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Results:
1-22
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Results: 22
Authors:
Makalowska, I
Ryan, JF
Baxevanis, AD
Citation: I. Makalowska et al., GeneMachine: gene prediction and sequence annotation, BIOINFORMAT, 17(9), 2001, pp. 843-844
Authors:
Sood, R
Bonner, TI
Makalowska, I
Stephan, DA
Robbins, CM
Connors, TD
Morgenbesser, SD
Su, K
Faruque, MU
Pinkett, H
Graham, C
Baxevanis, AD
Klinger, KW
Landes, GM
Trent, JM
Carpten, JD
Citation: R. Sood et al., Cloning and characterization of 13 novel transcripts and the human RC58 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus, GENOMICS, 73(2), 2001, pp. 211-222
Authors:
Banerjee-Basu, S
Baxevanis, AD
Citation: S. Banerjee-basu et Ad. Baxevanis, Molecular evolution of the homeodomain family of transcription factors, NUCL ACID R, 29(15), 2001, pp. 3258-3269
Authors:
Baxevanis, AD
Citation: Ad. Baxevanis, The Molecular Biology Database Collection: an updated compilation of biological database resources, NUCL ACID R, 29(1), 2001, pp. 1-10
Authors:
Banerjee-Basu, S
Sink, DW
Baxevanis, AD
Citation: S. Banerjee-basu et al., The Homeodomain Resource: sequences, structures, DNA binding sites and genomic information, NUCL ACID R, 29(1), 2001, pp. 291-293
Authors:
Saleem, RA
Banerjee-Basu, S
Berry, FB
Baxevanis, AD
Walter, MA
Citation: Ra. Saleem et al., Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1, AM J HU GEN, 68(3), 2001, pp. 627-641
Authors:
Stone, DL
Slavotinek, R
Bouffard, GG
Banerjee-Basu, S
Baxevanis, AD
Barr, M
Biesecker, LG
Citation: Dl. Stone et al., Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome, NAT GENET, 25(1), 2000, pp. 79-82
Authors:
Lipkin, SM
Wang, V
Jacoby, R
Banerjee-Basu, S
Baxevanis, AD
Lynch, HT
Elliott, RM
Collins, FS
Citation: Sm. Lipkin et al., MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability, NAT GENET, 24(1), 2000, pp. 27-35
Authors:
Carpten, JD
Makalowska, I
Robbins, CM
Scott, N
Sood, R
Connors, TD
Bonner, TI
Smith, JR
Faruque, MU
Stephan, DA
Pinkett, H
Morgenbesser, SD
Su, K
Graham, C
Gregory, SG
Williams, H
McDonald, L
Baxevanis, AD
Klingler, KW
Landes, GM
Trent, JM
Citation: Jd. Carpten et al., A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region, GENOMICS, 64(1), 2000, pp. 1-14
Authors:
Baxevanis, AD
Citation: Ad. Baxevanis, The Molecular Biology Database Collection: an online compilation of relevant database resources, NUCL ACID R, 28(1), 2000, pp. 1-7
The Histone Database: a comprehensive WWW resource for histones and histone fold-containing proteins
Authors:
Sullivan, SA
Aravind, L
Makalowska, I
Baxevanis, AD
Landsman, D
Citation: Sa. Sullivan et al., The Histone Database: a comprehensive WWW resource for histones and histone fold-containing proteins, NUCL ACID R, 28(1), 2000, pp. 320-322
Authors:
Banerjee-Basu, S
Ryan, JF
Baxevanis, AD
Citation: S. Banerjee-basu et al., The Homeodomain Resource: a prototype database for a large protein family, NUCL ACID R, 28(1), 2000, pp. 329-330
Authors:
Sood, R
Makalowska, I
Carpten, JD
Robbins, CM
Stephan, DA
Connors, TD
Morgenbesser, SD
Su, K
Pinkett, HW
Graham, CL
Quesenberry, MI
Baxevanis, AD
Klinger, KW
Trent, JM
Bonner, TI
Citation: R. Sood et al., The human RGL (RalGDS-like) gene: cloning, expression analysis and genomicorganization, BBA-GENE ST, 1491(1-3), 2000, pp. 285-288
Authors:
Ferlanti, ES
Ryan, JF
Makalowska, I
Baxevanis, AD
Citation: Es. Ferlanti et al., WebBLAST 2.0: an integrated solution for organizing and analyzing sequencedata, BIOINFORMAT, 15(5), 1999, pp. 422-423
Authors:
Southard-Smith, EM
Angrist, M
Ellison, JS
Agarwala, R
Baxevanis, AD
Chakravarti, A
Pavan, WJ
Citation: Em. Southard-smith et al., The Sox10(Dom) mouse: Modeling the genetic variation of Waardenburg-Shah (WS4) syndrome, GENOME RES, 9(3), 1999, pp. 215-225
Authors:
Banerjee-Basu, S
Baxevanis, AD
Citation: S. Banerjee-basu et Ad. Baxevanis, Threading analysis of the Pitx2 homeodomain: Predicted structural effects of mutations causing Rieger syndrome and iridogoniodysgenesis, HUM MUTAT, 14(4), 1999, pp. 312-319
Authors:
Southard-Smith, EM
Collins, JE
Ellison, JS
Smith, KJ
Baxevanis, AD
Touchman, JW
Green, ED
Dunham, I
Pavan, WJ
Citation: Em. Southard-smith et al., Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human, MAMM GENOME, 10(7), 1999, pp. 744-749
Authors:
Makalowska, I
Ferlanti, ES
Baxevanis, AD
Landsman, D
Citation: I. Makalowska et al., Histone sequence database: sequences, structures, post-translational modifications and genetic loci, NUCL ACID R, 27(1), 1999, pp. 323-324
Authors:
Banerjee-Basu, S
Ferlanti, ES
Ryan, JF
Baxevanis, AD
Citation: S. Banerjee-basu et al., The homeodomain resource: sequences, structures and genomic information, NUCL ACID R, 27(1), 1999, pp. 336-337
Authors:
Stephan, DA
Gillanders, E
Vanderveen, D
Freas-Lutz, D
Wistow, G
Baxevanis, AD
Robbins, CM
VanAuken, A
Quesenberry, MI
Bailey-Wilson, J
Juo, SHH
Trent, JM
Smith, L
Brownstein, MJ
Citation: Da. Stephan et al., Progressive juvenile-onset punctate cataracts caused by mutation of the gamma D-crystallin gene, P NAS US, 96(3), 1999, pp. 1008-1012
Authors:
Loftus, SE
Chen, Y
Gooden, G
Ryan, JF
Birznieks, G
Hilliard, M
Baxevanis, AD
Bittner, M
Meltzer, P
Trent, J
Pavan, W
Citation: Se. Loftus et al., Informatic selection of a neural crest-melanocyte cDNA set for microarray analysis, P NAS US, 96(16), 1999, pp. 9277-9280
Authors:
Baxevanis, AD
Boguski, MS
Ouellette, BFF
Citation: Ad. Baxevanis et al., Computational analysis of DNA and protein sequences, GENOME ANAL, 1, 1997, pp. 533-586
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1-22
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