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Isolation from Cochlea of a Novel Human Intronless Gene with Predominant Fetal Expression
Authors:Barbara L. Resendes  Sharon F. Kuo  Nahid G. Robertson  Anne B. S. Giersch  Dynio Honrubia  Osamu Ohara  Joe C. Adams  Cynthia C. Morton
Affiliation:(1) Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women"rsquo"s Hospital, Boston, MA 02115, USA;(2) Department of Pathology, Brigham and Women"rsquo"s Hospital, Boston, MA 02115, USA;(3) Speech and Hearing Bioscience and Technology Program, Harvard–MIT Division of Health Sciences and Technology, Cambridge, MA 02139, USA;(4) Harvard Medical School, Boston, MA 02115, USA;(5) Department of Neonatal Care, Children"rsquo"s Hospital, Boston, MA 02115, USA;(6) Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA;(7) Kazusa DNA Research Institute, Chiba 292-0812, Japan;(8) Laboratory of Immunogenomics, RIKEN Research Center for Allergy and Immunology, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan
Abstract:
Keywords:novel gene  intronless  GC-rich  cochlea  predominant fetal expression  tetramerization domain  unusually long 3  /content/wjbeqb9uwn003l1l/xxlarge8242.gif"   alt="  prime"   align="  BASELINE"   BORDER="  0"  > UTR  hair cells
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