Caroline Andrews Laboratory of Molecular Immunoregulation, Cancer and Inflammation Program, Center for Cancer Research National Cancer Institute, National Institutes of Health Biography Publications Institution JoVE Articles Caroline Andrews has not added a biography. If you are Caroline Andrews and would like to personalize this page please email our Author Liaison for assistance. Publications Interleukin-27 As a Novel Therapy for Inflammatory Bowel Disease: A Critical Review of the Literature Inflammatory Bowel Diseases. Sep, 2016 | Pubmed ID: 27243591 Two Unique TUBB3 Mutations Cause Both CFEOM3 and Malformations of Cortical Development American Journal of Medical Genetics. Part A. Feb, 2016 | Pubmed ID: 26639658 Generation of a De Novo Transcriptome from Equine Lamellar Tissue BMC Genomics. Oct, 2015 | Pubmed ID: 26432030 Expanding the Phenotypic Spectrum and Variability of Endocrine Abnormalities Associated with TUBB3 E410K Syndrome The Journal of Clinical Endocrinology and Metabolism. Mar, 2015 | Pubmed ID: 25559402 Diagnostic Distinctions and Genetic Analysis of Patients Diagnosed with Moebius Syndrome Ophthalmology. Jul, 2014 | Pubmed ID: 24612975 Pontine Malformation, Undecussated Pyramidal Tracts, and Regional Polymicrogyria: a New Syndrome Pediatric Neurology. Apr, 2014 | Pubmed ID: 24507697 Pathology in Practice. Compound Odontoma in a Horse Journal of the American Veterinary Medical Association. Feb, 2014 | Pubmed ID: 24479454 Autosomal-dominant Nystagmus, Foveal Hypoplasia and Presenile Cataract Associated with a Novel PAX6 Mutation European Journal of Human Genetics : EJHG. Mar, 2014 | Pubmed ID: 23942204 Complex Cytogenetic Rearrangements at the DURS1 Locus in Syndromic Duane Retraction Syndrome Clinical Case Reports. Oct, 2013 | Pubmed ID: 24416505 RYR1 Mutations As a Cause of Ophthalmoplegia, Facial Weakness, and Malignant Hyperthermia JAMA Ophthalmology. Dec, 2013 | Pubmed ID: 24091937 A Novel Syndrome Caused by the E410K Amino Acid Substitution in the Neuronal β-tubulin Isotype 3 Brain : a Journal of Neurology. Feb, 2013 | Pubmed ID: 23378218 An Inherited TUBB2B Mutation Alters a Kinesin-binding Site and Causes Polymicrogyria, CFEOM and Axon Dysinnervation Human Molecular Genetics. Dec, 2012 | Pubmed ID: 23001566 HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1-/- Mice American Journal of Human Genetics. Jul, 2012 | Pubmed ID: 22770981 The Response to Rapid Infusion of Fentanyl in the Human Brain Measured Using Pulsed Arterial Spin Labelling Magma (New York, N.Y.). Apr, 2012 | Pubmed ID: 22113518 Crystalline Cataract Caused by a Heterozygous Missense Mutation in γD-crystallin (CRYGD) Molecular Vision. 2011 | Pubmed ID: 22219628 Expansion of the CHN1 Strabismus Phenotype Investigative Ophthalmology & Visual Science. Aug, 2011 | Pubmed ID: 21715346 Two Novel CHN1 Mutations in 2 Families with Duane Retraction Syndrome Archives of Ophthalmology (Chicago, Ill. : 1960). May, 2011 | Pubmed ID: 21555619 Structural Grading of Foveal Hypoplasia Using Spectral-domain Optical Coherence Tomography a Predictor of Visual Acuity? Ophthalmology. Aug, 2011 | Pubmed ID: 21529956 KIF21A Mutations in Two Chinese Families with Congenital Fibrosis of the Extraocular Muscles (CFEOM) Molecular Vision. Oct, 2010 | Pubmed ID: 21042561 Which Patients with Dystonia Benefit from Deep Brain Stimulation? A Metaregression