Veasey,
John Schimenti and 1, 2, Maja Bucan
COMPLEMENTATION OF MOUSE NEURAL CREST DEFECTS
USING LINEAGE DIRECTED GENE TRANSFER
WJ Pavan, Dunn
KJ, Hou L, Loftus SK.
NEW ENU-INDUCED MUTANTS WITH HEARING AND BALANCE
DEFECTS FROM THE EUROPEAN MUTAGENESIS PROGRAMMES
Karen P Steel,
Kiernan AE, Erven AE, Rhodes C, Quint E,
Hawker K, Pau H,
Tsai H, Hardisty RE,
Nolan P, Peters J,
Hunter AJ, Ahituv N,
Hertzano R, Vreugde S,
Avraham KB, Fuchs H,
Balling R, Hrabé De Angelis M,
Brown SDM, Guénet JL
AN ENU MUTAGENESIS SCREEN TO IDENTIFY VARIANTS
THAT AFFECT GENE EXPRESSION FROM THE INACTIVE X CHROMOSOME
LH Chadwick, Willard
HF
EXTENSION AND EVALUATION OF “IN SILICO” MAPPING
OF COMPLEX TRAITS IN INBRED MICE
EJ Chesler,
Rodriguez-Zas SL Williams RW,
Mogil JS
GENETICS OF MALARIAL INFECTION IN MICE
S Foote, Vikki
Marshall, Rachel Burt, James Wagglen, Enmoore Lin
THE GENETIC ARCHITECTURE OF EXPLORATORY AND
FEAR-LIKE BEHAVIOR IN MICE: A COMPARISON OF THREE STRATEGIES FOR
FINE MAPPING QTLs
H Gershenfeld,
Lou Y, Zhang S, Amstein T, Anyango M,
Mohibullah N, Osoti A, King R,
Iraqi F
X-INACTIVATION MEDIATES AN EFFECT ON MATERNAL
RECOMBINATION AND MEIOTIC DRIVE
E. de la Casa-Esperon,
Loredo-Osti J C, Pardo-Manuel de Villena
F, Briscoe T L,
Malette J M, Vaughan J E,
Morgan K, Sapienza C
IDENTIFICATION OF 5-LIPOXYGENASE AS A MAJOR
GENE CONTRIBUTING TO ATHEROSCLEROSIS SUSCEPTIBILITY IN MICE
M Mehrabian,
Allayee H, Wong J, Shih W, Wang X-P,
Shaposhnik Z, Funk CD, Lusis AJ
PLASMACYTOMA SUSCEPTIBILITY/RESISTANCE LOCI,
PCTR1 AND PCTR2 RESULT FROM COMBINATIONS OF SINGLE NUCLEOTIDE POLYMORPHISMS
IN GENES THAT ALTER THEIR EFFICIENCY OF FUNCTION
B Mock,
Bliskovski V, Zhang S, Ramsay ES, Shi W,
Scott J, Qian X,
Lowy DR
A SUBPHENOTYPE BASED STRATEGY TO DISSECT A
GENE CLUSTER ON MOUSE CHROMOSOME 3 ASSOCIATED WITH SEVERAL AUTOIMMUNE
DISEASES
M Johannesson, Wester
L, Selva NK, Holmdahl M, Holmdahl R
MASSIVELY PARALLEL COMPLEX TRAIT ANALYSIS
OF TRANSCRIPTIONAL ACTIVITY IN MOUSE BRAIN
RW Williams,
Manly KF, Shou S, Chesler EJ, Hsu HC,
Mountz J, Threadgill DW,
Lu L
IDENTIFYING GENES THAT CONTRIBUTE TO CONTROL
OF AFRICAN TRYPANOSOMES USING A 27 THOUSAND GENE MICROARRAY
F Iraqi,
Naessens J, Quackenbush J,
Gaspard R, Nakamura Y,
Gibson J
GENETICS OF TESTICULAR DESCENT AND CRYPTORCHIDISM
A Agoulnik, Bogatcheva
N, Kamat A, Gorlov I
ABNORMAL DIAPHRAGMATIC DEVELOPMENT AND PULMONARY
HYPOPLASIA CAUSED BY AN ENU-INDUCED HYPOMORPHIC MUTATION OF FOG2
DR Beier,
Ackerman KG, Herron BJ, Rao C, Huang H,
Babiuk RP, Epstein JA,
Greer J
DNA METHYLATION AND CTCF BINDING SITES AT
THE CPG ISLAND OF SMCX: ROLE IN DEVELOPMENTAL ESCAPE FROM X INACTIVATION
C Disteche,
Filippova G, Truong J-P, Tsuchiya K
NOTCH SIGNALING REGULATES LEFT-RIGHT DETERMINATION
IN MICE
T. Gridley, Krebs
LT, Welsh IC, O'Brien TP
NEURODEGENERATION AND PIGMENTATION DEFECTS
IN ATTRACTIN AND MAHOGANOID MUTANTS
TM Gunn, He
L, Barsh GS
THE sasquatch MOUSE: DISCOVERY OF AN ENHANCER
ELEMENT ACTING OVER 1MB OF GENOMIC DNA
S Heaney, Hill
R, Lettice L, Purdie L, Taylor M
MESD PROMOTES SUBCELLULAR LOCALIZATION OF
THE WNT CO-RECEPTORS LRP5/6
L Lee, Hsieh
JC, Zhang L, Wefer S, Brown K, Holdener, BC.
