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de dchughes Schwartz [14 articles]

Recent papers posted to de dchughes library by the author Schwartz. You can also see Schwartz de everyone.
  • XLMR genes: update 2007
    European Journal of Human Genetics, Vol. aop, No. current.
    by Pietro Chiurazzi, Charles E Schwartz, Jozef Gecz, Giovanni Neri
    posted to x-linked-mental-retardation by dchughes on 2008-07-31 15:36:25 as **
  • Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism
    Hum. Mol. Genet., Vol. 17, No. 15. (1 August 2008), pp. 2405-2415.
    by Samuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, Alexander Sumaroka, Alejandro J Roman, Leigh M Gardner, Haydn M Prosser, Monalisa Mishra, Torben N Bech-Hansen, Waldo Herrera, Sharon B Schwartz, Xue-Zhong Liu, William J Kimberling, Karen P Steel, David S Williams
    posted to myo7a retina retinal-dystrophy retinitis-pigmentosa usher-syndrome by dchughes on 2008-07-16 09:38:22 as **
  • Mapping and sequencing of structural variation from eight human genomes
    Nature, Vol. 453, No. 7191., pp. 56-64.
    by Jeffrey M Kidd, Gregory M Cooper, William F Donahue, Hillary S Hayden, Nick Sampas, Tina Graves, Nancy Hansen, Brian Teague, Can Alkan, Francesca Antonacci, Eric Haugen, Troy Zerr, Alice N Yamada, Peter Tsang, Tera L Newman, Eray Tüzün, Ze Cheng, Heather M Ebling, Nadeem Tusneem, Robert David, Will Gillett, Karen A Phelps, Molly Weaver, David Saranga, Adrianne Brand, Wei Tao, Erik Gustafson, Kevin Mckernan, Lin Chen, Maika Malig, Joshua D Smith, Joshua M Korn, Steven A Mccarroll, David A Altshuler, Daniel A Peiffer, Michael Dorschner, John Stamatoyannopoulos, David Schwartz, Deborah A Nickerson, James C Mullikin, Richard K Wilson, Laurakay Bruhn, Maynard V Olson, Rajinder Kaul, Douglas R Smith, Evan E Eichler
    posted to human-genome human-variation by dchughes on 2008-05-01 17:06:26 as ** along with 16 people and 2 groups hpaces Ema chad_davis bpb djkt balicea shikin psique kintoki kaniko aprasad vplagnol maximilianh chrisamiller jyuh skoch3 GeneGo Koch_Lab
  • Alternative splicing of Alu exons--two arms are better than one.
    Nucleic Acids Res (14 February 2008)
    by Nurit Gal-Mark, Schraga Schwartz, Gil Ast
    posted to alternative-splicing alu alu-exonisation retrotransposon by dchughes on 2008-03-06 12:29:04 as ** along with 1 person and 1 group paulcartwright BergmanLab
  • Large-scale comparative analysis of splicing signals and their corresponding splicing factors in eukaryotes.
    Genome Res, Vol. 18, No. 1. (January 2008), pp. 88-103.
    by S Schwartz, J Silva, D Burstein, T Pupko, E Eyras, G Ast
    posted to comparative-analysis splice-site splicing by dchughes on 2008-01-15 13:14:58 as ** along with 3 people and 1 group stajich gjuggler GustavoLacerda Berkeley Mycology
  • Arf6 and microtubules in adhesion-dependent trafficking of lipid rafts
    Nature Cell Biology, Vol. 9, No. 12. (18 November 2007), pp. 1381-1391.
    by Nagaraj Balasubramanian, David W Scott, David J Castle, James E Casanova, Martin A Schwartz
    posted to arf6 by dchughes on 2007-12-04 13:03:10 as **
  • Structural and Functional Events on the Porcine Zona Pellucida During Maturation, Fertilization and Embryonic Development: a Scanning Electron Microscopy Analysis
    Reproduction in Domestic Animals, Vol. 42, No. 6. (December 2007), pp. 594-602.
    by Michelmann, Hw, Rath, , Topfer-Petersen, , Schwartz,
    posted to zona-pellucida by dchughes on 2007-11-06 11:21:13 as **
  • PCR amplification of animal DNA with human X-Y amelogenin primers used in gender determination.
