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Grußwort des Staatssekretärs im Thüringer Ministerium für Bildung, Wissenschaft und Kultur.
- Published in:
- Goethe-Jahrbuch, 2013, v. 130, p. 18
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- Publication type:
- Article
ZNF804A and Cortical Structure in Schizophrenia: In Vivo and Postmortem Studies.
- Published in:
- 2014
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- Publication type:
- Journal Article
ZNF804A and Cortical Structure in Schizophrenia: In Vivo and Postmortem Studies.
- Published in:
- Schizophrenia Bulletin, 2014, v. 40, n. 3, p. 532, doi. 10.1093/schbul/sbt123
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- Publication type:
- Article
A spastic paraplegia mouse model reveals REEP1-dependent ER shaping.
- Published in:
- 2013
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- Publication type:
- journal article
A spastic paraplegia mouse model reveals REEP1-dependent ER shaping.
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- Journal of Clinical Investigation, 2013, v. 123, n. 10, p. 4273, doi. 10.1172/JCI65665
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- Publication type:
- Article
Quantitation of serum free light chains does not compensate for serum immunofixation only when screening for monoclonal gammopathies.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2009, v. 47, n. 9, p. 1109, doi. 10.1515/CCLM.2009.254
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- Publication type:
- Article
Approaching clinical proteomics: current state and future fields of application in fluid proteomics.
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- Clinical Chemistry & Laboratory Medicine, 2009, v. 47, n. 6, p. 724, doi. 10.1515/CCLM.2009.167
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- Publication type:
- Article
Workflow restrictions on hematology analyzers XE-2100 and XS-800 when assaying pediatric samples with limited volume.
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- Clinical Chemistry & Laboratory Medicine, 2009, v. 47, n. 5, p. 607, doi. 10.1515/CCLM.2009.135
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- Publication type:
- Article
Correction of ventricular cerebrospinal fluid (CSF) samples for blood content does not increase sensitivity and specificity for the detection of CSF infection.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2008, v. 46, n. 6, p. 842, doi. 10.1515/CCLM.2008.167
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- Publication type:
- Article
Use of SELDI-TOF mass spectrometry for identification of new biomarkers: potential and limitations.
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- Clinical Chemistry & Laboratory Medicine, 2007, v. 45, n. 11, p. 1435, doi. 10.1515/CCLM.2007.351
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- Publication type:
- Article
Strong interference of hemoglobin concentration on CSF total protein measurement using the trichloroacetic acid precipitation method.
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- Clinical Chemistry & Laboratory Medicine, 2007, v. 45, n. 1, p. 112, doi. 10.1515/CCLM.2007.013
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- Publication type:
- Article
Rapid generation of detailed loss of heterozygosity profiles for routine diagnosis of gliomas.
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- Clinical Chemistry & Laboratory Medicine, 2004, v. 42, n. 6, p. 595, doi. 10.1515/CCLM.2004.103
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- Publication type:
- Article
Absence of Known Familial Hemiplegic Migraine (FHM) Mutations in the CACNA1A Gene in Patients with common Migraine: Implications for Genetic Testing.
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- Clinical Chemistry & Laboratory Medicine, 2003, v. 41, n. 3, p. 272, doi. 10.1515/CCLM.2003.042
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- Publication type:
- Article
External Quality Assessment of Molecular Biology-Based Methods Used in Laboratories of Clinical Chemistry and Human Genetics.
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- Clinical Chemistry & Laboratory Medicine, 1998, v. 36, n. 4, p. 234
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- Publication type:
- Article
Determination of Total Homocysteine in Human Plasma by Isocratic High-Performance Liquid Chromatography.
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- Clinical Chemistry & Laboratory Medicine, 1997, v. 35, n. 9, p. 687
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- Publication type:
- Article
Anwendung der SELDI-TOF-Massenspektrometrie zur Identifizierung neuer Biomarker: Möglichkeiten und Grenzen.
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- Journal of Laboratory Medicine / Laboratoriums Medizin, 2007, v. 31, n. 3, p. 93, doi. 10.1515/JLM.2007.021
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- Publication type:
- Article
A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large Brazilian pedigree.
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- European Journal of Human Genetics, 2007, v. 15, n. 12, p. 1276, doi. 10.1038/sj.ejhg.5201924
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- Publication type:
- Article
A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus.
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- European Journal of Human Genetics, 2001, v. 9, n. 3, p. 165
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- Publication type:
- Article
Synthesis, Structure, and Properties of Twofold Bridged Sesquinorbornenes.
- Published in:
- European Journal of Organic Chemistry, 1998, v. 1998, n. 9, p. 1759, doi. 10.1002/(SICI)1099-0690(199809)1998:9<1759::AID-EJOC1759>3.0.CO;2-I
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- Publication type:
- Article
1,7-Cyclopentenonorbornadiene: Synthesis and Crystal structure.
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- Angewandte Chemie International Edition, 1993, v. 32, n. 1, p. 97, doi. 10.1002/anie.199300971
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- Publication type:
- Article
Analysis of microsatellites by direct blotting electrophoresis and chemiluminescence detection.
