Search research articles
Contact Us
Filters
Showing results (11-20 of 14) with videos related to
Page
of 2
Sort By:
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 isomerase
E 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 abetalipoproteinemia
B 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 DSD
Kerstin N Walter, Frederike B Kienzle, Alexander Frankenschmidt, et al.
Nature
|
September 2, 1993
Cloning and gene defects in microsomal triglyceride transfer protein associated with abetalipoproteinaemia
D Sharp, L Blinderman, K A Combs, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 14) with videos related to
Sort By:
Page
of 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 isomerase
E 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 abetalipoproteinemia
B 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 DSD
Kerstin N Walter, Frederike B Kienzle, Alexander Frankenschmidt, et al.
Nature
|
September 2, 1993
Cloning and gene defects in microsomal triglyceride transfer protein associated with abetalipoproteinaemia
D Sharp, L Blinderman, K A Combs, et al.
Page
of 2