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Complex Genetics and Disease
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Gene Discovery *
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Mouse Models: Human Disease and Pharmacogenetics *
Sequence Annotation and Comparative Analysis
of Genomes *
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* Table
of Contents
* Photographs * Awards
33. DIALLEL ANALYSIS
OF THE LEYDIG CELL RESPONSIVENESS DURING THE POSTNATAL DEVELOPMENT
IN MICE
Ahmerova LG, Osadchuk AV
34. RECESSIVE SCREEN
AT DEL(1 SVEA36H
Bogani D, Davies J, Alexander E, Heines
H, Madge J, Napper H, Robertson L, McKeone R, Southwell
A, Denny P, 1 Arkell R
35. GENETIC AND BIOCHEMICAL
ANALYSIS OF A NEW PUTATIVE E3 LIGASE
Gao G, Wu J, Artzt K
36. MOLECULAR AND
GENETIC ANALYSIS OF THE MOUSE HOMOLOGUE OF A NOVEL ZEBRAFISH NEUROGENIC
MUTATION
Rajendra R, Wu J, Artzt K
37. RETINOIC ACID
REGULATES VASCULAR DEVELOPMENT
Bohnsack BL, Lai L, Niederreither K, Hirschi
KK
38. DESIGN AND VALIDATION
OF A NOVEL 22,000 FEATURE IN SITU-SYNTHESIZED 60-MER OLIGONUCLEOTIDE
MICROARRAY FOR STUDIES OF EARLY DEVELOPMENT AND STEM CELLS
Carter M, Hamatani T, Sharov A, Carmack
C, Qian Y, Brzoska P, Hwang S, Ko, M
39. NELL1, A GENE
CODING FOR A NOVEL PKC-BINDING PROTEIN IS A CANDIDATE FOR LATE-GESTATION
RECESSIVE LETHAL MUTATIONS AT THE L7R6 LOCUS
Desai J, Hughes L, Millsaps J, Stanford
B, Kerley M, Carpenter D, Rinchik E, Culiat C
40. A MUTATION IN
NKX INTERACTING PROTEIN 1 RESULTS IN ABNORMAL HEART AND SKIN DEVELOPMENT
AND DILATED CARDIOMYOPATHY IN WA3 MICE
Herron BJ, Rao C, Lien E, Lu J, Richardson
J, Semsarian C, Millar S, Stubbs L, Siedman C, Olson
E, and Beier DR
41. MOLECULAR ROLE
OF QUAKING IN BLOOD AND BLOOD VESSEL DEVELOPMENT
Bohnsack BL, Northrop JL, Lihua LL, Justice
MJ, Hirschi KK
42. NOVEL TRANSCRIPTS
WITHIN THE Gnas IMPRINTING CLUSTER
Holmes R, Wells C, Monk D, Williamson
C, Peters J
43. NODE AND MIDLINE
DEFECTS ARE ASSOCIATED WITH LEFT-RIGHT DEVELOPMENT IN DELTA1 MUTANT
EMBRYOS
Przemeck G, Heinzmann U, Beckers J Hrabe
de Angelis M
44. BIOINFORMATICS
IN MOUSE ENU MUTAGENESIS: A BRIDGE OF DATA GENERATION AND DATA
COMMUNICATION IN THE MOUSE COMMUNITY
Liu B, Zhong L, Tran N, Justice M
45. GENOMIC ANALYSIS
OF MOUSE PREIMPLANTATION DEVELOPMENT
Kimber W, Puri N, Borgmeyer C, Ritter
D, Seidman M, Ko, M
46. INVESTIGATION
OF THE ROLES OF WILMS’ TUMOUR SUPRESSOR 1 (WT ISOFORMS, WT1+KTS
AND WT1-KTS, IN MURINE UROGENITAL DEVELOPMENT
Lahiri D, Dutton J.R, Ward A
47. POG, GEMS AND
URF FORM A NOVEL INTERACTING PROTEIN COMPLEX WITH A ROLE IN GAMETE
DEVELOPMENT
Lu B, Truong C, Agoulnik A, , Bishop
C
48. NOVEL EMBRYONIC
FUNCTIONS FOR SMAD2 IDENTIFIED WITH AN ENU-INDUCED HYPOMORPHIC
ALLELE
Vivian JL, Chen Y, Magnuson T
49. A SENSITIZED
MUTAGENESIS SCREEN FOR NEURAL CREST DEFECTS
Elliott G, Baxter L.L., Pavan W.J.
50. HOMOLOGOUS RECOMBINATION
REPAIR AND GENOMIC STABILITY
Pittman, D, Smiraldo P, Gruver A
51. POSITIONAL CLONING
OF A PREAXIAL POLYDACTYLY MUTATION, HX, CLOSELY LINKED TO SONIC
HEDGEHOG GENE (SHH)
Sagai T, Masuya H, Shimizu K, Yada Y,
Tamura M, Shiroishi T
52. KLF4 IS SUFFICIENT
TO ESTABLISH EPIDERMAL BARRIER IN UTERO
Jaubert J, Cheng J, Segre
53. ANALYSIS OF CANDIDATE
GENE FOR A MOUSE MUTANT, RECOMBINATION-INDUCED MUTATION 3 (RIM ,
WITH IMPAIRED EPIDERMAL MORPHOGENESIS
Tanaka S, Aoki A, Sato H, Saeki N,
Tamura M, Shiroishi T
54. MOLECULAR AND
HISTOLOGICAL CHARACTERIZATION OF MURINE EPIDERMAL GROWTH FACTOR
RECEPTOR NULL PLACENTAE
Hovick M, Strunk KE, Clore J, threadgill DW
55. ABERRANT ANTERIOR-POSTERIOR
AXIS FORMATION IN A PREAXIAL POLYDACTYLY MUTANT, RECOMBINATION
INDUCED MUTATION (RIM
Yada Y, Masuya H, Makino S, Shiroishi
T
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