Munis Dundar: search on Z-Library

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51

Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome

Munis Dündar, Thomas Müller, Qi Zhang, Jing Pan, Beat Steinmann, Julia Vodopiutz, Robert Gruber, Tohru Sonoda, Birgit Krabichler, Gerd Utermann, Jacques U. Baenziger, Lijuan Zhang, Andreas R. Janecke

Journal:

The American Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 1.32 MB

english, 2009

52

Nitric oxide synthase in diabetic rat testicular tissue and the effects of pentoxifylline therapy

Sönmez, Mehmet Fatih, Kılıç, Eser, Karabulut, Derya, Çilenk, KübraTugce, Deligönül, Erkan, Dündar, Munis

Journal:

Systems Biology in Reproductive Medicine

Year:

2015

Language:

english

File:

PDF, 940 KB

english, 2015

53

The Association of Brain-Derived Neurotrophic Factor Gene Polymorphism with Obstructive Sleep Apnea Syndrome and Obesity

Yüksekkaya, Mehmet, Tutar, Nuri, Büyükoğlan, Hakan, Dündar, Munis, Yılmaz, İnsu, Gülmez, İnci, Oymak, Fatma Sema, Balta, Burhan, Korkmaz, Keziban, Demir, Ramazan

Journal:

Year:

2016

Language:

english

File:

PDF, 394 KB

english, 2016

54

Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases

Munis Dundar, Asli Subasioglu Uzak, Murat Erdogan, Yagut Akbarova

Journal:

The EPMA Journal

Year:

2011

Language:

english

File:

PDF, 465 KB

english, 2011

55

Inherited diseases and syndromes leading to aortic aneurysms and dissections

Caglayan, Ahmet Okay, Dundar, Munis

Journal:

European Journal of Cardio-Thoracic Surgery

Year:

2009

Language:

english

File:

PDF, 146 KB

english, 2009

56

Pharmacologically active fractions of Sideritis spp. and their use in inherited eye diseases

Abeshi, Andi, Precone, Vincenza, Beccari, Tommaso, Dundar, Munis, Falsini, Benedetto, Bertelli, Matteo

Journal:

The EuroBiotech Journal

Year:

2017

Language:

english

File:

PDF, 171 KB

english, 2017

57

Cleft palate in a patient with the 9p deletion syndrome

Asli Subasioglu Uzak, Serdar Ceylaner, Murat Erdogan, Yesim Karabulut, Burhan Balta, Oguzhan Bahadir, Fatma Kurt, Muhammed Dogan, Munis Dundar

Journal:

Current Opinion in Biotechnology

Year:

2011

Language:

english

File:

PDF, 82 KB

english, 2011

58

Adrenal axis functions in patients with familial Mediterranean fever

Tansu Sav, Omer Ozbakir, Fahrettin Kelestimur, Sebnem Gursoy, Mevlut Baskol, Mustafa Kula, Munis Dundar

Journal:

Clinical Rheumatology

Year:

2006

Language:

english

File:

PDF, 44 KB

english, 2006

59

A Novel COL4A3 Mutation Causes Autosomal-Recessive Alport Syndrome in a Large Turkish Family

Uzak, Asli Subasioglu, Tokgoz, Bulent, Dundar, Munis, Tekin, Mustafa

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2013

Language:

english

File:

PDF, 212 KB

english, 2013

60

The correlation of genotype–phenotype of FMF disease and its review of statistical data

Yavuz, Fatih, Bayramov, Ruslan, Kenanoglu, Sercan, Dogan, Muhammet Ensar, Gunes, Meltem Cerrah, Boz, Mehmet, Saatci, Çetin, Ozkul, Yusuf, Dundar, Munis

Journal:

Journal of Biotechnology

Year:

2017

Language:

english

File:

PDF, 70 KB

english, 2017

61

NF1 gene variant allele frequencies comparison of Turkish population with databases

Bayramov, Ruslan, Dogan, Muhammet Ensar, Gunes, Meltem Cerrah, Unal, Muge Gulcihan, Boz, Mehmet, Ada, Yasin, Eryılmaz, Havva Nur, Bayramov, Keziban Korkmaz, Saatçı, Çetin, Ozkul, Yusuf, Dundar, Munis

Journal:

Journal of Biotechnology

Year:

2017

Language:

english

File:

