18th International Mouse Genome Conference17-22 October 2004, Seattle, USA
Plenary Presentations * Oral
Presentations * Poster
Abstracts * Photos
Verne Chapman Memorial Lecture * Table
of Contents * Attendees * Awards
31. THE SEARCH
FOR HUNTINGTON'S DISEASE MODIFIERS IN THE MOUSE
Acevedo A 1, Chrobot N
1, Rubinsztein DC 2, Brown SD
1
1 MRC Mammalian Genetics Unit, Harwell, United
Kingdom, 2 Cambridge Institute for Medical
Research, Cambridge, United Kingdom
32. COORDINATION OF GROWTH
AND METABOLISM BY THE IMPRINTED GRB10 GENE
Ward A, Koumanov F, Charalambous M, Garfield A, Allsop
JE, Moorwood K, Smith FM
University of Bath, Bath, United Kingdom
33. SENSITIZED MUTAGENESIS
SCREEN FOR MODIFIERS OF THE DELTA/NOTCH PATHWAY IN THE MOUSE
Rubio-Aliaga I, Soewarto D, Wagner S, Przemeck G,
Fuchs H, Hrabé de Angelis M
GSF Research Center - Institute of Experimental Genetics,
Neuherberg/Munich, Germany
34. COORDINATION OF GROWTH
AND METABOLISM BY THE IMPRINTED GRB10 GENE
Smith FM 1, Charalambous
M 2, Koumanov F 1, Garfield
A 1, Ward A 1
1 Centre for Regenerative Medicine, University of
Bath, Bath, United Kingdom, 2 Centre for Diabetes
and Endocrinology, Division of Medicine, London, United
Kingdom
35. FINE MAPPING PRION
DISEASE INCUBATION TIME QTL USING HETEROGENEOUS STOCK MICE
Lloyd SE 1, Maytham ELG
1, Thompson S 1, Mott R 2,
Fisher EMC 1, Collinge J 1
1 MRC Prion Unit, London, United Kingdom,
2 The Wellcome Trust Centre for Human Genetics,
Oxford, United Kingdom
36. IDENTIFICATION OF
NOVEL IMPRINTED GENES ON MOUSE CHROMOSOMES 7 AND 18
Woodfine K 1, Choi
JD 1, Wood AJ 1, Collins
JN 2, Oakey RJ 1
1 Division of Medical Genetics, GKT School of
Medicine, London, United Kingdom, 2 Division of
Human Genetics, The Children’s Hospital of
Philadelphia, Philadelphia, United States
37. SUPPRESSORS AND ENHANCERS
OF TESTICULAR CANCER SUSCEPTIBILITY IN DOUBLE-MUTANT MICE
Lam MYJ, Youngren KK, Nadeau JH
Case Western Reserve University, Cleveland, United States
38. MODIFIERS OF THE
DDK SYNDROME RESULT IN THE DOMINANT RESCUE OF EMBRYONIC LETHALITY
Ideraabdullah FY, Kim K, Pardo-Manuel de Villena F
Dept of Genetics, UNC-Chapel Hill, Chapel Hill, United States
39. THE REQUIREMENT FOR
EED IN AUTOSOMAL GENOMIC IMPRINTING MAY BE TISSUE SPECIFIC
Chamberlain SJ, Montgomery ND, Kalantry S, Magnuson T
Department of Genetics, University of North Carolina-Chapel
Hill, Chapel Hill, NC, United States
40. PREDISPOSITION TO
MOUSE THYMIC LYMPHOMAS DEPENDS ON COMMON VARIANT ALLELES OF MTF-1 (METAL
RESPONSIVE TRANSCRIPTION FACTOR-1)
Kominami R 1, Tamura
Y 1, Maruyama M 1, Mishima
Y 1, Schaffner W 2
1 Niigata University, Graduate School of Medical
and Dental Sciences, Niigata, Japan, 2 Institute
for Molecular Biology, University of Zurich, Zurich,
Switzerland
41. EVOLUTIONARILY CONSERVED
SEQUENCE ELEMENTS THAT POSITIVELY REGULATE INTERFERON GAMMA EXPRESSION IN T
CELLS
Shnyreva M 1, Weaver
WM 1, Blanchette M 3, Taylor
SL 2, Fitzpatrick DR 2, Tompa
M 1, Wilson CB 1
1 University of Washington, Seattle, United
States, 2 Amgen Corporation, Seattle, United
States, 3 McGill University, Montreal, Canada
42. MODIFIER LOCI THAT
INFLUENCE TPA SKIN TUMOR PROMOTION SUSCEPTIBILITY IN GENETIC CROSSES OF DBA/2
WITH C57BL/6 MICE
Angel JM, Abel EL, Riggs PK, Elizondo L, Caballero M,
DiGiovanni J
Univ Texas, MD Anderson Cancer Center, Science Park-Research
Division, Smithville, United States
43. MOUSE HAIRY EARS
(EH) INVERSION MUTATION DISRUPTS NO GENE TRANSCRIPTS, BUT EXPRESSION
