scholarly journals Genetic map of seven polymorphic markers comprising a single linkage group on rat Chromosome 5

1993 ◽  
Vol 4 (11) ◽  
pp. 670-675 ◽  
Author(s):  
Ellen A. Goldmuntz ◽  
Elaine F. Remmers ◽  
Hongbin Zha ◽  
Peter Mathern ◽  
Ying Du ◽  
...  
Keyword(s):  
Linkage Group ◽  
Genetic Map ◽  
Polymorphic Markers ◽  
Chromosome 5 ◽  
Single Linkage

Genetic map of nine polymorphic loci comprising a single linkage group on rat chromosome 10: Evidence for linkage conservation with human chromosome 17 and mouse chromosome 11

Genomics ◽  
1992 ◽  
Vol 14 (3) ◽  
pp. 618-623 ◽  
Author(s):  
Elaine F. Remmers ◽  
Ellen A. Goldmuntz ◽  
Joseph M. Cash ◽  
Leslie J. Crofford ◽  
Barbara Misiewicz-Poltorak ◽  
...  
Keyword(s):  
Linkage Group ◽  
Human Chromosome ◽  
Mouse Chromosome ◽  
Genetic Map ◽  
Chromosome 17 ◽  
Chromosome 11 ◽  
Single Linkage ◽  
Human Chromosome 17 ◽  
Mouse Chromosome 11 ◽  
Linkage Conservation

Four polymorphic markers on rat chromosome 12 form a single linkage group

1993 ◽  
Vol 31 (9-10) ◽  
pp. 441-448 ◽  
Author(s):  
Peter Mathern ◽  
Ellen A. Goldmuntz ◽  
Hongbin Zha ◽  
Ying Du ◽  
Leslie J. Crofford ◽  
...  
Keyword(s):  
Linkage Group ◽  
Chromosome 12 ◽  
Polymorphic Markers ◽  
Single Linkage

A single linkage group comprising 11 polymorphic DNA markers on rat Chromosome 3

1994 ◽  
Vol 5 (9) ◽  
pp. 538-541 ◽  
Author(s):  
H. Zha ◽  
E. F. Remmers ◽  
Y. Du ◽  
E. A. Goldmuntz ◽  
P. Mathern ◽  
...  
Keyword(s):  
Linkage Group ◽  
Dna Markers ◽  
Chromosome 3 ◽  
Single Linkage

Genetic map of rat Chromosome 5 including the fatty (fa) locus

1995 ◽  
Vol 6 (1) ◽  
pp. 25-30 ◽  
Author(s):  
G. E. Truett ◽  
H. J. Jacob ◽  
J. Miller ◽  
G. Drouin ◽  
N. Bahary ◽  
...  
Keyword(s):  
Genetic Map ◽  
Chromosome 5

scholarly journals Centromere-Linkage Analysis and Consolidation of the Zebrafish Genetic Map

Genetics ◽  
1996 ◽  
Vol 142 (4) ◽  
pp. 1277-1288
Author(s):  
Stephen L Johnson ◽  
Michael A Gates ◽  
Michele Johnson ◽  
William S Talbot ◽  
Sally Horne ◽  
...  
Keyword(s):  
Linkage Group ◽  
Linkage Analysis ◽  
Genetic Analysis ◽  
Linkage Map ◽  
Rapid Method ◽  
Genetic Map ◽  
Dna Polymorphisms ◽  
Linkage Groups

Abstract The ease of isolating mutations in zebrafish will contribute to an understanding of a variety of processes common to all vertebrates. To facilitate genetic analysis of such mutations, we have identified DNA polymorphisms closely linked to each of the 25 centromeres of zebrafish, placed centromeres on the linkage map, increased the number of mapped PCR-based markers to 652, and consolidated the number of linkage groups to the number of chromosomes. This work makes possible centromere-linkage analysis, a novel, rapid method to assign mutations to a specific linkage group using half-tetrads.

