Nicole Meyer Experimental Obstetrics and Gynecology, Medical Faculty Otto-von-Guericke University Biography Publications Institution JoVE Articles Nicole Meyer has not added a biography. If you are Nicole Meyer and would like to personalize this page please email our Author Liaison for assistance. Publications Mast Cells-Good Guys with a Bad Image? American Journal of Reproductive Immunology (New York, N.Y. : 1989). Oct, 2018 | Pubmed ID: 29917288 Bisphenol A Exposure During Early Pregnancy Impairs Uterine Spiral Artery Remodeling and Provokes Intrauterine Growth Restriction in Mice Scientific Reports. Jun, 2018 | Pubmed ID: 29907759 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. Month, 2017 | Pubmed ID: 29375562 Safeguarding of Fetal Growth by Mast Cells and Natural Killer Cells: Deficiency of One Is Counterbalanced by the Other Frontiers in Immunology. Month, 2017 | Pubmed ID: 28670317 Chymase-producing Cells of the Innate Immune System Are Required for Decidual Vascular Remodeling and Fetal Growth Scientific Reports. 03, 2017 | Pubmed ID: 28327604 Transfer of Regulatory T Cells into Abortion-prone Mice Promotes the Expansion of Uterine Mast Cells and Normalizes Early Pregnancy Angiogenesis Scientific Reports. Sep, 2015 | Pubmed ID: 26355667 Economic Burden Associated with Adverse Events in Patients with Metastatic Melanoma Journal of Managed Care & Specialty Pharmacy. Feb, 2015 | Pubmed ID: 25615005 Treatment Patterns and Survival in Metastatic Breast Cancer Patients by Tumor Characteristics Current Medical Research and Opinion. Feb, 2015 | Pubmed ID: 25365467 Heme Oxygenase-1 is Critically Involved in Placentation, Spiral Artery Remodeling, and Blood Pressure Regulation During Murine Pregnancy Frontiers in Pharmacology. Month, 2014 | Pubmed ID: 25628565 Comparison of Direct and Indirect Costs of Abnormal Uterine Bleeding Treatment with Global Endometrial Ablation and Hysterectomy Journal of Comparative Effectiveness Research. Dec, 2014 | Pubmed ID: 25496448 Defining the Complement Biomarker Profile of C3 Glomerulopathy Clinical Journal of the American Society of Nephrology : CJASN. Nov, 2014 | Pubmed ID: 25341722 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. Month, 2014 | Pubmed ID: 25336979 Healthcare Resource Use and Expenditures Among Metastatic Breast Cancer Patients Treated with HER2-Targeted Agents International Journal of Breast Cancer. Month, 2014 | Pubmed ID: 25180099 A New Microfluidics-based Droplet Dispenser for ICPMS Analytical Chemistry. Jun, 2014 | Pubmed ID: 24805360 TBC1D24 Mutation Causes Autosomal-dominant Nonsyndromic Hearing Loss Human Mutation. Jul, 2014 | Pubmed ID: 24729539 Topiramate Use in Pregnancy and the Birth Prevalence of Oral Clefts Pharmacoepidemiology and Drug Safety. Oct, 2014 | Pubmed ID: 24692316 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. Mar, 2014 | Pubmed ID: 24492129 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). Mar, 2014 | Pubmed ID: 24103254 Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome Journal of the American Society of Nephrology : JASN. Jan, 2014 | Pubmed ID: 24029428 Soluble CR1 Therapy Improves Complement Regulation in C3 Glomerulopathy Journal of the American Society of Nephrology : JASN. Nov, 2013 | Pubmed ID: 23907509 A Novel Hybrid CFHR1/CFH Gene Causes Atypical Hemolytic Uremic Syndrome Pediatric Nephrology (Berlin, Germany). Nov, 2013 | Pubmed ID: 23880784 Atypical Postinfectious Glomerulonephritis is Associated with Abnormalities in the Alternative Pathway of Complement Kidney International. Feb, 2013 | Pubmed ID: 23235567 Impact of Chemotherapeutic Agents on the Immunostimulatory Properties of Human 6-sulfo LacNAc+ (slan) Dendritic Cells International Journal of Cancer. Journal International Du Cancer. Mar, 2013 | Pubmed ID: 22907335 A Comprehensive Study to Determine Heterogeneity of Autosomal Recessive Nonsyndromic Hearing Loss in Iran American Journal of Medical Genetics. Part A. Oct, 2012 | Pubmed ID: 22903915 The Spectrum of GJB2 Mutations in the Iranian Population with Non-syndromic Hearing Loss--a Twelve Year Study International Journal of Pediatric Otorhinolaryngology. Aug, 2012 | Pubmed ID: 22695344 Causes of Alternative Pathway Dysregulation in Dense Deposit Disease Clinical Journal of the American Society of Nephrology : CJASN. Feb, 2012 | Pubmed ID: 22223606 Paramedics Experiences and Expectations Concerning Advance Directives: a Prospective, Questionnaire-based, Bi-centre Study Palliative Medicine. Oct, 2012 | Pubmed ID: 21865293 Knowledge Levels of Pharmaceutical