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pro vyhledávání: '"Shirley I. Smith"'
Autor:
Shirley I. Smith, Kylie J. Ralston, Gordon F. Burns, Maryanne Power, Mark D. Spanevello, Andrew W. Boyd, Michelle Down
Publikováno v:
Gene Expression Patterns. 5:483-490
The cadherin superfamily members play an important role in mediating cell-cell contact and adhesion (Takeichi, M., 1991. Cadherin cell adhesion receptors as a morphogenetic regulator. Science 251, 1451-1455). A distinct subfamily, neither belonging t
Autor:
Shirley I. Smith, Colin G. Miles, Greg Elgar, Nicholas D. Hastie, Martina Niksic, Lesley Rankin
Publikováno v:
Nucleic Acids Research. 31:2795-2802
The teleost fish are widely used as model organisms in vertebrate biology. The compact genome of the pufferfish, Fugu rubripes, has proven a valuable tool in comparative genome analyses, aiding the annotation of mammalian genomes and the identificati
Publikováno v:
Blood
Blood, American Society of Hematology, 1998, 91 (3), pp.764-73
Europe PubMed Central
Blood, American Society of Hematology, 1998, 91 (3), pp.764-73
Europe PubMed Central
The Wilms' tumor gene, WT1, encodes a transcription factor of the Cys2-His2 zinc finger type. The functional significance of WT1 expression in leukemias, in addition to tissues and cell lines of hematopoietic origin, has not been determined. Using th
Publikováno v:
Europe PubMed Central
Blood
Blood, American Society of Hematology, 1997, 90 (11), pp.4332-40
Blood
Blood, American Society of Hematology, 1997, 90 (11), pp.4332-40
In the course of systematic cloning of protein tyrosine kinases (PTKs) expressed in hematopoietic stem and progenitor cells, we have identified the murine homologue of human Bmx. It encodes a protein containing the five domains characteristic of the
Autor:
Shirley I. Smith, Peter Kelehan, Wayne Lam, John Tolmie, Mohnish Suri, David O'Neill, Emma McCann, Shantala Vadeyar, William Reardon, S Faisal Ahmed, David R. FitzPatrick, Judith Grant, Nicholas D. Hastie
Publikováno v:
American journal of medical genetics. Part A. (19)
Meacham syndrome is a rare sporadically occurring multiple malformation syndrome characterized by male pseudohermaphroditism with abnormal internal female genitalia comprising a uterus and double or septate vagina, complex congenital heart defect and
Autor:
Lisa A. Simms, Shirley I. Smith, Yoshiki Kida, Mark T. Kenney, Elizabeth M. Algar, Peter J. Smith
Publikováno v:
Human mutation. 5(3)
We have examined a panel of 21 sporadic Wilms' tumours for rearrangements in the Wilms' tumour suppressor gene, WT1. In one tumour with specific allele loss in chromosome 11p13, a homozygous deletion in the 3' end of the gene, encompassing exon 10 an
Eight invited papers and 68 abstracts of volunteer presentations on gypsy moth biology, ecology, impacts, and management presented at the U. S. Department of Agriculture Interagency Gypsy Moth Research Review.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28194c96c36802af199fb2898a6ab221
https://doi.org/10.2737/ne-gtr-146
https://doi.org/10.2737/ne-gtr-146