Friedel Wenzel : rechercher sur Z-Library

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1

Effects of different freezing methods on estimates of soil microbial biomass N by fumigation-extraction

Friedel, Jürgen K., Kobel, Corinne, Pfeffer, Michael, Fitz, Walter J., Wenzel, Walter W.

Journal:

Journal of Plant Nutrition and Soil Science

Année:

2003

Langue:

english

Fichier:

PDF, 34 KB

english, 2003

2

Mosaic ring chromosome 8: Clinical and array-CGH findings in partial trisomy 8

Isabel Filges, Benno Röthlisberger, Friedel Wenzel, Karl Heinimann, Andreas R. Huber, Peter Miny

Journal:

American Journal of Medical Genetics Part A

Année:

2008

Langue:

english

Fichier:

PDF, 152 KB

english, 2008

3

Familial 14.5 Mb interstitial deletion 13q21.1–13q21.33: Clinical and array-CGH study of a benign phenotype in a three-generation family

Isabel Filges, Benno Röthlisberger, Christoph Noppen, Nemya Boesch, Friedel Wenzel, Judith Necker, Franz Binkert, Andreas R. Huber, Karl Heinimann, Peter Miny

Journal:

American Journal of Medical Genetics Part A

Année:

2009

Langue:

english

Fichier:

PDF, 142 KB

english, 2009

4

Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype–genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome

Isabel Filges, Benno Röthlisberger, Nemya Boesch, Peter Weber, Friedel Wenzel, Andreas R. Huber, Karl Heinimann, Peter Miny

Journal:

American Journal of Medical Genetics Part A

Année:

2010

Langue:

english

Fichier:

PDF, 231 KB

english, 2010

5

Genotyping fetal paternally inherited SNPs by MALDI-TOF MS using cell-free fetal DNA in maternal plasma: Influence of size fractionation

Ying Li, Friedel Wenzel, Wolfgang Holzgreve, Sinuhe Hahn

Journal:

ELECTROPHORESIS

Année:

2006

Langue:

english

Fichier:

PDF, 206 KB

english, 2006

6

aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis

Isabel Filges, Anjeung Kang, Vanessa Klug, Friedel Wenzel, Karl Heinimann, Sevgi Tercanli, Peter Miny

Journal:

Prenatal Diagnosis

Année:

2011

Langue:

english

Fichier:

PDF, 150 KB

english, 2011

7

Morphogenesis of the micropylar apparatus in ovarian follicles of the fungus gnatBradysia tritici(syn.Sciara ocellaris)

Friedel Wenzel, Herwig O. Gutzeit, Dieter Zissler

Journal:

Development Genes and Evolution

Année:

1990

Langue:

english

Fichier:

PDF, 3.36 MB

english, 1990

8

Cell-free foetal DNA in maternal plasma does not appear to be derived from the rich pool of cell-free foetal DNA in amniotic fluid

Xiao Yan Zhong, Wolfgang Holzgreve, Sevgi Tercanli, Friedel Wenzel, Sinuhe Hahn

Journal:

Archives of Gynecology and Obstetrics

Année:

2006

Langue:

english

Fichier:

PDF, 197 KB

english, 2006

9

Detection of SNPs in the Plasma of Pregnant Women and in the Urine of Kidney Transplant Recipients by Mass Spectrometry

YING LI, DEIRDRÉ HAHN, FRIEDEL WENZEL, WOLFGANG HOLZGREVE, SINUHE HAHN

Journal:

Annals of the New York Academy of Sciences

Année:

2006

Langue:

english

Fichier:

PDF, 131 KB

english, 2006

10

A novel missense mutation in the high mobility group domain of SRY drastically reduces its DNA-binding capacity and causes paternally transmitted 46,XY complete gonadal dysgenesis

Isabel Filges, Christophe Kunz, Peter Miny, Nemya Boesch, Gabor Szinnai, Friedel Wenzel, Sibil Tschudin, Urs Zumsteg, Karl Heinimann

Journal:

Fertility and Sterility

Année:

2011

Langue:

english

Fichier:

PDF, 722 KB

english, 2011

11

High resolution array in the clinical approach to chromosomal phenotypes

Isabel Filges, Luzia Suda, Peter Weber, Alexandre N. Datta, Dirk Fischer, Patricia Dill, Réné Glanzmann, Jörg Benzing, Lukas Hegi, Friedel Wenzel, Andreas R. Huber, Andrea Capone Mori, Peter Miny, Ben

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 386 KB

english, 2012

12

Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies

Isabel Filges, Anjeung Kang, Vanessa Klug, Friedel Wenzel, Karl Heinimann, Sevgi Tercanli, Peter Miny

Journal:

Molecular Cytogenetics

Année:

2012

Langue:

english

Fichier:

PDF, 177 KB

english, 2012

13

Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?

Miny, Peter, Wenzel, Friedel, Tercanli, Sevgi, Filges, Isabel

Journal:

Année:

2013

Langue:

english

Fichier:

PDF, 198 KB

english, 2013

14

The Use of Dopexamine after Cardiac Surgery: Acute and Long-Term Effects in Patients with Impaired Cardiac Function

Friedel, N., Wenzel, R., Matheis, G., Hetzer, R.

Journal:

The Thoracic and Cardiovascular Surgeon

Année:

1992

Langue:

english

Fichier:

PDF, 1.19 MB

english, 1992

15

Somatic alterations in juvenile polyps from BMPR1A and SMAD 4 mutation carriers

Blatter, Robert H. E., Plasilova, Martina, Wenzel, Friedel, Gokaslan, Sefik T., Terracciano, Luigi, Ashfaq, Raheela, Heinimann, Karl

Journal:

Genes, Chromosomes and Cancer

Année:

2015

Langue:

english

Fichier:

PDF, 99 KB

english, 2015

16

Sharing of aPTPN11mutation by myelodysplastic bone marrow and a mature plasmacytoid dendritic cell proliferation provides evidence for their common myelomonocytic origin

Bodmer, Andrea, Menter, Thomas, Juskevicius, Darius, Arranto, Christian, Wenzel, Friedel, Dirnhofer, Stephan, Tzankov, Alexandar

Journal:

Virchows Archiv

Année:

2017

Langue:

english

Fichier:

PDF, 6.56 MB

english, 2017

17

Reliable detection of Trisomy 21 using MALDI-TOF mass spectrometry

Huang, Dorothy J, Nelson, Matthew R, Zimmermann, Bernhard, Dudarewicz, Lech, Wenzel, Friedel, Spiegel, Roland, Nagy, Balint, Holzgreve, Wolfgang, Hahn, Sinuhe

Journal:

Genetics in Medicine

Année:

2006

Langue:

english

Fichier:

PDF, 530 KB

english, 2006

18

Clonogenic versus morphogenic mutations in myeloid neoplasms: chronologic observations in a U2AF1, TET2, CSF3R and JAK2 ‘co-mutated’ myeloproliferative neoplasm suggest a hierarchical order of mutations and potential predictive value for kinase inhibitor treatment response

Gerlach, Magdalena M., Lundberg, Pontus, Halter, Joerg, Arranto, Christian, Wenzel, Friedel, Dirnhofer, Stefan, Tzankov, Alexandar

Journal:

Leukemia and Lymphoma

Année:

2017

Langue:

english

Fichier:

PDF, 1.03 MB

english, 2017

19

Discordant Gene Expression Signatures and Related Phenotypic Differences in Lamin A- and A/C-Related Hutchinson-Gilford Progeria Syndrome (HGPS)

Plasilova, Martina, Chattopadhyay, Chandon, Ghosh, Apurba, Wenzel, Friedel, Demougin, Philippe, Noppen, Christoph, Schaub, Nathalie, Szinnai, Gabor, Terracciano, Luigi, Heinimann, Karl, Jeang, K. T.

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 547 KB

english, 2011

20

RUNX1 Mutations Can Lead to Aberrant Expression of CD79a and PAX5 in Acute Myelogenous Leukemias: A Potential Diagnostic Pitfall

Menter, Thomas, Lundberg, Pontus, Wenzel, Friedel, Dirks, Jan, Fernandez, Paula, Friess, Dorothea, Dirnhofer, Stefan, Tzankov, Alexandar

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 681 KB

english, 2018

21

Bedeutung der Tumorzytogenetik in der Tumordiagnostik

Wenzel, Friedel, Röthlisberger, Benno

Journal:

Therapeutische Umschau

Année:

2008

Fichier:

PDF, 286 KB

2008

22

Highly Substituted Hydroxyethyl Starch (HES 200/0.62) Leads to Type-l von Willebrand Syndrome after Repeated Administration

Treib, Johannes, Haass, Anton, Pindur, Gerhard, Miyachita, C., Grauer, Markus T., Jung, Friedel, Wenzel, Ernst, Schimrigk, Klaus

Journal:

Pathophysiology of Haemostasis and Thrombosis

Année:

1996

Fichier:

PDF, 538 KB

1996

23

Novel Real-Time Quantitative PCR Test for Trisomy 21

Zimmermann, Bernhard, Holzgreve, Wolfgang, Wenzel, Friedel, Hahn, Sinuhe

Journal:

Clinical Chemistry

Année:

2002

Fichier:

PDF, 105 KB

2002