Assouline Z - Search Results

1

The human gene for von Willebrand factor. Identification of repetitive Alu sequences 5' to the transcription initiation site.

Assouline Z, Kerbiriou-Nabias DM, Piétu G, Thomas N, Bahnak BR, Meyer D. Assouline Z, et al. Biochem Biophys Res Commun. 1988 Jun 30;153(3):1159-66. doi: 10.1016/s0006-291x(88)81349-4. Biochem Biophys Res Commun. 1988. PMID: 3260493

2

Expression of von Willebrand factor in porcine vessels: heterogeneity at the level of von Willebrand factor mRNA.

Bahnak BR, Wu QY, Coulombel L, Assouline Z, Kerbiriou-Nabias D, Piétu G, Drouet L, Caen JP, Meyer D. Bahnak BR, et al. Among authors: assouline z. J Cell Physiol. 1989 Feb;138(2):305-10. doi: 10.1002/jcp.1041380212. J Cell Physiol. 1989. PMID: 2783933

3

A Taq I polymorphism in the 5' region of the von Willebrand factor (vWF) gene.

Lavergne JM, Bahnak BR, Assouline Z, Piétu G, Kerbiriou-Nabias D, Meulien P, Pavirani A, Meyer D. Lavergne JM, et al. Among authors: assouline z. Nucleic Acids Res. 1988 Mar 25;16(6):2742. doi: 10.1093/nar/16.6.2742. Nucleic Acids Res. 1988. PMID: 2896339 Free PMC article. No abstract available.

4

Identification of a CpG mutation in the coagulation factor-IX gene by analysis of amplified DNA sequences.

Siguret V, Amselem S, Vidaud M, Assouline Z, Kerbiriou-Nabias D, Piétu G, Goossens M, Larrieu MJ, Bahnak B, Meyer D, et al. Siguret V, et al. Among authors: assouline z. Br J Haematol. 1988 Dec;70(4):411-6. doi: 10.1111/j.1365-2141.1988.tb02509.x. Br J Haematol. 1988. PMID: 3219291

5

The role of the 5'-flanking region in the cell-specific transcription of the human von Willebrand factor gene.

Ferreira V, Assouline Z, Schwachtgen JL, Bahnak BR, Meyer D, Kerbiriou-Nabias D. Ferreira V, et al. Among authors: assouline z. Biochem J. 1993 Aug 1;293 ( Pt 3)(Pt 3):641-8. doi: 10.1042/bj2930641. Biochem J. 1993. PMID: 8352730 Free PMC article.

6

Molecular dissection of the Schwann cell specific promoter of the PMP22 gene.

Sabéran-Djoneidi D, Sanguedolce V, Assouline Z, Lévy N, Passage E, Fontés M. Sabéran-Djoneidi D, et al. Among authors: assouline z. Gene. 2000 May 2;248(1-2):223-31. doi: 10.1016/s0378-1119(00)00116-5. Gene. 2000. PMID: 10806367

7

Toward genotype phenotype correlations in GFM1 mutations.

Galmiche L, Serre V, Beinat M, Zossou R, Assouline Z, Lebre AS, Chretien F, Shenhav R, Zeharia A, Saada A, Vedrenne V, Boddaert N, de Lonlay P, Rio M, Munnich A, Rötig A. Galmiche L, et al. Among authors: assouline z. Mitochondrion. 2012 Mar;12(2):242-7. doi: 10.1016/j.mito.2011.09.007. Epub 2011 Oct 1. Mitochondrion. 2012. PMID: 21986555

8

Characterization of the 5'-flanking region for the human fibrinogen beta gene.

Huber P, Dalmon J, Courtois G, Laurent M, Assouline Z, Marguerie G. Huber P, et al. Among authors: assouline z. Nucleic Acids Res. 1987 Feb 25;15(4):1615-25. doi: 10.1093/nar/15.4.1615. Nucleic Acids Res. 1987. PMID: 3029722 Free PMC article.

9

Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy.

Galmiche L, Serre V, Beinat M, Assouline Z, Lebre AS, Chretien D, Nietschke P, Benes V, Boddaert N, Sidi D, Brunelle F, Rio M, Munnich A, Rötig A. Galmiche L, et al. Among authors: assouline z. Hum Mutat. 2011 Nov;32(11):1225-31. doi: 10.1002/humu.21562. Epub 2011 Sep 14. Hum Mutat. 2011. PMID: 21786366

10

Improving post-natal detection of mitochondrial DNA mutations.

Barcia G, Assouline Z, Magen M, Pennisi A, Rötig A, Munnich A, Bonnefont JP, Steffann J. Barcia G, et al. Among authors: assouline z. Expert Rev Mol Diagn. 2020 Oct;20(10):1003-1008. doi: 10.1080/14737159.2020.1820326. Epub 2020 Sep 20. Expert Rev Mol Diagn. 2020. PMID: 32902337

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

42 results

Search Page