Holinski, P.: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia

K Brakensiek, H Frye-Boukhriss, M Mälzer, M Abramowicz, MJ Bahr, N Von Beckerath, C Bergmann, M Caselitz, E Holinski-Feder, P Muschke, K Oexle, G Strobl-Wildemann, G Wolff, EA El-Harith, M Stuhrmann

Journal:

Clinical Genetics

Year:

2008

Language:

english

File:

PDF, 103 KB

english, 2008

2

Single Cell Analysis of Mutations in the APC Gene

Mayer, Veronika, Schoen, Ulrike, Holinski-Feder, Elke, Koehler, Udo, Thalhammer, Stefan

Journal:

Fetal Diagnosis and Therapy

Year:

2009

Language:

english

File:

PDF, 428 KB

english, 2009

3

Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families

Dominguez-Valentin, Mev, Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Martins, Alexandra, Møller, Pål, Hovig, Eivind

Journal:

Familial Cancer

Year:

2017

Language:

english

File:

PDF, 1.42 MB

english, 2017

4

A study of solid lubricants in oils and greases under boundary conditions

J. Gänsheimer, R. Holinski

Journal:

Year:

1972

Language:

english

File:

PDF, 1.07 MB

english, 1972

5

The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1

Stefan Krüger, Christoph Engel, Andrea Bier, Ann-Sophie Silber, Heike Görgens, Elisabeth Mangold, Constanze Pagenstecher, Elke Holinski-Feder, Magnus von Knebel Doeberitz, Brigitte Royer-Pokora, Stefa

Journal:

Year:

2007

Language:

english

File:

PDF, 349 KB

english, 2007

6

SAE Technical Paper Series [SAE International 21st Annual Brake Colloquium & Exhibition - (OCT. 19, 2003)] SAE Technical Paper Series - Improvement of Friction Brake Lining Performance

Mcintyre, Gary, Holinski, Rudiger

Year:

2003

Language:

english

File:

PDF, 454 KB

english, 2003

7

Evidence for the Existence of Elaborate Enzyme Complexes in the Paleoarchean Era

Reisinger, Bernd, Sperl, Josef, Holinski, Alexandra, Schmid, Veronika, Rajendran, Chitra, Carstensen, Linn, Schlee, Sandra, Blanquart, Samuel, Merkl, Rainer, Sterner, Reinhard

Journal:

Journal of the American Chemical Society

Year:

2014

Language:

english

File:

PDF, 2.03 MB

english, 2014

8

Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer

Elisabeth Mangold, Constanze Pagenstecher, Waltraut Friedl, Micaela Mathiak, Reinhard Buettner, Christoph Engel, Markus Loeffler, Elke Holinski-Feder, Yvonne Müller-Koch, Gisela Keller, Hans K. Schack

Journal:

International Journal of Cancer

Year:

2005

Language:

english

File:

PDF, 126 KB

english, 2005

9

Advancements of tribological performance of carbon brushes in electrical motors

Groth, K., Heidenfelder, F., Holinski, R.

Journal:

Industrial Lubrication and Tribology

Year:

2001

Language:

english

File:

PDF, 315 KB

english, 2001

10

Carbon fiber on polyimide ultra-microelectrodes

Gillis, Winthrop F, Lissandrello, Charles A, Shen, Jun, Pearre, Ben W, Mertiri, Alket, Deku, Felix, Cogan, Stuart, Holinski, Bradley J, Chew, Daniel J, White, Alice E, Otchy, Timothy M, Gardner, Timot

Journal:

Journal of Neural Engineering

Year:

2017

Language:

english

File:

PDF, 16.41 MB

english, 2017

11

Fragiles X-assoziiertes Tremor-/Ataxie-Syndrom

C. Finke, R. Horváth, E. Holinski-Feder, C.J. Ploner

Journal:

Year:

2009

Language:

german

File:

PDF, 537 KB

german, 2009

12

Barth-Syndrom

I. Rost, A. Duroux, D. Toniolo, E. Holinski-Feder, R. Kozlik-Feldmann

Journal:

Monatsschrift Kinderheilkunde

Year:

2000

Language:

german

File:

PDF, 110 KB

german, 2000

13

Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis

Isabel Spier, Sukanya Horpaopan, Stefanie Vogt, Siegfried Uhlhaas, Monika Morak, Dietlinde Stienen, Markus Draaken, Michael Ludwig, Elke Holinski-Feder, Markus M. Nöthen, Per Hoffmann, Stefan Aretz

Journal:

