Jamet D - Search Results

1

Identification of novel variant A alleles within the ABO gene.

Fichou Y, Hennion M, Dupont I, Jamet D, Le Maréchal C, Férec C. Fichou Y, et al. Among authors: jamet d. Transfusion. 2016 May;56(5):1244-6. doi: 10.1111/trf.13542. Epub 2016 Feb 26. Transfusion. 2016. PMID: 26920498 No abstract available.

2

Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles.

Fichou Y, Le Maréchal C, Bryckaert L, Guerry C, Bénech C, Dupont I, Jamet D, Férec C, Chen JM. Fichou Y, et al. Among authors: jamet d. Transfusion. 2012 Apr;52(4):759-64. doi: 10.1111/j.1537-2995.2011.03350.x. Epub 2011 Sep 26. Transfusion. 2012. PMID: 21950494

3

Weak D caused by a founder deletion in the RHD gene.

Fichou Y, Chen JM, Le Maréchal C, Jamet D, Dupont I, Chuteau C, Durousseau C, Loirat MJ, Bailly P, Férec C. Fichou Y, et al. Among authors: jamet d. Transfusion. 2012 Nov;52(11):2348-55. doi: 10.1111/j.1537-2995.2012.03606.x. Epub 2012 Mar 15. Transfusion. 2012. PMID: 22420867

4

Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms.

Chen JM, Fichou Y, Jamet D, Dupont I, Cooper DN, Le Maréchal C, Férec C. Chen JM, et al. Among authors: jamet d. Transfusion. 2013 Jan;53(1):206-10. doi: 10.1111/j.1537-2995.2012.03713.x. Epub 2012 May 21. Transfusion. 2013. PMID: 22612274

5

Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare alleles.

Fichou Y, Le Maréchal C, Jamet D, Bryckaert L, Ka C, Audrézet MP, Le Gac G, Dupont I, Chen JM, Férec C. Fichou Y, et al. Among authors: jamet d. Transfusion. 2013 Aug;53(8):1821-8. doi: 10.1111/trf.12009. Epub 2012 Dec 11. Transfusion. 2013. PMID: 23228153 Clinical Trial.

6

A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.

Fichou Y, Le Maréchal C, Bryckaert L, Dupont I, Jamet D, Chen JM, Férec C. Fichou Y, et al. Among authors: jamet d. Transfusion. 2013 Nov;53(11 Suppl 2):2974-82. doi: 10.1111/trf.12179. Epub 2013 Apr 3. Transfusion. 2013. PMID: 23550903

7

Insights into RHCE Molecular Analysis in Samples with Partial D Variants: the Experience of Western France.

Fichou Y, Le Maréchal C, Scotet V, Jamet D, Férec C. Fichou Y, et al. Among authors: jamet d. Transfus Med Hemother. 2015 Nov;42(6):372-7. doi: 10.1159/000382086. Epub 2015 Jul 23. Transfus Med Hemother. 2015. PMID: 26733768 Free PMC article.

8

A proposal for a rational transfusion strategy in patients of European and North African descent with weak D type 4.0 and 4.1 phenotypes.

Flegel WA, Peyrard T, Chiaroni J, Tournamille C, Jamet D, Pirenne F. Flegel WA, et al. Among authors: jamet d. Blood Transfus. 2019 Mar;17(2):89-90. doi: 10.2450/2018.0059-18. Epub 2018 May 3. Blood Transfus. 2019. PMID: 31013249 Free PMC article. No abstract available.

9

Jumping translocations in multiple myeloma.

Jamet D, Marzin Y, Douet-Guilbert N, Morel F, Le Bris MJ, Herry A, Banzakour S, Bourquard P, Morice P, Abgrall JF, Berthou C, De Braekeleer M. Jamet D, et al. Cancer Genet Cytogenet. 2005 Sep;161(2):159-63. doi: 10.1016/j.cancergencyto.2005.01.017. Cancer Genet Cytogenet. 2005. PMID: 16102587

10

Chromosome 1 abnormalities in multiple myeloma.

Marzin Y, Jamet D, Douet-Guilbert N, Morel F, Le Bris MJ, Morice P, Abgrall JF, Berthou C, De Braekeleer M. Marzin Y, et al. Among authors: jamet d. Anticancer Res. 2006 Mar-Apr;26(2A):953-9. Anticancer Res. 2006. PMID: 16619492 Free article.

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