Investigation of MEFV gene polymorphisms (G138G and A165A) in adult patients with familial Mediterranean fever

Authors: Öksuz, Mustafa Ferhat, Karkucak, Mutlu, Görukmez, Orhan, Ocakoğlu, Gökhan, Yıldız, Abdulmecit, Ture, Mehmet, Yakut, Tahsin, Dilek, Kamil

Source: Revista Brasileira de Reumatologia. December 2017 57(6)

Subject Terms: Familial Mediterranean fever, MEFV gene, Polymorphism

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Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencing

Authors: Bastida, Jose María, Morais, Sara, Palma-Barqueros, Veronica, Benito, Rocio, Bermejo, Nuria, Karkucak, Mutlu, Trapero-Marugan, Maria, Bohdan, Natalia, Pereira, Mónica, Marin-Quilez, Ana, Oliveira, Jorge, Yucel, Yusuf, Santos, Rosario, Padilla, Jose, Janusz, Kamila, Lau, Catarina, Martin-Izquierdo, Marta, Couto, Eduarda, Francisco Ruiz-Pividal, Juan, Vicente, Vicente, Hernández-Rivas, Jesus Maria, González-Porras, Jose Ramon, Luisa Lozano, Maria, Lima, Margarida, Rivera, Jose

Source: Annals of medicine. 51(2):141-148

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SPINK5 mutation and FLG gene deletion in an infant with Netherton syndrome

Authors: Hacıhamdioğlu, Duygu Övünç, Altan Ferhatoğlu, Zeynep, Karkucak, Mutlu, Fişek İzci, Neslihan Müge, Yakut, Tahsin

Source: Pediatrics international. 64(1)

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Evaluation of TNF-alpha gene (G308A) and MBL2 gene codon 54 polymorphisms in Turkish patients with tuberculosis

Authors: Ceylan, Esma, Karkucak, Mutlu, Coban, Hikmet, Karadag, Mehmet, Yakut, Tahsin

Source: In Journal of Infection and Public Health November-December 2017 10(6):774-777

Glutathione S-Transferase M1 and T1 Gene Polymorphisms in Patients with Chronic Plaque-Type Psoriasis: A Case-Control Study

Authors: Solak, Berna, Karkucak, Mutlu, Turan, Hakan, Ocakoğlu, Gökhan, Özemri Sağ, Şebnem, Uslu, Esma, Yakut, Tahsin, Erdem, Teoman

Source: Medical principles and practice. 25(2):155-158

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100096019501.0x000001&indx=1&recIds=ETOCvdc_100096019501.0x000001

Jacobsen syndrome: a case report and clinical features of a rare genetic syndrome.

Authors: Öztarhan, Kazım, Kaptaç, Talya, Karkucak, Mutlu, Öztarhan, Ece, Gedikbaş, Ali

Source: Perinatal Journal; Dec2022, Vol. 30 Issue 3, p320-325, 6p

Subject Terms: CHROMOSOME abnormalities, INTELLECTUAL disabilities, HOSPITAL care, GESTATIONAL age, AMNIOCENTESIS

TNFRSF11A (RANK) Gen Mutasyonu Saptanan Bir Ailede Prenatal Tanı: Bir Olgu Sunumu.

Alternate Title: Prenatal Diagnosis in a Family of TNFRSF11A (RANK) Gene Mutation Detection: A Case Report.

Authors: Karkucak, Mutlu¹ mutlukarkucak@hotmail.com, Hafızoğlu, Demet², Sağ, Şebnem Özemri¹, Başaranoğlu, Sevgen Tanır², Görükmez, Orhan¹, Kılıç, Şebnem Sara², Gülten, Tuna¹, Yakut, Tahsin¹, Kimya, Yalçın³, Gül, Davut⁴

Source: Journal of Current Pediatrics / Guncel Pediatri. 8/1/2014, Vol. 12 Issue 2, p123-126. 4p.

Association between p16(CDKN2A) C540G polymorphism and tumor behavior in prolactinoma: A single-center study.