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- Electrophoresis, 1995, v. 16, n. 1, p. 1886, doi. 10.1002/elps.11501601309
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- Publication type:
- Article
Reduced Cortical Thickness is Associated with the Glutamatergic Regulatory Gene Risk Variant DAOA Arg30Lys in Schizophrenia.
- Published in:
- Neuropsychopharmacology, 2011, v. 36, n. 8, p. 1747, doi. 10.1038/npp.2011.56
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- Publication type:
- Article
Direct analysis of clinical relevant single bacterial cells from cerebrospinal fluid during bacterial meningitis by means of micro-Raman spectroscopy.
- Published in:
- Journal of Biophotonics, 2009, v. 2, n. 1/2, p. 70, doi. 10.1002/jbio.200810068
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- Publication type:
- Article
Effects of Fat-Modified Dairy Products on Blood Lipids in Humans in Comparison with Other Fats.
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- Annals of Nutrition & Metabolism, 2005, v. 49, n. 1, p. 42, doi. 10.1159/000084176
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- Publication type:
- Article
Immediate diagnosis of ventriculits: evaluation of parameters independent of microbiological culture.
- Published in:
- Acta Neurochirurgica, 2011, v. 153, n. 9, p. 1797, doi. 10.1007/s00701-011-1079-1
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- Publication type:
- Article
A paediatric supratentorial primitive neuroectodermal tumour associated with malignant astrocytic transformation and a clonal origin of both components.
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- Neurosurgical Review, 2007, v. 30, n. 2, p. 143, doi. 10.1007/s10143-007-0069-5
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- Publication type:
- Article
Methylation-specific multiplex ligation-dependent probe amplification in meningiomas.
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- Journal of Neuro-Oncology, 2008, v. 90, n. 3, p. 267, doi. 10.1007/s11060-008-9672-8
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- Publication type:
- Article
Functional Mutation Analysis Provides Evidence for a Role of REEP1 in Lipid Droplet Biology.
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- Human Mutation, 2014, v. 35, n. 4, p. 497, doi. 10.1002/humu.22521
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- Publication type:
- Article
Linkage to a known gene but no mutation identified: comprehensive reanalysis of SPG4 HSP pedigrees reveals large deletions as the sole cause.
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- Human Mutation, 2007, v. 28, n. 7, p. 739, doi. 10.1002/humu.20508
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- Publication type:
- Article
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
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- Human Molecular Genetics, 2005, v. 14, n. 3, p. 461, doi. 10.1093/hmg/ddi044
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- Publication type:
- Article
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 4, p. 637, doi. 10.1093/hmg/9.4.637
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- Publication type:
- Article
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia.
- Published in:
- Neurogenetics, 2009, v. 10, n. 2, p. 97, doi. 10.1007/s10048-008-0158-9
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- Publication type:
- Article
An SPG3A whole gene deletion neither co-segregates with disease nor modifies phenotype in a hereditary spastic paraplegia family with a pathogenic SPG4 deletion.
- Published in:
- 2007
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- Publication type:
- Letter
Analysis of the CTNS gene in patients of German and Swiss origin with nephropathic cystinosis.
- Published in:
- Human Mutation, 2002, v. 20, n. 3, p. 237, doi. 10.1002/humu.9063
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- Publication type:
- Article
Three novel mutations (I506S, S466X, 1651A→T) in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) detected in patients of Southern German Descent.
- Published in:
- Human Mutation, 1994, v. 3, n. 1, p. 64, doi. 10.1002/humu.1380030111
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- Publication type:
- Article
Identification of a novel missense mutation (G314E) in exon 7 of the cystic fibrosis transmembrane conductance regulator gene identified in a CF patient with pancreatic sufficiency.
- Published in:
- Human Mutation, 1994, v. 3, n. 1, p. 67, doi. 10.1002/humu.1380030112
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- Publication type:
- Article
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency: The Prevalent Mutation G985 (K304E) Is Subject to a Strong Founder Effect from Northwestern Europe.
- Published in:
- Human Heredity, 1993, v. 43, n. 6, p. 342, doi. 10.1159/000154157
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- Publication type:
- Article
A Genome Wide Search for Susceptibility Loci in Three European Malignant Hyperthermia Pedigrees.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 6, p. 953, doi. 10.1093/hmg/6.6.953
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- Publication type:
- Article
In frame deletion (ΔF311) within a short trinucleotide repeat of the first transmembrane region of the cystic fibrosis gene.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 12, p. 2173
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- Publication type:
- Article
No Influence of 5-HTTLPR Gene Polymorphism on Migraine Symptomatology, Comorbid Depression, and Chronification.
- Published in:
- Headache: The Journal of Head & Face Pain, 2010, v. 50, n. 3, p. 420, doi. 10.1111/j.1526-4610.2009.01428.x
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- Publication type:
- Article
Gene for integrin-associated protein (IAP, CD47): Physical mapping, genomic structure, and expression studies in skeletal muscle.
- Published in:
- Biochemistry & Cell Biology, 2002, v. 80, n. 2, p. 169, doi. 10.1139/o01-210
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- Publication type:
- Article
Carnitine Metabolism in Isolated Rat Kidney Cortex Tubules.
- Published in:
- Biological Chemistry, 1986, v. 367, n. 1, p. 75
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- Publication type:
- Article