of Individual Patient Outcomes Journal of Neurology, Neurosurgery, and Psychiatry. Dec, 2010 | Pubmed ID: 20841370 HOXA1 Mutations Are Not a Common Cause of Möbius Syndrome Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus. Feb, 2010 | Pubmed ID: 20227628 Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance Cell. Jan, 2010 | Pubmed ID: 20074521 CHN1 Mutations Are Not a Common Cause of Sporadic Duane's Retraction Syndrome American Journal of Medical Genetics. Part A. Jan, 2010 | Pubmed ID: 20034095 Human CHN1 Mutations Hyperactivate Alpha2-chimaerin and Cause Duane's Retraction Syndrome Science (New York, N.Y.). Aug, 2008 | Pubmed ID: 18653847 Magnetic Resonance Imaging of the Endophenotype of a Novel Familial Möbius-like Syndrome Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus. Aug, 2008 | Pubmed ID: 18455936 Three Novel Mutations in KIF21A Highlight the Importance of the Third Coiled-coil Stalk Domain in the Etiology of CFEOM1 BMC Genetics. May, 2007 | Pubmed ID: 17511870 Two Pedigrees Segregating Duane's Retraction Syndrome As a Dominant Trait Map to the DURS2 Genetic Locus Investigative Ophthalmology & Visual Science. Jan, 2007 | Pubmed ID: 17197532 HOXA1 Mutations Are Not a Common Cause of Duane Anomaly American Journal of Medical Genetics. Part A. Apr, 2006 | Pubmed ID: 16528738 A Novel KIF21A Mutation in a Patient with Congenital Fibrosis of the Extraocular Muscles and Marcus Gunn Jaw-winking Phenomenon Archives of Ophthalmology (Chicago, Ill. : 1960). Sep, 2005 | Pubmed ID: 16157808 Homozygous HOXA1 Mutations Disrupt Human Brainstem, Inner Ear, Cardiovascular and Cognitive Development Nature Genetics. Oct, 2005 | Pubmed ID: 16155570 Autosomal Dominant Hereditary Hemochromatosis Associated with a Novel Ferroportin Mutation and Unique Clinical Features Blood Cells, Molecules & Diseases. Mar-Apr, 2005 | Pubmed ID: 15727899 Identification of KIF21A Mutations As a Rare Cause of Congenital Fibrosis of the Extraocular Muscles Type 3 (CFEOM3) Investigative Ophthalmology & Visual Science. Jul, 2004 | Pubmed ID: 15223798 Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis Science (New York, N.Y.). Jun, 2004 | Pubmed ID: 15105459 Heterozygous Mutations of the Kinesin KIF21A in Congenital Fibrosis of the Extraocular Muscles Type 1 (CFEOM1) Nature Genetics. Dec, 2003 | Pubmed ID: 14595441 Duane Radial Ray Syndrome (Okihiro Syndrome) Maps to 20q13 and Results from Mutations in SALL4, a New Member of the SAL Family American Journal of Human Genetics. Nov, 2002 | Pubmed ID: 12395297 Evidence for a Dual Mechanism for IL-10 Suppression of TNF-alpha Production That Does Not Involve Inhibition of P38 Mitogen-activated Protein Kinase or NF-kappa B in Primary Human Macrophages Journal of Immunology (Baltimore, Md. : 1950). May, 2002 | Pubmed ID: 11994432 Visualization of IL-22-expressing Lymphocytes Using Reporter Mice Wei Shen1, Wenqing Li1, Julie A. Hixon1, Caroline Andrews1, Scott K. Durum1 1Laboratory of Molecular Immunoregulation, Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health JoVE 54710 Immunologia e infezioni
Visualization of IL-22-expressing Lymphocytes Using Reporter Mice Wei Shen1, Wenqing Li1, Julie A. Hixon1, Caroline Andrews1, Scott K. Durum1 1Laboratory of Molecular Immunoregulation, Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health JoVE 54710 Immunologia e infezioni