Year:

2012

Language:

english

File:

PDF, 213 KB

english, 2012

14

Lubrication Mechanism of Solid Lubricants in Oils

Holinski, Rüdiger

Journal:

A S L E Transactions

Year:

1975

Language:

english

File:

PDF, 1.52 MB

english, 1975

15

MUTYH-associated polyposis – variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations

M Morak, A Laner, U Bacher, C Keiling, E Holinski-Feder

Journal:

Clinical Genetics

Year:

2010

Language:

english

File:

PDF, 647 KB

english, 2010

16

MRX42: Two linkage intervals, one in the pericentromeric region and one in Xq26, and the impact for carrier risk estimation

Astrid Golla, Imma Rost, Kerry Baldwin Jedele, Angelika Albert, Jan Murken, Elke Holinski-Feder

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 255 KB

english, 2002

17

Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population-based study in northern Sweden

Kristina Cederquist, Monica Emanuelsson, Ingela Göransson, Elke Holinski-Feder, Yvonne Müller-Koch, Irina Golovleva, Henrik Grönberg

Journal:

International Journal of Cancer

Year:

2004

Language:

english

File:

PDF, 105 KB

english, 2004

18

A new interphase fluorescence in situ hybridization approach for genomic rearrangements involving MLH1 and MSH6 in hereditary nonpolyposis colorectal cancer-suspected mutation-negative patients

Udo Koehler, Monika Grabowski, Ulrike Bacher, Elke Holinski-Feder

Journal:

Cancer Genetics and Cytogenetics

Year:

2007

Language:

english

File:

PDF, 252 KB

english, 2007

19

Preoperative serum levels of the carcinoembryonic antigen in hereditary non-polyposis colorectal cancer compared to levels in sporadic colorectal cancer

Uwe Schiemann, Silke Günther, Manfred Gross, Gaby Henke, Yvonne Müller-Koch, August König, Michael Muders, Christian Folwaczny, Thomas Mussack, Elke Holinski-Feder

Journal:

Cancer Detection and Prevention

Year:

2005

Language:

english

File:

PDF, 130 KB

english, 2005

20

Clinical and neuropathological findings in patients with TACO1 mutations

Jürgen Seeger, Bertold Schrank, Angela Pyle, Rolf Stucka, Ulrich Lörcher, Solvig Müller-Ziermann, Angela Abicht, Birgit Czermin, Elke Holinski-Feder, Hanns Lochmüller, Rita Horvath

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 468 KB

english, 2010

21

Hereditäre Syndrome: von der Familienanamnese zur genetischen Diagnostik

Holinski-Feder, E

Journal:

Zeitschrift für Gastroenterologie

Year:

2003

Language:

german

File:

PDF, 100 KB

german, 2003

22

Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing

Dominguez-Valentin, Mev, Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Holth, Arild, Capella, Gabriel, Davidson, Ben, Evans, D.

Journal:

Scientific Reports

Year:

2019

File:

PDF, 1.80 MB

2019

23

Intrafamilial variability in fragile X–associated tremor/ataxia syndrome

Nils Peters, Christoph Kamm, Friedrich Asmus, Elke Holinski-Feder, Eduard Kraft, Martin Dichgans, Roland Brüning, Thomas Gasser, Kai Bötzel

Journal:

Movement Disorders

Year:

2006

Language:

english

File:

PDF, 167 KB

english, 2006

24

Die Kristallstruktur von β-KZnBr3·2 H2O

B. Brehler, R. Holinski

Journal:

Naturwissenschaften (The Science of Nature)

Year:

1967

File:

PDF, 114 KB

1967

25

Mentale Retardierung

E. Holinski-Feder

Journal:

Monatsschrift Kinderheilkunde

Year:

2008

Language:

german

File:

PDF, 760 KB

german, 2008

26

YbiB from Escherichia coli , the Defining Member of the Novel TrpD2 Family of Prokaryotic DNA-binding Proteins

D. Schneider, W. Kaiser, C. Stutz, A. Holinski, O. Mayans, P. Babinger

Year:

2015

Language:

english

File:

PDF, 3.56 MB

english, 2015

27

Successful Treatment of VAD Pump Thrombosis in Four Pediatric Patients

Chetan, D., Buchholz, H., Bauman, M., Anand, V., Holinski, P., Conway, J.

Journal:

The Journal of Heart and Lung Transplantation

Year:

2016

Language:

english

File:

PDF, 322 KB

english, 2016

28

ABSTRACT 645

Mickiewicz, B., Holinski, P., Vogel, H.J., Winston, B.W., Wong, J., Thompson, G., Blackwood, J., Joffe, A.R.

