Nader Chalhoub

Nader Chalhoub

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Nader Chalhoub

Nader Chalhoub

Publications by authors named "Nader Chalhoub"

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12Publications

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NT5C2 novel splicing variant expands the phenotypic spectrum of Spastic Paraplegia (SPG45): case report of a new member of thin corpus callosum SPG-Subgroup.

BMC Med Genet 2017 Mar 21;18(1):33. Epub 2017 Mar 21.

Neurogenetics Research program, Neurology Department, Weill Cornell Medical College, Qatar Foundation- Education City, 24144, Doha, Qatar.

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http://dx.doi.org/10.1186/s12881-017-0395-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359868PMC
March 2017

Cell type specificity of PI3K signaling in Pdk1- and Pten-deficient brains.

Genes Dev 2009 Jul;23(14):1619-24

Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

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http://genesdev.cshlp.org/cgi/doi/10.1101/gad.1799609
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http://dx.doi.org/10.1101/gad.1799609DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714713PMC
July 2009

PTEN and the PI3-kinase pathway in cancer.

Annu Rev Pathol 2009 ;4:127-50

Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105-2794, USA.

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http://dx.doi.org/10.1146/annurev.pathol.4.110807.092311DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2710138PMC
May 2009

Recurrent genomic alterations characterize medulloblastoma arising from DNA double-strand break repair deficiency.

Proc Natl Acad Sci U S A 2009 Feb 21;106(6):1880-5. Epub 2009 Jan 21.

Department of Genetics and Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

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http://dx.doi.org/10.1073/pnas.0806882106DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2644132PMC
February 2009

S6k1 is not required for Pten-deficient neuronal hypertrophy.

Brain Res 2006 Jul 13;1100(1):32-41. Epub 2006 Jun 13.

Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 332 North Lauderdale, Memphis, TN 38105, USA.

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http://dx.doi.org/10.1016/j.brainres.2006.05.013DOI Listing
July 2006

Severe malignant osteopetrosis caused by a GL gene mutation.

J Bone Miner Res 2004 Jul 12;19(7):1194-9. Epub 2004 Apr 12.

Dipartimento di Scienze Pediatriche, Università di Torino, Turin, Italy.

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http://doi.wiley.com/10.1359/JBMR.040407
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http://dx.doi.org/10.1359/JBMR.040407DOI Listing
July 2004

Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human.

Nat Med 2003 Apr 10;9(4):399-406. Epub 2003 Mar 10.

Institut de Recherches Cliniques de Montréal, Faculté de Médecine de l'Université de Montréal, Montréal, Québec, Canada.

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http://www.nature.com/articles/nm842
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http://dx.doi.org/10.1038/nm842DOI Listing
April 2003

Linkage disequilibrium and founder effect analysis of the NF1 gene in French Canadians from the Quebec population.

Ann Genet 2002 Jan-Mar;45(1):39-44

Département de microbiologie et d'infectiologie, faculté de médecine, Université de Sherbrooke, Sherbrooke, PQ J1H 5N4, Canada.

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October 2002