-
1
-
-
0030200869
-
A yeast artificial chromosome contig and NotI restriction map that spans the tumor suppressor gene(s) locus, 11q22.2-q23.3
-
Arai, Y., F. Hosoda, K. Nakayama, and M. Ohki. 1996. A yeast artificial chromosome contig and NotI restriction map that spans the tumor suppressor gene(s) locus, 11q22.2-q23.3. Genomics 35: 195-206.
-
(1996)
Genomics
, vol.35
, pp. 195-206
-
-
Arai, Y.1
Hosoda, F.2
Nakayama, K.3
Ohki, M.4
-
2
-
-
0031238583
-
A high resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23
-
Baysal, B.E., E.M. van Schothorst, J.E. Farr, M.R. James, P. Devilee, and C.W. Richard III. 1997. A high resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23. Genomics 44: 214-221.
-
(1997)
Genomics
, vol.44
, pp. 214-221
-
-
Baysal, B.E.1
Van Schothorst, E.M.2
Farr, J.E.3
James, M.R.4
Devilee, P.5
Richard C.W. III6
-
3
-
-
0028952956
-
A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet alpha-granules and chromosome 11 deletion at 11q
-
Breton-Gorius, J., R. Favier, J. Guichard, D. Cherif, R. Berger, N. Debili, W. Vainchenker, and L. Douay. 1995. A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet alpha-granules and chromosome 11 deletion at 11q. Blood 85: 1805-1814.
-
(1995)
Blood
, vol.85
, pp. 1805-1814
-
-
Breton-Gorius, J.1
Favier, R.2
Guichard, J.3
Cherif, D.4
Berger, R.5
Debili, N.6
Vainchenker, W.7
Douay, L.8
-
4
-
-
0028295479
-
Hunting 11q23 deletions with fluorescence in situ hybridization (FISH)
-
Cherif, D., O. Bernard, S. Paulien, M.R. James, D. Le Paslier, and R. Berger. 1994. Hunting 11q23 deletions with fluorescence in situ hybridization (FISH). Leukemia 8: 578-586.
-
(1994)
Leukemia
, vol.8
, pp. 578-586
-
-
Cherif, D.1
Bernard, O.2
Paulien, S.3
James, M.R.4
Le Paslier, D.5
Berger, R.6
-
5
-
-
0027723477
-
A first generation physical map of the human genome
-
Cohen, D., I. Chumakov, and J. Weissenbach. 1993. A first generation physical map of the human genome. Nature 366: 398-400.
-
(1993)
Nature
, vol.366
, pp. 398-400
-
-
Cohen, D.1
Chumakov, I.2
Weissenbach, J.3
-
6
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib, C., S. Fauré, C. Fizames, D. Samson, N. Drouot, A. Vignal, P. Millasseau, S. Marc, J. Hazan, E. Seboun et al. 1996. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380: 152-154.
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Fauré, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
-
7
-
-
1842328565
-
11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis
-
Döhner, H., S. Stilgenbauer, M.R. James, A. Benner, T. Weilguni, M. Bentz, K. Fischer, W. Hunstein, and P. Lichter. 1997. 11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis. Blood 89: 2516-2522.
-
(1997)
Blood
, vol.89
, pp. 2516-2522
-
-
Döhner, H.1
Stilgenbauer, S.2
James, M.R.3
Benner, A.4
Weilguni, T.5
Bentz, M.6
Fischer, K.7
Hunstein, W.8
Lichter, P.9
-
8
-
-
0020793569
-
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
-
Feinberg, A.P. and B. Vogelstein. 1983. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 132: 6-13.
-
(1983)
Anal. Biochem.
, vol.132
, pp. 6-13
-
-
Feinberg, A.P.1
Vogelstein, B.2
-
10
-
-
0028318417
-
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments
-
Ioannou, P.A., C.T. Amemiya, J. Garnes, P.M. Kroisel, H. Shizuya, C. Chen, M.A. Batzer, and P.J. De Jong. 1994. A new bacteriophage P1-derived vector for the propagation of large human DNA fragments. Nat. Genet. 6: 84-89.
-
(1994)
Nat. Genet.
, vol.6
, pp. 84-89
-
-
Ioannou, P.A.1
Amemiya, C.T.2
Garnes, J.3
Kroisel, P.M.4
Shizuya, H.5
Chen, C.6
Batzer, M.A.7
De Jong, P.J.8
-
11
-
-
20244377832
-
A radiation hybrid map of 506 STS markers spanning human chromosome 11
-
James, M.R., C.W. Richard III, J.J. Schott, C. Yousry, K. Clark, J. Bell, J.D. Terwilliger, J. Hazan, C. Dubay, A. Vignal et al. 1994. A radiation hybrid map of 506 STS markers spanning human chromosome 11. Nat. Genet. 9: 70-76.