PDF, 60 KB

english, 2017

62

Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema

Michelini, Sandro, Amato, Bruno, Ricci, Maurizio, Kenanoglu, Sercan, Veselenyiova, Dominika, Kurti, Danjela, Baglivo, Mirko, Manara, Elena, Dundar, Munis, Krajcovic, Juraj, Basha, Syed Hussain, Priya,

Journal:

Year:

2020

File:

PDF, 3.81 MB

2020

63

A case with de novo Y;1 translocation causing male infertility

Burhan Balta, Murat Erdogan, Sevda Yesim Karabulut, Oguzhan Bahadir, Fatma Colak, Asli Subasioglu Uzak, Muhammet Dogan, Cetin Saatci, Munis Dundar

Journal:

Current Opinion in Biotechnology

Year:

2011

Language:

english

File:

PDF, 93 KB

english, 2011

64

Common Familial Mediterranean Fever gene mutations in a Turkish cohort

Munis Dundar, Elif Funda Emirogullari, Aslihan Kiraz, Serpil Taheri, Mevlut Baskol

Journal:

Molecular Biology Reports

Year:

2011

Language:

english

File:

PDF, 1.56 MB

english, 2011

65

IS IDIOPATHIC HIRSUTISM REALLY IDIOPATHIC? mRNA EXPRESSIONS OF SKIN STEROIDOGENIC ENZYMES IN WOMEN WITH IDIOPATHIC HIRSUTISM

Taheri, Serpil, Zararsız, Gökmen, Karaburgu, Sulbiye, Borlu, Murat, Özgün, Tuncay, Karaca, Zuleyha, Tanriverdi, Fatih, Dundar, Munis, Kelestimur, Fahrettin, Unluhizarci, Kursad

Journal:

European Journal of Endocrinology

Year:

2015

Language:

english

File:

PDF, 1.21 MB

english, 2015

66

Perspectives of biotechnology

Gartland, Kevan M.A., Dundar, Munis, Beccari, Tommaso, Magni, Mariapia Viola, Gartland, Jill S.

Journal:

Journal of Biotechnology

Year:

2016

Language:

english

File:

PDF, 96 KB

english, 2016

67

A novel nonsense mutation in GALNS gene in family with MPS4A diagnosed child

Gunes, Meltem Cerrah, Bayramov, Ruslan, Boyukoglan, Ruksan, Dogan, Muhammet Ensar, Bayramov, Keziban Korkmaz, Dundar, Munis

Journal:

Journal of Biotechnology

Year:

2016

Language:

english

File:

PDF, 60 KB

english, 2016

68

Prenatal diagnosis of upper extremity malformations with ultrasonography: Diagnostic features and perinatal outcome

Kutuk, Mehmet Serdar, Altun, Ozguc, Tutus, Sadan, Dogan, Muhammet Ensar, Ozgun, Mahmut Tuncay, Dundar, Munis

Journal:

Journal of Clinical Ultrasound

Year:

2016

Language:

english

File:

PDF, 470 KB

english, 2016

69

Loss of dermatan-4-sulfotransferase 1 (D4ST1/CHST14) function represents the first dermatan sulfate biosynthesis defect, “dermatan sulfate-deficient adducted thumb–clubfoot syndrome”

Andreas R. Janecke, Jacques U. Baenziger, Thomas Müller, Munis Dündar

Journal:

Year:

2011

Language:

english

File:

PDF, 90 KB

english, 2011

70

Current State of Biotechnology in Turkey

Munis Dundar, Yagut Akbarova

Journal:

Current Opinion in Biotechnology

Year:

2011

Language:

english

File:

PDF, 120 KB

english, 2011

71

An autosomal recessive adducted thumb-club foot syndrome observed in Turkish cousins

Munis Dundar, Fatma Demiryilmaz, Ilhan Demiryilmaz, Sefer Kumandas, Kuddusi Erkilic, Mustafa Kendirci, Mehmet Tuncel, Isilay Ozyazgan, John L Tolmie

Journal:

Clinical Genetics

Year:

1997

Language:

english

File:

PDF, 1.07 MB

english, 1997

72

How the I1307K adenomatous polyposis coli gene variant contributes in the assessment of risk of colorectal cancer, but not stomach cancer, in a Turkish population

Munis Dundar, Ahmet Okay Caglayan, Cetin Saatci, Hatice Karaca, Mevlut Baskol, Serpil Tahiri, Yusuf Ozkul

Journal:

Cancer Genetics and Cytogenetics

Year:

2007

Language:

english

File:

PDF, 75 KB

english, 2007

73

Ameliorative effects of pentoxifylline on NOS induced by diabetes in rat kidney

Sönmez, Mehmet Fatih, Dündar, Munis

Journal:

Year:

2016

Language:

english

File:

PDF, 2.94 MB

english, 2016

74

A case of 46, XX, t(2;17)(q37.1;q25) with recurrent miscarriage

Fatma Colak, Muhammet Ensar Dogan, Asli Subasioglu Uzak, Murat Erdogan, Sevda Yesim Karabulut, Burhan Balta, Oguzhan Bahadir, Yusuf Ozkul, Munis Dundar

Journal:

Current Opinion in Biotechnology

Year:

2011

Language:

english

File:

PDF, 83 KB

english, 2011

75

Isolated congenital anonychia cases with coincident chromosomal fragility

İrfan Özyazgan, Işılay Özyazgan, Munis Dündar

Journal:

Annales de Génétique

Year:

2004

Language:

english

File:

PDF, 209 KB

english, 2004

76

Is there relation betweenCOL4A1/A2mutations and antenatally detected fetal intraventricular hemorrhage?

Kutuk, Mehmet Serdar, Balta, Burhan, Kodera, Hirofumi, Matsumoto, Naomichi, Saitsu, Hirotomo, Doganay, Selim, Canpolat, Mehmet, Dolanbay, Mehmet, Unal, Ekrem, Dundar, Munis

Journal:

Child's Nervous System

Year:

2014

Language:

english

File:

PDF, 249 KB

english, 2014

77

Prenatally detected de novo 46, XX, t(21;21)(p12;p12) at chorionic villus sampling

Muhammet Ensar Dogan, Fatma Colak, Asli Subasioglu Uzak, Murat Erdogan, Sevda Yesim Karabulut, Burhan Balta, Oguzhan Bahadir, Cetin Saatci, Munis Dundar

Journal:

Current Opinion in Biotechnology

Year:

2011

Language:

english

File:

PDF, 83 KB

english, 2011

78

Sexing Greater Flamingo Chicks from Feather Bulb DNA

Balkiz, Özge, Dano, Stéphanie, Barbraud, Christophe, Tekin, Serpil, Özesmi, Uygar, Dündar, Munis, Béchet, Arnaud

Journal:

Year:

2007

Language:

english

File:

PDF, 106 KB

english, 2007

79

Innovations in biotechnology

Gartland, Kevan M.A., Beccari, Tommaso, Bruschi, Fabrizio, Dundar, Munis, Magni, Mariapia Viola, Gartland, Jill S.

Journal:

Journal of Biotechnology

Year:

2015

Language:

english

File:

PDF, 106 KB

english, 2015

80

A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia

Mastushita, Masaki, Kitoh, Hiroshi, Subasioglu, Asli, Kurt Colak, Fatma, Dundar, Munis, Mishima, Kenichi, Nishida, Yoshihiro, Ishiguro, Naoki

Journal:

Molecular Syndromology

Year:

2015

File:

PDF, 356 KB

2015

81

Retrospective results of 18 years prenatal diagnosis cases and its evaluation

Bayramov, Ruslan, Kutuk, Mehmet Serdar, Kenanoglu, Sercan, Gunes, Meltem Cerrah, Dogan, Muhammet Ensar, Ozkul, Yusuf, Saatçi, Çetin, Dundar, Munis

Journal:

Journal of Biotechnology

Year:

2017

Language:

english

File:

PDF, 59 KB

english, 2017

82

Biotechnological opportunities

Gartland, Kevan M.A., Dundar, Munis, Beccari, Tommaso, Gartland, Jill S.

Journal:

Journal of Biotechnology

Year:

2018

Language:

english

File:

PDF, 84 KB

english, 2018

83

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

84

Genetic testing for aortic valve stenosis

Rakhmanov, Yeltay, Maltese, Paolo Enrico, Zulian, Alessandra, Paolacci, Stefano, Beccari, Tommaso, Dundar, Munis, Bertelli, Matteo

Journal:

The EuroBiotech Journal

Year:

2018

Language:

english

File:

PDF, 272 KB

english, 2018

85

A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype

Yusuf Ozkul, M. Emre Atabek, Munis Dundar, Selim Kurtoglu, Cetin Saatci

Journal:

Annales de Génétique

Year:

2002

Language:

english

File:

PDF, 130 KB

english, 2002

86

A de novo SRCAP mutation associated with Floating-Harbor syndrome

Uzak, Asli Subasioglu, Jackson, Andrew P, Murray, Jennie E, Bicknell, Louise S, Dundar, Munis