Journal:

Pediatric Critical Care Medicine

Year:

2014

Language:

english

File:

PDF, 414 KB

english, 2014

29

Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation

von Salomé, Jenny, Liu, Tao, Keihäs, Markku, Morak, Moni, Holinski-Feder, Elke, Berry, Ian R., Moilanen, Jukka S., Baert-Desurmont, Stéphanie, Lindblom, Annika, Lagerstedt-Robinson, Kristina

Journal:

Familial Cancer

Year:

2017

Language:

english

File:

PDF, 981 KB

english, 2017

30

Mitochondrial and nuclear disease panel (Mito-aND-Panel): Combined sequencing of mitochondrial and nuclear DNA by a cost-effective and sensitive NGS-based method

Abicht, Angela, Scharf, Florentine, Kleinle, Stephanie, Schön, Ulrike, Holinski-Feder, Elke, Horvath, Rita, Benet-Pagès, Anna, Diebold, Isabel

Journal:

Molecular Genetics & Genomic Medicine

Year:

2018

Language:

english

File:

PDF, 618 KB

english, 2018

31

Diagnostik seltener Erkrankungen mit „next generation sequencing“ – angekommen oder abgewehrt?; Diagnostics of rare diseases with next generation sequencing—arrived at the patients or rejected?;

Abicht, Angela, Neuhann, Teresa, Mehnert, Laura, Rost, Imma, Reis, André, Zweier, Christiane, Holinski-Feder, Elke

Journal:

medizinische genetik

Year:

2019

Language:

german

File:

PDF, 389 KB

german, 2019

32

BTKbase, mutation database for X-linked agammaglobulinemia (XLA)

Vihinen, M., Belohradsky, B. H., Haire, R. N., Holinski-Feder, E., Kwan, S.-P., Lappalainen, I., Lehvaslaiho, H., Lester, T., Meindl, A., Ochs, H. D., Ollila, J., Vorechovsky, I., Weiss, M., Smith, C.

Journal:

Nucleic Acids Research

Year:

1997

Language:

english

File:

PDF, 90 KB

english, 1997

33

Changes of olfactory and gustatory function in the course of disease in patients with multiple sclerosis

Schmidt, F., Uecker, F., Gerz, C., Holinski, F., Göktas, O., Harms, L.

Journal:

Journal of the Neurological Sciences

Year:

2015

Language:

english

File:

PDF, 52 KB

english, 2015

34

Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database

Møller, Pål, Seppälä, Toni, Bernstein, Inge, Holinski-Feder, Elke, Sala, Paola, Evans, D Gareth, Lindblom, Annika, Macrae, Finlay, Blanco, Ignacio, Sijmons, Rolf, Jeffries, Jacqueline, Vasen, Hans, Bu

Journal:

Year:

2016

Language:

english

File:

PDF, 628 KB

english, 2016

35

EDC-crosslinking of decellularized tissue - A promising approach?

Lehmann, Nadine, Christ, Torsten, Daugs, Aila, Bloch, Oliver, Holinski, Sebastian

Journal:

Tissue Engineering Part A

Year:

2017

Language:

english

File:

PDF, 837 KB

english, 2017

36

ERN GENTURIS – Europäisches Referenznetzwerk für erbliche Tumorerkrankungen; ERN GENTURIS: European Reference Network for Genetic Tumour Risk Syndromes;

Steinke-Lange, Verena, Aretz, Stefan, Schröck, Evelin, Holinski-Feder, Elke

Journal:

medizinische genetik

Year:

2017

Language:

german

File:

PDF, 172 KB

german, 2017

37

Noninvasive monitoring of cardiac function in a chronic ischemic heart failure model in the rat: Assessment with tissue Doppler and non-Doppler 2D strain echocardiography

Sebastian Holinski, Fabian Knebel, Georg Heinze, Wolfgang Konertz, Gert Baumann, Adrian C Borges

Journal:

Cardiovascular Ultrasound

Year:

2011

Language:

english

File:

PDF, 3.97 MB

english, 2011

38

A novel 1p31.3p32.2 deletion involving theNFIAgene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum

Udo Koehler, Elke Holinski-Feder, Birgit Ertl-Wagner, Juergen Kunz, Arpad von Moers, Hubertus von Voss, Chayim Schell-Apacik

Journal:

European Journal of Pediatrics

Year:

2010

Language:

english

File:

