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P‐IG‐11 | Apparent RHCE Phenotype Discrepancy in a Mother and Child Due to a Shared RHCECE‐D(3‐9)‐CE Allele

Transfusion (Philadelphia, Pa.), 2023-10, Vol.63 (S5), p.176A-176A

2023

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NGS and blood group systems: State of the art and perspectives

Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine, 2017-09, Vol.24 (3), p.240-244

2017

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The experience of extended blood group genotyping by next-generation sequencing (NGS): investigation of patients with sickle-cell disease

Vox sanguinis, 2016-11, Vol.111 (4), p.418-424

2016

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Weak D type 1, 2 and 3 subtype alleles are rare in the Western French population

Transfusion medicine (Oxford, England), 2019-06, Vol.29 (3), p.209-210

2019

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From genetic variability to phenotypic expression of blood group systems

Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine, 2017-11, Vol.24 (4), p.472-475

2017

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The RHDweak D type 4.0 allele is predominantly but not exclusively cis-associated with the altered RHCEce(c.48C, c.105T, c.733G, c.744C, c.1025T) allele in the French population

Transfusion medicine (Oxford, England), 2014-04, Vol.24 (2), p.120-122

2014

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Cell cloning‐based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes

Journal of cellular and molecular medicine, 2010-07, Vol.14 (7), p.1962-1974

2010

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Next‐generation sequencing for blood group genotyping

ISBT science series, 2017-02, Vol.12 (1), p.184-190

2017

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Intérêt et application du NGS pour le génotypage des groupes sanguins : étude d’une cohorte de patients drépanocytaires

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2015-09, Vol.22 (4), p.204-204

2015

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WS17.1 The ancient origin of F508del-CF: When and where the mutation arose

Journal of cystic fibrosis, 2015-06, Vol.14, p.S31-S31

2015

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Le séquençage de nouvelle génération pour le génotypage des groupes sanguins

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2013-06, Vol.20 (3), p.293-293

2013

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Identification de nouveaux variants dans le gène ABO

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2013-06, Vol.20 (3), p.317-317

2013

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The potential of oligonucleotides for therapeutic applications

Trends in biotechnology (Regular ed.), 2006-12, Vol.24 (12), p.563-570

2006

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De l’estran à la digue: Histoire des aménagements portuaires et littoraux, xvie-xxe siècle

2018

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The RHD weak D type 4.0 allele is predominantly but not exclusively cis ‐associated with the altered RHCE ce ( c. 48C , c. 105T , c. 733G , c. 744C , c. 1025T ) allele in the French population

Transfusion medicine (Oxford, England), 2014-04, Vol.24 (2), p.120-122

2014

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Extensive genetic analysis in non-classic CF patients

Journal of cystic fibrosis, 2008-06, Vol.7, p.S7-S7

2008

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Analysis of High-Frequency Modulation Response of Strongly Injection-Locked Cascaded Semiconductor Ring Lasers

IEEE journal of quantum electronics, 2012-12, Vol.48 (12), p.1568-1577

2012

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403 Estimating the age of common CFTR mutations in Brittany (western France)

Journal of cystic fibrosis, 2007, Vol.6, p.S98-S98

2007

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Weak D caused by a founder deletion in the RHD gene

Transfusion (Philadelphia, Pa.), 2012-11, Vol.52 (11), p.2348-2355

2012

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ENaC mutations in patients with CF-like disease

Journal of cystic fibrosis, 2008-06, Vol.7, p.S1-S1

2008

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CDKL5 MUTATIONS IN BOYS WITH SEVERE ENCEPHALOPATHY AND EARLY-ONSET INTRACTABLE EPILEPSY

Neurology, 2009-07, Vol.73 (1), p.77-78

2009

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Interaction of dystrophin rod domain with membrane phospholipids. Evidence of a close proximity between tryptophan residues and lipids

The Journal of biological chemistry, 2003-02, Vol.278 (8), p.5993-6001

2003

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KLN-5: a safe monocationic lipophosphoramide to transfect efficiently haematopoietic cell lines and human CD34 + cells

Biochimica et biophysica acta. Biomembranes, 2004, Vol.1665 (1), p.118-133

2004

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Re: CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy

Neurology, 2009-07, Vol.73 (1), p.77

2009

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KLN-5: a safe monocationic lipophosphoramide to transfect efficiently haematopoietic cell lines and human CD34+ cells

Biochimica et biophysica acta, 2004-10, Vol.1665 (1-2), p.118

2004

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P‐IG‐11 | Apparent RHCE Phenotype Discrepancy in a Mother and Child Due to a Shared RHCECE‐D(3‐9)‐CE Allele

NGS and blood group systems: State of the art and perspectives

The experience of extended blood group genotyping by next-generation sequencing (NGS): investigation of patients with sickle-cell disease

Weak D type 1, 2 and 3 subtype alleles are rare in the Western French population

From genetic variability to phenotypic expression of blood group systems

The RHDweak D type 4.0 allele is predominantly but not exclusively cis-associated with the altered RHCEce(c.48C, c.105T, c.733G, c.744C, c.1025T) allele in the French population

Cell cloning‐based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes

Next‐generation sequencing for blood group genotyping

Intérêt et application du NGS pour le génotypage des groupes sanguins : étude d’une cohorte de patients drépanocytaires

WS17.1 The ancient origin of F508del-CF: When and where the mutation arose

Le séquençage de nouvelle génération pour le génotypage des groupes sanguins

Identification de nouveaux variants dans le gène ABO

The potential of oligonucleotides for therapeutic applications

De l’estran à la digue: Histoire des aménagements portuaires et littoraux, xvie-xxe siècle

The RHD weak D type 4.0 allele is predominantly but not exclusively cis ‐associated with the altered RHCE ce ( c. 48C , c. 105T , c. 733G , c. 744C , c. 1025T ) allele in the French population

Extensive genetic analysis in non-classic CF patients

Analysis of High-Frequency Modulation Response of Strongly Injection-Locked Cascaded Semiconductor Ring Lasers

403 Estimating the age of common CFTR mutations in Brittany (western France)

Weak D caused by a founder deletion in the RHD gene

ENaC mutations in patients with CF-like disease

CDKL5 MUTATIONS IN BOYS WITH SEVERE ENCEPHALOPATHY AND EARLY-ONSET INTRACTABLE EPILEPSY

Interaction of dystrophin rod domain with membrane phospholipids. Evidence of a close proximity between tryptophan residues and lipids

KLN-5: a safe monocationic lipophosphoramide to transfect efficiently haematopoietic cell lines and human CD34 + cells

Re: CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy

KLN-5: a safe monocationic lipophosphoramide to transfect efficiently haematopoietic cell lines and human CD34+ cells

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