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Nature Communications
|
April 11, 2015
Autoprocessing of neutrophil elastase near its active site reduces the efficiency of natural and synthetic elastase inhibitors
T Dau, R S J Sarker, A O Yildirim, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1992
Three human elastase-like genes coordinately expressed in the myelomonocyte lineage are organized as a single genetic locus on 19pter
M Zimmer, R L Medcalf, T M Fink, et al.
European Journal of Human Genetics : EJHG
|
July 6, 2000
Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene
S Tinschert, I Naumann, E Stegmann, et al.
Genomics
|
September 2, 1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers syndrome
R D Kortschak, H Reimann, M Zimmer, et al.
Biochemistry
|
September 19, 1989
Isolation and complete structure of the lymphocyte serine protease granzyme G, a novel member of the granzyme multigene family in murine cytolytic T lymphocytes. Evolutionary origin of lymphocyte proteases
D E Jenne, D Masson, M Zimmer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 25, 1996
A new isoleucine substitution of Val-20 in transthyretin tetramers selectively impairs dimer-dimer contacts and causes systemic amyloidosis
D E Jenne, K Denzel, P Blätzinger, et al.
American Journal of Human Genetics
|
July 27, 2001
Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions
D E Jenne, S Tinschert, H Reimann, et al.
Genomics
|
December 1, 1994
The human Met-ase gene (GZMM): structure, sequence, and close physical linkage to the serine protease gene cluster on 19p13.3
D Pilat, T Fink, B Obermaier-Skrobanek, et al.
Scientific Reports
|
October 15, 2016
Quantitative analysis of protease recognition by inhibitors in plasma using microscale thermophoresis
T Dau, E V Edeleva, S A I Seidel, et al.
The Journal of Biological Chemistry
|
September 10, 1999
Generation of catalytically active granzyme K from Escherichia coli inclusion bodies and identification of efficient granzyme K inhibitors in human plasma
E Wilharm, M A Parry, R Friebel, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 42) with videos related to
Sort By:
Page
of 5
Nature Communications
|
April 11, 2015
Autoprocessing of neutrophil elastase near its active site reduces the efficiency of natural and synthetic elastase inhibitors
T Dau, R S J Sarker, A O Yildirim, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1992
Three human elastase-like genes coordinately expressed in the myelomonocyte lineage are organized as a single genetic locus on 19pter
M Zimmer, R L Medcalf, T M Fink, et al.
European Journal of Human Genetics : EJHG
|
July 6, 2000
Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene
S Tinschert, I Naumann, E Stegmann, et al.
Genomics
|
September 2, 1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers syndrome
R D Kortschak, H Reimann, M Zimmer, et al.
Biochemistry
|
September 19, 1989
Isolation and complete structure of the lymphocyte serine protease granzyme G, a novel member of the granzyme multigene family in murine cytolytic T lymphocytes. Evolutionary origin of lymphocyte proteases
D E Jenne, D Masson, M Zimmer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 25, 1996
A new isoleucine substitution of Val-20 in transthyretin tetramers selectively impairs dimer-dimer contacts and causes systemic amyloidosis
D E Jenne, K Denzel, P Blätzinger, et al.
American Journal of Human Genetics
|
July 27, 2001
Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions
D E Jenne, S Tinschert, H Reimann, et al.
Genomics
|
December 1, 1994
The human Met-ase gene (GZMM): structure, sequence, and close physical linkage to the serine protease gene cluster on 19p13.3
D Pilat, T Fink, B Obermaier-Skrobanek, et al.
Scientific Reports
|
October 15, 2016
Quantitative analysis of protease recognition by inhibitors in plasma using microscale thermophoresis
T Dau, E V Edeleva, S A I Seidel, et al.
The Journal of Biological Chemistry
|
September 10, 1999
Generation of catalytically active granzyme K from Escherichia coli inclusion bodies and identification of efficient granzyme K inhibitors in human plasma
E Wilharm, M A Parry, R Friebel, et al.
Page
of 5