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Neoplasia (New York, N.Y.)
|
August 9, 2001
Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography
D J Marsh, G Theodosopoulos, V Howell, et al.
American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses
|
July 3, 2018
Correlation Between mMINDS and CIWA-Ar Scoring Tools in Patients With Alcohol Withdrawal Syndrome
Audrey J Littlefield, Mojdeh S Heavner, Claire C Eng, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 19, 1997
P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase
M P Myers, J P Stolarov, C Eng, et al.
Genes, Chromosomes & Cancer
|
August 10, 1999
Genomic organization and chromosomal localization of the human CUL2 gene and the role of von Hippel-Lindau tumor suppressor-binding protein (CUL2 and VBP1) mutation and loss in renal-cell carcinoma development
S C Clifford, S Walsh, K Hewson, et al.
Oncogene
|
February 18, 1999
Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation
O Gimm, D S Neuberg, D J Marsh, et al.
American Journal of Hematology
|
January 24, 2015
Genome-wide association study follow-up identifies cyclin A2 as a regulator of the transition through cytokinesis during terminal erythropoiesis
Leif S Ludwig, Hyunjii Cho, Aoi Wakabayashi, et al.
Journal of Medical Genetics
|
October 22, 2003
PTEN hamartoma tumour syndrome: variability of an entity
J H M Merks, L S de Vries, X-P Zhou, et al.
Human Molecular Genetics
|
August 1, 1995
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease
T Attié, A Pelet, P Edery, et al.
Human Molecular Genetics
|
June 1, 1996
Mutational scanning of large genes by extensive PCR multiplexing and two-dimensional electrophoresis: application to the RB1 gene
N J Van Orsouw, D Li, P van der Vlies, et al.
Biochemical and Biophysical Research Communications
|
May 9, 2000
Analysis of hABC1 gene 5' end: additional peptide sequence, promoter region, and four polymorphisms
C R Pullinger, H Hakamata, P N Duchateau, et al.
Page
of 39
Search research articles
Search
Showing results (251-260 of 385) with videos related to
Sort By:
Page
of 39
Neoplasia (New York, N.Y.)
|
August 9, 2001
Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography
D J Marsh, G Theodosopoulos, V Howell, et al.
American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses
|
July 3, 2018
Correlation Between mMINDS and CIWA-Ar Scoring Tools in Patients With Alcohol Withdrawal Syndrome
Audrey J Littlefield, Mojdeh S Heavner, Claire C Eng, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 19, 1997
P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase
M P Myers, J P Stolarov, C Eng, et al.
Genes, Chromosomes & Cancer
|
August 10, 1999
Genomic organization and chromosomal localization of the human CUL2 gene and the role of von Hippel-Lindau tumor suppressor-binding protein (CUL2 and VBP1) mutation and loss in renal-cell carcinoma development
S C Clifford, S Walsh, K Hewson, et al.
Oncogene
|
February 18, 1999
Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation
O Gimm, D S Neuberg, D J Marsh, et al.
American Journal of Hematology
|
January 24, 2015
Genome-wide association study follow-up identifies cyclin A2 as a regulator of the transition through cytokinesis during terminal erythropoiesis
Leif S Ludwig, Hyunjii Cho, Aoi Wakabayashi, et al.
Journal of Medical Genetics
|
October 22, 2003
PTEN hamartoma tumour syndrome: variability of an entity
J H M Merks, L S de Vries, X-P Zhou, et al.
Human Molecular Genetics
|
August 1, 1995
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease
T Attié, A Pelet, P Edery, et al.
Human Molecular Genetics
|
June 1, 1996
Mutational scanning of large genes by extensive PCR multiplexing and two-dimensional electrophoresis: application to the RB1 gene
N J Van Orsouw, D Li, P van der Vlies, et al.
Biochemical and Biophysical Research Communications
|
May 9, 2000
Analysis of hABC1 gene 5' end: additional peptide sequence, promoter region, and four polymorphisms
C R Pullinger, H Hakamata, P N Duchateau, et al.
Page
of 39