The genetic and RFLP characterization of the left end of linkage group III in Caenorhabditis elegans

Genome ◽  
1993 ◽  
Vol 36 (4) ◽  
pp. 712-724 ◽  
Author(s):  
Dave Pilgrim
Keyword(s):  
Caenorhabditis Elegans ◽  
Linkage Group ◽  
Genetic Map ◽  
Physical Map ◽  
Group Iii ◽  
C Elegans ◽  
Genomic Regions ◽  
Caenorhabditis Elegans Genome ◽  
Selection Of

A genetic approach was taken to identify new transposable element Tc1 -dependent polymorphisms on the left end of linkage group III in the nematode Caenorhabditis elegans. The cloning of the genomic DNA surrounding the Tc1 allowed the selection of overlapping clones (from the collection being used to assemble the physical map of the C. elegans genome). A contig of approximately 600–800 kbp in the region has been identified, the genetic map of the region has been refined, and 10 new RFLPs as well as at least four previously characterized genetic loci have been positioned onto the physical map, to the resolution of a few cosmids. This analysis demonstrated the ability to combine physical and genetic mapping for the rapid analysis of large genomic regions (0.5–1 Mbp) in genetically amenable eukaryotes.Key words: Caenorhabditis elegans, genome analysis, RFLP, physical map, genetic map.

Genetic map of 16 polymorphic markers forming three linkage groups assigned to rat Chromosome 4

1995 ◽  
Vol 6 (7) ◽  
pp. 459-463 ◽  
Author(s):  
E. A. Goldmuntz ◽  
E. F. Remmers ◽  
Y. Du ◽  
H. Zha ◽  
P. Mathern ◽  
...  
Keyword(s):  
Genetic Map ◽  
Polymorphic Markers ◽  
Chromosome 4 ◽  
Linkage Groups

A long-range restriction map of the interleukin-4 and interleukin-5 linkage group on chromosome 5

Genomics ◽  
1990 ◽  
Vol 6 (1) ◽  
pp. 94-99 ◽  
Author(s):  
Settara C. Chandrasekharappa ◽  
Michelle S. Rebelsky ◽  
Thomas A. Firak ◽  
Michelle M. Le Beau ◽  
Carol A. Westbrook
Keyword(s):  
Linkage Group ◽  
Long Range ◽  
Interleukin 4 ◽  
Restriction Map ◽  
Chromosome 5 ◽  
Range Restriction ◽  
Interleukin 5

scholarly journals Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families

Genomics ◽  
2006 ◽  
Vol 87 (1) ◽  
pp. 1-29 ◽  
Author(s):  
June E. Swinburne ◽  
Mike Boursnell ◽  
Gemma Hill ◽  
Louise Pettitt ◽  
Twink Allen ◽  
...  
Keyword(s):  
Linkage Group ◽  
Linkage Map ◽  
Genetic Linkage ◽  
Genetic Linkage Map ◽  
Single Linkage ◽  
Full Sibling

scholarly journals The Mouse Clock Mutation Behaves as an Antimorph and Maps Within the W19H Deletion, Distal of Kit

Genetics ◽  
1997 ◽  
Vol 146 (3) ◽  
pp. 1049-1060 ◽  
Author(s):  
David P King ◽  
Martha Hotz Vitaterna ◽  
Anne-Marie Chang ◽  
William F Dove ◽  
Lawrence H Pinto ◽  
...  
Keyword(s):  
High Resolution ◽  
Mouse Chromosome ◽  
Genetic Map ◽  
Circadian System ◽  
Complementation Analysis ◽  
Chromosome 5 ◽  
Mutagenesis Screen ◽  
Circadian Behavior

Clock is a semidominant mutation identified from an N-ethyl-N-nitrosourea mutagenesis screen in mice. Mice carrying the Clock mutation exhibit abnormalities of circadian behavior, including lengthening of endogenous period and loss of rhythmicity. To identify the gene affected by this mutation, we have generated a high-resolution genetic map (>1800 meioses) of the Clock locus. We report that Clock is 0.7 cM distal of Kit on mouse chromosome 5. Mapping shows that Clock lies within the W19H deletion. Complementation analysis of different Clock and W19H compound genotypes indicates that the Clock mutation behaves as an antimorph. This antimorphic behavior of Clock strongly argues that Clock defines a gene centrally involved in the mammalian circadian system.

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