Authors: CANDER, SONER^1,2 drcander@gmail.com, KARKUCAK, MUTLU³, GUL, OZEN OZ¹, SAG, SEBNEM OZEMRI³, YAKUT, TAHSIN³, ERSOY, CANAN¹, TUNCEL, ERCAN¹, ERTURK, ERDINC¹

Source: Biomedical Reports. 2014, Vol. 2 Issue 4, p589-595. 7p.

Subject Terms: *PROLACTINOMA, *TUMOR suppressor genes, *GENETIC polymorphism research, *EXONS (Genetics), *CANCER invasiveness, *POLYMERASE chain reaction, *RESTRICTION fragment length polymorphisms

Investigation of Monnose-Binding Lectin gene Polymorphism in Patients with Erythema Multiforme, Stevens-Johnson Syndrome and Stevens- Johnson Syndrome/Toxic Epidermal Necrolysis Overlap Syndrome.

Authors: Karkucak, Mutlu¹, Bülbül, Emel Başkan, Turan, Hakan² drhakanturan@gmail.com, Yakut, Tahsin¹, Toka, Sevil, Sarıcaoğlu, Hayriye

Source: Balkan Medical Journal. Sep2012, Vol. 29 Issue 3, p301-303. 4p.

Subject Terms: *STEVENS-Johnson Syndrome, *TOXIC epidermal necrolysis, *ERYTHEMA multiforme, *CHI-squared test, *GENETIC polymorphisms, *RESEARCH methodology, *GENETICS

Geographic Terms: TURKEY

Molecular Cytogenetic Findings in Cases with Childhood Acute Lymphoblastic Leukemia.

Alternate Title: Çocukluk Çaği Akut Lenfoblastik Lösemi'li Olgularda Moleküler Sitogenetik Bulgular.

Authors: KARKUCAK, Mutlu¹, GORUKMEZ, Orhan¹, YAKUT, Tahsin¹ tyakut@uludag.edu.tr, BAYTAN, Birol², GORUKMEZ, Ozlem¹, GUNES, A. Meral²

Source: UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi. 2012, Vol. 22 Issue 2, p67-72. 6p. 1 Color Photograph, 3 Charts.

Subject Terms: *LYMPHOBLASTIC leukemia in children, *CHILDHOOD cancer, *FLUORESCENCE in situ hybridization, *ANEUPLOIDY, *CHROMOSOME abnormalities, *PLOIDY

Childhood Acute Lymphoblastic Leukemia with Near-Tetraplody And t(12; 21) (p13;q22) Translocation: A Case Report.

Alternate Title: t(12;21)(p13;q22) translokasyonu ve Near Tetraplodi Bulunan Çocukluk Çağı Akut Lenfoblastik Lösemili Bir Olgu Sunumu.

Authors: KARKUCAK, Mutlu¹, YAKUT, Tahsin¹ tyakut@uludag.edu.tr, BAYTAN, Birol², GULTEN, Tuna¹, GUNES, A. Meral²

Source: UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi. Sep2011, Vol. 21 Issue 3, p192-195. 4p. 1 Color Photograph.

Subject Terms: *LYMPHOBLASTIC leukemia in children, *CHROMOSOMAL translocation, *HEMATOLOGY, *ONCOLOGY

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The potential utility of real-time PCR of the 16S-rRNA gene in the diagnosis of neonatal sepsis.

Authors: İstanbullu, Kenan, Köksal, Nilgün, Çetinkaya, Merih, Özkan, Hilal, Yakut, Tahsin, Karkucak, Mutlu, Doğan, Haldun

Source: Turkish Journal of Pediatrics; 2019, Vol. 61 Issue 4, p493-499, 7p

Investigação de polimorfismos no gene MEFV (G138G e A165A) em pacientes adultos com febre mediterrânica familiar

Authors: Öksuz, Mustafa Ferhat, Karkucak, Mutlu, Görukmez, Orhan, Ocakoğlu, Gökhan, Yıldız, Abdulmecit, Ture, Mehmet, Yakut, Tahsin, Dilek, Kamil

Source: Revista Brasileira de Reumatologia; 20240101, Issue: Preprints

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