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 비보에 태아 및 태 반 개발의 분석에 대 한 높은 주파수 초음파 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 Developmental Biology ICPMS 샘플 소개를위한 미세 유체 칩 Pascal E. Verboket1, Olga Borovinskaya1, Nicole Meyer1, Detlef Günther1, Petra S. Dittrich1 1Department of Chemistry and Applied Biosciences, ETH Zurich JoVE 52525 Bioengineering
비보에 태아 및 태 반 개발의 분석에 대 한 높은 주파수 초음파 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 Developmental Biology
ICPMS 샘플 소개를위한 미세 유체 칩 Pascal E. Verboket1, Olga Borovinskaya1, Nicole Meyer1, Detlef Günther1, Petra S. Dittrich1 1Department of Chemistry and Applied Biosciences, ETH Zurich JoVE 52525 Bioengineering