Arnaud L - Search Results

1

SMIM1 is a type II transmembrane phosphoprotein and displays the Vel blood group antigen at its carboxyl-terminus.

Arnaud L, Kelley LP, Helias V, Cartron JP, Ballif BA. Arnaud L, et al. FEBS Lett. 2015 Nov 30;589(23):3624-30. doi: 10.1016/j.febslet.2015.09.029. Epub 2015 Oct 9. FEBS Lett. 2015. PMID: 26452714 Free PMC article.

2

Disruption of SMIM1 causes the Vel- blood type.

Ballif BA, Helias V, Peyrard T, Menanteau C, Saison C, Lucien N, Bourgouin S, Le Gall M, Cartron JP, Arnaud L. Ballif BA, et al. Among authors: arnaud l. EMBO Mol Med. 2013 May;5(5):751-61. doi: 10.1002/emmm.201302466. Epub 2013 Apr 15. EMBO Mol Med. 2013. PMID: 23505126 Free PMC article.

3

Dimerization of small integral membrane protein 1 promotes cell surface presentation of the Vel blood group epitope.

Kelley LP, Nylander A, Arnaud L, Schmoker AM, St Clair RM, Gleason LA, Souza JM, Storry JR, Olsson ML, Ballif BA. Kelley LP, et al. Among authors: arnaud l. FEBS Lett. 2020 Apr;594(8):1261-1270. doi: 10.1002/1873-3468.13726. Epub 2020 Jan 14. FEBS Lett. 2020. PMID: 31879955 Free article.

4

Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization.

Daniels G, Ballif BA, Helias V, Saison C, Grimsley S, Mannessier L, Hustinx H, Lee E, Cartron JP, Peyrard T, Arnaud L. Daniels G, et al. Among authors: arnaud l. Blood. 2015 Jun 4;125(23):3651-4. doi: 10.1182/blood-2015-03-631598. Epub 2015 Apr 20. Blood. 2015. PMID: 25896650 Free PMC article.

5

A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group system.

Arnaud L, Helias V, Menanteau C, Peyrard T, Lucien N, Ripoche P, Lapègue R, Pham BN, Le Pennec PY, Moulds JJ, Cartron JP. Arnaud L, et al. Transfusion. 2010 Oct;50(10):2106-16. doi: 10.1111/j.1537-2995.2010.02687.x. Epub 2010 Oct 4. Transfusion. 2010. PMID: 20492605

6

Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior.

Saison C, Helias V, Ballif BA, Peyrard T, Puy H, Miyazaki T, Perrot S, Vayssier-Taussat M, Waldner M, Le Pennec PY, Cartron JP, Arnaud L. Saison C, et al. Among authors: arnaud l. Nat Genet. 2012 Jan 15;44(2):174-7. doi: 10.1038/ng.1070. Nat Genet. 2012. PMID: 22246505 Free PMC article.

7

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis.

Helias V, Saison C, Ballif BA, Peyrard T, Takahashi J, Takahashi H, Tanaka M, Deybach JC, Puy H, Le Gall M, Sureau C, Pham BN, Le Pennec PY, Tani Y, Cartron JP, Arnaud L. Helias V, et al. Among authors: arnaud l. Nat Genet. 2012 Jan 15;44(2):170-3. doi: 10.1038/ng.1069. Nat Genet. 2012. PMID: 22246506 Free PMC article.

8

Molecular analysis of the rare in(Lu) blood type: toward decoding the phenotypic outcome of haploinsufficiency for the transcription factor KLF1.

Helias V, Saison C, Peyrard T, Vera E, Prehu C, Cartron JP, Arnaud L. Helias V, et al. Among authors: arnaud l. Hum Mutat. 2013 Jan;34(1):221-8. doi: 10.1002/humu.22218. Epub 2012 Nov 2. Hum Mutat. 2013. PMID: 23125034

9

The ABCB6 mutation p.Arg192Trp is a recessive mutation causing the Lan- blood type.

Saison C, Helias V, Peyrard T, Merad L, Cartron JP, Arnaud L. Saison C, et al. Among authors: arnaud l. Vox Sang. 2013 Feb;104(2):159-65. doi: 10.1111/j.1423-0410.2012.01650.x. Epub 2012 Sep 10. Vox Sang. 2013. PMID: 22958180

10

Deletion of Exons 3 through 5 of ABCG2 causes the Jr(a-) phenotype in a West African woman.

Saison C, Cartron JP, Arnaud L. Saison C, et al. Among authors: arnaud l. Transfusion. 2015 Nov;55(11):2766-7. doi: 10.1111/trf.13223. Epub 2015 Jul 14. Transfusion. 2015. PMID: 26173500 No abstract available.

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