Literature DB >> 10939805

Clinical manifestations, management, and molecular genetics in congenital factor VII deficiency: the International Registry on Congenital Factor VII Deficiency (IRF7)

G Mariani, F H Herrmann, F Bernardi, J F Schved, G Auerswald, J Ingerslev.   

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Year:  2000        PMID: 10939805

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


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  5 in total

1.  No Dataset Left Behind: Mechanistic Insights into Thyroid Receptor Signaling Through Transcriptomic Consensome Meta-Analysis.

Authors:  Scott A Ochsner; Neil J McKenna
Journal:  Thyroid       Date:  2020-01-29       Impact factor: 6.568

2.  Functional and Molecular Characterization of C91S Mutation in the Second Epidermal Growth Factor-Like Domain of Factor VII.

Authors:  Amir Mashayekhi; Shirin Shahbazi; Mirdavood Omrani
Journal:  Iran J Biotechnol       Date:  2018-04-18       Impact factor: 1.671

Review 3.  Phenotypical variability in congenital FVII deficiency follows the ISTH-SSC severity classification guidelines: a review with illustrative examples from the clinic.

Authors:  Shilpa Jain; Jennifer Donkin; Mary-Jane Frey; Skye Peltier; Sriya Gunawardena; David L Cooper
Journal:  J Blood Med       Date:  2018-11-19

4.  An engineered tale-transcription factor rescues transcription of factor VII impaired by promoter mutations and enhances its endogenous expression in hepatocytes.

Authors:  Elena Barbon; Silvia Pignani; Alessio Branchini; Francesco Bernardi; Mirko Pinotti; Matteo Bovolenta
Journal:  Sci Rep       Date:  2016-06-24       Impact factor: 4.379

5.  Novel factor VII gene mutations in six families with hereditary coagulation factor VII deficiency.

Authors:  Xiaoyu Zhang; Shuwen Wang; Shaoqiu Leng; Qi Feng; Yanqi Zhang; Shuqian Xu; Lei Zhang; Xinsheng Zhang; Yunhai Fang; Jun Peng; Zi Sheng
Journal:  J Clin Lab Anal       Date:  2021-08-02       Impact factor: 2.352

  5 in total

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