Department of Chemistry and Applied Biosciences
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[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 , 2002 | Pubmed ID: 12512224
Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequences.
Human mutation Jun, 2004 | Pubmed ID: 15146463
C. elegans PAR proteins function by mobilizing and stabilizing asymmetrically localized protein complexes.
Current biology : CB May, 2004 | Pubmed ID: 15186741
The PGL family proteins associate with germ granules and function redundantly in Caenorhabditis elegans germline development.
Genetics Jun, 2004 | Pubmed ID: 15238518
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
Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data.
BMC genetics , 2005 | Pubmed ID: 15713228
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
A novel DFNA5 mutation does not cause hearing loss in an Iranian family.
Journal of human genetics , 2007 | Pubmed ID: 17427029
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
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
Genetic analysis of the Caenorhabditis elegans GLH family of P-granule proteins.
Genetics Apr, 2008 | Pubmed ID: 18430929
Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.
The Laryngoscope Apr, 2009 | Pubmed ID: 19274735
Human male infertility caused by mutations in the CATSPER1 channel protein.
American journal of human genetics Apr, 2009 | Pubmed ID: 19344877
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 , 2009 | Pubmed ID: 19886594
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
[Quality characteristics concerning pain therapy].
Anästhesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS Feb, 2010 | Pubmed ID: 20155638
Genetic male infertility and mutation of CATSPER ion channels.
European journal of human genetics : EJHG Nov, 2010 | Pubmed ID: 20648059
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
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
American journal of human genetics Feb, 2011 | Pubmed ID: 21255762
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
The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.
The Laryngoscope Jun, 2011 | Pubmed ID: 21495045
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
Human mutation Jul, 2011 | Pubmed ID: 21520338
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
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
Paramedics experiences and expectations concerning advance directives: a prospective, questionnaire-based, bi-centre study.
Palliative medicine Oct, 2012 | Pubmed ID: 21865293
Causes of alternative pathway dysregulation in dense deposit disease.
Clinical journal of the American Society of Nephrology : CJASN Feb, 2012 | Pubmed ID: 22223606
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
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
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
Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement.
Kidney international Feb, 2013 | Pubmed ID: 23235567
A novel hybrid CFHR1/CFH gene causes atypical hemolytic uremic syndrome.
Pediatric nephrology (Berlin, Germany) Nov, 2013 | Pubmed ID: 23880784
Soluble CR1 therapy improves complement regulation in C3 glomerulopathy.
Journal of the American Society of Nephrology : JASN Nov, 2013 | Pubmed ID: 23907509
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
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
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
Topiramate use in pregnancy and the birth prevalence of oral clefts.
Pharmacoepidemiology and drug safety Oct, 2014 | Pubmed ID: 24692316
TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss.
Human mutation Jul, 2014 | Pubmed ID: 24729539
A new microfluidics-based droplet dispenser for ICPMS.
Analytical chemistry Jun, 2014 | Pubmed ID: 24805360
Healthcare Resource Use and Expenditures among Metastatic Breast Cancer Patients Treated with HER2-Targeted Agents.
International journal of breast cancer , 2014 | Pubmed ID: 25180099
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 , 2014 | Pubmed ID: 25336979
Defining the complement biomarker profile of C3 glomerulopathy.
Clinical journal of the American Society of Nephrology : CJASN Nov, 2014 | Pubmed ID: 25341722
Treatment patterns and survival in metastatic breast cancer patients by tumor characteristics.
Current medical research and opinion Feb, 2015 | Pubmed ID: 25365467
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
Economic burden associated with adverse events in patients with metastatic melanoma.
Journal of managed care & specialty pharmacy Feb, 2015 | Pubmed ID: 25615005
Heme oxygenase-1 is critically involved in placentation, spiral artery remodeling, and blood pressure regulation during murine pregnancy.
Frontiers in pharmacology , 2014 | Pubmed ID: 25628565
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
Chymase-producing cells of the innate immune system are required for decidual vascular remodeling and fetal growth.
Scientific reports 03, 2017 | Pubmed ID: 28327604
Safeguarding of Fetal Growth by Mast Cells and Natural Killer Cells: Deficiency of One Is Counterbalanced by the Other.
Frontiers in immunology , 2017 | Pubmed ID: 28670317
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 , 2017 | Pubmed ID: 29375562
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
Mast cells-Good guys with a bad image?
American journal of reproductive immunology (New York, N.Y. : 1989) Oct, 2018 | Pubmed ID: 29917288
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