A ROLE FOR A MOUSE POLYCOMB GROUP GENE IN
GENOMIC IMPRINTING
J.C. Mager, Montgomery
N, Pardo-Manuel de Villena F,
Magnuson T
Fgf9 ACTS IN THE SEX DETERMINING PATHWAY BY
UP-REGULATING Sox9 EXPRESSION
Y Qin, Troung
C, Bishop CE
ALTERATION OF EARLY CEREBELLAR DEVELOPMENT
IN THE Ts65Dn MOUSE MODEL OF DOWN SYNDROME
RJ Roper,
Baxter LL, Klinedinst DK,
Mullaney BC, 2, Blue ME,
Reeves RH
ISOLATION AND IDENTIFICATION OF RECESSIVE
MUTATIONS AFFECTING MURINE HEMATOPOIESIS USING A BALANCER CHROMOSOME.
BT Kile,
Ross M, Mason-Garrison CL,
Salinger AP, Bradley A,
Behringer RR, Justice MJ
MOUSEEXPRESS: IN SILICO ANALYSIS OF EXPRESSION
PATTERNS IN MOUSE MUTANTS
J Beckers,
Seltmann M, Horsch M, Drobyshev A, Mader M, Tornow S,
Frohme M, Korica T,
Vingron M, Mewes W,
Hoheisel J, Hrabe de Angelis M
FUNCTIONAL AND MICROARRAY ANALYSIS OF KY,
A TRANSGLUTAMINASE-LIKE PROTEIN UNDERLYING THE KYPHOSCOLIOTIC NEUROMUSCULAR
DYSTROPHY IN THE MOUSE
G Blanco, Wright
E, Pritchard C, Brown SDM
EMAGE -THE EDINBURGH MOUSE ATLAS OF GENE EXPRESSION
J Christiansen, Armit
C, Venkataraman S, Stark M, Waterhouse A,
Houghton D, Burton N,
Yang Y, Hill B, Feng G, Rao J, Sharpe J, Stevenson P,
Baldock R, Davidson D
MOLECULAR MAPPING OF THE MOUSE BRAIN
M. de Chaldée,
Gaillard MC, Bizat N, Aude JC, Buhler JM,
Manzoni O, Bockaert J,
Hantraye P, Brouillet E,
Elalouf JM
ELUCIDATING GENE REGULATORY NETWORKS INVOLVED
IN HAIR AND SKIN PHYSIOLOGY BY INTEGRATING EXPERIMENTAL AND COMPUTATIONAL
APPROACHES
B. Jones, Leuze
M, Snoddy J, Schmoyer D, Baker E,
Das S, Hoyt P, Doktycz M, Culiat C,
Michaud E
MICROARRAY EXPRESSION PROFILING APPLIED TO
GENES FOR NEURAL CREST DEVELOPMENT IDENTIFIES RAB38, THE GENE MUTATED
IN CHOCOLATE MICE
S. Loftus, Larson
D, Antonellis A, Baxter L, Wolfsberg T,
Pavan W.
GENETIC AND PHYSIOLOGICAL PERTURBATIONS OF
THE HOMOCYSTEINE AND FOLATE PATHWAYS IN A MOUSE MODEL OF HUMAN
DISEASE
S Ernest,
Carter M, Hosack A, Rosenblatt D, Ross E, Nadeau J
STRUCTURE AND EXPRESSION OF AN UNUSUAL AXONEMAL
DYNEIN HEAVY CHAIN GENE, Dnahc8, A Mouse T Complex Distorter/Sterility
2 (Tcd/Tcs CANDIDATE
S Samant, Pilder
S.
FUNCTIONAL STUDIES OF PROTEINS THAT INTERACT
WITH TRAF ADAPTOR PROTEINS
H Suzuki, Kanamori
M, Saito R, Kai C, Hayashizaki Y
SNP MAPPING IN THE MOUSE
T Wiltshire,
Pletcher M, Barnes W, Tarantino L, Cooke M, Wu H,
Smylie K, Santrosyan A,
Batalov S, Copeland N,
Jenkins N, Kay S,
Fletcher C.
A NOVEL MOUSE MODEL OF HYPOGONADISM
RR Behringer,
Pask AJ, Wang Y, Salinger AP, Justice MJ
MUTATED GLYCOSYLTRANSFERASE AND HYPOGLYCOSYLATION
OF ALPHA-DYSTROGLYCAN IN THE LARGEMYD MOUSE: A MODEL FOR GLYCOSYLATION-DEFICIENT
MUSCULAR DYSTROPHIES
P Grewal,
Holzfiend P, Reitsamer H,
Kechvar J, Lassmann H,
Höger H, Bittner R,
Hewitt J
Cx32 KNOCKOUT MOUSE AND LEUKEMOGENESIS
Y Hirabayashi,
Yoon BI, Tsuboi I, Huo Y, Kodama Y,
Otto T, Kanno J,
Willecke K, Trosko JE,
and Inoue T.
MOOD DISORDER IN MICE LACKING a1G T-type Ca2+
CHANNELS
H-S Shin,
Kim D, Park D, Lee J-R, Lee S, Kim H-T
MICE WITH A PARTIAL TRISOMY OF CHROMOSOME
17 AS A MODEL OF HUMAN ANEUPLOIDY SYNDROMES
J Forejt,
Vacik T, Gregorova S, Ort M, Bures J,
Yaspo ML, Lehrach H
GENERATION OF SEGMENTAL ANEUPLOIDY TO CREATE
A MOUSE MODEL OF DOWN SYNDROME
L.E. Olson, Reeves
RH
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