Nicole Meyer

Department of Chemistry and Applied Biosciences, ETH Zurich

Affiliated withETH Zurich Otto-von-Guericke University

Research Area

BioengineeringDevelopmental Biology

Biography

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JoVE Journal Publications

ArticleTotal : 2	Year
Publication title Cited by 4	2015
Publication title Cited by 9	2018

Other Publications

Article	Year
[The use of medical services and the utilization rate in screening programs in relation to social class: results of a representative survey in Bavaria]. Sozial- und Präventivmedizin\| PubMed ID: 12512224	2002
Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequences. Human mutation\| PubMed ID: 15146463	2004
C. elegans PAR proteins function by mobilizing and stabilizing asymmetrically localized protein complexes. Current biology : CB\| PubMed ID: 15186741	2004
The PGL family proteins associate with germ granules and function redundantly in Caenorhabditis elegans germline development. Genetics\| PubMed ID: 15238518	2004
Four and one-half-year follow-up of the effectiveness of diphtheria-tetanus toxoids-acellular pertussis/Haemophilus influenzae type b and diphtheria-tetanus toxoids-acellular pertussis-inact... The Pediatric infectious disease journal\| PubMed ID: 15602195	2004
Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data. BMC genetics\| PubMed ID: 15713228	2005
Personal dosimetry of exposure to mobile telephone base stations? An epidemiologic feasibility study comparing the Maschek dosimeter prototype and the Antennessa SP-090 system. Bioelectromagnetics\| PubMed ID: 16304690	2006
A novel DFNA5 mutation does not cause hearing loss in an Iranian family. Journal of human genetics\| PubMed ID: 17427029	2007
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus. American journal of medical genetics. Part A\| PubMed ID: 17431902	2007
Sonographic measurement of the lower uterine segment thickness: is it truly predictive of uterine rupture? Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstétrique et gynécologie du Canada : JOGC\| PubMed ID: 18430377	2008
Genetic analysis of the Caenorhabditis elegans GLH family of P-granule proteins. Genetics\| PubMed ID: 18430929	2008
Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss. The Laryngoscope\| PubMed ID: 19274735	2009
Human male infertility caused by mutations in the CATSPER1 channel protein. American journal of human genetics\| PubMed ID: 19344877	2009
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations. Human genetics\| PubMed ID: 19847460	2010
[Validity of the axis "conflicts" of the Operationalized Psychodynamic Diagnostics (OPD)]. Zeitschrift für Psychosomatische Medizin und Psychotherapie\| PubMed ID: 19886594	2009
Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population. American journal of medical genetics. Part A\| PubMed ID: 20034061	2010
[Quality characteristics concerning pain therapy]. Anästhesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS\| PubMed ID: 20155638	2010
Genetic male infertility and mutation of CATSPER ion channels. European journal of human genetics : EJHG\| PubMed ID: 20648059	2010
A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association\| PubMed ID: 20974643	2011
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42. American journal of human genetics\| PubMed ID: 21255762	2011
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss. American journal of medical genetics. Part A\| PubMed ID: 21484990	2011
The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population. The Laryngoscope\| PubMed ID: 21495045	2011
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss. Human mutation\| PubMed ID: 21520338	2011
Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian population. DNA and cell biology\| PubMed ID: 21612410	2011
Knowledge levels of pharmaceutical sales representatives in pain therapy: a descriptive questionnaire-based study. European journal of clinical pharmacology\| PubMed ID: 21805161	2012
Rotavirus shedding in premature infants following first immunization. Vaccine\| PubMed ID: 21856359	2011
Paramedics experiences and expectations concerning advance directives: a prospective, questionnaire-based, bi-centre study. Palliative medicine\| PubMed ID: 21865293	2012
Causes of alternative pathway dysregulation in dense deposit disease. Clinical journal of the American Society of Nephrology : CJASN\| PubMed ID: 22223606	2012
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study. International journal of pediatric otorhinolaryngology\| PubMed ID: 22695344	2012
A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran. American journal of medical genetics. Part A\| PubMed ID: 22903915	2012
Impact of chemotherapeutic agents on the immunostimulatory properties of human 6-sulfo LacNAc+ (slan) dendritic cells. International journal of cancer. Journal international du cancer\| PubMed ID: 22907335	2013
Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement. Kidney international\| PubMed ID: 23235567	2013
A novel hybrid CFHR1/CFH gene causes atypical hemolytic uremic syndrome. Pediatric nephrology (Berlin, Germany)\| PubMed ID: 23880784	2013
Soluble CR1 therapy improves complement regulation in C3 glomerulopathy. Journal of the American Society of Nephrology : JASN\| PubMed ID: 23907509	2013
Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome. Journal of the American Society of Nephrology : JASN\| PubMed ID: 24029428	2014
Pharmacokinetic and pharmacodynamic effects of methylphenidate and MDMA administered alone or in combination. The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP)\| PubMed ID: 24103254	2014
Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology\| PubMed ID: 24492129	2014
Topiramate use in pregnancy and the birth prevalence of oral clefts. Pharmacoepidemiology and drug safety\| PubMed ID: 24692316	2014
TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss. Human mutation\| PubMed ID: 24729539	2014
A new microfluidics-based droplet dispenser for ICPMS. Analytical chemistry\| PubMed ID: 24805360	2014
Healthcare Resource Use and Expenditures among Metastatic Breast Cancer Patients Treated with HER2-Targeted Agents. International journal of breast cancer\| PubMed ID: 25180099	2014
Retrospective database analysis of clinical outcomes and costs for treatment of abnormal uterine bleeding among women enrolled in US Medicaid programs. ClinicoEconomics and outcomes research : CEOR\| PubMed ID: 25336979	2014
Defining the complement biomarker profile of C3 glomerulopathy. Clinical journal of the American Society of Nephrology : CJASN\| PubMed ID: 25341722	2014
Treatment patterns and survival in metastatic breast cancer patients by tumor characteristics. Current medical research and opinion\| PubMed ID: 25365467	2015
Comparison of direct and indirect costs of abnormal uterine bleeding treatment with global endometrial ablation and hysterectomy. Journal of comparative effectiveness research\| PubMed ID: 25496448	2014
Economic burden associated with adverse events in patients with metastatic melanoma. Journal of managed care & specialty pharmacy\| PubMed ID: 25615005	2015
Heme oxygenase-1 is critically involved in placentation, spiral artery remodeling, and blood pressure regulation during murine pregnancy. Frontiers in pharmacology\| PubMed ID: 25628565	2014
Transfer of regulatory T cells into abortion-prone mice promotes the expansion of uterine mast cells and normalizes early pregnancy angiogenesis. Scientific reports\| PubMed ID: 26355667	2015
Chymase-producing cells of the innate immune system are required for decidual vascular remodeling and fetal growth. Scientific reports\| PubMed ID: 28327604	2017
Safeguarding of Fetal Growth by Mast Cells and Natural Killer Cells: Deficiency of One Is Counterbalanced by the Other. Frontiers in immunology\| PubMed ID: 28670317	2017
Simultaneous Ablation of Uterine Natural Killer Cells and Uterine Mast Cells in Mice Leads to Poor Vascularization and Abnormal Doppler Measurements That Compromise Fetal Well-being. Frontiers in immunology\| PubMed ID: 29375562	2017
Bisphenol A exposure during early pregnancy impairs uterine spiral artery remodeling and provokes intrauterine growth restriction in mice. Scientific reports\| PubMed ID: 29907759	2018
Mast cells-Good guys with a bad image? American journal of reproductive immunology (New York, N.Y. : 1989)\| PubMed ID: 29917288	2018