Sirmaci, N: search on Z-Library

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1

Pre-service teachers’ views on school experience and teaching practice courses

Journal:

Procedia - Social and Behavioral Sciences

Year:

2010

Language:

english

File:

PDF, 282 KB

english, 2010

2

The relationship between the attitudes towards mathematics and learning styles

Journal:

Procedia - Social and Behavioral Sciences

Year:

2010

Language:

english

File:

PDF, 231 KB

english, 2010

3

The effects of cognitive awareness strategies taught with cognitive coaching method on achievement, attitudes and cognitive awareness skills of students

Sirmaci, Nur, Ceylan, Mehriban

Journal:

International Journal of Academic Research

Year:

2014

Language:

english

File:

PDF, 1.28 MB

english, 2014

4

A complex TFAP2A allele is associated with branchio-oculo-facial syndrome and inner ear malformation in a deaf child

Mustafa Tekin, Aslı Sırmacı, Berrin Yüksel-Konuk, Suat Fitoz, Levent Sennaroğlu

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 212 KB

english, 2009

5

The c.IVS1+1G>A mutation intheGJB2gene is prevalent and large deletions involving theGJB6gene are not present in the Turkish population

Asli Sirmaci, Duygu Akcayoz-Duman, Mustafa Tekin

Journal:

Journal of Genetics

Year:

2006

Language:

english

File:

PDF, 118 KB

english, 2006

6

Homozygous mutations in the 15-hydroxyprostaglandin dehydrogenase gene in patients with primary hypertrophic osteoarthropathy

Berrin Yüksel-Konuk, Aslı Sırmacı, Gülen Ece Ayten, Mustafa Özdemir, İdil Aslan, Ülkü Yılmaz-Turay, Yurdanur Erdoğan, Mustafa Tekin

Journal:

Rheumatology International

Year:

2009

Language:

english

File:

PDF, 346 KB

english, 2009

7

A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia

A Sırmacı, H Öztürkmen-Akay, S Erbek, A İncesulu, D Duman, S Taşır-Yılmaz, H Özdağ, M Tekin

Journal:

Clinical Genetics

Year:

2009

Language:

english

File:

PDF, 187 KB

english, 2009

8

A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

Aslı Sırmacı, Seyra Erbek, Justin Price, Mingqian Huang, Duygu Duman, F. Başak Cengiz, Güney Bademci, Suna Tokgöz-Yılmaz, Burcu Hişmi, Hilal Özdağ, Banu Öztürk, Sevsen Kulaksızoğlu, Erkan Yıldırım, Ha

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 1.11 MB

english, 2010

9

MASP1 Mutations in Patients with Facial, Umbilical, Coccygeal, and Auditory Findings of Carnevale, Malpuech, OSA, and Michels Syndromes

Asli Sirmaci, Tom Walsh, Hatice Akay, Michail Spiliopoulos, Yıldırım Bayezit Şakalar, Aylin Hasanefendioğlu-Bayrak, Duygu Duman, Amjad Farooq, Mary-Claire King, Mustafa Tekin

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 1000 KB

english, 2010

10

Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia

Asli Sirmaci, Michail Spiliopoulos, Francesco Brancati, Eric Powell, Duygu Duman, Alex Abrams, Guney Bademci, Emanuele Agolini, Shengru Guo, Berrin Konuk, Asli Kavaz, Susan Blanton, Maria Christina Di

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 703 KB

english, 2011

11

GPSM2 mutations in Chudley–McCullough syndrome

Oscar Diaz-Horta, Asli Sirmaci, Dan Doherty, Walter Nance, Kathleen Arnos, Arti Pandya, Mustafa Tekin

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 113 KB

english, 2012

12

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations

Aslı Sırmacı, Duygu Duman, Hatice Öztürkmen-Akay, Seyra Erbek, Armağan İncesulu, Burcu Öztürk-Hişmi, Z. Serap Arıcı, E. Berrin Yüksel-Konuk, Seda Taşır-Yılmaz, Suna Tokgöz-Yılmaz, Filiz Başak Cengiz,

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2009

Language:

english

File:

PDF, 436 KB

english, 2009

13

Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

Mustafa Tekin, Burcu Öztürk Hişmi, Suat Fitoz, Hilal Özdağ, Filiz Başak Cengiz, Aslı Sırmacı, İdil Aslan, Bora İnceoğlu, E. Berrin Yüksel-Konuk, Seda Taşır Yılmaz, Öztan Yasun, Nejat Akar

Journal:

The American Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 5.56 MB

english, 2007

14

Unique spectrum of GJB2 mutations in Mexico

Maria de la Luz Arenas-Sordo, Ibis Menendez, Edgar Hernández-Zamora, Asli Sirmaci, Diana Gutiérrez-Tinajero, Molly McGetrick, Paulina Murphy-Ruiz, Xolotl Leyva-Juárez, Fabiola Huesca-Hernández, Juan D

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2012

Language:

english

File:

PDF, 149 KB

english, 2012

15

Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

Kemal O. Yariz, Duygu Duman, Celia Zazo Seco, Julia Dallman, Mingqian Huang, Theo A. Peters, Asli Sirmaci, Na Lu, Margit Schraders, Isaac Skromne, Jaap Oostrik, Oscar Diaz-Horta, Juan I. Young, Suna T

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 1.19 MB

english, 2012

16

Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population

Cengiz, F. Basak, Duman, Duygu, Sırmacı, Aslı, Tokgöz-Yilmaz, Suna, Erbek, Seyra, Öztürkmen-Akay, Hatice, İncesulu, Armaḡan, Edwards, Yvonne J.K., Özdaḡ, Hilal, Liu, Xue Z., Tekin, Mustafa

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2010

Language:

english

File:

PDF, 1.83 MB

english, 2010

17

Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in Turkey

Duman, Duygu, Sirmaci, Asli, Cengiz, F. Basak, Ozdag, Hilal, Tekin, Mustafa

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2011

Language:

english

File:

PDF, 109 KB

english, 2011

18

Mutation of the ATP-gated P2X2 receptor leads to progressive hearing loss and increased susceptibility to noise

Yan, D., Zhu, Y., Walsh, T., Xie, D., Yuan, H., Sirmaci, A., Fujikawa, T., Wong, A. C. Y., Loh, T. L., Du, L., Grati, M., Vlajkovic, S. M., Blanton, S., Ryan, A. F., Chen, Z.-Y., Thorne, P. R., Kachar

Journal:

Proceedings of the National Academy of Sciences

Year:

2013

Language:

english

File:

PDF, 1.01 MB

english, 2013

19

Oxygen extraction rate of the myocardium at rest and on exercise in various conditions.

Binak, K, Harmanci, N, Sirmaci, N, Ataman, N, Ogan, H

Journal:

Heart (BMJ Pub. Group)

Year:

1967

Language:

english

File:

PDF, 705 KB

english, 1967

20

Biochemical Evaluation of Oxidative Stress during Exercise in Patients with Coronary Heart Disease

Andican, Gülnur, Koldaş, Lale, Seven, Arzu, Ayan, Faruk, Sirmaci, Necati, Burçak, Gülden

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2001

Language:

english

File:

PDF, 93 KB

english, 2001

21

Circulatory changes in acute glomerulonephritis at rest and during exercise.

Binak, K, Sirmaci, N, Ucak, D, Harmanci, N

Journal:

Heart (BMJ Pub. Group)

Year:

1975

Language:

english

File:

PDF, 908 KB

english, 1975

22

Fishnet based metamaterial loaded THz patch antenna

Sirmaci, Y. Denizhan, Akin, Cagdas K., Sabah, Cumali

Journal:

Optical and Quantum Electronics

Year:

2016

Language:

english

File:

PDF, 1.49 MB

english, 2016

23

Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss

Diaz-Horta, Oscar, Duman, Duygu, Foster, Joseph, Sırmacı, Aslı, Gonzalez, Michael, Mahdieh, Nejat, Fotouhi, Nikou, Bonyadi, Mortaza, Cengiz, Filiz Başak, Menendez, Ibis, Ulloa, Rick H., Edwards, Yvonn

Journal:

Year:

2012

Language:

english

File:

PDF, 275 KB

english, 2012

24

Comparison of the First Dose Response of Fosinopril and Captopril in Congestive Heart Failure.

Eryonucu, Beyhan, Koldas, Lale, Ayan, Faruk, Keser, Nurgul, Sirmaci, Necati

Journal:

Japanese Heart Journal

Year:

2001

Language:

english

File:

PDF, 71 KB

english, 2001

25

Research of genetic bases of hereditary non-syndromic hearing loss

Subasioglu, Asli, Duman, Duygu, Sirmaci, Asli, Bademci, Guney, Carkit, Fehime, Somdas, Mehmet Akif, Erkan, Mustafa, Tekin, Mustafa, Dundar, Munis

Journal:

Türk Pediatri Arşivi

Year:

2017

Language:

english

File:

PDF, 326 KB

english, 2017

26

Research of genetic bases of hereditary non-syndromic hearing loss

Subasioglu, Asli, Duman, Duygu, Sirmaci, Asli, Bademci, Guney, Carkit, Fehime, Somdas, Mehmet Akif, Erkan, Mustafa, Tekin, Mustafa, Dundar, Munis

Journal:

Türk Pediatri Arşivi

Year:

2017

File:

PDF, 326 KB

2017

27

[IEEE 2019 Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC) - Munich, Germany (2019.6.23-2019.6.27)] 2019 Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC) - Ultra-Thin Plasmonic Metasurfaces Based on Carbon Nanomembranes

Sirmaci, Yunus Denizhan, Fasold, Stefan, Neumann, Christof, Tang, Zian, Pertsch, Thomas, Turchanin, Andrey, Staude, Isabelle

Year:

2019

Language:

english

File:

PDF, 132 KB

english, 2019

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