International Mammalian Genome Society

The 16th International Mouse Genome Conference (2002)


Oral Presentations

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

A PROPOSAL FOR A COMMUNITY EFFORT TO ANNOTATE THE STRUCTURE, FUNCTION AND EVOLUTION OF BIOLOGICAL PATHWAYS IN A PUBLIC DATABASE
J Nadeau

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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