Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Susan J Hinze"'
Autor:
Susan J Hinze, Christopher P. Barnett, Ching Moey, Cheryl Shoubridge, Jozef Gecz, Jillian Nicholl, Nicola Brunetti-Pierri, Louise Brueton, Jenny Morton, Dominic J. McMullan, Benjamin Kamien
Copy number variations are a common cause of intellectual disability (ID). Determining the contribution of copy number variants (CNVs), particularly gains, to disease remains challenging. Here, we report four males with ID with sub-microscopic duplic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f166ceea2760a187ef802626b5553d8
http://hdl.handle.net/11588/682818
http://hdl.handle.net/11588/682818
Autor:
Michael R. Beard, Ljiljana Semendric, Erin M. McCartney, Susan J Hinze, Steven A. Weinman, Brett Jones, Karla J. Helbig
Publikováno v:
The Journal of Infectious Diseases. 198:1766-1775
The interactions between hepatitis C virus (HCV) and alcohol metabolism are not well understood. To determine the effect that alcohol metabolism has on HCV replication and the antiviral action of interferon (IFN), Huh-7 cells that harbor HCV replicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::891eaac4a1f332d56ff523775fa0a5ea
https://doi.org/10.1086/593216
https://doi.org/10.1086/593216
Simplex PCR Assay for Positive Identification of Genetic Sex in the Japanese Medaka, Oryzias latipes
Autor:
Susan J. Hinze, Jawahar G. Patil
Publikováno v:
Marine Biotechnology. 10:641-644
The medaka, Oryzias latipes, is a very popular model in biomedical research, particularly for elucidating sex differentiation and determination mechanisms and effects of endocrine disruptors among others. These studies require a sensitive, accurate,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2244c6d1e4a1c494c04cde18d31c6512
https://doi.org/10.1007/s10126-008-9106-9
https://doi.org/10.1007/s10126-008-9106-9
Autor:
Jason A. Powell, Grant R. Sutherland, David F. Callen, S.A. Whitmore, Susan J. Hinze, Hayley E. Spendlove, Gabriel Kremmidiotis, Alison Gardner, Elizabeth Baker, Marina Kochetkova, Anthony John Bais, Norman A. Doggett, Joanna Crawford
Publikováno v:
Genomics. 80:303-310
Loss of heterozygosity (LOH) of chromosome 16q24.3 is a common genetic alteration observed in invasive ductal and lobular breast carcinomas. We constructed a physical map and generated genomic DNA sequence data spanning 2.4 Mb in this region. Detaile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f1530cc3daaf3a532d5ed450609a836
https://doi.org/10.1006/geno.2002.6828
https://doi.org/10.1006/geno.2002.6828
Autor:
Susan J Hinze, Shervi Lie, Matilda R. Jackson, Simon C. Barry, Lachlan A. Jolly, Robert J. Harvey, Cheryl Shoubridge, Michael Field
Publikováno v:
Translational Psychiatry
There is considerable genetic and phenotypic heterogeneity associated with intellectual disability (ID), specific learning disabilities, attention-deficit hyperactivity disorder, autism and epilepsy. The intelligence quotient (IQ) motif and SEC7 doma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72920293f6ca44d12a0ee903a6c05ec5
https://doi.org/10.1038/tp.2017.81
https://doi.org/10.1038/tp.2017.81
Autor:
Xianxian Yang, Jodie T. Hatfield, Susan J Hinze, Peter J. Anderson, Xiongzheng Mu, Barry C. Powell
Publikováno v:
BMC Research Notes, Vol 5, Iss 1, p 222 (2012)
BMC Research Notes
BMC Research Notes
Background RT-qPCR is a common tool for quantification of gene expression, but its accuracy is dependent on the choice and stability (steady state expression levels) of the reference gene/s used for normalization. To date, in the bone field, there ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef31725a84286dfafe127a4c20eb1a0f
http://www.biomedcentral.com/1756-0500/5/222
http://www.biomedcentral.com/1756-0500/5/222
Autor:
Marina, Kochetkova, Olivia L D, McKenzie, Anthony J, Bais, Julie M, Martin, Genevieve A, Secker, Ram, Seshadri, Jason A, Powell, Susan J, Hinze, Alison E, Gardner, Hayley E, Spendlove, Nathan J, O'Callaghan, Anne-Marie, Cleton-Jansen, Cees, Cornelisse, Scott A, Whitmore, Joanna, Crawford, Gabriel, Kremmidiotis, Grant R, Sutherland, David F, Callen
Publikováno v:
Cancer research. 62(16)
Numerous cytogenetic and molecular studies of breast cancer have identified frequent loss of heterozygosity (LOH) of the long arm of human chromosome 16. On the basis of these data, the likely locations of breast cancer tumor suppressor genes are ban
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3308c501f10481822fa9bb9f47747f98
https://pubmed.ncbi.nlm.nih.gov/12183414
https://pubmed.ncbi.nlm.nih.gov/12183414
Autor:
Patil, Jawahar, Hinze, Susan
Publikováno v:
Marine Biotechnology; Nov/Dec2008, Vol. 10 Issue 6, p641-644, 4p, 1 Black and White Photograph, 1 Diagram