    J Forensic Sci, Vol. 40, No. 4. (July 1995), pp. 641-644.
    by E Buel, G Wang, M Schwartz
    posted to amelogenin sex-determination by dchughes on 2007-11-02 14:45:03 as **
  • Centrosomal-ciliary gene <I>CEP290/NPHP6</I> mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis
    Human Mutation, Vol. 28, No. 11. (2007), pp. 1074-1083.
    by Artur V Cideciyan, Tomas S Aleman, Samuel G Jacobson, Hemant Khanna, Alexander Sumaroka, Geoffrey K Aguirre, Sharon B Schwartz, Elizabeth AM Windsor, Shirley He, Bo Chang, Edwin M Stone, Anand Swaroop
    posted to cep290 jouberts-syndrome by dchughes on 2007-10-15 16:06:25 as **
  • Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome
    Genome Res., Vol. 17, No. 6. (1 June 2007), pp. 760-774.
    by Elliott H Margulies, Gregory M Cooper, George Asimenos, Daryl J Thomas, Colin N Dewey, Adam Siepel, Ewan Birney, Damian Keefe, Ariel S Schwartz, Minmei Hou, James Taylor, Sergey Nikolaev, Juan I Montoya-Burgos, Ari Loytynoja, Simon Whelan, Fabio Pardi, Tim Massingham, James B Brown, Peter Bickel, Ian Holmes, James C Mullikin, Abel Ureta-Vidal, Benedict Paten, Eric A Stone, Kate R Rosenbloom, James W Kent, Gerard G Bouffard, Xiaobin Guan, Nancy F Hansen, Jacquelyn R Idol, Valerie V Maduro, Baishali Maskeri, Jennifer C Mcdowell, Morgan Park, Pamela J Thomas, Alice C Young, Robert W Blakesley, Donna M Muzny, Erica Sodergren, David A Wheeler, Kim C Worley, Huaiyang Jiang, George M Weinstock, Richard A Gibbs, Tina Graves, Robert Fulton, Elaine R Mardis, Richard K Wilson, Michele Clamp, James Cuff, Sante Gnerre, David B Jaffe, Jean L Chang, Kerstin Lindblad-Toh, Eric S Lander, Angie Hinrichs, Heather Trumbower, Hiram Clawson, Ann Zweig, Robert M Kuhn, Galt Barber, Rachel Harte, Donna Karolchik, Matthew A Field, Richard A Moore, Carrie A Matthewson, Jacqueline E Schein, Marco A Marra, Stylianos E Antonarakis, Serafim Batzoglou, Nick Goldman, Ross Hardison, David Haussler, Webb Miller, Lior Pachter, Eric D Green, Arend Sidow
    posted to comparative-analysis encode mammal by dchughes on 2007-09-17 13:08:35 as ** along with 7 people and 4 groups dpollard AaronDarling djkt ghattem Garamonfok gjuggler elfar Bioinformatics EisenLab G4ID Genetics-of-Gambling
  • A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation
    Human Genetics, Vol. 122, No. 2. (2007), pp. 191-199.
    by Christian Babbs, Raoul Heller, David Everman, Mark Crocker, Stephen Twigg, Charles Schwartz, Henk Giele, Andrew Wilkie
    posted to dominant-hemimelia by dchughes on 2007-08-15 15:24:40 as ** along with 2 groups G4ID Genetics-of-Gambling
  • Genome sequence of the Brown Norway rat yields insights into mammalian evolution.
    Nature, Vol. 428, No. 6982. (1 April 2004), pp. 493-521.
