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R Critcher

Explore the profile of R Critcher including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 19
Citations 325
Followers 0
Related Specialties
Genetics
Molecular Biology
Cell Biology
Top 10 Co-Authors
P N Goodfellow
C J Farr
L C McCarthy
K Schmitt
M E Davis
S L Kiguwa
W Mills
T Takagi
A Tsuji
J Browne
Published In
Genomics
Cytogenet Cell Genet
Hum Mol Genet
Mamm Genome
Chromosoma
Affiliations
Soon will be listed here.
Recent Articles
1.
Assignment of TERF1 to chicken chromosome 2q32 and TERF2 to chicken microchromosome 11 by fluorescence in situ hybridization
Fillon V, Critcher R, Baird K, Konrad J, Vignal A, Farr C
Cytogenet Cell Genet . 2001 Apr; 92(1-2):175-6. PMID: 11306824
No abstract available.
2.
Distribution of gamma satellite DNA on the human X and Y chromosomes suggests that it is not required for mitotic centromere function
Lee C, Critcher R, Zhang J, Mills W, Farr C
Chromosoma . 2000 Nov; 109(6):381-9. PMID: 11072793
The bulk of the DNA found at human centromeres is composed of tandemly arranged repeats, the most abundant of which is alpha satellite. Other human centromeric repetitive families have been...
3.
A horse whole-genome-radiation hybrid panel: chromosome 1 and 10 preliminary maps
Kiguwa S, Hextall P, Smith A, Critcher R, Swinburne J, Millon L, et al.
Mamm Genome . 2000 Sep; 11(9):803-5. PMID: 10967144
No abstract available.
4.
A whole-genome radiation hybrid panel and framework map of the rat genome
McCarthy L, Bihoreau M, Kiguwa S, Browne J, Watanabe T, Hishigaki H, et al.
Mamm Genome . 2000 Sep; 11(9):791-5. PMID: 10967141
No abstract available.
5.
Genomic characterisation and fine mapping of the human SOX13 gene
Argentaro A, Olsson J, Critcher R, McDowall S, Harley V
Gene . 2000 Jun; 250(1-2):181-9. PMID: 10854791
SOX13 is the member of the SOX (Sry related HMG BOX) family of transcription factors which encodes the type-1 diabetes autoantigen, ICA12, and is expressed in a number of tissues...
6.
A radiation hybrid map of the rat genome containing 5,255 markers
Watanabe T, Bihoreau M, McCarthy L, Kiguwa S, Hishigaki H, Tsuji A, et al.
Nat Genet . 1999 May; 22(1):27-36. PMID: 10319858
A whole-genome radiation hybrid (RH) panel was used to construct a high-resolution map of the rat genome based on microsatellite and gene markers. These include 3,019 new microsatellite markers described...
7.
Generation of an approximately 2.4 Mb human X centromere-based minichromosome by targeted telomere-associated chromosome fragmentation in DT40
Mills W, Critcher R, Lee C, Farr C
Hum Mol Genet . 1999 Apr; 8(5):751-61. PMID: 10196364
A linear mammalian artificial chromosome (MAC) will require at least three types of functional element: a centromere, two telomeres and origins of replication. As yet, our understanding of these elements,...
8.
Construction and characterization of zebrafish whole genome radiation hybrids
Kwok C, Critcher R, Schmitt K
Methods Cell Biol . 1999 Jan; 60:287-302. PMID: 9891343
No abstract available.
9.
Assignment of Sox4 to mouse chromosome 13 bands A3-A5 by fluorescence in situ hybridization; refinement of the human SOX4 location to 6p22.3 and of SOX20 to chromosome 17p12.3
Critcher R, Stitson R, Wade-Martins R, Easty D, Farr C
Cytogenet Cell Genet . 1998 Sep; 81(3-4):294-5. PMID: 9730625
No abstract available.
10.
Deletion of long-range regulatory elements upstream of SOX9 causes campomelic dysplasia
Wunderle V, Critcher R, Hastie N, Goodfellow P, Schedl A
Proc Natl Acad Sci U S A . 1998 Sep; 95(18):10649-54. PMID: 9724758
Campomelic dysplasia (CD) is a rare, neonatal human chondrodysplasia characterized by bowing of the long bones and often associated with male-to-female sex-reversal. Patients present with either heterozygous mutations in the...