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A low-power CMOS 155 Mb/s transceiver for SONET/SDH over co-ax and fibre

Proceedings of the IEEE 2001 Custom Integrated Circuits Conference (Cat. No.01CH37169), 2001, p.127-130

2001

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Evolution and present varietal situation of the leek

Journal d'agriculture traditionnelle et de botanique appliquée, 1986

Morle, R. (Centre de Recherche Tezier S.A., Valence (France))

1986

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2018 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations Summary

Resuscitation, 2018-12, Vol.133, p.194-206

2018

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Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3

Blood, 2000-08, Vol.96 (4), p.1602-1604

2000

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Service delivery model of extracorporeal membrane oxygenation in an Australian regional hospital

Critical care and resuscitation, 2016-12, Vol.18 (4), p.235-241

2016

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Localization of a non-syndromic X-linked mental retardation gene (MRX80) to Xq22-q24

American journal of medical genetics, 2003-09, Vol.122A (1), p.37-41

2003

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Targeted Inactivation of the Major Positive Regulatory Element (HS-40) of the Human α-Globin Gene Locus

Blood, 1995-08, Vol.86 (3), p.1202-1211

1995

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Non-erythroid Genes Inserted on Either Side of Human HS-40 Impair the Activation of Its Natural α-Globin Gene Targets without Being Themselves Preferentially Activated

The Journal of biological chemistry, 2000-08, Vol.275 (33), p.25831-25839

2000

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Gain and loss of function mutations of ataxin-7 cause cilia pathology in mouse and zebrafish models

Cilia (London), 2015-07, Vol.4 (S1), p.P13-P13, Article P13

2015

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Disruption of the mechanism of long range activation within the human alpha-globin complex

The Journal of biological chemistry, 2004-05, Vol.279 (21), p.21793-21801

2004

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A new α chain variant Hb Sallanches [α2 104(G11) Cys→Tyr] associated with HbH disease in one homozygous patient

British journal of haematology, 1995-11, Vol.91 (3), p.608-611

1995

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Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

Blood, 1989-08, Vol.74 (2), p.828-832

1989

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Targeted inactivation of the major positive regulatory element (HS-40) of the human alpha-globin gene locus

Blood, 1995-08, Vol.86 (3), p.1202-1211

1995

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Human chronic myeloid leukemic cell line with positive Philadelphia chromosome exhibits megakaryocytic and erythroid characteristics

Experimental hematology, 1987-09, Vol.15 (8), p.822

1987

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Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis

British journal of haematology, 1997-12, Vol.99 (3), p.522-530

1997

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Occurrence of the αI 22 Arg→His (CGT→CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis

British journal of haematology, 1991-05, Vol.78 (1), p.108-113

1991

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Expression of human colony-stimulating factor-I (CSF-1) receptor in murine pluripotent hematopoietic NFS-60 cells induces long-term proliferation in response to CSF-1 without loss of erythroid differentiation potential

Blood, 1993-05, Vol.81 (10), p.2511-2520

1993

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Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG)

Haematologica (Roma), 2000-01, Vol.85 (1), p.19

2000

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Spectrin Tunis (SpαI/78), an elliptocytogenic variant, is due to the CGG→TGG codon change (Arg→Trp) at position 35 of the αI domain

Blood, 1989-08, Vol.74 (2), p.828-832

1989

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Reduction of membrane band 7 and activation of volume stimulated (K+, Cl−)‐cotransport in a case of congenital stomatocytosis

British journal of haematology, 1989-01, Vol.71 (1), p.141-146

1989

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Two distinct truncated variants of ankyrin associated with hereditary spherocytosis

American journal of hematology, 1998-05, Vol.58 (1), p.36-41

1998

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Expression of Human Colony-Stimulating Factor-1 (CSF-1) Receptor in Murine Pluripotent Hematopoietic NFS-60 Cells Induces Long-Term Proliferation in Response to CSF-1 Without Loss of Erythroid Differentiation Potential

Blood, 1993-05, Vol.81 (10), p.2511-2520

1993

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SpαV/41 : a common spectrin polymorphism at the αIV-αV domain junction : relevance to the expression level of hereditary elliptocytosis due to α-spectrin variants located in trans

The Journal of clinical investigation, 1991-06, Vol.87 (6), p.2169-2177

1991

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Disruption of the mechanism of long range activation within the human alpha-globin complexe

The Journal of biological chemistry, 2004 (279), p.21793-21801

2004

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Two elliptocytogenic alpha super(I/74) variants of the spectrin alpha I domain. Spectrin Culoz (GGT arrow right GTT; alpha I 40 Gly arrow right Val) and spectrin Lyon (CTT arrow right TTT; alpha I 43 Leu arrow right Phe)

The Journal of clinical investigation, 1990-01, Vol.86 (2), p.548-554

1990

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A low-power CMOS 155 Mb/s transceiver for SONET/SDH over co-ax and fibre

Evolution and present varietal situation of the leek

2018 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations Summary

Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3

Service delivery model of extracorporeal membrane oxygenation in an Australian regional hospital

Localization of a non-syndromic X-linked mental retardation gene (MRX80) to Xq22-q24

Targeted Inactivation of the Major Positive Regulatory Element (HS-40) of the Human α-Globin Gene Locus

Non-erythroid Genes Inserted on Either Side of Human HS-40 Impair the Activation of Its Natural α-Globin Gene Targets without Being Themselves Preferentially Activated

Gain and loss of function mutations of ataxin-7 cause cilia pathology in mouse and zebrafish models

Disruption of the mechanism of long range activation within the human alpha-globin complex

A new α chain variant Hb Sallanches [α2 104(G11) Cys→Tyr] associated with HbH disease in one homozygous patient

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

Targeted inactivation of the major positive regulatory element (HS-40) of the human alpha-globin gene locus

Human chronic myeloid leukemic cell line with positive Philadelphia chromosome exhibits megakaryocytic and erythroid characteristics

Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis

Occurrence of the αI 22 Arg→His (CGT→CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis

Expression of human colony-stimulating factor-I (CSF-1) receptor in murine pluripotent hematopoietic NFS-60 cells induces long-term proliferation in response to CSF-1 without loss of erythroid differentiation potential

Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG)

Spectrin Tunis (SpαI/78), an elliptocytogenic variant, is due to the CGG→TGG codon change (Arg→Trp) at position 35 of the αI domain

Reduction of membrane band 7 and activation of volume stimulated (K+, Cl−)‐cotransport in a case of congenital stomatocytosis

Two distinct truncated variants of ankyrin associated with hereditary spherocytosis

Expression of Human Colony-Stimulating Factor-1 (CSF-1) Receptor in Murine Pluripotent Hematopoietic NFS-60 Cells Induces Long-Term Proliferation in Response to CSF-1 Without Loss of Erythroid Differentiation Potential

SpαV/41 : a common spectrin polymorphism at the αIV-αV domain junction : relevance to the expression level of hereditary elliptocytosis due to α-spectrin variants located in trans

Disruption of the mechanism of long range activation within the human alpha-globin complexe

Two elliptocytogenic alpha super(I/74) variants of the spectrin alpha I domain. Spectrin Culoz (GGT arrow right GTT; alpha I 40 Gly arrow right Val) and spectrin Lyon (CTT arrow right TTT; alpha I 43 Leu arrow right Phe)

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