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B Kienzle

Showing results (11-20 of 14) with videos related to

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The Journal of Biological Chemistry|November 22, 1996
A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomeraseE F Rehberg, M E Samson-Bouma, B Kienzle, et al.
The Journal of Biological Chemistry|June 16, 1995
A 30-amino acid truncation of the microsomal triglyceride transfer protein large subunit disrupts its interaction with protein disulfide-isomerase and causes abetalipoproteinemiaB Ricci, D Sharp, E O'Rourke, et al.
Hormone Research in Paediatrics|April 17, 2010
Difficulties in diagnosis and treatment of 5alpha-reductase type 2 deficiency in a newborn with 46,XY DSDKerstin N Walter, Frederike B Kienzle, Alexander Frankenschmidt, et al.
Nature|September 2, 1993
Cloning and gene defects in microsomal triglyceride transfer protein associated with abetalipoproteinaemiaD Sharp, L Blinderman, K A Combs, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
The Journal of Biological Chemistry|November 22, 1996
A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomeraseE F Rehberg, M E Samson-Bouma, B Kienzle, et al.
The Journal of Biological Chemistry|June 16, 1995
A 30-amino acid truncation of the microsomal triglyceride transfer protein large subunit disrupts its interaction with protein disulfide-isomerase and causes abetalipoproteinemiaB Ricci, D Sharp, E O'Rourke, et al.
Hormone Research in Paediatrics|April 17, 2010
Difficulties in diagnosis and treatment of 5alpha-reductase type 2 deficiency in a newborn with 46,XY DSDKerstin N Walter, Frederike B Kienzle, Alexander Frankenschmidt, et al.
Nature|September 2, 1993
Cloning and gene defects in microsomal triglyceride transfer protein associated with abetalipoproteinaemiaD Sharp, L Blinderman, K A Combs, et al.
Pageof 2