    by RA Gibbs, GM Weinstock, ML Metzker, DM Muzny, EJ Sodergren, S Scherer, G Scott, D Steffen, KC Worley, PE Burch, G Okwuonu, S Hines, L Lewis, C DeRamo, O Delgado, S Dugan-Rocha, G Miner, M Morgan, A Hawes, R Gill, Celera, RA Holt, MD Adams, PG Amanatides, H Baden-Tillson, M Barnstead, S Chin, CA Evans, S Ferriera, C Fosler, A Glodek, Z Gu, D Jennings, CL Kraft, T Nguyen, CM Pfannkoch, C Sitter, GG Sutton, JC Venter, T Woodage, D Smith, HM Lee, E Gustafson, P Cahill, A Kana, L Doucette-Stamm, K Weinstock, K Fechtel, RB Weiss, DM Dunn, ED Green, RW Blakesley, GG Bouffard, PJ De Jong, K Osoegawa, B Zhu, M Marra, J Schein, I Bosdet, C Fjell, S Jones, M Krzywinski, C Mathewson, A Siddiqui, N Wye, J McPherson, S Zhao, CM Fraser, J Shetty, S Shatsman, K Geer, Y Chen, S Abramzon, WC Nierman, PH Havlak, R Chen, KJ Durbin, A Egan, Y Ren, XZ Song, B Li, Y Liu, X Qin, S Cawley, KC Worley, AJ Cooney, LM D'Souza, K Martin, JQ Wu, ML Gonzalez-Garay, AR Jackson, KJ Kalafus, MP McLeod, A Milosavljevic, D Virk, A Volkov, DA Wheeler, Z Zhang, JA Bailey, EE Eichler, E Tuzun, E Birney, E Mongin, A Ureta-Vidal, C Woodwark, E Zdobnov, P Bork, M Suyama, D Torrents, M Alexandersson, BJ Trask, JM Young, H Huang, H Wang, H Xing, S Daniels, D Gietzen, J Schmidt, K Stevens, U Vitt, J Wingrove, F Camara, M Mar Albà, JF Abril, R Guigo, A Smit, I Dubchak, EM Rubin, O Couronne, A Poliakov, N Hübner, D Ganten, C Goesele, O Hummel, T Kreitler, YA Lee, J Monti, H Schulz, H Zimdahl, H Himmelbauer, H Lehrach, HJ Jacob, S Bromberg, J Gullings-Handley, MI Jensen-Seaman, AE Kwitek, J Lazar, D Pasko, PJ Tonellato, S Twigger, CP Ponting, JM Duarte, S Rice, L Goodstadt, SA Beatson, RD Emes, EE Winter, C Webber, P Brandt, G Nyakatura, M Adetobi, F Chiaromonte, L Elnitski, P Eswara, RC Hardison, M Hou, D Kolbe, K Makova, W Miller, A Nekrutenko, C Riemer, S Schwartz, J Taylor, S Yang, Y Zhang, K Lindpaintner, TD Andrews, M Caccamo, M Clamp, L Clarke, V Curwen, R Durbin, E Eyras, SM Searle, GM Cooper, S Batzoglou, M Brudno, A Sidow, EA Stone, JC Venter, BA Payseur, G Bourque, C López-Otín, XS Puente, K Chakrabarti, S Chatterji, C Dewey, L Pachter, N Bray, VB Yap, A Caspi, G Tesler, PA Pevzner, D Haussler, KM Roskin, R Baertsch, H Clawson, TS Furey, AS Hinrichs, D Karolchik, WJ Kent, KR Rosenbloom, H Trumbower, M Weirauch, DN Cooper, PD Stenson, B Ma, M Brent, M Arumugam, D Shteynberg, RR Copley, MS Taylor, H Riethman, U Mudunuri, J Peterson, M Guyer, A Felsenfeld, S Old, S Mockrin, F Collins,
    posted to genome rat-genome by dchughes on 2006-08-01 19:05:25 as ** along with 5 people and 4 groups aprasad ccots rvosa djkt stajich FAB-lab G4ID Genetics-of-Gambling Berkeley Mycology
  • Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B.
    Genomics, Vol. 36, No. 3. (15 September 1996), pp. 440-448.
    by ZY Chen, T Hasson, PM Kelley, BJ Schwender, MF Schwartz, M Ramakrishnan, WJ Kimberling, MS Mooseker, DP Corey
    posted to deafness mir myosin-viia by dchughes on 2006-07-04 17:21:35 as ** along with 2 groups G4ID Genetics-of-Gambling
  • Segmental duplications and copy-number variation in the human genome.
    Am J Hum Genet, Vol. 77, No. 1. (July 2005), pp. 78-88.
    by AJ Sharp, DP Locke, SD McGrath, Z Cheng, JA Bailey, RU Vallente, LM Pertz, RA Clark, S Schwartz, R Segraves, VV Oseroff, DG Albertson, D Pinkel, EE Eichler
    posted to copy-number-variation human-genome segmental-duplications by dchughes on 2006-07-03 11:03:14 as ** along with 3 people and 4 groups pcahan1 balicea giovanni Bioinformatics G4ID GeschwindLab Genetics-of-Gambling
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