-
1
-
-
0027141519
-
Number of CpG islands and genes in human and mouse
-
Antequera F, Bird A (1993) Number of CpG islands and genes in human and mouse. Proc Natl Acad Sci USA 90:11995-11999.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 11995-11999
-
-
Antequera, F.1
Bird, A.2
-
2
-
-
0342788462
-
Analysis of the FACC and XPAC genes as candidate genes for the basal cell nevus syndrome
-
Program and Abstract
-
Bare JW, Xie J, Quinn AG, Epstein Jr EH (1995) Analysis of the FACC and XPAC genes as candidate genes for the basal cell nevus syndrome. Am J Hum Genet 57: Program and Abstract 312.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 312
-
-
Bare, J.W.1
Xie, J.2
Quinn, A.G.3
Epstein E.H., Jr.4
-
3
-
-
0024393234
-
The human genome contains hundreds of gene encoding zinc finger proteins of the Kruppel type
-
Bellefroid EJ, Lecocq PJ, Benhida A, Poncelet DA, Belayew A, Martial JA (1989) The human genome contains hundreds of gene encoding zinc finger proteins of the Kruppel type. DNA 8:377-387.
-
(1989)
DNA
, vol.8
, pp. 377-387
-
-
Bellefroid, E.J.1
Lecocq, P.J.2
Benhida, A.3
Poncelet, D.A.4
Belayew, A.5
Martial, J.A.6
-
4
-
-
0025920615
-
The evolutionary conserved kruppel-associated box domain defines a subfamily of eukaryotic multifingered proteins
-
Bellefroid EJ, Poncelet DA, Lecocq, PJ, Revelant O, Martial JA (1991) The evolutionary conserved kruppel-associated box domain defines a subfamily of eukaryotic multifingered proteins. Proc Natl Acad Sci USA 88:3608-3612.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 3608-3612
-
-
Bellefroid, E.J.1
Poncelet, D.A.2
Lecocq, P.J.3
Revelant, O.4
Martial, J.A.5
-
5
-
-
0028219676
-
Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients
-
Bonifas JM, Bare JW, Kerschmann RL, Master SP, Epstein EH Jr (1994) Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients. Hum Mol Genet 3:447-448.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 447-448
-
-
Bonifas, J.M.1
Bare, J.W.2
Kerschmann, R.L.3
Master, S.P.4
Epstein E.H., Jr.5
-
6
-
-
0024986272
-
Rapid cloning and characterization of new chromosome 10 DNA markers by Alu-element mediated PCR
-
Brooks-Wilson AR, Goodfellow PN, Povey S, Nevalinna HA, deJong PJ, Goodfellow PJ (1990) Rapid cloning and characterization of new chromosome 10 DNA markers by Alu-element mediated PCR. Genomics 7:617-620.
-
(1990)
Genomics
, vol.7
, pp. 617-620
-
-
Brooks-Wilson, A.R.1
Goodfellow, P.N.2
Povey, S.3
Nevalinna, H.A.4
DeJong, P.J.5
Goodfellow, P.J.6
-
7
-
-
0027436115
-
Kurther localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: Linkage and loss of hererozygosity
-
Chenevix-Trench G, Wicking C, Berkman J, Sharpe H, Goldgar D, Searle J, Wainright B (1993) Kurther localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: Linkage and loss of hererozygosity. Am J Hum Genet 53:760-767.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 760-767
-
-
Chenevix-Trench, G.1
Wicking, C.2
Berkman, J.3
Sharpe, H.4
Goldgar, D.5
Searle, J.6
Wainright, B.7
-
8
-
-
0028348712
-
Structure, function and chromosome mapping of the growth suppressing human homologue of the murine GAS1 gene
-
Del Sal G, Collavin L, Ruaro ME, Edomi P, Saccone S, Della Valle G, Schneider C (1994) Structure, function and chromosome mapping of the growth suppressing human homologue of the murine GAS1 gene. Proc Natl Acad Sci, USA 91:1848-1852.
-
(1994)
Proc Natl Acad Sci, USA
, vol.91
, pp. 1848-1852
-
-
Del Sal, G.1
Collavin, L.2
Ruaro, M.E.3
Edomi, P.4
Saccone, S.5
Della Valle, G.6
Schneider, C.7
-
9
-
-
0021760092
-
A comprehensive set of sequence analysis programs for the VAX
-
Devereaux J, Haberli P, Smithies O (1984) A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res 12:387-395.
