D. Kamnasaran

发表

Tumorigenesis and Neoplastic Progression NPAS 3 Demonstrates Features of a Tumor Suppressive Role in Driving the Progression of Astrocytomas

Tim-Rasmus Kiehl, T. Kiehl, F. Moreira, 2011 .

Immunohistochemical Analyses of NPAS3 Expression in the Developing Human Fetal Brain

D. Kamnasaran, P. Gould, 2011, Anatomia, histologia, embryologia.

Prenatal diagnosis and identification of heterozygous frameshift mutation in PRRX1 in an infant with agnathia‐otocephaly

E. Todd, V. Winn, D. Kamnasaran, 2012, Prenatal diagnosis.

PRRX1 is mutated in an otocephalic newborn infant conceived by consanguineous parents

O. Ozyuncu, B. Talim, G. Utine, 2012, Clinical genetics.

Current perspectives on the etiology of agnathia-otocephaly.

B. Li, J. Gekas, D. Kamnasaran, 2010, European journal of medical genetics.

The microtubule binding drug EM011 inhibits the growth of paediatric low grade gliomas.

H. Joshi, N. Ajeawung, D. Kamnasaran, 2013, Cancer letters.

Medulloblastomas: Clinically Important MicroRNA Genes

D. Kamnasaran, 2012 .

Pathological and molecular progression of astrocytomas in a GFAP:12 V-Ha-Ras mouse astrocytoma model.

D. Gutmann, P. Shannon, A. Guha, 2005, The American journal of pathology.

Corpus Callosum: Agenesis

D. Kamnasaran, 2009 .

Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes.

K. Devriendt, Chih-ping Chen, D. Cox, 2005, Genomics.

Preclinical evaluation of dipotassium bisperoxo (picolinato) oxovanadate V for the treatment of pediatric low-grade gliomas.

Chris Jones, R. Faure, N. Ajeawung, 2013, Future oncology.

Expression of GATA6 in the human and mouse central nervous system.

A. Guha, D. Kamnasaran, 2005, Brain research. Developmental brain research.

An efficient approach to Enrich Glioma Stem Cells from Glioma Cell Lines in Culture

N. Ajeawung, D. Kamnasaran, 2010 .

Rearrangement in the PITX2 and MIPOL1 genes in a patient with a t(4;14) chromosome

E. Zackai, M. Ferguson-Smith, M. Muenke, 2003, European Journal of Human Genetics.

Human schwannomas express activated platelet-derived growth factor receptors and c-kit and are growth inhibited by Gleevec (Imatinib Mesylate).

T. Kiehl, G. Zadeh, A. Guha, 2009, Cancer research.

Stem cells and models of astrocytomas.

D. Kamnasaran, 2009, Clinical and investigative medicine. Medecine clinique et experimentale.

Disruption of the neuronal PAS3 gene in a family affected with schizophrenia

D W Cox, M A Ferguson-Smith, W. Muir, 2003, Journal of medical genetics.

Comparative mapping of human Chromosome 14q11.2-q13 genes with mouse homologous gene regions

M. Ferguson-Smith, D. Cox, P. O’Brien, 2000, Mammalian Genome.

Progress from clinical trials and emerging non-conventional therapies for the treatment of Medulloblastomas.

N. Ajeawung, D. Kamnasaran, H. Wang, 2013, Cancer letters.

Translational applications of microRNA genes in medulloblastomas.

N. Ajeawung, D. Kamnasaran, Ben Li, 2010, Clinical and investigative medicine. Medecine clinique et experimentale.

Epigenetic inheritance associated with human chromosome 14.

D. Kamnasaran, 2001, Clinical and investigative medicine. Medecine clinique et experimentale.

Advances in molecular targets for the treatment of medulloblastomas.

N. Ajeawung, P. Gould, D. Kamnasaran, 2012, Clinical and investigative medicine. Medecine clinique et experimentale.

Investigation of Targetin, a Microtubule Binding Agent which Regresses the Growth of Pediatric High and Low Grade Gliomas

H. Joshi, N. Ajeawung, D. Kamnasaran, 2013, Journal of pediatric oncology.

GATA6 is an astrocytoma tumor suppressor gene identified by gene trapping of mouse glioma model

C. Hawkins, W. Stanford, A. Guha, 2007, Proceedings of the National Academy of Sciences.

Current status of human chromosome 14

D. Cox, D. Kamnasaran, 2002, Journal of medical genetics.

Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomes.

J. Lupski, S. Schuffenhauer, M. Ferguson-Smith, 2001, American journal of medical genetics.

Characterization and transformation potential of “Synthetic” astrocytes differentiated from murine embryonic stem cells

C. Hawkins, A. Guha, D. Kamnasaran, 2008, Glia.

NPAS3 demonstrates features of a tumor suppressive role in driving the progression of Astrocytomas.

T. Kiehl, F. Moreira, R. Pieper, 2011, The American journal of pathology.

393 NPAS3 is a novel late-stage acting progression factor in gliomas with tumour suppressive functions

D. Kamnasaran, P. Gould, M. Rana, 2010 .

In-Vitro and Ex-Vivo Investigations of the Microtubule Binding Drug Targetin on Angiogenesis

J. Huot, H. Joshi, N. Ajeawung, 2013, Journal of pediatric oncology.

Complete Maxillo-Mandibular Syngnathia in a Newborn with Multiple Congenital Malformations.

C. Sergi, Y. Vial, M. Broome, 2016, Pediatrics and neonatology.

The adjuvant use of lansoprazole, clonazepam and dimenhydrinate for treating intractable hiccups in a patient with gastritis and reflux esophagitis complicated with myocardial infarction: a case report

D. Kamnasaran, G. Maximov, 2013, BMC Research Notes.

Recurrent anencephaly: A case report and examination of the VANGL1 and FOXN1 genes

C. Sergi, J. Gekas, D. Kamnasaran, 2013, Fetal and pediatric pathology.

Recurrent agnathia–otocephaly caused by DNA replication slippage in PRRX1

B. Andrews, M. Dasouki, D. Kamnasaran, 2013, American journal of medical genetics. Part A.

Agenesis of the corpus callosum: lessons from humans and mice.

D. Kamnasaran, 2005, Clinical and investigative medicine. Medecine clinique et experimentale.

Viability screen on pediatric low grade glioma cell lines unveils a novel anti-cancer drug of the steroid biosynthesis inhibitor family.

Chris Jones, Chris Jones, D. Poirier, 2013, Cancer letters.

Holoprosencephaly-Polydactyly (Pseudotrisomy 13) Syndrome: Case Report and Diagnostic Criteria

C. Sergi, J. Gekas, D. Kamnasaran, 2012, Fetal and pediatric pathology.

Molecular prenatal diagnosis of a sporadic alobar holoprosencephalic fetus: genotype-phenotype correlations.

C. Sergi, J. Gekas, D. Kamnasaran, 2012, Journal of prenatal medicine.

PRENATAL DIAGNOSIS AND MOLECULAR GENETIC STUDIES ON A NEW CASE OF AGNATHIA-OTOCEPHALY

J. Gekas, D. Kamnasaran, F. Morin, 2010, Fetal and pediatric pathology.

PRRX1 is mutated in a fetus with agnathia‐otocephaly

C. Sergi, D. Kamnasaran, 2011, Clinical genetics.

343 Brominated Noscapine Inhibits the Growth of Pediatric Low Grade Astrocytomas

H. Joshi, N. Ajeawung, D. Kamnasaran, 2012 .