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Oncogene
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April 14, 2009
Galectin-1 is a major effector of TrkB-mediated neuroblastoma aggressiveness
F Cimmino, J H Schulte, M Zollo, et al.
Genomics
|
August 1, 1996
Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)
N Mastroianni, M De Fusco, M Zollo, et al.
Biotechniques
|
September 4, 2003
Method to express and purify nm23-H2 protein from baculovirus-infected cells
L Garzia, A André, A Amoresano, et al.
Molecular and Cellular Probes
|
July 17, 1998
A method for point mutation analysis that links SSCP and dye primer fluorescent sequencing
I Chiarelli, B Porfirio, P L Mattiuz, et al.
Cytogenetics and Cell Genetics
|
November 27, 1999
Identification of two paralogous regions mapping to the short and long arms of human chromosome 2 comprising LIS1 pseudogenes
A Fogli, S Giglio, G Arrigo, et al.
Genomics
|
May 23, 1998
The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome
M P Sperandeo, G Borsani, B Incerti, et al.
Genomics
|
April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation
M Piccini, F Vitelli, M Bruttini, et al.
Oncogene
|
October 2, 2007
Phosphorylation of nm23-H1 by CKI induces its complex formation with h-prune and promotes cell motility
L Garzia, A D'Angelo, A Amoresano, et al.
Genomics
|
January 1, 1989
Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels
A Ballabio, R Carrozzo, G Parenti, et al.
Nature Genetics
|
June 1, 1996
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching
S Banfi, G Borsani, E Rossi, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 4
Oncogene
|
April 14, 2009
Galectin-1 is a major effector of TrkB-mediated neuroblastoma aggressiveness
F Cimmino, J H Schulte, M Zollo, et al.
Genomics
|
August 1, 1996
Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)
N Mastroianni, M De Fusco, M Zollo, et al.
Biotechniques
|
September 4, 2003
Method to express and purify nm23-H2 protein from baculovirus-infected cells
L Garzia, A André, A Amoresano, et al.
Molecular and Cellular Probes
|
July 17, 1998
A method for point mutation analysis that links SSCP and dye primer fluorescent sequencing
I Chiarelli, B Porfirio, P L Mattiuz, et al.
Cytogenetics and Cell Genetics
|
November 27, 1999
Identification of two paralogous regions mapping to the short and long arms of human chromosome 2 comprising LIS1 pseudogenes
A Fogli, S Giglio, G Arrigo, et al.
Genomics
|
May 23, 1998
The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome
M P Sperandeo, G Borsani, B Incerti, et al.
Genomics
|
April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation
M Piccini, F Vitelli, M Bruttini, et al.
Oncogene
|
October 2, 2007
Phosphorylation of nm23-H1 by CKI induces its complex formation with h-prune and promotes cell motility
L Garzia, A D'Angelo, A Amoresano, et al.
Genomics
|
January 1, 1989
Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels
A Ballabio, R Carrozzo, G Parenti, et al.
Nature Genetics
|
June 1, 1996
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching
S Banfi, G Borsani, E Rossi, et al.
Page
of 4