Arif B. Ekici: search on Z-Library

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

Don't use scam websites

1

The healing effect of goal-oriented dance and movement therapy in schizophrenia: A rater-blinded randomized controlled trial

GÃ¶kcen, Arif, Ekici, Gamze, AbaoÄlu, Hatice, Tiryaki Åen, Duygu

Journal:

The Arts in Psychotherapy

Year:

2020

File:

PDF, 715 KB

2020

2

Evaluation of conserved and ultra-conserved non-genic sequences in chromosome 15q15-linked periodic catatonia

Denny Schanze, Arif B. Ekici, Bruno Pfuhlmann, André Reis, Gerald Stöber

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2012

Language:

english

File:

PDF, 246 KB

english, 2012

3

Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders

Reuter, Miriam S., Tawamie, Hasan, Buchert, Rebecca, Hosny Gebril, Ola, Froukh, Tawfiq, Thiel, Christian, Uebe, Steffen, Ekici, Arif B., Krumbiegel, Mandy, Zweier, Christiane, Hoyer, Juliane, Eberlein

Journal:

JAMA Psychiatry

Year:

2017

Language:

english

File:

PDF, 194 KB

english, 2017

4

Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome

Vasileiou, Georgia, Vergarajauregui, Silvia, Endele, Sabine, Popp, Bernt, Büttner, Christian, Ekici, Arif B., Gerard, Marion, Bramswig, Nuria C., Albrecht, Beate, Clayton-Smith, Jill, Morton, Jenny, T

Journal:

The American Journal of Human Genetics

Year:

2018

Language:

english

File:

PDF, 2.05 MB

english, 2018

5

AIP Conference Proceedings [Author(s) TURKISH PHYSICAL SOCIETY 33RD INTERNATIONAL PHYSICS CONGRESS (TPS33) - Bodrum, Turkey (6–10 September 2017)] - The importance of pre-annealing treatment for ESR dating of mollusc shells: A key study for İsmil in Konya closed Basin/Turkey

Ekici, Gamze, Sayin, Ulku, Aydin, Hulya, Isik, Mesut, Kapan, Sevinc, Demir, Ahmet, Engin, Birol, Delikan, Arif, Orhan, Hukmu, Biyik, Recep, Ozmen, Ayhan

Year:

2018

Language:

english

File:

PDF, 913 KB

english, 2018

6

Single molecule real time sequencing in ADTKD-MUC1 allows complete assembly of the VNTR and exact positioning of causative mutations

Wenzel, Andrea, Altmueller, Janine, Ekici, Arif B., Popp, Bernt, Stueber, Kurt, Thiele, Holger, Pannes, Alois, Staubach, Simon, Salido, Eduardo, Nuernberg, Peter, Reinhardt, Richard, Reis, André, Rump

Journal:

Scientific Reports

Year:

2018

Language:

english

File:

PDF, 3.06 MB

english, 2018

7

BRCA mutations and their influence on pathological complete response and prognosis in a clinical cohort of neoadjuvantly treated breast cancer patients

Wunderle, Marius, Gass, Paul, Häberle, Lothar, Flesch, Vivien M., Rauh, Claudia, Bani, Mayada R., Hack, Carolin C., Schrauder, Michael G., Jud, Sebastian M., Emons, Julius, Erber, Ramona, Ekici, Arif

Journal:

Breast Cancer Research and Treatment

Year:

2018

Language:

english

File:

PDF, 1.14 MB

english, 2018

8

The polynucleotide kinase 3′-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25

Leal, Alejandro, Bogantes-Ledezma, Sixto, Ekici, Arif B., Uebe, Steffen, Thiel, Christian T., Sticht, Heinrich, Berghoff, Martin, Berghoff, Corinna, Morera, Bernal, Meisterernst, Michael, Reis, André

Journal:

Year:

2018

Language:

english

File:

PDF, 3.97 MB

english, 2018

9

Analyses of association of psoriatic arthritis and psoriasis vulgaris with functional NCF1 variants

Löhr, Sabine, Ekici, Arif B, Uebe, Steffen, Büttner, Christian, Köhm, Michaela, Behrens, Frank, Böhm, Beate, Sticherling, Michael, Schett, Georg, Simon, David, Mössner, Rotraut, Nimeh, Ali, Oji, Vinze

