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PMID |
Sentence |
1 |
11178400
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[Abnormal toxicity - a relevant safety test under GLP- and GMP-conditions in the production of vaccines?]
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2 |
11178400
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This paper deals with the relevance of abnormal toxicity after the introduction of GMP- and GLP-conditions in the production of veterinary biologicals.
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3 |
11178400
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[Abnormal toxicity - a relevant safety test under GLP- and GMP-conditions in the production of vaccines?]
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4 |
11178400
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This paper deals with the relevance of abnormal toxicity after the introduction of GMP- and GLP-conditions in the production of veterinary biologicals.
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5 |
11178440
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The purpose of this project was to investigate the relevance of ATT after the introduction of GMP- and GLP-principles in the manufacturing of biological products.
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6 |
15496321
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Thus it has become imperative that, in concert with other quality control measures, a potency test be utilized for the GMP/GLP lot-release of DC products for preclinical and clinical studies.
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7 |
23629948
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Affinity purification also was used to identify the distinct composition of the h-CDYLa or h-CDYLb protein complex. h-CDYLb was found in a multiprotein complex with G9a and GLP, while the h-CDYLa complex did not contain these two enzymes.
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8 |
25483693
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To meet the time constraint imposed on this project, we used a distributed R&D model involving experts in the fields of protein engineering and production, bioinformatics, peptide synthesis/design and GMP/GLP manufacturing and testing standards.
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9 |
25637356
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GLP and G9a are major H3K9 dimethylases and are essential for mouse early embryonic development.
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10 |
25637356
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GLP and G9a both harbor ankyrin repeat domains that are capable of binding H3K9 methylation.
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11 |
25637356
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Here, we report that the histone methyltransferase activities of GLP and G9a are stimulated by neighboring nucleosomes that are premethylated at H3K9.
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12 |
25637356
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These stimulation events function in cis and are dependent on the H3K9 methylation binding activities of ankyrin repeat domains of GLP and G9a.
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13 |
25637356
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In mouse embryonic stem cells (ESCs) harboring a mutant GLP that lacks H3K9me1-binding activity, critical pluripotent genes, including Oct4 and Nanog, display inefficient establishment of H3K9me2 and delayed gene silencing during differentiation.
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14 |
25637356
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Collectively, our study reveals a new activation mechanism for GLP and G9a that plays an important role in ESC differentiation and mouse viability.
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15 |
25637356
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GLP and G9a are major H3K9 dimethylases and are essential for mouse early embryonic development.
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16 |
25637356
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GLP and G9a both harbor ankyrin repeat domains that are capable of binding H3K9 methylation.
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17 |
25637356
|
Here, we report that the histone methyltransferase activities of GLP and G9a are stimulated by neighboring nucleosomes that are premethylated at H3K9.
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18 |
25637356
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These stimulation events function in cis and are dependent on the H3K9 methylation binding activities of ankyrin repeat domains of GLP and G9a.
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19 |
25637356
|
In mouse embryonic stem cells (ESCs) harboring a mutant GLP that lacks H3K9me1-binding activity, critical pluripotent genes, including Oct4 and Nanog, display inefficient establishment of H3K9me2 and delayed gene silencing during differentiation.
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20 |
25637356
|
Collectively, our study reveals a new activation mechanism for GLP and G9a that plays an important role in ESC differentiation and mouse viability.
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21 |
25637356
|
GLP and G9a are major H3K9 dimethylases and are essential for mouse early embryonic development.
|
22 |
25637356
|
GLP and G9a both harbor ankyrin repeat domains that are capable of binding H3K9 methylation.
|
23 |
25637356
|
Here, we report that the histone methyltransferase activities of GLP and G9a are stimulated by neighboring nucleosomes that are premethylated at H3K9.
|
24 |
25637356
|
These stimulation events function in cis and are dependent on the H3K9 methylation binding activities of ankyrin repeat domains of GLP and G9a.
|
25 |
25637356
|
In mouse embryonic stem cells (ESCs) harboring a mutant GLP that lacks H3K9me1-binding activity, critical pluripotent genes, including Oct4 and Nanog, display inefficient establishment of H3K9me2 and delayed gene silencing during differentiation.
|
26 |
25637356
|
Collectively, our study reveals a new activation mechanism for GLP and G9a that plays an important role in ESC differentiation and mouse viability.
|
27 |
25637356
|
GLP and G9a are major H3K9 dimethylases and are essential for mouse early embryonic development.
|
28 |
25637356
|
GLP and G9a both harbor ankyrin repeat domains that are capable of binding H3K9 methylation.
|
29 |
25637356
|
Here, we report that the histone methyltransferase activities of GLP and G9a are stimulated by neighboring nucleosomes that are premethylated at H3K9.
|
30 |
25637356
|
These stimulation events function in cis and are dependent on the H3K9 methylation binding activities of ankyrin repeat domains of GLP and G9a.
|
31 |
25637356
|
In mouse embryonic stem cells (ESCs) harboring a mutant GLP that lacks H3K9me1-binding activity, critical pluripotent genes, including Oct4 and Nanog, display inefficient establishment of H3K9me2 and delayed gene silencing during differentiation.
|
32 |
25637356
|
Collectively, our study reveals a new activation mechanism for GLP and G9a that plays an important role in ESC differentiation and mouse viability.
|
33 |
25637356
|
GLP and G9a are major H3K9 dimethylases and are essential for mouse early embryonic development.
|
34 |
25637356
|
GLP and G9a both harbor ankyrin repeat domains that are capable of binding H3K9 methylation.
|
35 |
25637356
|
Here, we report that the histone methyltransferase activities of GLP and G9a are stimulated by neighboring nucleosomes that are premethylated at H3K9.
|
36 |
25637356
|
These stimulation events function in cis and are dependent on the H3K9 methylation binding activities of ankyrin repeat domains of GLP and G9a.
|
37 |
25637356
|
In mouse embryonic stem cells (ESCs) harboring a mutant GLP that lacks H3K9me1-binding activity, critical pluripotent genes, including Oct4 and Nanog, display inefficient establishment of H3K9me2 and delayed gene silencing during differentiation.
|
38 |
25637356
|
Collectively, our study reveals a new activation mechanism for GLP and G9a that plays an important role in ESC differentiation and mouse viability.
|