Caroline Andrews

Laboratory of Molecular Immunoregulation, National Cancer Institute, National Institutes of Health

Affiliated withNational Cancer Institute, National Institutes of Health

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 2	2017

Other Publications

Article	Year
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 macrophage... Journal of immunology (Baltimore, Md. : 1950)\| PubMed ID: 11994432	2002
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\| PubMed ID: 12395297	2002
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). Nature genetics\| PubMed ID: 14595441	2003
Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. Science (New York, N.Y.)\| PubMed ID: 15105459	2004
Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3). Investigative ophthalmology & visual science\| PubMed ID: 15223798	2004
Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features. Blood cells, molecules & diseases\| PubMed ID: 15727899	2005
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development. Nature genetics\| PubMed ID: 16155570	2005
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)\| PubMed ID: 16157808	2005
HOXA1 mutations are not a common cause of Duane anomaly. American journal of medical genetics. Part A\| PubMed ID: 16528738	2006
Two pedigrees segregating Duane's retraction syndrome as a dominant trait map to the DURS2 genetic locus. Investigative ophthalmology & visual science\| PubMed ID: 17197532	2007
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1. BMC genetics\| PubMed ID: 17511870	2007
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\| PubMed ID: 18455936	2008
Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome. Science (New York, N.Y.)\| PubMed ID: 18653847	2008
CHN1 mutations are not a common cause of sporadic Duane's retraction syndrome. American journal of medical genetics. Part A\| PubMed ID: 20034095	2010
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. Cell\| PubMed ID: 20074521	2010
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\| PubMed ID: 20227628	2010
Which patients with dystonia benefit from deep brain stimulation? A metaregression of individual patient outcomes. Journal of neurology, neurosurgery, and psychiatry\| PubMed ID: 20841370	2010
KIF21A mutations in two Chinese families with congenital fibrosis of the extraocular muscles (CFEOM). Molecular vision\| PubMed ID: 21042561	2010
Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity? Ophthalmology\| PubMed ID: 21529956	2011
Two novel CHN1 mutations in 2 families with Duane retraction syndrome. Archives of ophthalmology (Chicago, Ill. : 1960)\| PubMed ID: 21555619	2011
Expansion of the CHN1 strabismus phenotype. Investigative ophthalmology & visual science\| PubMed ID: 21715346	2011
The response to rapid infusion of fentanyl in the human brain measured using pulsed arterial spin labelling. Magma (New York, N.Y.)\| PubMed ID: 22113518	2012
Crystalline cataract caused by a heterozygous missense mutation in γD-crystallin (CRYGD). Molecular vision\| PubMed ID: 22219628	2011
HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice. American journal of human genetics\| PubMed ID: 22770981	2012
An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation. Human molecular genetics\| PubMed ID: 23001566	2012
A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3. Brain : a journal of neurology\| PubMed ID: 23378218	2013
Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation. European journal of human genetics : EJHG\| PubMed ID: 23942204	2014
RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermia. JAMA ophthalmology\| PubMed ID: 24091937	2013
Complex cytogenetic rearrangements at the DURS1 locus in syndromic Duane retraction syndrome. Clinical case reports\| PubMed ID: 24416505	2013
Pathology in practice. Compound odontoma in a horse. Journal of the American Veterinary Medical Association\| PubMed ID: 24479454	2014
Pontine malformation, undecussated pyramidal tracts, and regional polymicrogyria: a new syndrome. Pediatric neurology\| PubMed ID: 24507697	2014
Diagnostic distinctions and genetic analysis of patients diagnosed with moebius syndrome. Ophthalmology\| PubMed ID: 24612975	2014
Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndrome. The Journal of clinical endocrinology and metabolism\| PubMed ID: 25559402	2015
Generation of a de novo transcriptome from equine lamellar tissue. BMC genomics\| PubMed ID: 26432030	2015
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development. American journal of medical genetics. Part A\| PubMed ID: 26639658	2016
Interleukin-27 as a Novel Therapy for Inflammatory Bowel Disease: A Critical Review of the Literature. Inflammatory bowel diseases\| PubMed ID: 27243591	2016