PDF, 270 KB

english, 2010

39

Functional Significance and Clinical Phenotype of Nontruncating Mismatch Repair Variants of MLH1

Tiina E. Raevaara, Mari K. Korhonen, Hannes Lohi, Heather Hampel, Elly Lynch, Karin E. Lönnqvist, Elke Holinski-Feder, Christian Sutter, Wendy McKinnon, Sekhar Duraisamy, Anne-Marie Gerdes, Päivi Pelt

Journal:

Gastroenterology

Year:

2005

Language:

english

File:

PDF, 553 KB

english, 2005

40

[IEEE 2011 33rd Annual International Conference of the IEEE Engineering in Medicine and Biology Society - Boston, MA (2011.08.30-2011.09.3)] 2011 Annual International Conference of the IEEE Engineering in Medicine and Biology Society - Restoring stepping after spinal cord injury using intraspinal microstimulation and novel control strategies

Holinski, B. J., Mazurek, K. A., Everaert, D. G., Stein, R. B., Mushahwar, V. K.

Year:

2011

Language:

english

File:

PDF, 1.21 MB

english, 2011

41

Fundamentals of dry friction and some practical examples

Journal:

Industrial Lubrication and Tribology

Year:

2001

Language:

english

File:

PDF, 337 KB

english, 2001

42

Disease-causing gene-flanking genomic rearrangements in HNPCC patients

Monika Morak, Trisari Massdorf, Melanie Locher, Elke Holinski-Feder

Journal:

Hereditary Cancer in Clinical Practice

Year:

2011

Language:

english

File:

PDF, 166 KB

english, 2011

43

Age dependent rejection after heterotopic experimental heart transplantation

S. Holinski, D. Modersohn, C. Proch, R. Meyer, W. Konertz

Journal:

The Journal of Heart and Lung Transplantation

Year:

2005

Language:

english

File:

PDF, 63 KB

english, 2005

44

In vitro supplementation with deoxynucleoside monophosphates rescues mitochondrial DNA depletion

Stefanie Bulst, Elke Holinski-Feder, Brendan Payne, Angela Abicht, Sabine Krause, Hanns Lochmüller, Patrick F. Chinnery, Maggie C. Walter, Rita Horvath

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 981 KB

english, 2012

45

[IEEE 2010 3rd Electronic System-Integration Technology Conference (ESTC) - Berlin, Germany (2010.09.13-2010.09.16)] 3rd Electronics System Integration Technology Conference ESTC - Future high security ID documents based on innovative microsystem technologies

Kloeser, Joachim, Holinski, Denis, Ferber, Alexander, Muth, Oliver, Fischer, Jorg, Paeschke, Manfred

Year:

2010

Language:

english

File:

PDF, 460 KB

english, 2010

46

A simple meningococcal sepsis prognostic score: focusing on the human animal

Paula Holinski,Ari R Joffe

Journal:

Critical Care (BioMed Central)

Year:

2013

Language:

english

File:

PDF, 84 KB

english, 2013

47

In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromes

Bulst, S., Abicht, A., Holinski-Feder, E., Muller-Ziermann, S., Koehler, U., Thirion, C., Walter, M. C., Stewart, J. D., Chinnery, P. F., Lochmuller, H., Horvath, R.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 421 KB

english, 2009

48

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

Møller, Pål, Seppälä, Toni T, Bernstein, Inge, Holinski-Feder, Elke, Sala, Paulo, Gareth Evans, D, Lindblom, Annika, Macrae, Finlay, Blanco, Ignacio, Sijmons, Rolf H, Jeffries, Jacqueline, Vasen, Hans

Journal:

Year:

2017

Language:

english

File:

PDF, 493 KB

english, 2017

49

[Tribology Series] The Third Body Concept Interpretation of Tribological Phenomena Volume 31 || Significance of transfer layers for dry frictional applications

Holinski, Rüdiger

Year:

1996

Language:

english

File:

PDF, 633 KB

english, 1996

50

Comprehensive analysis of the MLH1 promoter region in 480 patients with colorectal cancer and 1150 controls reveals new variants including one with a heritable constitutional MLH1 epimutation

Morak, Monika, Ibisler, Ayseguel, Keller, Gisela, Jessen, Ellen, Laner, Andreas, Gonzales-Fassrainer, Daniela, Locher, Melanie, Massdorf, Trisari, Nissen, Anke M, Benet-Pagès, Anna, Holinski-Feder, El

Journal:

Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 470 KB

english, 2018

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски