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Human Genetics
|
January 1, 1985
Variant of ataxia-telangiectasia with low-level radiosensitivity
M Fiorilli, A Antonelli, G Russo, et al.
Mutation Research
|
July 1, 1987
The pR plasmid: a tool for discriminating between DNA lesions induced by different types of cytotoxic agents in cultured mammalian cells
R Elli, A Antonelli, P Petrinelli, et al.
European Journal of Pediatrics
|
July 1, 1993
Neurological and cytogenetic study in early-onset ataxia-telangiectasia patients
V Leuzzi, R Elli, A Antonelli, et al.
Blood
|
January 1, 1988
Establishment of a new Epstein-Barr virus-immortalized cell line from chronic lymphocytic leukemia with trisomy of chromosome 12 that produces monoclonal IgM against a sheep RBC antigen
M Crescenzi, M Napolitano, M Carbonari, et al.
Acta Anaesthesiologica Scandinavica
|
August 19, 2004
Chromosome instability in T-cells cultured in the presence of pancuronium or fentanyl
G Delogu, A Antonelli, M Signore, et al.
American Journal of Medical Genetics
|
March 1, 1992
Heterogeneity in ataxia-telangiectasia: classical phenotype associated with intermediate cellular radiosensitivity
L Chessa, P Petrinelli, A Antonelli, et al.
Journal of Endocrinological Investigation
|
November 30, 2000
Chromosomal alterations and male infertility
A Antonelli, L Gandini, P Petrinelli, et al.
Environmental and Molecular Mutagenesis
|
August 26, 1998
Effects of poly(ADP-ribose) polymerase inhibition on cell death and chromosome damage induced by VP16 and bleomycin
I D'Agnano, A Antonelli, B Bucci, et al.
British Journal of Cancer
|
September 11, 2003
Telomerase activity, apoptosis and cell cycle progression in ataxia telangiectasia lymphocytes expressing TCL1
C Gabellini, A Antonelli, P Petrinelli, et al.
The American Journal of the Medical Sciences
|
January 14, 1998
Erythrocyte uroporphyrinogen decarboxylase activity: diagnostic value and relationship with clinical features in hereditary porphyria cutanea tarda
A Camagna, P Del Duca, P Petrinelli, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Human Genetics
|
January 1, 1985
Variant of ataxia-telangiectasia with low-level radiosensitivity
M Fiorilli, A Antonelli, G Russo, et al.
Mutation Research
|
July 1, 1987
The pR plasmid: a tool for discriminating between DNA lesions induced by different types of cytotoxic agents in cultured mammalian cells
R Elli, A Antonelli, P Petrinelli, et al.
European Journal of Pediatrics
|
July 1, 1993
Neurological and cytogenetic study in early-onset ataxia-telangiectasia patients
V Leuzzi, R Elli, A Antonelli, et al.
Blood
|
January 1, 1988
Establishment of a new Epstein-Barr virus-immortalized cell line from chronic lymphocytic leukemia with trisomy of chromosome 12 that produces monoclonal IgM against a sheep RBC antigen
M Crescenzi, M Napolitano, M Carbonari, et al.
Acta Anaesthesiologica Scandinavica
|
August 19, 2004
Chromosome instability in T-cells cultured in the presence of pancuronium or fentanyl
G Delogu, A Antonelli, M Signore, et al.
American Journal of Medical Genetics
|
March 1, 1992
Heterogeneity in ataxia-telangiectasia: classical phenotype associated with intermediate cellular radiosensitivity
L Chessa, P Petrinelli, A Antonelli, et al.
Journal of Endocrinological Investigation
|
November 30, 2000
Chromosomal alterations and male infertility
A Antonelli, L Gandini, P Petrinelli, et al.
Environmental and Molecular Mutagenesis
|
August 26, 1998
Effects of poly(ADP-ribose) polymerase inhibition on cell death and chromosome damage induced by VP16 and bleomycin
I D'Agnano, A Antonelli, B Bucci, et al.
British Journal of Cancer
|
September 11, 2003
Telomerase activity, apoptosis and cell cycle progression in ataxia telangiectasia lymphocytes expressing TCL1
C Gabellini, A Antonelli, P Petrinelli, et al.
The American Journal of the Medical Sciences
|
January 14, 1998
Erythrocyte uroporphyrinogen decarboxylase activity: diagnostic value and relationship with clinical features in hereditary porphyria cutanea tarda
A Camagna, P Del Duca, P Petrinelli, et al.
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of 2