-
(1984)
Nucleic Acids Res
, vol.12
, pp. 387-395
-
-
Devereaux, J.1
Haberli, P.2
Smithies, O.3
-
10
-
-
0027968936
-
Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anaemia Group C in a 2.6-cM interval and contributes to the fine map of 9q22.3
-
Farndon PA, Morris DJ, Hardy C, McConville CM, Weissenbach J, Kilpatrick MW, Reis A (1994) Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anaemia Group C in a 2.6-cM interval and contributes to the fine map of 9q22.3. Genomics 23:486-489.
-
(1994)
Genomics
, vol.23
, pp. 486-489
-
-
Farndon, P.A.1
Morris, D.J.2
Hardy, C.3
McConville, C.M.4
Weissenbach, J.5
Kilpatrick, M.W.6
Reis, A.7
-
11
-
-
0026627965
-
Developmental defects in gorlin syndrome related to a purative tumor suppressor gene on chromosome 9
-
Gailani MR, Bale SJ, Leffell DJ, DiGiovanna JJ, Peck GL, Poliack S, Drum MA, Pastakia B, McBride OW, Kase R, Green M, Mulvihill JJ, Bale AE (1992) Developmental defects in gorlin syndrome related to a purative tumor suppressor gene on chromosome 9. Cell 69:111-117.
-
(1992)
Cell
, vol.69
, pp. 111-117
-
-
Gailani, M.R.1
Bale, S.J.2
Leffell, D.J.3
DiGiovanna, J.J.4
Peck, G.L.5
Poliack, S.6
Drum, M.A.7
Pastakia, B.8
McBride, O.W.9
Kase, R.10
Green, M.11
Mulvihill, J.J.12
Bale, A.E.13
-
12
-
-
0027269608
-
Sun exposure and basal cell carcinomas in the nevoid basal cell carcinoma syndrome
-
Goldstein AM, Bale SJ, Peck GL, DiGiovanna JJ (1993) Sun exposure and basal cell carcinomas in the nevoid basal cell carcinoma syndrome. J Am Acad Dermatol 29:34-41.
-
(1993)
J Am Acad Dermatol
, vol.29
, pp. 34-41
-
-
Goldstein, A.M.1
Bale, S.J.2
Peck, G.L.3
DiGiovanna, J.J.4
-
13
-
-
0028316105
-
Localization of the gene for the nevoid basal cell carcinoma syndrome
-
Goldstein AM, Stewart C, Bale AE, Bale SJ, Dean M (1994) Localization of the gene for the nevoid basal cell carcinoma syndrome. Am J Hum Genet 54:765-773.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 765-773
-
-
Goldstein, A.M.1
Stewart, C.2
Bale, A.E.3
Bale, S.J.4
Dean, M.5
-
14
-
-
0023222358
-
Nevoid basal-cell carcinoma syndrome
-
Gorlin RJ (1987) Nevoid basal-cell carcinoma syndrome. Medicine 66:98-113.
-
(1987)
Medicine
, vol.66
, pp. 98-113
-
-
Gorlin, R.J.1
-
15
-
-
0027479494
-
Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry
-
Goudie DR, Yuille MAR, Leversha MA, Furlong RA, Carter NA, Lush M J, Affara NA, Ferguson-Smith MA (1993) Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry. Nature Genet 3:165-169.
-
(1993)
Nature Genet
, vol.3
, pp. 165-169
-
-
Goudie, D.R.1
Yuille, M.A.R.2
Leversha, M.A.3
Furlong, R.A.4
Carter, N.A.5
Lush, M.J.6
Affara, N.A.7
Ferguson-Smith, M.A.8
-
16
-
-
15844382075
-
A mammalian patched homolog is expressed in target tissues of sonic hedgehog and maps to a region associated with developmental abnormalities
-
Hahn H, Christiansen J, Wicking C, Zaphiropoulos PG, Chidambaram A, Gerrard B, Vorechovsky I, Bale AK, Toftgard R, Dean M, Wainwright B (1996a) A mammalian patched homolog is expressed in target tissues of sonic hedgehog and maps to a region associated with developmental abnormalities. J Biol Chem 271:12125-12128.
-
(1996)
J Biol Chem
, vol.271
, pp. 12125-12128
-
-
Hahn, H.1
Christiansen, J.2
Wicking, C.3
Zaphiropoulos, P.G.4
Chidambaram, A.5
Gerrard, B.6
Vorechovsky, I.7
Bale, A.K.8
Toftgard, R.9
Dean, M.10
Wainwright, B.11
-
17
-
-
15844386165
-
Mutations of the human homolog of drosophila patched in the nevoid basal cell carcinoma syndrome
-
Hahn H, Wicking G, Zaphiropoulos PG, Gailani MR, Shanley S, Chidambaram A, Vorechovsky I, Holmberg E, Unden AB, Gillies S, Negus K, Smyth I, Pressman C, Leffell DJ, Gerrard B, Goldstein AM, Dean M, Toftgard R, Chenevix-Trench G, Wainwright B, Bale AE (1996b) Mutations of the human homolog of drosophila patched in the nevoid basal cell carcinoma syndrome. Cell 85:841-851.