Sales Representatives in Pain Therapy: a Descriptive Questionnaire-based Study European Journal of Clinical Pharmacology. Feb, 2012 | Pubmed ID: 21805161 Rotavirus Shedding in Premature Infants Following First Immunization Vaccine. Oct, 2011 | Pubmed ID: 21856359 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. Sep, 2011 | Pubmed ID: 21612410 DFNA8/12 Caused by TECTA Mutations is the Most Identified Subtype of Nonsyndromic Autosomal Dominant Hearing Loss Human Mutation. Jul, 2011 | Pubmed ID: 21520338 The Prevalence of Mitochondrial Mutations Associated with Aminoglycoside-induced Sensorineural Hearing Loss in an NICU Population The Laryngoscope. Jun, 2011 | Pubmed ID: 21495045 Two Iranian Families with a Novel Mutation in GJB2 Causing Autosomal Dominant Nonsyndromic Hearing Loss American Journal of Medical Genetics. Part A. May, 2011 | Pubmed ID: 21484990 Loss-of-function Mutations of ILDR1 Cause Autosomal-recessive Hearing Impairment DFNB42 American Journal of Human Genetics. Feb, 2011 | Pubmed ID: 21255762 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. Feb, 2011 | Pubmed ID: 20974643 Genetic Male Infertility and Mutation of CATSPER Ion Channels European Journal of Human Genetics : EJHG. Nov, 2010 | Pubmed ID: 20648059 [Quality Characteristics Concerning Pain Therapy] Anästhesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS. Feb, 2010 | Pubmed ID: 20155638 Polymorphisms in KCNE1 or KCNE3 Are Not Associated with Ménière Disease in the Caucasian Population American Journal of Medical Genetics. Part A. Jan, 2010 | Pubmed ID: 20034061 Genetic Variants in the RELN Gene Are Associated with Otosclerosis in Multiple European Populations Human Genetics. Feb, 2010 | Pubmed ID: 19847460 [Validity of the Axis "conflicts" of the Operationalized Psychodynamic Diagnostics (OPD)] Zeitschrift Für Psychosomatische Medizin Und Psychotherapie. Month, 2009 | Pubmed ID: 19886594 Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein American Journal of Human Genetics. Apr, 2009 | Pubmed ID: 19344877 Mutations in the First MyTH4 Domain of MYO15A Are a Common Cause of DFNB3 Hearing Loss The Laryngoscope. Apr, 2009 | Pubmed ID: 19274735 Genetic Analysis of the Caenorhabditis Elegans GLH Family of P-granule Proteins Genetics. Apr, 2008 | Pubmed ID: 18430929 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. Apr, 2008 | Pubmed ID: 18430377 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. Jul, 2007 | Pubmed ID: 17431902 A Novel DFNA5 Mutation Does Not Cause Hearing Loss in an Iranian Family Journal of Human Genetics. Month, 2007 | Pubmed ID: 17427029 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. Jan, 2006 | Pubmed ID: 16304690 Comparative Linkage Analysis and Visualization of High-density Oligonucleotide SNP Array Data BMC Genetics. Month, 2005 | Pubmed ID: 15713228 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-inactivated Poliovirus/H. Influenzae Type B Combination Vaccines in Germany The Pediatric Infectious Disease Journal. Oct, 2004 | Pubmed ID: 15602195 The PGL Family Proteins Associate with Germ Granules and Function Redundantly in Caenorhabditis Elegans Germline Development Genetics. Jun, 2004 | Pubmed ID: 15238518 C. Elegans PAR Proteins Function by Mobilizing and Stabilizing Asymmetrically Localized Protein Complexes Current Biology : CB. May, 2004 | Pubmed ID: 15186741 Branchio-oto-renal Syndrome: the Mutation Spectrum in EYA1 and Its Phenotypic Consequences Human Mutation. Jun, 2004 | Pubmed ID: 15146463 [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. Month, 2002 | Pubmed ID: 12512224 高频超声在胎儿和胎盘发育分析中的影响 Nicole Meyer1, Thomas Schüler2, Ana Claudia Zenclussen1 1Experimental Obstetrics and Gynecology, Medical Faculty, Otto-von-Guericke University, 2Institute of Molecular and Clinical Immunology, Medical Faculty, Otto-von-Guericke University JoVE 58616 Biologia dello sviluppo 微流体芯片ICPMS进样 Pascal E. Verboket1, Olga Borovinskaya1, Nicole Meyer1, Detlef Günther1, Petra S. Dittrich1 1Department of Chemistry and Applied Biosciences, ETH Zurich JoVE 52525 Bioingegneria
高频超声在胎儿和胎盘发育分析中的影响 Nicole Meyer1, Thomas Schüler2, Ana Claudia Zenclussen1 1Experimental Obstetrics and Gynecology, Medical Faculty, Otto-von-Guericke University, 2Institute of Molecular and Clinical Immunology, Medical Faculty, Otto-von-Guericke University JoVE 58616 Biologia dello sviluppo
微流体芯片ICPMS进样 Pascal E. Verboket1, Olga Borovinskaya1, Nicole Meyer1, Detlef Günther1, Petra S. Dittrich1 1Department of Chemistry and Applied Biosciences, ETH Zurich JoVE 52525 Bioingegneria