Genetics of ion homeostasis in Ménière’s Disease

[1]  L. Citterio,et al.  Lanosterol Synthase Gene Polymorphisms and Changes in Endogenous Ouabain in the Response to Low Sodium Intake , 2016, Hypertension.

[2]  F. Kraemer,et al.  A Novel Role of Salt-Inducible Kinase 1 (SIK1) in the Post-Translational Regulation of Scavenger Receptor Class B Type 1 Activity. , 2015, Biochemistry.

[3]  H. Struijker‐Boudier,et al.  Inactive matrix Gla protein is causally related to adverse health outcomes: a Mendelian randomization study in a Flemish population. , 2015, Hypertension.

[4]  J. Lopez-Escamez,et al.  Accompanying Symptoms Overlap during Attacks in Menière’s Disease and Vestibular Migraine , 2014, Front. Neurol..

[5]  G. Vriend,et al.  A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine , 2014, European Journal of Human Genetics.

[6]  R. Ohrbach,et al.  The International Classification of Headache Disorders, 3rd edition (beta version) , 2013, Cephalalgia : an international journal of headache.

[7]  D. Khananshvili,et al.  The SLC8 gene family of sodium-calcium exchangers (NCX) - structure, function, and regulation in health and disease. , 2013, Molecular aspects of medicine.

[8]  M. Männikkö,et al.  A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies , 2012, International journal of audiology.

[9]  C. Hoggart,et al.  Genomewide Association Study Using a High-Density Single Nucleotide Polymorphism Array and Case-Control Design Identifies a Novel Essential Hypertension Susceptibility Locus in the Promoter Region of Endothelial NO Synthase , 2012, Hypertension.

[10]  O. Melander,et al.  Salt-inducible kinase 1 influences Na+,K+-ATPase activity in vascular smooth muscle cells and associates with variations in blood pressure , 2011, Journal of hypertension.

[11]  S. Lindberg,et al.  Identification of New Signaling Components in the Sensory Epithelium of Human Saccule , 2011, Front. Neur..

[12]  Erika Salvi,et al.  Genes Involved in Vasoconstriction and Vasodilation System Affect Salt-Sensitive Hypertension , 2011, PloS one.

[13]  Erika Salvi,et al.  Adducin- and Ouabain-Related Gene Variants Predict the Antihypertensive Activity of Rostafuroxin, Part 2: Clinical Studies , 2010, Science Translational Medicine.

[14]  J. Vrabec Genetic investigations of Meniere's disease. , 2010, Otolaryngologic clinics of North America.

[15]  N. Gürtler,et al.  Molecular Analysis of Aquaporin Genes 1 to 4 in Patients with Menière’s Disease , 2010, Cellular Physiology and Biochemistry.

[16]  H. Brismar,et al.  Functional and molecular interactions between aquaporins and Na,K-ATPase , 2010, Neuroscience.

[17]  M. Blaustein,et al.  Knockout of Na+/Ca2+ exchanger in smooth muscle attenuates vasoconstriction and L-type Ca2+ channel current and lowers blood pressure. , 2010, American journal of physiology. Heart and circulatory physiology.

[18]  A. Kakigi,et al.  Hormonal Aspects of Ménière’s Disease on the Basis of Clinical and Experimental Studies , 2010, ORL.

[19]  L. Zagato,et al.  Endogenous Ouabain in Ménière's Disease , 2010, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

[20]  E. Stone,et al.  Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population , 2010, American journal of medical genetics. Part A.

[21]  A. Lalwani,et al.  Aquaporin-2 and -4: Single nucleotide polymorphisms in Ménière's disease patients , 2010 .

[22]  A. Katz,et al.  Blocking the salt-inducible kinase 1 network prevents the increases in cell sodium transport caused by a hypertension-linked mutation in human α-adducin , 2009, Journal of hypertension.

[23]  Jae Young Choi,et al.  Functional and Molecular Expression of Epithelial Sodium Channels in Cultured Human Endolymphatic Sac Epithelial Cells , 2009, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

[24]  M. Triggiani,et al.  Expression and function of Na+/Ca2+ exchangers 1 and 3 in human macrophages and monocytes , 2009, European journal of immunology.

[25]  L. Zagato,et al.  Gly460Trp &agr;-Adducin Mutation as a Possible Mechanism Leading to Endolymphatic Hydrops in Ménière's Syndrome , 2008, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

[26]  M. Paparella,et al.  Meniere's disease , 2008, The Lancet.

[27]  S. Cohen,et al.  TORCing up metabolic control in the brain. , 2008, Cell metabolism.

[28]  J. Olesen The International Classification of Headache Disorders , 2008, Headache.

[29]  C. Marshall,et al.  Gene Structure Evolution of the Na+-Ca2+ Exchanger (NCX) Family , 2008, BMC Evolutionary Biology.

[30]  M. Knipper,et al.  Functional significance of channels and transporters expressed in the inner ear and kidney. , 2007, American journal of physiology. Cell physiology.

[31]  A. Ambesi-Impiombato,et al.  Permanent Focal Brain Ischemia Induces Isoform-Dependent Changes in the Pattern of Na+/Ca2+ Exchanger Gene Expression in the Ischemic Core, Periinfarct Area, and Intact Brain Regions , 2006, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[32]  N. Matsushiro,et al.  Ménière’s Disease Is Associated with Single Nucleotide Polymorphisms in the Human Potassium Channel Genes, KCNE1 and KCNE3 , 2005, ORL.

[33]  Joe C. Adams,et al.  Pathophysiology of Ménière's Syndrome: Are Symptoms Caused by Endolymphatic Hydrops? , 2005, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

[34]  A. Tortiglione,et al.  Two Sodium/Calcium Exchanger Gene Products, NCX1 and NCX3, Play a Major Role in the Development of Permanent Focal Cerebral Ischemia , 2004, Stroke.

[35]  Takahiro Iwamoto,et al.  Salt-sensitive hypertension is triggered by Ca2+ entry via Na+/Ca2+ exchanger type-1 in vascular smooth muscle , 2004, Nature Medicine.

[36]  A. Bronstein,et al.  Migraine and Ménière’s disease , 2002, Neurology.

[37]  J. Ruppersberg,et al.  Expression pattern of aquaporin water channels in the inner ear of the rat The molecular basis for a water regulation system in the endolymphatic sac , 1999, Hearing Research.

[38]  K. Livak,et al.  Allelic discrimination using fluorogenic probes and the 5' nuclease assay. , 1999, Genetic analysis : biomolecular engineering.

[39]  M. Knepper,et al.  Regulation of aquaporin-2 water channel trafficking by vasopressin. , 1997, Current opinion in cell biology.

[40]  G. Gates,et al.  Committee on Hearing and Equilibrium Guidelines for the Diagnosis and Evaluation of Therapy in Meniere's Disease ∗ , 1995 .

[41]  G. Fraser,et al.  Pathology of the Ear in the Cardio-Auditory Syndrome of Jervell and Lange-Nielsen (Recessive Deafness with Electrocardiographic Abnormalities) , 1966, The Journal of Laryngology & Otology.

[42]  J. Olesen,et al.  Vestibular migraine: diagnostic criteria. , 2012, Journal of vestibular research : equilibrium & orientation.

[43]  A. W. Morrison,et al.  Familial Ménière's disease: clinical and genetic aspects. , 2009, The Journal of laryngology and otology.

[44]  T Foitzi,et al.  Allelic discrimination using fluorogenic probes and the 5' nuclease assay , 1999 .