Ramsden, Simon C., Deans, Zandra, Robinson, David O., Mountford, Roger, Sistermans, Erik A., Grody, Wayne W., ...
Molecular genetic techniques have entered many areas of clinical practice. Public expectations from this technology are understandably high. To maintain confidence in this technology, laboratories...
Arginase: A Novel Proliferative Determinant in Prostate Cancer (2006)
This project is an investigation of the involvement of the enzyme arginase type II (AII) in the pathogenesis and growth of prostate cancer. Having cloned the AII gene in our laboratory, we...
Cystic Fibrosis Mutations in Costa Rica (2003)
Venegas, Patricia B., Novak, Jessica M., Oscar, Castro A., Sanchez, Felix L., Gutierrez, Ines G., Rivera, Julio M., ...
Human Biology - Volume 75, Number 2, April 2003
Arginase: A Novel Proliferative Determinant in Prostate Cancer (1998)
This project is an investigation of the involvement of the enzyme arginase type II (All) in the pathogenesis and growth of prostate cancer. Having recently cloned the All gene in our laboratory, we...
Arginase: A Novel Proliferative Determinant in Prostate Cancer (1998)
This project is an investigation of the involvement of the enzyme arginase type II (All) in the pathogenesis and growth of prostate cancer. Having cloned the All gene in our laboratory, we...
Thesis (Ph. D.)--Baylor College of Medicine. Dept. of Cell Biology.
Huang, Tony Jun, Liu, Minghsun, Knight, Linda D., Grody, Wayne W., Miller, Jeff F., Ho, Chih-Ming
Single nucleotide polymorphisms are implicated as having a significant role in regulating growth, development and, thereby, human health and disease. We have developed a method for identifying single...
Mouse Model for Human Arginase Deficiency
Iyer, Ramaswamy K., Yoo, Paul K., Kern, Rita M., Rozengurt, Nora, Tsoa, Rosemarie, O'Brien, William E., ...
Deficiency of liver arginase (AI) causes hyperargininemia (OMIM 207800), a disorder characterized by progressive mental impairment, growth retardation, and spasticity and punctuated by sometimes...
Molecular genetic study of human arginase deficiency
Grody, Wayne W., Klein, Deborah, Dodson, Amy E., Kern, Rita M., Wissmann, Paul B., Goodman, Barbara K., ...
We have explored the molecular pathology in 28 individuals homozygous or heterozygous for liver arginase deficiency (hyperargininemia) by a combination of Southern analysis, western blotting, DNA...
Huang, Tony Jun, Liu, Minghsun, Knight, Linda D., Grody, Wayne W., Miller, Jeff F., Ho, Chih-Ming
Single nucleotide polymorphisms are implicated as having a significant role in regulating growth, development and, thereby, human health and disease. We have developed a method for identifying single...
Mouse Model for Human Arginase Deficiency
Iyer, Ramaswamy K., Yoo, Paul K., Kern, Rita M., Rozengurt, Nora, Tsoa, Rosemarie, O'Brien, William E., ...
Deficiency of liver arginase (AI) causes hyperargininemia (OMIM 207800), a disorder characterized by progressive mental impairment, growth retardation, and spasticity and punctuated by sometimes...
Molecular genetic study of human arginase deficiency
Grody, Wayne W., Klein, Deborah, Dodson, Amy E., Kern, Rita M., Wissmann, Paul B., Goodman, Barbara K., ...
We have explored the molecular pathology in 28 individuals homozygous or heterozygous for liver arginase deficiency (hyperargininemia) by a combination of Southern analysis, western blotting, DNA...
Jarvis, Michael, Iyer, Ramaswamy K., Williams, Laurina O., Noll, Walter W., Thomas, Kirk, Telatar, Milhan, ...
The lack of readily available, patient-derived materials for molecular genetic testing of many heterozygous or rare disorders creates a major impediment for laboratory proficiency and quality control...