OF HOXC GENES IN SKIN IS DISTURBED
Mentzer S 1, Sundberg J 2,
Cacheiro N 1, Chao H 3,
Carpenter D 1, Johnson D 1,
Rinchik E 3, You Y
1
1 Oak Ridge National Laboratory, Oak Ridge, United
States, 2 The Jackson Laboratory, Bar Harbor,
United States, 3 University of Tennessee,
Knoxville, United States
44. DEVELOPMENTAL PROFILE
OF DNA METHYLATION AND GENE EXPRESSION AT THE H19 LOCUS IN MICE LACKING
SEQUENCE REQUIRED FOR GENOMIC IMPRINTING
Thorvaldsen J , Fedoriw A , Yang
G , Bartolomei M
University of Pennsylvania, Philadelphia, United States
45. CURRENT PROGRESS
IN SCREENING FOR MUTANTS AFFECTING GENOMIC IMPRINTING IN THE RIKEN-GSC PROJECT
Suzuki T 1, Furuumi
H 2, Hashimoto M 3, Kyouno
S 4, Nagashima A 1, Kumaki
K 2, Kaneda H 1, Gondo
Y 5, Noda T 1, Wakana
S 1, Ishino F 4, Sasaki
H 2, Shiroishi T 1
1 Mouse Functional Genomics Research Group,
Genomics Science Center (GSC), RIKEN Yokohama Institute,
Yokohama, Japan, 2 Department of Integrated
Genetics, National Institute of Genetics, Mishima, Japan,
3 Gene Research Center, Tokyo Institute of
Technology, Yokohama, Japan, 4 Department of
Epigenetics, Medical Research Center, Tokyo Medical and
Dental University, Tokyo, Japan, 5 Population and
Quantitative Genomics Team, GSC, RIKEN, Yokohama, Japan
46. ANALYSIS OF THE CANDIDATE
REGION AND CANDIDATE GENES RESPONSIBLE FOR THE DDK SYNDROME OF EMBRYONIC LETHALITY
de la Casa-Esperon E 1,
Gimelbrant A 3, Adey B 1,
Briscoe T 1, Hao L 1,
Wu G 1, Chess A 3,
Pardo-Manuel de Villena F 2, Sapienza
C 1
1 Fels Institute, Temple University School of
Medicine, Philadelphia, PA, United States, 2
Department of Genetics, UNC-Chapel Hill, Chapel Hill, NC,
United States, 3 Whitehead Institute for
Biomedical Research, MIT, Cambridge, MA, United States
47. GENOME-WIDE ASSOCIATION
ANALYSIS IDENTIFIES NOVEL MODIFIER LOCI OF HIRSCHSPRUNG DISEASE IN SOX10DOM
MICE
Owens SE 1, Broman
KW 2, Smith JR 1,
Southard-Smith EM 1
1 Vanderbilt University, Nashville, United States,
2 Johns Hopkins University, Baltimore, United
States
48. A SENSITIZED ENU
MUTAGENESIS SCREEN FOR DOMINANT GENETIC MODIFIERS OF THROMBOSIS IN THE FACTOR
V LEIDEN MOUSE
Westrick RJ 1, Manning
SL 2, Dobies SL 1, Peterson
AL 2, Siemieniak DR 2,
Korepta LM 1, Ginsburg D 2
1 University of Michigan, Ann Arbor, United
States, 2 Howard Hughes Medical Institute, Ann
Arbor, United States
49. MODIFIERS OF AGANGLIONIC
MEGACOLON IDENTIFIED BY EVALUATION OF CANDIDATE GENES IN THE SOX10DOM
HIRSCHSPRUNG DISEASE MODEL
Cantrell VA, Owens SE, Chandler RL, Bradley KM, Smith JR,
Southard-Smith EM
Vanderbilt University, Nashville, United States
50. CHROMATIN DOMAINS
THAT ESCAPE X INACTIVATION CHARACTERIZED BY CTCF BINDING AND HISTONE MODIFICATIONS
Cheng MK 1, Filippova
GN 2, Disteche CM 1
1 University of Washington, Seattle, United
States, 2 Fred Hutchinson Cancer Research Center,
Seattle, United States
51. SNP AND SSLP HAPLOTYPES,
TUMOR MICROARRAYS, AND CONGENIC RECOMBINANTS IN THE IDENTIFICATION OF HCS7,
A POTENT LIVER CANCER MODIFIER
Bilger A, Schneider A, Leutkehoelter K, Sundlov T,
Drinkwater N
University of Wisconsin Medical School, Madison, United
States
52. IDENTIFICATION OF
GENES INFLUENCING PLASMA VON WILLEBRAND FACTOR LEVELS IN MICE
Lemmerhirt HL 1, Ginsburg
D 2
1 Department of Human Genetics, The University of
Michigan, Ann Arbor, United States, 2 Howard
Hughes Medical Institutue, Ann Arbor, United States
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