Journal:

Current Opinion in Biotechnology

Year:

2013

Language:

english

File:

PDF, 63 KB

english, 2013

87

A case of SRY positive 46, XX male with speaking disorder

Bayramov, Ruslan, Güneş, Meltem Cerrah, Erdem, Yagut, Dündar, Munis

Journal:

Journal of Biotechnology

Year:

2015

Language:

english

File:

PDF, 62 KB

english, 2015

88

Prenatal diagnosis of a foetus with partial monosomy 4p and partial trisomy 13q

Dogan, Muhammet E., Kutuk, Mehmet Serdar, Bayramov, Ruslan, Saatci, Cetin, Ozkul, Yusuf, Dundar, Munis

Journal:

Journal of Biotechnology

Year:

2017

Language:

english

File:

PDF, 59 KB

english, 2017

89

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

90

A case of ambiguous genitalia presenting with a 45,X/46,Xr(Y)(p11.2;q11.23)/47,X,idic(Y)(p11.2),idic(Y)(p11.2) karyotype

Munis Dundar, Gordon Lowther, Hasan Acar, Selim Kurtoglu, Fatma Demiryilmaz, Mustafa Kucukaydin

Journal:

Annales de Génétique

Year:

2001

Language:

english

File:

PDF, 240 KB

english, 2001

91

Alcohol withdrawal investigation of Cytochrome P450 CYP1A2, CYP2D6, CYP2E1 and CYP3A4 expression and gene polymorphism

Nazife Tascioglu, Cetin Saatci, Ertugrul Esel, Munis Dundar

Journal:

Journal of Biotechnology

Year:

2012

Language:

english

File:

PDF, 64 KB

english, 2012

92

Apolipoprotein E3/E3 Genotype Decreases the Risk of Pituitary Dysfunction after Traumatic Brain Injury due to Various Causes: Preliminary Data

Tanriverdi, Fatih, Taheri, Serpil, Ulutabanca, Halil, Caglayan, Ahmet Okay, Ozkul, Yusuf, Dundar, Munis, Selcuklu, Ahmet, Unluhizarci, Kursad, Casanueva, Felipe F., Kelestimur, Fahrettin

Journal:

Journal of Neurotrauma

Year:

2008

Language:

english

File:

PDF, 86 KB

english, 2008

93

Polycystic kidney disease, biliary dysgenesis in a patient with Larsen's syndrome

Selim Kurtoglu, Munis Dundar, I. Kuttulus. Hallaç, Kazim Üzüm, Yüksel Okumus, Turhan Öktem

Journal:

Clinical Genetics

Year:

1997

Language:

english

File:

PDF, 1.24 MB

english, 1997

94

A new syndrome of microtia with unilateral renal agenesis and short stature

Ahmet Okay Caglayan, Servi J.C. Stevens, Jozefa C.M. Albrechts, Munis Dundar, John Engelen

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 115 KB

english, 2012

95

Congenital alacrima in a patient with G (Opitz Frias) syndrome

Munis Dundar,Kuddusi Erkiliç,Fatma Demiryilmaz,Mustafa Küçükaydin…

Journal:

Year:

1996

Language:

english

File:

PDF, 197 KB

english, 1996

96

Polymorphisms of TNF-alpha and coagulation genes in the etiopathogenesis of Sheehan's Syndrome

Tascioglu, Nazife, Sener, Elif Funda, Onal, Müge Gülcihan, Diri, Halit, Bayram, Fahri, Dundar, Munis

Journal:

Current Opinion in Biotechnology

Year:

2013

Language:

english

File:

PDF, 73 KB

english, 2013

97

The prevalence of non-classic adrenal hyperplasia among Turkish women with hyperandrogenism

Unluhizarci, Kursad, Kula, Mustafa, Dundar, Munis, Tanriverdi, Fatih, Israel, Shoshana, Colak, Ramis, Dokmetas, Hatice Sebila, Atmaca, Hulusi, Bahceci, Mithat, Balci, Mustafa Kemal, Comlekci, Abdurrah

Journal:

Gynecological Endocrinology

Year:

2010

Language:

english

File:

PDF, 161 KB

english, 2010

98

Novel FBN1 gene frameshift mutation in patient with type 1 Chiari malformation

Güneş, Meltem Cerrah, Bayramov, Ruslan, Erdem, Yagut, Dündar, Munis

Journal:

Journal of Biotechnology

Year:

2015

Language:

english

File:

PDF, 70 KB

english, 2015

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