-
(1994)
Nat. Genet.
, vol.9
, pp. 70-76
-
-
James, M.R.1
Richard C.W. III2
Schott, J.J.3
Yousry, C.4
Clark, K.5
Bell, J.6
Terwilliger, J.D.7
Hazan, J.8
Dubay, C.9
Vignal, A.10
-
12
-
-
0028557941
-
Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3
-
Jones, C., P. Slijepcevic, S. Marsh, E. Baker, W.Y. Langdon, R.I. Richards, and A. Tunnacliffe. 1994. Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3. Hum. Mol. Genet. 3: 2123-2130.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 2123-2130
-
-
Jones, C.1
Slijepcevic, P.2
Marsh, S.3
Baker, E.4
Langdon, W.Y.5
Richards, R.I.6
Tunnacliffe, A.7
-
13
-
-
0028896099
-
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2
-
Jones, C., L. Penny, T. Mattina, S. Yu, E. Baker, L. Voullaire, W.Y. Langdon, G.R. Sutherland, R.I. Richards, and A. Tunnacliffe. 1995. Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2. Nature 376: 145-149.
-
(1995)
Nature
, vol.376
, pp. 145-149
-
-
Jones, C.1
Penny, L.2
Mattina, T.3
Yu, S.4
Baker, E.5
Voullaire, L.6
Langdon, W.Y.7
Sutherland, G.R.8
Richards, R.I.9
Tunnacliffe, A.10
-
14
-
-
0033521961
-
11q23.1 and 11q25-qter YACs suppress tumor growth in vivo
-
in press
-
Koreth, J., C.J. Bakkenist, Z. Larin, N.C.A. Hunt, M.R. James, and J.O.D. McGee. 1999. 11q23.1 and 11q25-qter YACs suppress tumor growth in vivo. Oncogene (in press).
-
(1999)
Oncogene
-
-
Koreth, J.1
Bakkenist, C.J.2
Larin, Z.3
Hunt, N.C.A.4
James, M.R.5
McGee, J.O.D.6
-
15
-
-
0025800165
-
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
-
Kremer, E.J., M. Pritchard, M. Lynch, S. Yu, K. Holman, E. Baker, S.T. Warren, D. Schlessinger, G.R. Sutherland, and R.J. Richards. 1991. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n. Science 252: 1711-1714.
-
(1991)
Science
, vol.252
, pp. 1711-1714
-
-
Kremer, E.J.1
Pritchard, M.2
Lynch, M.3
Yu, S.4
Holman, K.5
Baker, E.6
Warren, S.T.7
Schlessinger, D.8
Sutherland, G.R.9
Richards, R.J.10
-
16
-
-
0032546337
-
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B
-
Michaelis, R.C., G.V.N. Velagaleti, C. Jones, E.K. Pivnick, M.C. Phelan, E. Boyd, J. Tarleton, R.S. Wilroy, A. Tunnacliffe, and A.T. Tharapel. 1998. Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B. Am. J. Med. Genet. 76: 222-228.
-
(1998)
. Am. J. Med. Genet.
, vol.76
, pp. 222-228
-
-
Michaelis, R.C.1
Velagaleti, G.V.N.2
Jones, C.3
Pivnick, E.K.4
Phelan, M.C.5
Boyd, E.6
Tarleton, J.7
Wilroy, R.S.8
Tunnacliffe, A.9
Tharapel, A.T.10
-
17
-
-
0028910140
-
Clinical and molecular characterization of patients with distal 11q deletions
-
Penny, L.A., M. Dell'Aquila, M.C. Jones, J. Bergoffen, C. Cunniff, J.-P. Fryns, E. Grace, J.M. Graham, Jr., B. Kousseff, T. Mattina et al. 1995. Clinical and molecular characterization of patients with distal 11q deletions. Am. J. Hum. Genet. 56: 676-683.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 676-683
-
-
Penny, L.A.1
Dell'Aquila, M.2
Jones, M.C.3
Bergoffen, J.4
Cunniff, C.5
Fryns, J.-P.6
Grace, E.7
Graham J.M., Jr.8
Kousseff, B.9
Mattina, T.10
-
18
-
-
0029745041
-
Jacobsen syndrome: Report of a patient with severe eye anomalies, growth hormone deficiency, hypothyroidism associated with deletion 11(q23q25) and review of 52 cases
-
Pivnick, E.K., G.V.N. Velagaleti, R.S. Wilroy, M.E. Smith, S.R. Rose, R.E. Tipton, and A.T. Tharapel. 1996. Jacobsen syndrome: Report of a patient with severe eye anomalies, growth hormone deficiency, hypothyroidism associated with deletion 11(q23q25) and review of 52 cases. J. Med. Genet. 33: 772-778.
