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1

Two novel alpha-galactosidase A mutations causing Fabry disease: A missense mutation M11V in a heterozygote woman and a nonsense mutation R190X in a hemizygote man

Basak Celtikci, Meral Topçu, Hatice Asuman Ozkara

Journal:

Clinical Biochemistry

Year:

2011

Language:

english

File:

PDF, 265 KB

english, 2011

2

Biochemical and molecular characterization of mutant hexosaminidase A in a Turkish family

İNCİLAY SİNİCİ, H.ASUMAN ÖZKARA, MERAL TOPÇU, GÖNENÇ CİLİV

Journal:

Pediatrics International

Year:

2003

Language:

english

File:

PDF, 522 KB

english, 2003

3

Alcohol determination via covalent enzyme immobilization on magnetic beads

Senem Kiralp, Asuman Topcu, Gülay Bayramoğlu, M. Yakup Arıca, Levent Toppare

Journal:

Sensors and Actuators B: Chemical

Year:

2008

Language:

english

File:

PDF, 769 KB

english, 2008

4

Antioxidant and anti-apoptotic effects of onion (Allium cepa) extract on doxorubicin-induced cardiotoxicity in rats

Seref Alpsoy, Cevat Aktas, Ramazan Uygur, Birol Topcu, Mehmet Kanter, Mustafa Erboga, Osman Karakaya, Asuman Gedikbasi

Journal:

Journal of Applied Toxicology

Year:

2012

Language:

english

File:

PDF, 10.68 MB

english, 2012

5

The effects of onion (Allium cepa) extract on doxorubicin-induced apoptosis in aortic endothelial cells

Seref Alpsoy, Ramazan Uygur, Cevat Aktas, Birol Topcu, Mehmet Kanter, Mustafa Erboga, Osman Karakaya, Asuman Gedikbasi

Journal:

Journal of Applied Toxicology

Year:

2012

Language:

english

File:

PDF, 214 KB

english, 2012

6

Sphingolipidoses in Turkey

Hatice Asuman Özkara, Meral Topçu

Journal:

Brain and Development

Year:

2004

Language:

english

File:

PDF, 109 KB

english, 2004

7

Sandhoff disease in the Turkish population

Hatice Asuman Özkara, Meral Topçu, Yavuz Renda

Journal:

Brain and Development

Year:

1997

Language:

english

File:

PDF, 44 KB

english, 1997

8

Four novel mutations in the β-galactosidase gene identified in infantile type of GM1 gangliosidosis

Başak Çeltikçi, Halil İbrahim Aydın, Serap Sivri, Müjgan Sönmez, Meral Topçu, Hatice Asuman Özkara

Journal:

Clinical Biochemistry

Year:

2012

Language:

english

File:

PDF, 398 KB

english, 2012

9

Identification of two novel arylsulfatase A mutations with a polymorphism as a cause of metachromatic leukodystrophy

Önder, Evren, Sinici, Incilay, Sönmez, F. Müjgan, Topçu, Meral, Özkara, H. Asuman

Journal:

Neurological Research

Year:

2009

Language:

english

File:

PDF, 314 KB

english, 2009

10

Niemann-Pick disease type C in the newborn period: Reflections from 10 patients

Yuce, Aysel, Gumus, Ersin, Haliloglu, Goknur, Karhan, Asuman N., Ardicli, Didem, Demir, Hulya, Gurakan, Figen, Topcu, Meral

Journal:

Molecular Genetics and Metabolism

Year:

2016

Language:

english

File:

PDF, 53 KB

english, 2016

11

EFFECT OF 12 bp DELETION MUTATION IN EXON 10 OF β HEXOSAMINIDASE α SUBUNIT GENE ON ENZYMES OF HETEROZYGOTE PARENTS

Sinici, Incilay, Özkara, H. Asuman, Topcu, Meral, Ciliv, Gönenç

Journal:

Biochemical Society Transactions

Year:

2000

Language:

english

File:

PDF, 143 KB

english, 2000

12

Niemann-Pick disease type C in the newborn period: a single-center experience

Gumus, Ersin, Haliloglu, Goknur, Karhan, Asuman Nur, Demir, Hulya, Gurakan, Figen, Topcu, Meral, Yuce, Aysel

Journal:

European Journal of Pediatrics

Year:

2017

Language:

english

File:

PDF, 435 KB

english, 2017

13

Amplification of the C-MYC Oncogene in Non-small Cell Lung Cancer

Özkara, H. Asuman, Özkara, Şeref, Topçu, Salih, Criss, Wayne E.

Journal:

Year:

1999

Language:

english

File:

PDF, 598 KB

english, 1999

14

Prenatal Enzymatic Diagnosis of Lysosomal Storage Diseases using cultured amniotic cells, uncultured chorionic villus samples and fetal blood cells: Hacettepe experience

Unal, Canan, Ozkara, Hatice Asuman, Tanacan, Atakan, Fadiloglu, Erdem, Lay, Incilay, Topçu, Meral, Cakar, Ayse Nur, Beksac, Mehmet Sinan

Journal:

Prenatal Diagnosis

Year:

2019

File:

PDF, 548 KB

2019

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