Zobrazeno 1 - 10
of 84
pro vyhledávání: '"L. Hanel'"'
Publikováno v:
Journal of Ichthyology. 58:633-661
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::739465251799b208882805188757978e
https://doi.org/10.1134/s0032945218050053
https://doi.org/10.1134/s0032945218050053
Akademický článek
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Autor:
Steven W. Long, Derek J. Milner, Peter L. Jones, Chia Yun Jessica Sun, Simona Zanotti, Meredith L. Hanel, Takako I. Jones
Publikováno v:
Differentiation. 81:107-118
Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a candidate gene for mediating FSHD pathophysiology, however, very little is known about the endogenous FRG1 protein. This study uses immunocytochemistry (ICC) and histology to pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac5060429acdfa95f93de316fb9626d6
https://doi.org/10.1016/j.diff.2010.09.185
https://doi.org/10.1016/j.diff.2010.09.185
Publikováno v:
Russian Journal of Biological Invasions. 1:172-175
In this paper, we record the introduction or invasion of 41 non-indigenous fish species into natural ecosystems of the Czech Republic over the past two centuries. Of these, only 12 species have survived to the present day. Fully naturalised species t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8ec43b1da3f45f805cf498ac67d4407
https://doi.org/10.1134/s2075111710030057
https://doi.org/10.1134/s2075111710030057
Publikováno v:
Developmental Dynamics. 238:1502-1512
The leading candidate gene responsible for facioscapulohumeral muscular dystrophy (FSHD) is FRG1 (FSHD region gene 1). However, the correlation of altered FRG1 expression levels with disease pathology has remained controversial and the precise functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7d87b4d5d5ffa5ff076cd8da1e187ff
https://doi.org/10.1002/dvdy.21830
https://doi.org/10.1002/dvdy.21830
Publikováno v:
Journal of Cellular Biochemistry. 94:1046-1057
Allele-specific transcription is a characteristic feature of imprinted genes. Many imprinted genes are also transcribed in a tissue- or cell type-specific manner. Overlapping epigenetic signals must, therefore, modulate allele-specific and tissue-spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::588e33e9f3002d06360b0d8b341a7d7a
https://doi.org/10.1002/jcb.20365
https://doi.org/10.1002/jcb.20365
Autor:
Rachel Wevrick, Meredith L. Hanel
Publikováno v:
Clinical Genetics. 59:156-164
Normal human development involves a delicate interplay of gene expression in specific tissues at narrow windows of time. Temporally and spatially regulated gene expression is controlled both by gene-specific factors and chromatin-specific factors. Ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1236b9c76ef7c4330483452473be73af
https://doi.org/10.1034/j.1399-0004.2001.590303.x
https://doi.org/10.1034/j.1399-0004.2001.590303.x
Akademický článek
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Akademický článek
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Publikováno v:
International journal of clinical and experimental pathology. 3(4)
The genetic lesion leading to facioscapulohumeral muscular dystrophy (FSHD) is a dominant deletion at the 4q35 locus. The generally accepted disease model involves an epigenetic dysregulation in the region resulting in the upregulation of one or more
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::41675dee768af3f902daad1c277b2a1f
https://pubmed.ncbi.nlm.nih.gov/20490329
https://pubmed.ncbi.nlm.nih.gov/20490329