1992 - Fellow of the American Association for the Advancement of Science (AAAS)
His primary scientific interests are in Genetics, Molecular biology, Sister chromatid exchange, DNA and Chromosome. Chromosome 19, Cytogenetics, Gene mapping, Chromosome 16 and Chromosome 22 are the subjects of his Genetics studies. His Molecular biology research includes elements of Cosmid, Mitosis, Complementary DNA, Restriction fragment and Restriction digest.
His Sister chromatid exchange research incorporates themes from Nucleotide excision repair, DNA damage, Chinese hamster ovary cell, Mutation and Mutant. His DNA study integrates concerns from other disciplines, such as Metaphase, Mitomycin C and Hypoxanthine Phosphoribosyltransferase. His study in Chromosome is interdisciplinary in nature, drawing from both Sperm, Andrology and Flow cytometry.
Anthony V. Carrano mainly focuses on Genetics, Molecular biology, Chromosome, Sister chromatid exchange and DNA. His Genetics and Gene mapping, Cosmid, Chromosome 19, Contig and Chromosome 22 investigations all form part of his Genetics research activities. Anthony V. Carrano has researched Chromosome 22 in several fields, including Chromosome 21, Chromosome 15 and Chromosome 17.
His Molecular biology research integrates issues from Metaphase, Chinese hamster ovary cell, Gene, Cytophotometry and Chinese hamster. His Chromosome research is multidisciplinary, relying on both Sperm, Andrology and Flow cytometry. In his work, Chemotherapy is strongly intertwined with Immunology, which is a subfield of Sister chromatid exchange.
Anthony V. Carrano spends much of his time researching Genetics, Cosmid, Gene mapping, Chromosome 19 and Contig. Genetics and Molecular biology are frequently intertwined in his study. His research investigates the connection with Molecular biology and areas like DNA which intersect with concerns in Cytogenetics and Normal limit.
He has researched Gene mapping in several fields, including clone, Restriction map, genomic DNA and Locus. His Chromosome 19 study combines topics in areas such as Chromosome 15, Sequence-tagged site, Chromosome 4, Chromosome 3 and Fluorescence in situ hybridization. Anthony V. Carrano has included themes like Restriction fragment and Yeast artificial chromosome in his Contig study.
Genetics, Chromosome 19, Alu element, Chromosome 22 and Chromosome 16 are his primary areas of study. His study explores the link between Genetics and topics such as Molecular biology that cross with problems in Transcription Factor TFIIH. His work deals with themes such as Consensus sequence, DNA sequencing and Genomic library, which intersect with Alu element.
His Chromosome 22 research is multidisciplinary, incorporating elements of Chromosome 21, Chromosome 15, Chromosome 4, Chromosome 3 and Chromosome 17. His Gene mapping study integrates concerns from other disciplines, such as EcoRI, Restriction map, Contig and Euchromatin. He combines subjects such as Coding region, Exon, Intron and Gene map with his study of Cosmid.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Considerations for population monitoring using cytogenetic techniques
A.V. Carrano;A.T. Natarajan.
Mutation Research/genetic Toxicology (1988)
Sister chromatid exchange as an indicator of mutagenesis
A V Carrano;L H Thompson;P A Lindl;J L Minkler.
Nature (1978)
Molecular cloning of the human XRCC1 gene, which corrects defective DNA strand break repair and sister chromatid exchange.
Larry H. Thompson;Kerry W. Brookman;Nigel J. Jones;Susan A. Allen.
Molecular and Cellular Biology (1990)
Sister-chromatid exchanges: a report of the GENE-TOX program.
Samuel A. Latt;James Allen;Stephen E. Bloom;Anthony Carrano.
Mutation Research/reviews in Genetic Toxicology (1981)
Silicon-based sleeve devices for chemical reactions
Northrup M Allen;Mariella Raymond P;Carrano Anthony;Balch Joseph W.
(1996)
A CHO-cell strain having hypersensitivity to mutagens, a defect in DNA strand-break repair, and an extraordinary baseline frequency of sister-chromatid exchange
L.H. Thompson;K.W. Brookman;L.E. Dillehay;A.V. Carrano.
Mutation Research (1982)
The DNA sequence and biology of human chromosome 19
Jane Grimwood;Laurie A. Gordon;Laurie A. Gordon;Anne Olsen;Anne Olsen;Astrid Terry.
Nature (2004)
Chromosome measurement and sorting by flow systems.
J. W. Gray;A. V. Carrano;L. L. Steinmetz;M. A. van Dilla.
Proceedings of the National Academy of Sciences of the United States of America (1975)
Human ret proto-oncogene mapped to chromosome 10q11.2.
Y Ishizaka;F Itoh;T Tahira;I Ikeda.
Oncogene (1989)
Chapter 10 – The Rationale and Methodology for Quantifying Sister Chromatid Exchange in Humans
Anthony V. Carrano;Dan H. Moore.
Mutagenicity#R##N#New Horizons in Genetic Toxicology (1982)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Lawrence Livermore National Laboratory
Oregon Health & Science University
Wayne State University
University of California, San Francisco
Lawrence Livermore National Laboratory
Louisiana State University
Boston Children's Hospital
Sorbonne University
University of Göttingen
The University of Texas MD Anderson Cancer Center
Intel (United States)
Chinese Academy of Sciences
University of Rostock
Linnaeus University
The University of Texas Health Science Center at San Antonio
ExxonMobil (United States)
Beijing Institute of Technology
University of Toledo
University of California, Berkeley
Arizona State University
Fudan University
National Research University Higher School of Economics
University of New Hampshire
University of Eastern Finland
University of Melbourne
Arizona State University