Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ruiqin Pan"'
Publikováno v:
Planta. 220:156-164
During plant cytokinesis, kinesin-related motor proteins are believed to play critical roles in microtubule organization and vesicle transport in the phragmoplast. Previously, we reported that the motor AtPAKRP1 was associated with the plus end of ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c112dcc5e5995b94cb4ccf19e926cf0
https://doi.org/10.1007/s00425-004-1324-4
https://doi.org/10.1007/s00425-004-1324-4
Publikováno v:
Journal of Biological Chemistry. 275:5739-5747
The small proline-rich protein, SPRR1, is a marker gene whose expression in conducting airway epithelium is elevated under a variety of conditions that enhance squamous differentiation. The purpose of this study is to elucidate the nature of the SPRR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37de941848379c21159b1a981e2dc9ff
https://doi.org/10.1074/jbc.275.8.5739
https://doi.org/10.1074/jbc.275.8.5739
Publikováno v:
Current Nanoscience. 5:503-505
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc4280dcd3b55b124c59013a90c9f811
https://doi.org/10.2174/157341309789378005
https://doi.org/10.2174/157341309789378005
Autor:
Andrew Hadd, Stela Filipovic-Sadic, Timothy T. Stenzel, Julie Krosting, Paul J. Hagerman, Flora Tassone, Sachin Sah, Liangjing Chen, Gary J. Latham, Ruiqin Pan, Edward Sekinger
Publikováno v:
The Journal of molecular diagnostics : JMD. 12(5)
(CGG)(n) repeat expansion in the FMR1 gene is associated with fragile X syndrome and other disorders. Current methods for FMR1 molecular testing rely on Southern blot analysis to detect expanded alleles too large to be PCR-amplified and to identify f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03db1b2efcacf464ebe1314f95e85a98
https://pubmed.ncbi.nlm.nih.gov/20616364
https://pubmed.ncbi.nlm.nih.gov/20616364
Autor:
E. Melina Casillas, Wenting Zhang, Ruiqin Pan, Randi J Hagerman, Jennifer Yuhas, Flora Tassone, Paulina Walichiewicz
Publikováno v:
Genetic testing and molecular biomarkers. 13(6)
Background: Because fragile X syndrome (FXS) is prevalent, it has become the subject of newborn and high-risk screening efforts. International screening, however, can be financially and logistically prohibitive, particularly in countries where resour
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::718a0c1146c6dc87e3ef83194a656be7
https://pubmed.ncbi.nlm.nih.gov/19810826
https://pubmed.ncbi.nlm.nih.gov/19810826
Autor:
Blanca Lopez Posadas, Paul J. Hagerman, Flora Tassone, Isabel Fernandez-Carvajal, Christopher Raske, Ruiqin Pan
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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Fragile X Syndrome is caused by the expansion of an unstable CGG-repeat tract in the 5′-UTR of the FMR1 gene, which generally results in transcriptional silencing and consequent absence of the FMR1 protein. To date, the smallest premutation allele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c6f749c8d9424bdf393a926404d679a
https://pubmed.ncbi.nlm.nih.gov/19525339
https://pubmed.ncbi.nlm.nih.gov/19525339
Autor:
Gianni Pezzoli, Jeremy Kraff, Ruiqin Pan, Margherita Canesi, Paul J. Hagerman, Roberto Cilia, Hiu Tung Tang, Flora Tassone, Stefano Goldwurm, Khalid Amiri
Publikováno v:
Archives of Neurology. 66
Background Fragile X−associated tremor/ataxia syndrome (FXTAS) is a progressive, late-onset neurodegenerative disease that affects older carriers of premutation (CGG) repeat expansions of the fragile X mental retardation 1 ( FMR1 ) gene. Clinical f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fa228ca979496c2e43be3ca59ac3409
https://doi.org/10.1001/archneurol.2008.548
https://doi.org/10.1001/archneurol.2008.548
Autor:
Paul J. Hagerman, Flora Tassone, Paulina Walichiewicz, Xie Xiaosen, Isabel Fernandez-Carvajal, Ruiqin Pan
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Fragile X syndrome, which is caused by expanded CGG repeats of the FMR1 gene, is associated with a broad spectrum of clinical involvement and is the most common inherited form of intellectual disability. Early diagnosis and intervention are likely to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa8918abf1ffcabf76547b825419e388
http://hdl.handle.net/10261/72758
http://hdl.handle.net/10261/72758
Publikováno v:
The Journal of molecular diagnostics : JMD. 10(1)
Fragile X syndrome, the most common inherited cause of intellectual impairment and the most common single gene associated with autism, generally occurs for fragile X mental retardation 1 (FMR1) alleles that exceed 200 CGG repeats (full-mutation range
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd2937eddffe1572183b1fcb4a432b0f
https://pubmed.ncbi.nlm.nih.gov/18165273
https://pubmed.ncbi.nlm.nih.gov/18165273
Publikováno v:
Molecular and cellular neurosciences. 36(3)
A cDNA encoding a novel protein was cloned from ischemic rat brain and found to be homologous to testis Mea-2 Golgi-associated protein (Golga3). The sequence predicted a 165-kDa protein, and in vitro translated protein exhibited a molecular mass of 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d561d1e5c7b6a75cfc8df530a4f6262
https://pubmed.ncbi.nlm.nih.gov/17888676
https://pubmed.ncbi.nlm.nih.gov/17888676