Mohammad Shboul

Mohammad Shboul

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Mohammad Shboul

Mohammad Shboul

Publications by authors named "Mohammad Shboul"

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27Publications

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Bone matrix hypermineralization associated with low bone turnover in a case of Nasu-Hakola disease.

Bone 2019 Jun 11;123:48-55. Epub 2018 Oct 11.

Ludwig Boltzmann Institute of Osteology at Hanusch Hospital of WGKK and AUVA Trauma Centre Meidling, 1st Med. Dept. Hanusch Hospital, Vienna, Austria; Orthopedic Hospital of Speising, Pediatric Department, Vienna, Austria.

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http://dx.doi.org/10.1016/j.bone.2018.10.008DOI Listing
June 2019

Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan.

Medicines (Basel) 2019 May 29;6(2). Epub 2019 May 29.

Department of Medical Chemistry, Medical University of Vienna, Vienna 1090, Austria.

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http://dx.doi.org/10.3390/medicines6020060DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631815PMC
May 2019

Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis.

Turk J Pediatr 2019 ;61(1):130-133

Department of Pediatric, School of Medicine, The University of Jordan, Jordan, Amman.

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http://dx.doi.org/10.24953/turkjped.2019.01.022DOI Listing
January 2019

Genome-wide CRISPR-Cas9 Screen Identifies Leukemia-Specific Dependence on a Pre-mRNA Metabolic Pathway Regulated by DCPS.

Cancer Cell 2018 03 22;33(3):386-400.e5. Epub 2018 Feb 22.

Division of Hematology, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA; Center for Cellular and Molecular Medicine, Kyushu University Hospital, Fukuoka 812-8582, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.ccell.2018.01.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849534PMC
March 2018

Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem Cells.

Stem Cell Reports 2017 06;8(6):1675-1688

Institute of Medical Biology, Agency for Science Technology and Research (A(∗)STAR), 8a Biomedical Grove, #06-06 Immunos, Singapore 138648, Singapore; Lee Kong Chian School of Medicine, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798, Singapore; School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, Singapore 637551, Singapore. Electronic address:

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http://dx.doi.org/10.1016/j.stemcr.2017.05.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470345PMC
June 2017

Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization.

Bone Rep 2016 Dec 13;5:86-95. Epub 2016 Apr 13.

Department of Medicine, Division of Endocrinology and Metabolism, Institute for Human Genetics, Program in Craniofacial Biology, University of California, San Francisco, San Francisco, CA 94143-0794, USA.

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http://dx.doi.org/10.1016/j.bonr.2016.02.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926823PMC
December 2016

Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defects.

Hum Mol Genet 2015 Jun 24;24(11):3163-71. Epub 2015 Feb 24.

Institute of Medical Biology, A*STAR, 8A Biomedical Grove, Singapore 138648, Singapore Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore

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http://dx.doi.org/10.1093/hmg/ddv067DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424953PMC
June 2015

Katanin p80 regulates human cortical development by limiting centriole and cilia number.

Neuron 2014 Dec;84(6):1240-57

Division of Genetics and Genomics, Department of Medicine, Boston Children's Hospital, Boston, MA 02115, USA; Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA; Program in Neuroscience, Harvard Medical School, Boston, MA 02115, USA; Harvard MD-PhD MSTP Program, Harvard Medical School, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA; Department of Neurology, Harvard Medical School, Boston, MA 02115, USA. Electronic address:

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http://dx.doi.org/10.1016/j.neuron.2014.12.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485387PMC
December 2014

The snRNA-processing complex, Integrator, is required for ciliogenesis and dynein recruitment to the nuclear envelope via distinct mechanisms.

Biol Open 2013 Dec 15;2(12):1390-6. Epub 2013 Dec 15.

Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN 37232-8240, USA.

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http://dx.doi.org/10.1242/bio.20136981DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863424PMC
December 2013

Nuclear-localized Asunder regulates cytoplasmic dynein localization via its role in the integrator complex.

Mol Biol Cell 2013 Sep 31;24(18):2954-65. Epub 2013 Jul 31.

Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN 37232-8240 Department of Biochemistry and Molecular Biology, University of Texas Medical School at Houston, Houston, TX 77030 Institute of Medical Biology, A*STAR, Singapore 138648 Department of Pediatrics, National University of Singapore, Singapore 119228.

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http://dx.doi.org/10.1091/mbc.E13-05-0254DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771956PMC
September 2013

Human Asunder promotes dynein recruitment and centrosomal tethering to the nucleus at mitotic entry.

Mol Biol Cell 2012 Dec 24;23(24):4713-24. Epub 2012 Oct 24.

Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN 37232-8240, USA.

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http://dx.doi.org/10.1091/mbc.E12-07-0558DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521680PMC
December 2012

Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1.

Nat Genet 2012 May 13;44(6):709-13. Epub 2012 May 13.

Institute of Medical Biology, Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.

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http://dx.doi.org/10.1038/ng.2259DOI Listing
May 2012