-
(1996)
Cell
, vol.85
, pp. 841-851
-
-
Hahn, H.1
Wicking, G.2
Zaphiropoulos, P.G.3
Gailani, M.R.4
Shanley, S.5
Chidambaram, A.6
Vorechovsky, I.7
Holmberg, E.8
Unden, A.B.9
Gillies, S.10
Negus, K.11
Smyth, I.12
Pressman, C.13
Leffell, D.J.14
Gerrard, B.15
Goldstein, A.M.16
Dean, M.17
Toftgard, R.18
Chenevix-Trench, G.19
Wainwright, B.20
Bale, A.E.21
more..
-
18
-
-
44049115577
-
Choice of enzymes for mapping based on CpG islands in the human genome
-
Larsen F, Gundersen G, Prydz H (1992) Choice of enzymes for mapping based on CpG islands in the human genome. GATA 9:80-85.
-
(1992)
GATA
, vol.9
, pp. 80-85
-
-
Larsen, F.1
Gundersen, G.2
Prydz, H.3
-
19
-
-
0028049612
-
A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia Group C, and xeroderma pigmentosum Group a loci on chromosome 9q
-
Morris DJ, Reis A (1994) A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia Group C, and xeroderma pigmentosum Group A loci on chromosome 9q. Genomics 23: 23-29.
-
(1994)
Genomics
, vol.23
, pp. 23-29
-
-
Morris, D.J.1
Reis, A.2
-
20
-
-
1542471167
-
Alu polymerase chain reaction: A method for rapid isolation of human specific sequences from complex DNA sources
-
Nelson DL, Ledbetter SA, Corbo L, Victoria MF, Ramirez-Solis R, Webster TD, Ledbetter DH, Caskey CT (1989) Alu polymerase chain reaction: A method for rapid isolation of human specific sequences from complex DNA sources. Proc Natl Acad Sci USA 86:6686-6690.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 6686-6690
-
-
Nelson, D.L.1
Ledbetter, S.A.2
Corbo, L.3
Victoria, M.F.4
Ramirez-Solis, R.5
Webster, T.D.6
Ledbetter, D.H.7
Caskey, C.T.8
-
21
-
-
43949167467
-
Methods for finding genes a major rate limiting step in positional cloning
-
Parrish JK, Nelson DL (1993) Methods for finding genes a major rate limiting step in positional cloning. GATA 10:29-11.
-
(1993)
GATA
, vol.10
, pp. 29-111
-
-
Parrish, J.K.1
Nelson, D.L.2
-
22
-
-
0028476207
-
Report on the 3rd International Workshop on Chromosome 9
-
Report on the 3rd International Workshop on Chromosome 9 (1994) Ann Hum Genet 58:177-250.
-
(1994)
Ann Hum Genet
, vol.58
, pp. 177-250
-
-
-
23
-
-
0028801755
-
Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas
-
Shanley SM, Dawkins H, Wainwright BJ, Wicking C, Heenan P, Eldon M, Searle J, Chenevix-Trench G (1995) Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas. Hum Mol Genet 4:129-133.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 129-133
-
-
Shanley, S.M.1
Dawkins, H.2
Wainwright, B.J.3
Wicking, C.4
Heenan, P.5
Eldon, M.6
Searle, J.7
Chenevix-Trench, G.8
-
24
-
-
0029010375
-
Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders
-
Tommerup N, Vissing H (1995) Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders. Genomics 27:259-264.
-
(1995)
Genomics
, vol.27
, pp. 259-264
-
-
Tommerup, N.1
Vissing, H.2
-
25
-
-
0028966074
-
The human growth arrest specific gene GAS1 maps outside the candidate region of the gene for nevoid basal cell carcinoma syndrome
-
Wicking C, Breen M, Negus K, Berkman J, Evdokion A, Cowled P, Chenevix-Trench G, Wainright B (1995) The human growth arrest specific gene GAS1 maps outside the candidate region of the gene for nevoid basal cell carcinoma syndrome. Cytogenet Cell Genet 68:119-121.
-
(1995)
Cytogenet Cell Genet
, vol.68
, pp. 119-121
-
-
Wicking, C.1
Breen, M.2
Negus, K.3
Berkman, J.4
Evdokion, A.5
Cowled, P.6
Chenevix-Trench, G.7
Wainright, B.8
|