Journal:

Year:

2019

Language:

english

File:

PDF, 91 KB

english, 2019

10

The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy

Hebebrand, Moritz, Hüffmeier, Ulrike, Trollmann, Regina, Hehr, Ute, Uebe, Steffen, Ekici, Arif B., Kraus, Cornelia, Krumbiegel, Mandy, Reis, André, Thiel, Christian T., Popp, Bernt

Journal:

Orphanet Journal of Rare Diseases

Year:

2019

Language:

english

File:

PDF, 6.17 MB

english, 2019

11

T>C transition in codon 72 (TCG→CCG), S72P, a putative hotspot in PMP22

Arif B. Ekici, Oksoon Park, Rudolf Korinthenberg, Holger Grehl, Bernd Rautenstrauß

Journal:

Year:

2001

Language:

english

File:

PDF, 8 KB

english, 2001

12

MicroRNA profiles of prostate carcinoma detected by multiplatform microRNA screening

Sven Wach, Elke Nolte, Jaroslaw Szczyrba, Robert Stöhr, Arndt Hartmann, Torben Ørntoft, Lars Dyrskjøt, Elke Eltze, Wolf Wieland, Bastian Keck, Arif B. Ekici, Friedrich Grässer, Bernd Wullich

Journal:

International Journal of Cancer

Year:

2012

Language:

english

File:

PDF, 601 KB

english, 2012

13

Heterologous expression of wildtype and mutant myocilin in High Five™ insect cells shows comparable effects to cultivated trabecular meshwork cells

Sevinc Oezbey, Corinna Stengel, Ursula Schlötzer-Schrehardt, Arif Ekici, Bernd Rautenstrauss

Journal:

Biomolecular Engineering

Year:

2007

Language:

english

File:

PDF, 1.13 MB

english, 2007

14

Tracing Myelin Protein Zero (P0)in vivoby construction of P0-GFP fusion proteins

Arif B Ekici, Sevinc Oezbey, Christina Fuchs, Eva Nelis, Christine Van Broeckhoven, Melitta Schachner, Bernd Rautenstrauss

Journal:

BMC Cell Biology

Year:

2002

Language:

english

File:

PDF, 2.96 MB

english, 2002

15

Expanding the clinical spectrum associated with defects inCNTNAP2andNRXN1

Anne Gregor, Beate Albrecht, Ingrid Bader, Emilia K Bijlsma, Arif B Ekici, Hartmut Engels, Karl Hackmann, Denise Horn, Juliane Hoyer, Jakub Klapecki, Jürgen Kohlhase, Isabelle Maystadt, Sandra Nagl, E

Journal:

BMC Medical Genetics

Year:

2011

Language:

english

File:

PDF, 531 KB

english, 2011

16

Genpolymorphismus bei der verkalkten Aortenklappenstenose

Thomas Anger, Arif B. Ekici, Werner G. Daniel, Christoph D. Garlichs

Journal:

Year:

2006

Language:

german

File:

PDF, 342 KB

german, 2006

17

Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion

T. Liehr, B. Rautenstrauss, Holger Grehl, Klaus Dieter Bathke, Arif Ekici, Anita Rauch, Hans-Dieter Rott

Journal:

Year:

1996

Language:

english

File:

PDF, 143 KB

english, 1996

18

Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models

Alejandro Leal, Kathrin Huehne, Finn Bauer, Heinrich Sticht, Philipp Berger, Ueli Suter, Bernal Morera, Gerardo Del Valle, James R. Lupski, Arif Ekici, Francesca Pasutto, Sabine Endele, Ramiro Barrant

Journal:

Year:

2009

Language:

english

File:

PDF, 558 KB

english, 2009

19

Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models

Alejandro Leal, Kathrin Huehne, Finn Bauer, Heinrich Sticht, Philipp Berger, Ueli Suter, Bernal Morera, Gerardo Del Valle, James R. Lupski, Arif Ekici, Francesca Pasutto, Sabine Endele, Ramiro Barrant

Journal:

Year:

2009

Language:

english

File:

PDF, 48 KB

english, 2009

20

Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: aSacIpolymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis

Christina Fuchs, Thomas Liehr, Sevinc Özbey, Arif Ekici, Holger Grehl, B. Rautenstrauss

Journal:

Year:

1998

Language:

english

File:

PDF, 263 KB

english, 1998

21

De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardation

Grasshoff, Ute, Bonin, Michael, Goehring, Ina, Ekici, Arif, Dufke, Andreas, Cremer, Kirsten, Wagner, Nicholas, Rossier, Eva, Jauch, Anna, Walter, Michael

Journal:

European Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 666 KB

english, 2011

22

Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis

Hüffmeier, Ulrike, Uebe, Steffen, Ekici, Arif B, Bowes, John, Giardina, Emiliano, Korendowych, Eleanor, Juneblad, Kristina, Apel, Maria, McManus, Ross, Ho, Pauline

Journal:

Nature Genetics

Year:

2010

Language:

english

File:

PDF, 472 KB

english, 2010

23

A new quantitative PCR multiplex assay for rapid analysis of chromosome 17p11.2-12 duplications and deletions leading to HMSN/HNPP

Thiel, Christian T, Kraus, Cornelia, Rauch, Anita, Ekici, Arif B, Rautenstrauss, Bernd, Reis, André

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 293 KB

english, 2003

24

Periodic catatonia: confirmation of linkage to chromosome

St&#x000F6, ber, Gerald, Seelow, Dominik, R&#x000FC, schendorf, Franz, Ekici, Arif, Beckmann, Helmut, Reis, Andr&#x000E9,

Journal:

Year:

2002

Language:

english

File:

PDF, 694 KB

english, 2002

25

CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila

Christiane Zweier, Eiko K. de Jong, Markus Zweier, Alfredo Orrico, Lilian B. Ousager, Amanda L. Collins, Emilia K. Bijlsma, Merel A.W. Oortveld, Arif B. Ekici, André Reis, Annette Schenck, Anita Rauch

Journal:

The American Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 1.15 MB

english, 2009

26

NEK1 Mutations Cause Short-Rib Polydactyly Syndrome Type Majewski

Christian Thiel, Kristin Kessler, Andreas Giessl, Arno Dimmler, Stavit A. Shalev, Sigrun von der Haar, Martin Zenker, Diana Zahnleiter, Hartmut Stöss, Ernst Beinder, Rami Abou Jamra, Arif B. Ekici, Na

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 1.88 MB

english, 2011

27

Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature

Rami Abou Jamra, Orianne Philippe, Annick Raas-Rothschild, Sebastian H. Eck, Elisabeth Graf, Rebecca Buchert, Guntram Borck, Arif Ekici, Felix F. Brockschmidt, Markus M. Nöthen, Arnold Munnich, Tim M.

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 882 KB

english, 2011

28

Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability

Juliane Hoyer, Arif B. Ekici, Sabine Endele, Bernt Popp, Christiane Zweier, Antje Wiesener, Eva Wohlleber, Andreas Dufke, Eva Rossier, Corinna Petsch, Markus Zweier, Ina Göhring, Alexander M. Zink, Gu

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 704 KB

english, 2012

29

The 5-HTTLPR polymorphism modulates the influence on environmental stressors on peripartum depression symptoms

Divya Mehta, Carina Quast, Peter A. Fasching, Anna Seifert, Franziska Voigt, Matthias W. Beckmann, Florian Faschingbauer, Pascal Burger, Arif B. Ekici, Johannes Kornhuber, Elisabeth B. Binder, Tamme W

Journal:

Journal of Affective Disorders

Year:

2012

Language:

english

File:

PDF, 324 KB

english, 2012

30

Assay of transfection rate in insect cells on a single cell level

Bernd Rautenstrauss, Christina Fuchs, Arif Ekici, Eva Nelis, Christine Van Broeckhoven, Thomas Liehr

Journal:

Genetic Analysis: Biomolecular Engineering

Year:

1998

Language:

english

File:

PDF, 213 KB

english, 1998

31

An adhesion test system based on Schneider cells to determine genotype–phenotype correlations for mutated P0 proteins

Arif Bülent Ekici, Christina Fuchs, Eva Nelis, Rainer Hillenbrand, Melitta Schachner, Christine Van Broeckhoven, Bernd Rautenstrauss

Journal:

Genetic Analysis: Biomolecular Engineering

Year:

1998

Language:

english

File:

PDF, 58 KB

english, 1998

32

One-tube, two-stage PCR-directed in vitro mutagenesis using megaprimers

Arif Bülent Ekici, Ok Soon Park, Christina Fuchs, Bernd Rautenstrauss

Journal:

Technical Tips Online

Year:

1997

Language:

english

File:

PDF, 127 KB

english, 1997

33

Fatty acid elongation in yeast : Biochemical characteristics of the enzyme system and isolation of elongation-defective mutants

Franziska Dittrich, Dirk Zajonc, Kathrin Hühne, Ursula Hoja, Arif Ekici, Eva Greiner, Hans Klein, Jörg Hofmann, Jean-Jacques Bessoule, Petra Sperling, Eckhart Schweizer

Journal:

Year:

1998

Language:

english

File:

PDF, 239 KB

english, 1998

34

GPFrontend and GPGraphics: graphical analysis tools for genetic association studies

Steffen Uebe, Francesca Pasutto, Mandy Krumbiegel, Denny Schanze, Arif B Ekici, André Reis

Journal:

BMC Bioinformatics

Year:

2010

Language:

english

File:

PDF, 1.11 MB

english, 2010

35

A 15 Mb duplication of 6q24.1–q25.3 associated with typical but milder features of the duplication 6q syndrome

Christiane Zweier, Udo Trautmann, Arif Ekici, Anita Rauch

Journal:

European Journal of Medical Genetics

Year:

2008

Language:

english

File:

PDF, 440 KB

english, 2008

36

A de novo 7.6 Mb tandem duplication of 14q32.2-qter associated with primordial short stature with neurosecretory growth hormone dysfunction, distinct facial anomalies and mild developmental delay

Christian T. Thiel, Helmuth-Günther Dörr, Udo Trautmann, Juliane Hoyer, Kristin Hofmann, Cornelia Kraus, Arif B. Ekici, André Reis, Anita Rauch

Journal:

European Journal of Medical Genetics

Year:

2008

Language:

english

File:

PDF, 360 KB

english, 2008

37

6.7 Mb interstitial duplication in chromosome band 11q24.2q25 associated with infertility, minor dysmorphic features and normal psychomotor development

Ina Göhring, Hans-Martin Blümlein, Juliane Hoyer, Arif B. Ekici, Udo Trautmann, Anita Rauch

Journal:

European Journal of Medical Genetics

Year:

2008

Language:

english

File:

PDF, 172 KB

english, 2008

38

7 Mb de novo deletion within 8q21 in a patient with distal arthrogryposis type 2B (DA2B)

Kristin Hofmann, Jutta Becker, Raoul Heller, Odile Boute, Joris Andrieux, Juliane Hoyer, Arif B. Ekici, André Reis, Anita Rauch

Journal:

European Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 1021 KB

english, 2011

39

Familial short stature due to a 5q22.1–q23.2 duplication refines the 5q duplication spectrum

Diana Zahnleiter, Udo Trautmann, Arif B. Ekici, Ina Goehring, André Reis, Helmuth-Günther Dörr, Anita Rauch, Christian T. Thiel

Journal:

European Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 528 KB

english, 2011

40

Genetic variants in the tryptophan hydroxylase 2 gene (TPH2) and depression during and after pregnancy

Peter A. Fasching, Florian Faschingbauer, Tamme W. Goecke, Anne Engel, Lothar Häberle, Anna Seifert, Franziska Voigt, Manuela Amann, Dirk Rebhan, Pascal Burger, Johannes Kornhuber, Arif B. Ekici, Matt

Journal:

Journal of Psychiatric Research

Year:

2012

Language:

english

File:

PDF, 479 KB

english, 2012

41

Severely Incapacitating Mutations in Patients with Extreme Short Stature Identify RNA-Processing Endoribonuclease RMRP as an Essential Cell Growth Regulator

Christian T. Thiel, Denise Horn, Bernhard Zabel, Arif B. Ekici, Kelly Salinas, Erich Gebhart, Franz Rüschendorf, Heinrich Sticht, Jürgen Spranger, Dietmar Müller, Christiane Zweier, Mark E. Schmitt, A

Journal:

The American Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 1.48 MB

english, 2005

42

FcγRIIa genotype is associated with acute coronary syndromes as first manifestation of coronary artery disease

Dorette Raaz, Martin Herrmann, Arif B. Ekici, Lutz Klinghammer, Berthold Lausen, Reinhard E. Voll, Jeanette H.W. Leusen, Jan G.J. van de Winkel, Werner G. Daniel, André Reis, Christoph D. Garlichs

Journal:

Atherosclerosis

Year:

2009

Language:

english

File:

PDF, 141 KB

english, 2009

43

Two naturally occurring variants of the serotonin receptor gene HTR3C are associated with nausea in pregnancy

TAMME W. GOECKE, ARIF B. EKICI, BEATE NIESLER, CHRISTIAN R. LOEHBERG, CHRISTIAN HAMMER, GUDRUN RAPPOLD, DENNY SCHANZE, VERICA STRAUB, HANS-HARALD ALTMANN, PAMELA STRISSEL, REINER STRICK, MATTHIAS W. B

Journal:

Acta Obstetricia et Gynecologica Scandinavica

Year:

2010

Language:

english

File:

PDF, 130 KB

english, 2010

44

De Novo Mutations in the Genome Organizer CTCF Cause Intellectual Disability

Gregor, Anne, Oti, Martin, Kouwenhoven, Evelyn N., Hoyer, Juliane, Sticht, Heinrich, Ekici, Arif B., Kjaergaard, Susanne, Rauch, Anita, Stunnenberg, Hendrik G., Uebe, Steffen, Vasileiou, Georgia, Reis

Journal:

The American Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 1.08 MB

english, 2013

45

Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA

Earp, Madalene A., Kelemen, Linda E., Magliocco, Anthony M., Swenerton, Kenneth D., Chenevix-Trench, Georgia, Lu, Yi, Hein, Alexander, Ekici, Arif B., Beckmann, Matthias W., Fasching, Peter A., Lambre

Journal:

Year:

2014

Language:

english

File:

PDF, 882 KB

english, 2014

46

HER2andTOP2Aamplification in a hospital-based cohort of breast cancer patients: associations with patient and tumor characteristics

Fasching, Peter A., Weihbrecht, Sebastian, Haeberle, Lothar, Gasparyan, Armen, Villalobos, Ivonne E., Ma, Yanling, Ekici, Arif B., Wachter, David L., Hartmann, Arndt, Beckmann, Matthias W., Slamon, De

Journal:

Breast Cancer Research and Treatment

Year:

2014

Language:

english

File:

PDF, 342 KB

english, 2014

47

Premature Osteoarthritis as Presenting Sign of Type II Collagenopathy: A Case Report and Literature Review

Husar-Memmer, Emma, Ekici, Arif, Al Kaissi, Ali, Sticht, Heinrich, Manger, Bernhard, Schett, Georg, Zwerina, Jochen

Journal:

Seminars in Arthritis and Rheumatism

Year:

2013

Language:

english

File:

PDF, 440 KB

english, 2013

48

SCOTTISH POOR-LAW MEDICAL OFFICERS' ASSOCIATION.

Husar-Memmer, Emma, Ekici, Arif, Al Kaissi, Ali, Sticht, Heinrich, Manger, Bernhard, Schett, Georg, Zwerina, Jochen

Journal:

Year:

1896

Language:

english

File:

PDF, 201 KB

english, 1896

49

A defect of CD16-positive monocytes can occur without disease

Frankenberger, Marion, Ekici, Arif B., Angstwurm, Matthias W., Hoffmann, Harald, Hofer, Thomas P.J., Heimbeck, Irene, Meyer, Peter, Lohse, Peter, Wjst, Matthias, Häussinger, Karl, Reis, André, Ziegler

Journal:

Year:

2013

Language:

english

File:

PDF, 456 KB

english, 2013

50

HOXA10 and HOXA13 sequence variations in human female genital malformations including congenital absence of the uterus and vagina

Ekici, Arif B., Strissel, Pamela L., Oppelt, Patricia G., Renner, Stefan P., Brucker, Sara, Beckmann, Matthias W., Strick, Reiner

Journal:

Year:

2013

Language:

english

File:

PDF, 459 KB

english, 2013

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@z-lib.do

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