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Author Details
Full Name
Rama Rao Damerla
Affiliation
Kasturba Medical College, Manipal Academy of Higher Education (MAHE)
ORCID
Career Start Year
2010
Papers
19
H Index
12
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36269850
A Mechanistic Review of Methotrexate and Celecoxib as a Potential Metronomic Chemotherapy for Oral Squamous Cell Carcinoma.
Cancer Invest
2023
37559688
Prostaglandin-endoperoxide synthase 2 (PTGS2) gene expression and its association with genes regulating the VEGF signaling pathway in head and neck squamous cell carcinoma.
J Oral Biol Craniofac Res
2023
37949487
Circulating cell-free DNA as a diagnostic and prognostic marker for cervical cancer.
Int J Gynecol Cancer
2023
37947608
Increased Gene Expression of <i>C1orf74</i> Is Associated with Poor Prognosis in Cervical Cancer.
Cells
2023
33429428
Precision Radiotherapy: Reduction in Radiation for Oropharyngeal Cancer in the 30 ROC Trial.
J Natl Cancer Inst
2021
33877327
Measuring nonhomologous end-joining, homologous recombination and alternative end-joining simultaneously at an endogenous locus in any transfectable human cell.
Nucleic Acids Res
2021
33029702
Liquid biopsy approaches for pleural effusion in lung cancer patients.
Mol Biol Rep
2020
31591214
Human papillomavirus 16 promotes microhomology-mediated end-joining.
Proc Natl Acad Sci U S A
2019
31485558
Detection of Early Human Papillomavirus-Associated Cancers by Liquid Biopsy.
JCO Precis Oncol
2019
29521606
Coincident myelomeningocele and gastroschisis: report of 2 cases.
J Neurosurg Pediatr
2018
26918822
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.
PLoS Genet
2016
26883626
Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects.
Biol Open
2016
25807483
Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
Nature
2015
25877302
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies.
Hum Mol Genet
2015
24306492
Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis.
Mamm Genome
2014
24975753
Role of cilia in structural birth defects: insights from ciliopathy mutant mouse models.
Birth Defects Res C Embryo Today
2014
23849778
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry.
Am J Hum Genet
2013
22871734
Werner syndrome protein suppresses the formation of large deletions during the replication of human telomeric sequences.
Cell Cycle
2012
20800555
Telomeric repeat mutagenicity in human somatic cells is modulated by repeat orientation and G-quadruplex stability.
DNA Repair (Amst)
2010
1 - 19 of 19
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