Prescott L. Deininger

ORCID: 0000-0002-1067-3028
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About
Contact & Profiles
Research Areas
  • Chromosomal and Genetic Variations
  • RNA and protein synthesis mechanisms
  • CRISPR and Genetic Engineering
  • Genomics and Phylogenetic Studies
  • RNA Research and Splicing
  • Genomics and Chromatin Dynamics
  • DNA Repair Mechanisms
  • Molecular Biology Techniques and Applications
  • DNA and Nucleic Acid Chemistry
  • Forensic and Genetic Research
  • Genomic variations and chromosomal abnormalities
  • Advanced biosensing and bioanalysis techniques
  • Plant Virus Research Studies
  • RNA modifications and cancer
  • RNA Interference and Gene Delivery
  • Bacteriophages and microbial interactions
  • Viral-associated cancers and disorders
  • Polyomavirus and related diseases
  • T-cell and Retrovirus Studies
  • Genetic diversity and population structure
  • Glycosylation and Glycoproteins Research
  • Hearing, Cochlea, Tinnitus, Genetics
  • Cancer-related molecular mechanisms research
  • Mitochondrial Function and Pathology
  • Lymphoma Diagnosis and Treatment

Tulane University
2012-2022

University of New Orleans
1991-2015

Louisiana State University
1991-2010

Changwon National University
2010

University of Tennessee at Knoxville
2010

Ochsner Health System
2006

University Medical Center New Orleans
1992-2004

Tulane Medical Center
1999-2004

University Medical Center
1999-2003

University Hospital and Clinics
1999-2003

10.1016/0003-2697(90)90595-z article EN Analytical Biochemistry 1990-04-01

10.1016/0003-2697(91)90283-y article EN Analytical Biochemistry 1991-11-01

DNA base sequence comparisons demonstrate that the principal family of 300-nucleotide interspersed human sequences, repetitive double-strand regions HeLa cell heterogeneous nuclear RNA, and specific RNA polymerase III in vitro transcripts cloned sequences are all representatives a closely related sequences. A segment approximately 30 residues these is highly conserved mammalian evolution because it also present repeated Chinese hamsters. Further portion this mamalian similar to found within...

10.1073/pnas.77.3.1398 article EN Proceedings of the National Academy of Sciences 1980-03-01

Alu insertion polymorphisms (polymorphisms consisting of the presence/absence an element at a particular chromosomal location) offer several advantages over other nuclear DNA for human evolution studies. First, they are typed by rapid, simple, PCR-based assays; second, stable polymorphisms—newly inserted elements rarely undergo deletion; third, presence represents identity descent—the probability that different would independently insert into exact same location is negligible; and fourth,...

10.1101/gr.7.11.1061 article EN cc-by-nc Genome Research 1997-11-01

10.1007/bf02102862 article EN Journal of Molecular Evolution 1991-10-01
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