-
(1996)
J. Med. Genet.
, vol.33
, pp. 772-778
-
-
Pivnick, E.K.1
Velagaleti, G.V.N.2
Wilroy, R.S.3
Smith, M.E.4
Rose, S.R.5
Tipton, R.E.6
Tharapel, A.T.7
-
19
-
-
0030664357
-
Dynamic mutation: Possible mechanisms and significance in human disease
-
Richards, R.I. and G.R. Sutherland. 1997. Dynamic mutation: Possible mechanisms and significance in human disease. Trends Biochem. Sci. 22: 432-436.
-
(1997)
Trends Biochem. Sci.
, vol.22
, pp. 432-436
-
-
Richards, R.I.1
Sutherland, G.R.2
-
20
-
-
0025339588
-
A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones
-
Riley, J., R. Butler, D. Ogilvie, R. Finniear, D. Jenner, S. Powell, R. Anand, J.C. Smith, and A.F. Markham. 1990. A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones. Nucleic Acids Res. 18: 2887-2890.
-
(1990)
Nucleic Acids Res.
, vol.18
, pp. 2887-2890
-
-
Riley, J.1
Butler, R.2
Ogilvie, D.3
Finniear, R.4
Jenner, D.5
Powell, S.6
Anand, R.7
Smith, J.C.8
Markham, A.F.9
-
21
-
-
0004136246
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Sambrook, J., E.F. Fritsch, and T. Maniatis. 1989. Molecular cloning: A laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
22
-
-
0029792056
-
Report of the fifth international workshop on human chromosome 11 mapping
-
Shows, T.B., M. Alders, S. Bennet, D. Burbee, P. Cartwright, S. Chandrasekharappa, P. Cooper, A. Courseaux, C. Davies, M.-D. Devignes et al. 1996. Report of the fifth international workshop on human chromosome 11 mapping. Cytogenet. Cell Genet. 74: 1-56.
-
(1996)
Cytogenet. Cell Genet.
, vol.74
, pp. 1-56
-
-
Shows, T.B.1
Alders, M.2
Bennet, S.3
Burbee, D.4
Cartwright, P.5
Chandrasekharappa, S.6
Cooper, P.7
Courseaux, A.8
Davies, C.9
Devignes, M.-D.10
-
23
-
-
0029969111
-
Molecular cytogenetic delineation of a novel critical genomic region in chromosome bands 11q22.3-23.1 in lymphoproliferative disorders
-
Stilgenbauer, S., P. Liebisch, M.R. James, M. Schröder, B. Schlegelberger, K. Fischer, M. Bentz, P. Lichter, and H. Döhner. 1996. Molecular cytogenetic delineation of a novel critical genomic region in chromosome bands 11q22.3-23.1 in lymphoproliferative disorders. Proc. Natl. Acad. Sci. 93: 11837-11841.
-
(1996)
Proc. Natl. Acad. Sci.
, vol.93
, pp. 11837-11841
-
-
Stilgenbauer, S.1
Liebisch, P.2
James, M.R.3
Schröder, M.4
Schlegelberger, B.5
Fischer, K.6
Bentz, M.7
Lichter, P.8
Döhner, H.9
-
25
-
-
0029862406
-
Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes
-
van Schothorst, E.M., J.C. Jansen, A.F.J. Bardoel, A.G.L. van der Mey, M.R. James, H. Sobol, J. Weissenbach, G.-J.B. van Ommen, C.J. Cornelisse, and P. Devilee. 1996. Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes. Eur. J. Hum. Genet. 4: 267-273.
-
(1996)
Eur. J. Hum. Genet.
, vol.4
, pp. 267-273
-
-
Van Schothorst, E.M.1
Jansen, J.C.2
Bardoel, A.F.J.3
Van Der Mey, A.G.L.4
James, M.R.5
Sobol, H.6
Weissenbach, J.7
Van Ommen, G.-J.B.8
Cornelisse, C.J.9
Devilee, P.10
-
26
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk, A.J.M.H., M. Pieretti, J.S. Sutcliffe, Y.-H. Fu, D.P.A. Kuhl, A. Pizzuti, O. Reiner, S. Richards, M.F. Victoria, F. Zhang et al. 1991. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65: 905-914.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.-H.4
Kuhl, D.P.A.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.10
-
27
-
-
85070037709
-
Mapping of human chromosome 11qter
-
in press
-
Yousry, C., D. Browne, D. Cherif, C.W. Richard III, N. Janin, V. Baud, M. Lipinski, U. Claussen, B. Horsthemke, M. Birdsall et al. 1999. Mapping of human chromosome 11qter. Cytogenet. Cell Genet. (in press).
-
(1999)
Cytogenet. Cell Genet.
-
-
Yousry, C.1
Browne, D.2
Cherif, D.3
Richard C.W. III4
Janin, N.5
Baud, V.6
Lipinski, M.7
Claussen, U.8
Horsthemke, B.9
Birdsall, M.10
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