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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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M J Tanner

Showing results (141-150 of 150) with videos related to

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Blood|August 15, 1994

Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypesD M Lublin, G Mallinson, J Poole, et al.

Blood|July 1, 1997

Modulation of clinical expression and band 3 deficiency in hereditary spherocytosisN Alloisio, P Texier, A Vallier, et al.

Transfusion|January 1, 1981

Studies on the blood of an MiV homozygoteV Vengelen-Tyler, D J Anstee, P D Issitt, et al.

The Biochemical Journal|April 15, 1988

Monoclonal antibodies that recognize different membrane proteins that are deficient in Rhnull human erythrocytes. One group of antibodies reacts with a variety of cells and tissues whereas the other group is erythroid-specificN Avent, P A Judson, S F Parsons, et al.

The Biochemical Journal|March 1, 1984

Two individuals with elliptocytic red cells apparently lack three minor erythrocyte membrane sialoglycoproteinsD J Anstee, S F Parsons, K Ridgwell, et al.

Blood|January 3, 2001

Lutheran blood group glycoprotein and its newly characterized mouse homologue specifically bind alpha5 chain-containing human laminin with high affinityS F Parsons, G Lee, F A Spring, et al.

Journal of Molecular Biology|February 20, 1992

Basis of unique red cell membrane properties in hereditary ovalocytosisA E Schofield, M J Tanner, J C Pinder, et al.

Journal of Immunology (Baltimore, Md. : 1950)|April 15, 1990

Preferential expression of the complement regulatory protein decay accelerating factor at the fetomaternal interface during human pregnancyC H Holmes, K L Simpson, S D Wainwright, et al.

The Biochemical Journal|August 6, 2000

Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cellsL J Bruce, O Wrong, A M Toye, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 30, 1998

Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosisF E Karet, F J Gainza, A Z Györy, et al.

Pageof 15

Search research articles

Showing results (141-150 of 150) with videos related to

Sort By:

Pageof 15

You have reached the last page of results.This site can display upto 150 results.

Blood|August 15, 1994

Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypesD M Lublin, G Mallinson, J Poole, et al.

Blood|July 1, 1997

Modulation of clinical expression and band 3 deficiency in hereditary spherocytosisN Alloisio, P Texier, A Vallier, et al.

Transfusion|January 1, 1981

Studies on the blood of an MiV homozygoteV Vengelen-Tyler, D J Anstee, P D Issitt, et al.

The Biochemical Journal|April 15, 1988

The Biochemical Journal|March 1, 1984

Two individuals with elliptocytic red cells apparently lack three minor erythrocyte membrane sialoglycoproteinsD J Anstee, S F Parsons, K Ridgwell, et al.

Blood|January 3, 2001

Lutheran blood group glycoprotein and its newly characterized mouse homologue specifically bind alpha5 chain-containing human laminin with high affinityS F Parsons, G Lee, F A Spring, et al.

Journal of Molecular Biology|February 20, 1992

Basis of unique red cell membrane properties in hereditary ovalocytosisA E Schofield, M J Tanner, J C Pinder, et al.

Journal of Immunology (Baltimore, Md. : 1950)|April 15, 1990

Preferential expression of the complement regulatory protein decay accelerating factor at the fetomaternal interface during human pregnancyC H Holmes, K L Simpson, S D Wainwright, et al.

The Biochemical Journal|August 6, 2000

Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cellsL J Bruce, O Wrong, A M Toye, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 30, 1998

Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosisF E Karet, F J Gainza, A Z Györy, et al.

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