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Neurogenetics
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April 8, 2006
Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein
Ashraf U Mannan, Johann Boehm, Simone M Sauter, et al.
Cancer Research
|
October 1, 1996
Specificity of antibodies directed against Env protein of human endogenous retroviruses in patients with germ cell tumors
M Sauter, K Roemer, B Best, et al.
Virus Research
|
September 1, 1993
Molecular and biological characteristics of a novel HIV-2 isolate, HIV-2HOM
S Nick, C A Diniz, G Born, et al.
The Plant Journal : for Cell and Molecular Biology
|
October 13, 2000
Activation of CDK-activating kinase is dependent on interaction with H-type cyclins in plants
M Yamaguchi, T Fabian, M Sauter, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
October 29, 2000
Expression of cell volume-regulated kinase h-sgk in pancreatic tissue
K Klingel, S Wärntges, J Bock, et al.
American Journal of Human Genetics
|
July 11, 2006
ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia
Ashraf U Mannan, Philip Krawen, Simone M Sauter, et al.
European Journal of Human Genetics : EJHG
|
August 15, 2008
Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia
Moneef Shoukier, Juergen Neesen, Simone M Sauter, et al.
BMC Veterinary Research
|
May 26, 2020
Spatial distribution and incidence of bovine neonatal pancytopenia in Bavaria, Germany
Carola M Sauter-Louis, Christoph Staubach, Frederike Reichmann, et al.
Oncogene
|
September 12, 2000
Human endogenous retrovirus protein cORF supports cell transformation and associates with the promyelocytic leukemia zinc finger protein
A Boese, M Sauter, U Galli, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2005
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay
G von Beust, S M Sauter, T Liehr, et al.
Page
of 14
Search research articles
Search
Showing results (101-110 of 133) with videos related to
Sort By:
Page
of 14
Neurogenetics
|
April 8, 2006
Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein
Ashraf U Mannan, Johann Boehm, Simone M Sauter, et al.
Cancer Research
|
October 1, 1996
Specificity of antibodies directed against Env protein of human endogenous retroviruses in patients with germ cell tumors
M Sauter, K Roemer, B Best, et al.
Virus Research
|
September 1, 1993
Molecular and biological characteristics of a novel HIV-2 isolate, HIV-2HOM
S Nick, C A Diniz, G Born, et al.
The Plant Journal : for Cell and Molecular Biology
|
October 13, 2000
Activation of CDK-activating kinase is dependent on interaction with H-type cyclins in plants
M Yamaguchi, T Fabian, M Sauter, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
October 29, 2000
Expression of cell volume-regulated kinase h-sgk in pancreatic tissue
K Klingel, S Wärntges, J Bock, et al.
American Journal of Human Genetics
|
July 11, 2006
ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia
Ashraf U Mannan, Philip Krawen, Simone M Sauter, et al.
European Journal of Human Genetics : EJHG
|
August 15, 2008
Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia
Moneef Shoukier, Juergen Neesen, Simone M Sauter, et al.
BMC Veterinary Research
|
May 26, 2020
Spatial distribution and incidence of bovine neonatal pancytopenia in Bavaria, Germany
Carola M Sauter-Louis, Christoph Staubach, Frederike Reichmann, et al.
Oncogene
|
September 12, 2000
Human endogenous retrovirus protein cORF supports cell transformation and associates with the promyelocytic leukemia zinc finger protein
A Boese, M Sauter, U Galli, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2005
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay
G von Beust, S M Sauter, T Liehr, et al.
Page
of 14