A refined physical map of the long arm of human chromosome 16

Genomics ◽  
1991 ◽  
Vol 10 (2) ◽  
pp. 308-312 ◽  
Author(s):  
L.Z. Chen ◽  
P.C. Harris ◽  
S. Apostolou ◽  
E. Baker ◽  
K. Holman ◽  
...  
Keyword(s):  
Human Chromosome ◽  
Physical Map ◽  
Chromosome 16

Human chromosome 16 physical map: Mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sites

Genomics ◽  
1991 ◽  
Vol 10 (4) ◽  
pp. 1047-1052 ◽  
Author(s):  
Robert I. Richards ◽  
Katherine Holman ◽  
Sharon Lane ◽  
Grant R. Sutherland ◽  
David F. Callen
Keyword(s):  
Human Chromosome ◽  
Somatic Cell ◽  
Multiplex Pcr ◽  
Physical Map ◽  
Deletion Analysis ◽  
Somatic Cell Hybrids ◽  
Chromosome 16 ◽  
Cell Hybrids ◽  
Sequence Tagged Sites

Evaluation of a cosmid contig physical map of human chromosome 16

Genomics ◽  
1992 ◽  
Vol 13 (4) ◽  
pp. 1031-1039 ◽  
Author(s):  
Raymond L. Stallings ◽  
Norman A. Doggett ◽  
David Callen ◽  
Sinoula Apostolou ◽  
L.Zhong Chen ◽  
...  
Keyword(s):  
Human Chromosome ◽  
Physical Map ◽  
Chromosome 16 ◽  
Cosmid Contig

High-resolution cytogenetic-based physical map of human chromosome 16

Genomics ◽  
1992 ◽  
Vol 13 (4) ◽  
pp. 1178-1185 ◽  
Author(s):  
D.F. Callen ◽  
N.A. Doggett ◽  
R.L. Stallings ◽  
L.Z. Chen ◽  
S.A. Whitmore ◽  
...  
Keyword(s):  
High Resolution ◽  
Human Chromosome ◽  
Physical Map ◽  
Chromosome 16

Integration of 28 STSs into the Physical Map of Human Chromosome 18

Genomics ◽  
1994 ◽  
Vol 24 (3) ◽  
pp. 612-613 ◽  
Author(s):  
Steve Gerken ◽  
Kimberlee Fish ◽  
Denise Uyar ◽  
Mihael H. Polymeropoulos ◽  
Paige Bradley ◽  
...  
Keyword(s):  
Human Chromosome ◽  
Physical Map ◽  
Chromosome 18

scholarly journals Regulatory factors specific for adult and embryonic globin genes may govern their expression in erythroleukemia cells

Blood ◽  
1985 ◽  
Vol 65 (3) ◽  
pp. 705-712 ◽  
Author(s):  
NP Anagnou ◽  
TY Yuan ◽  
E Lim ◽  
J Helder ◽  
S Wieder ◽  
...  
Keyword(s):  
Gene Expression ◽  
Human Chromosome ◽  
Globin Gene ◽  
Globin Genes ◽  
Chromosome 16 ◽  
Regulatory Factors ◽  
Erythroleukemia Cells ◽  
Erythroleukemia Cell ◽  
Globin Gene Expression ◽  
Mouse Erythroleukemia

Abstract In order to test if trans-acting regulatory factors specific for globin genes of the adult and embryonic stages of development exist in erythroid cells, transcriptionally active embryonic and adult globin genes on the same chromosome were transferred by cell fusion from the human leukemia cell K562 into phenotypically adult mouse erythroleukemia cells. Restriction-fragment-length polymorphisms of the K562 zeta (embryonic) globin genes were used to establish that all three copies of human chromosome 16 present in the K562 cell showed the same pattern of human globin gene expression after transfer to the mouse erythroleukemia cell. Adult (alpha) but not embryonic (zeta) human globin mRNA was detected in all nine of the independently derived mouse erythroleukemia hybrid cells, each of which contained human chromosome 16. Restriction endonuclease studies of the K562 alpha- and zeta-globin genes after transfer into the mouse erythroleukemia cell showed no evidence of rearrangements or deletions that could explain this loss of zeta-globin gene expression. These data suggest that regulation of globin gene expression in these erythroleukemia cells involves trans-acting regulatory factors specific for the adult and embryonic stages of development.

Report of the Fourth International Workshop on Human Chromosome 16 Mapping 1995

1996 ◽  
Vol 72 (4) ◽  
pp. 271-293 ◽  
Author(s):  
Martijn H. Breuning ◽  
Norman A. Doggett ◽  
David F. Callen
Keyword(s):  
Human Chromosome ◽  
International Workshop ◽  
Chromosome 16

A 2.8 megabase YAC contig spanning D8S339, which is tightly linked to the Werner syndrome locus

Genome ◽  
1997 ◽  
Vol 40 (1) ◽  
pp. 77-83
Author(s):  
R. Bruskiewich ◽  
M. Schertzer ◽  
S. Wood
Keyword(s):  
Human Chromosome ◽  
Genetic Marker ◽  
Yeast Artificial Chromosome ◽  
Werner Syndrome ◽  
Physical Map ◽  
Artificial Chromosome ◽  
Sequence Tagged Sites ◽  
Yeast Artificial Chromosome Contig ◽  
Yac Contig ◽  
Chromosome 8P

A number of gene loci, including the locus for Werner syndrome (WRN), map to proximal human chromosome 8p near the genetic marker D8S339. In this report, we present a long range physical map of an approximately 2.8 megabase yeast artificial chromosome contig centred on D8S339. In this map, we localize the WRN-linked polymorphic sequence-tagged sites (STS) D8S339 and D8S1055, as well as a novel polymorphic STS, D8S2297. We also refine the positions of three known gene loci, GTF2E2, GSR, and PPP2CB, relative to the location of WRN within the map.Key words: WRN, GTF2E2, GSR, PPP2CB, physical map, human chromosome 8p.

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