| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A Methylation Imprint Mark in the Mouse Imprinted GeneGrf1/Cdc25MmLocus Shares a Common Feature with theU2afbp-rsGene: An Association with a Short Tandem Repeat and a Hypermethylated Region
|
Shibata, Hideo
|
|
1998
|
49 |
1 |
p. 30-37
8 p.
|
article
|
| 2 |
A Microdeletion of D6S305 in a Family of Autosomal Recessive Juvenile Parkinsonism (PARK2)
|
Matsumine, Hiroto
|
|
1998
|
49 |
1 |
p. 143-146
4 p.
|
article
|
| 3 |
Analysis of HomologousXRCC1-Linked Zinc-Finger Gene Families in Human and Mouse: Evidence for Orthologous Genes
|
Shannon, Mark
|
|
1998
|
49 |
1 |
p. 112-121
10 p.
|
article
|
| 4 |
A New Isoform of Human Myosin Phosphatase Targeting/Regulatory Subunit (MYPT2): cDNA Cloning, Tissue Expression, and Chromosomal Mapping
|
Fujioka, Masaki
|
|
1998
|
49 |
1 |
p. 59-68
10 p.
|
article
|
| 5 |
A Novel Unstable Mouse VNTR Family Expanded from SINE B1 Elements
|
Bois, Philippe
|
|
1998
|
49 |
1 |
p. 122-128
7 p.
|
article
|
| 6 |
Assignment of the MurineNotch2andNotch3Genes to Chromosomes 3 and 17
|
Gao, Xiang
|
|
1998
|
49 |
1 |
p. 160-161
2 p.
|
article
|
| 7 |
Characterization of Human and Mouse Rod cGMP Phosphodiesterase δ Subunit (PDE6D) and Chromosomal Localization of the Human Gene
|
Li, Ning
|
|
1998
|
49 |
1 |
p. 76-82
7 p.
|
article
|
| 8 |
Characterization ofSCML1,a New Gene in Xp22, with Homology to Developmental Polycomb Genes
|
van de Vosse, Esther
|
|
1998
|
49 |
1 |
p. 96-102
7 p.
|
article
|
| 9 |
Cloning of a Novel Human Putative Type Ia Integral Membrane Protein Mapping to 21q22.3
|
Yaspo, Marie-Laure
|
|
1998
|
49 |
1 |
p. 133-136
4 p.
|
article
|
| 10 |
Construction of a 2.5-Mb Integrated Physical and Gene Map of Distal 21q22.3
|
Lapenta, Vincenza
|
|
1998
|
49 |
1 |
p. 1-13
13 p.
|
article
|
| 11 |
Divergently Transcribed Overlapping Genes Expressed in Liver and Kidney and Located in the 11p15.5 Imprinted Domain
|
Cooper, Paul R.
|
|
1998
|
49 |
1 |
p. 38-51
14 p.
|
article
|
| 12 |
Generation of a 3-Mb PAC Contig Spanning the Miyoshi Myopathy/Limb-Girdle Muscular Dystrophy (MM/LGMD2B) Locus on Chromosome 2p13
|
Liu, Jing
|
|
1998
|
49 |
1 |
p. 23-29
7 p.
|
article
|
| 13 |
Genotype in the 24-kDa Subunit Gene (NDUFV2) of Mitochondrial Complex I and Susceptibility to Parkinson Disease
|
Hattori, Nobutaka
|
|
1998
|
49 |
1 |
p. 52-58
7 p.
|
article
|
| 14 |
Identification, Characterization, and Genetic Mapping ofRad51d,a New Mouse and HumanRAD51/RecA-Related Gene
|
Pittman, Douglas L.
|
|
1998
|
49 |
1 |
p. 103-111
9 p.
|
article
|
| 15 |
Localization of 67 Exons on a YAC Contig Spanning 1.5 Mb around the Multidrug Resistance Gene Region of Human Chromosome 7q21.1
|
Torigoe, Kiyoyuki
|
|
1998
|
49 |
1 |
p. 14-22
9 p.
|
article
|
| 16 |
Mapping of theCYP2JCytochrome P450 Genes to Human Chromosome 1 and Mouse Chromosome 4
|
Ma, Jixiang
|
|
1998
|
49 |
1 |
p. 152-155
4 p.
|
article
|
| 17 |
Organization of the Human Glucokinase Regulator GeneGCKR
|
Hayward, B.E.
|
|
1998
|
49 |
1 |
p. 137-142
6 p.
|
article
|
| 18 |
Radiation Hybrid Mapping ofEPB41L1,a Novel Protein 4.1 Homologue, to Human Chromosome 20q11.2–q12
|
Kim, Anthony C.
|
|
1998
|
49 |
1 |
p. 165-166
2 p.
|
article
|
| 19 |
StchMaps to Mouse Chromosome 16, Extending the Conserved Synteny with Human Chromosome 21
|
Reeves, Roger H.
|
|
1998
|
49 |
1 |
p. 156-157
2 p.
|
article
|
| 20 |
Structure and Chromosomal Localization of Mouse G Protein Subunit γ4 Gene
|
Kalyanaraman, S.
|
|
1998
|
49 |
1 |
p. 147-151
5 p.
|
article
|
| 21 |
Structure and Expression of the Gene Encoding Murine M-Protein, a Sarcomere-Specific Member of the Immunoglobulin Superfamily
|
Steiner, Frank
|
|
1998
|
49 |
1 |
p. 83-95
13 p.
|
article
|
| 22 |
Structure, Chromosomal Locus, and Promoter of MouseHes2Gene, a Homologue ofDrosophila hairyandEnhancer of split
|
Nishimura, Masataka
|
|
1998
|
49 |
1 |
p. 69-75
7 p.
|
article
|
| 23 |
The Gene Encoding Guanidinoacetate Methyltransferase (GAMT) Maps to Human Chromosome 19 at Band p13.3 and to Mouse Chromosome 10
|
Chae, Young-Jin
|
|
1998
|
49 |
1 |
p. 162-164
3 p.
|
article
|
| 24 |
The Periplakin Gene Maps to 16p13.3 in Human and 16A–B1 in Mouse
|
Ruhrberg, Christiana
|
|
1998
|
49 |
1 |
p. 157-159
3 p.
|
article
|
| 25 |
The Protein Kinase N (PKN) GenePRKCL1/Prkcl1Maps to Human Chromosome 19p12–p13.1 and Mouse Chromosome 8 with Close Linkage to the Myodystrophy (myd) Mutation
|
Bartsch, Jörg W.
|
|
1998
|
49 |
1 |
p. 129-132
4 p.
|
article
|
Journal description