PMC:1584416 / 5429-5648 JSONTXT

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{"project":"craft-ca-core-dev","denotations":[{"id":"T458","span":{"begin":28,"end":33},"obj":"NCBITaxon:10088"},{"id":"T459","span":{"begin":41,"end":44},"obj":"PR:000007164"},{"id":"T460","span":{"begin":72,"end":77},"obj":"NCBITaxon:9606"},{"id":"T461","span":{"begin":147,"end":150},"obj":"PR:000007164"},{"id":"T462","span":{"begin":151,"end":158},"obj":"SO:0001023"}],"text":"viously, we generated a TTD mouse model (XPDR722W) that phenocopies the human syndrome [15,21]. Here we report the generation of additional mutant Xpd alleles that fail to support viability on their own but nevertheless"}

{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T554","span":{"begin":28,"end":33},"obj":"NCBITaxon:10088"},{"id":"T555","span":{"begin":41,"end":44},"obj":"PR_EXT:000007164"},{"id":"T556","span":{"begin":72,"end":77},"obj":"NCBITaxon:9606"},{"id":"T557","span":{"begin":140,"end":146},"obj":"SO_EXT:sequence_altered_entity_or_alteration_process"},{"id":"T558","span":{"begin":147,"end":150},"obj":"PR_EXT:000007164"},{"id":"T559","span":{"begin":151,"end":158},"obj":"SO_EXT:0001023"}],"text":"viously, we generated a TTD mouse model (XPDR722W) that phenocopies the human syndrome [15,21]. Here we report the generation of additional mutant Xpd alleles that fail to support viability on their own but nevertheless"}

{"project":"2_test","denotations":[{"id":"17020410-11950998-84795137","span":{"begin":88,"end":90},"obj":"11950998"},{"id":"17020410-9651581-84795138","span":{"begin":91,"end":93},"obj":"9651581"},{"id":"T24869","span":{"begin":88,"end":90},"obj":"11950998"},{"id":"T77326","span":{"begin":91,"end":93},"obj":"9651581"}],"text":"viously, we generated a TTD mouse model (XPDR722W) that phenocopies the human syndrome [15,21]. Here we report the generation of additional mutant Xpd alleles that fail to support viability on their own but nevertheless"}