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P Texier

Showing results (21-30 of 27) with videos related to

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Blood|January 1, 1995
A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemiaS Hayette, D Dhermy, M E dos Santos, et al.
The European Journal of Medicine|April 1, 1992
Asymptomatic renal-vein thrombosis in adult nephrotic syndrome ultrasonography and urinary fibrin-fibrinogen products: a prospective studyG Rostoker, J P Texier, B Jeandel, et al.
Blood|August 15, 1993
Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin CN Alloisio, N Dalla Venezia, A Rana, et al.
Blood|May 15, 1996
The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulumN Alloisio, P Texier, L Denoroy, et al.
British Journal of Haematology|December 1, 1995
Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11P Maillet, A Vallier, W H Reinhart, et al.
Blood|July 1, 1997
Modulation of clinical expression and band 3 deficiency in hereditary spherocytosisN Alloisio, P Texier, A Vallier, et al.
Blood|August 15, 2000
Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3M L Ribeiro, N Alloisio, H Almeida, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Blood|January 1, 1995
A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemiaS Hayette, D Dhermy, M E dos Santos, et al.
The European Journal of Medicine|April 1, 1992
Asymptomatic renal-vein thrombosis in adult nephrotic syndrome ultrasonography and urinary fibrin-fibrinogen products: a prospective studyG Rostoker, J P Texier, B Jeandel, et al.
Blood|August 15, 1993
Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin CN Alloisio, N Dalla Venezia, A Rana, et al.
Blood|May 15, 1996
The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulumN Alloisio, P Texier, L Denoroy, et al.
British Journal of Haematology|December 1, 1995
Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11P Maillet, A Vallier, W H Reinhart, et al.
Blood|July 1, 1997
Modulation of clinical expression and band 3 deficiency in hereditary spherocytosisN Alloisio, P Texier, A Vallier, et al.
Blood|August 15, 2000
Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3M L Ribeiro, N Alloisio, H Almeida, et al.
Pageof 3