Rao, Ercole Dr. rer. nat.Universität HeidelbergHeidelberg
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Co-Autoren (Uni Heidelberg)
Co-Autoren (extern)
- Muroya, Koji (2)
- Mertz, Andrea (2)
- Gianfrancesco, Fernando (2)
- Forabosco, Antonino (2)
- Esposito, Teresa (2)
- Klink, Albrecht (2)
- Strachan, Tom (2)
- D'Urso, Marco (1)
- Scherer, Gerd (1)
- Richter, Alexandra (1)
- Ried, Thomas (1)
- Ranke, Michael B. (1)
- Rump, Andreas (1)
- Horsthemke, Bernhard (1)
- Claussen, Uwe (1945-2008) (1)
- Zeller, Rolf (1)
- Zuniga, Aimée (1)
- Robson, Stephen C. (1)
- Ogata, T. (1)
- Glass, Ian (1)
- Padilla-Nash, Hesed (1)
- Monaghan, A. Paula (1)
- Matsuo, N. (1)
- Geschwind, Daniel H. (1)
- Woods, R. (1)
- Winkelmann, Martina (1)
- Swerdloff, R. (1)
- Pawlikowska‐Haddal, Anna (1)
- Nelson, S. F. (1)
- Mumm, Steven (1)
- Montanini, Luisa (1)
- Mazzarella, Richard (1)
- Karrim, J. (1)
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Neueste Publikationen in heiBIB 
(ingesamt sind 16 Publikationen erfasst)
- Rao, Ercole: Shox homeobox gene and Turner syndrome / E. Rao and G.A. Rappold, 2002. - 7 S.
In: Genomics and proteomics. (2002), Seite 149-155
DOI: 10.1007/0-306-46823-9_13
- Gianfrancesco, Fernando: Differential divergence of three human pseudoautosomal genes and their mouse homologs : implications for sex chromosome evolution / Fernando Gianfrancesco, Remo Sanges, Teresa Esposito, Sergio Tempesta, Ercole Rao, Gudrun Rappold, N… , 2001. - 6 S.
In: Genome research, ISSN 1549-5469. 11(2001), 12, Seite 2095-2100
DOI: 10.1101/gr.197001
- Rao, Ercole: The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator / Ercole Rao, Rüdiger J. Blaschke, Antonio Marchini, Beate Niesler, Michael Burnett and Gudrun A. Rapp… , 15 December 2001. - 10 S.
In: Human molecular genetics, ISSN 1460-2083. 10(2001), 26, Seite 3083-3091
DOI: 10.1093/hmg/10.26.3083
- Fukami, Maki: A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation / Maki Fukami, Stefan Kirsch, Simone Schiller, Alexandra Richter, Vladimir Benes, Brunella Franco, Koj… , 2000 Jul 20. - 11 S.
In: The American journal of human genetics, ISSN 1537-6605. 67(2000), 3, Seite 563-573
DOI: 10.1086/303047
- Rappold, Gudrun: The short stature homeobox gene is involved in the skeletal abnormalities in Turner syndrome / G.A. Rappold, R. Blaschke, E. Rao, S. Schiller, M. Clement-Jones, S. Lindsay, T. Strachan, 2000. - 6 S.
In: Optimizing health care for Turner patients in the 21st century. (2000), Seite 3-8
- Clement-Jones, Mark: The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome / Mark Clement-Jones, Simone Schiller, Ercole Rao, Rüdiger J. Blaschke, Aimee Zuniga, Rolf Zeller, Ste… , 22 March 2000. - 8 S.
In: Human molecular genetics, ISSN 1460-2083. 9(2000), 5, Seite 695-702
DOI: 10.1093/hmg/9.5.695
- Rappold, Gudrun: Pulsed-Field gel electrophoresis : protocols / Gudrun A. Rappold, Karin Ried, Albrecht Klink, Ercole Rao and Birgit Weiss, 1999. - 11 S.
In: Techniques in molecular medicine. (1999), Seite 103-113
DOI: 10.1007/978-3-642-59811-1_8
- Geschwind, Daniel H.: Klinefelter's syndrome as a model of anomalous cerebral laterality : testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray / D.H. Geschwind, J. Gregg, K. Boone, J. Karrim, Anna Pawlikowska‐Haddal, E. Rao, J. Ellison, A. Cicco… , 29 December 1998. - 15 S.
In: Genesis, ISSN 1526-968X. 23(1998), 3, Seite 215-229
DOI: 10.1002/(SICI)1520-6408(1998)23:3<215::AID-DVG7>3.0.CO;2-X
- Ried, Karin: Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1 : isolation of the gene ASMTL / K. Ried, E. Rao, K. Schiebel, G.A. Rappold, 01 October 1998. - 8 S.
In: Human molecular genetics, ISSN 1460-2083. 7(1998), 11, Seite 1771-1778
DOI: 10.1093/hmg/7.11.1771
- Gianfrancesco, Fernando: A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere / Fernando Gianfrancesco, Teresa Esposito, Luisa Montanini, Alfredo Ciccodicola, Steven Mumm, Richard … , 01 March 1998. - 8 S.
In: Human molecular genetics, ISSN 1460-2083. 7(1998), 3, Seite 407-414
DOI: 10.1093/hmg/7.3.407
