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MBG publications 2008 - 2003


2009

  • Mapping of Class I and Class II Odorant Receptors to Glomerular Domains by Two Distinct Types of Olfactory Sensory Neurons in the Mouse.
    Bozza T, Vassalli A, Fuss S, Zhang JJ, Weiland B, Pacifico R, Feinstein, P, and Mombaerts P.
    Neuron2009,61(2):220-233.
  • A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype.
    Pirkevi C, Lesage S, Condroyer C, Tomiyama H, Hattori N, Ertan S, Brice A, Başak AN .
    Neurogenetics. 2009 Jan 27.

  • A Multiplexed ARMS-PCR Approach for the Detection of Common MECP2 Mutations.
    Baris I, Battaloglu E.
    Genet Test. 2009 Jan 2.


2008

  • Prenatal Expressions of Hyperpolarization-activated Cyclic-Nucleotide-Gated Channel (HCN) Genes in Dysplastic Hippocampi in Rats.
    Işler C, Tanriverdı T, Kavak E, Sanus GZ, Ulu MO, Erkanli G, Koman A, Iyıson NB, Uzan M.
    Turk Neurosurg. 2008;18(4):327-335.

  • Two Young Sisters with Spinocerebellar Ataxia Type 2 Showing Different Clinical Progression of Disease.
    Yiş U, Dirik E, Kurul SH, Eken AG, Başak AN.
    Cerebellum. 2008 Nov 21

  • Delayed diagnosis of a neuroBehçet patient with only brainstem and cerebellar atrophy: Literature review.
    Taskapilioglu O, Seferoglu M, Akkaya C, Hakyemez B, Yusufoglu C, Basak AN, Gundogdu A, Bora I.
    J Neurol Sci. 2008 Nov 10.

  • Coinheritance of sickle cell anemia and hereditary spherocytosis.
    Selcuk Duru N, Celkan T, Civilibal M, Ozbek NO, Basak AN, Elevli M.
    Pediatr Blood Cancer. 2008 Oct;51(4):560-3.

  • Phenotypic differences in a large family with Kennedy's disease from the Middle Black Sea region of Turkey.
    Karaer H, Kaplan Y, Kurt S, Gundogdu A, Erdoğan B, Basak NA.
    Amyotroph Lateral Scler. 2008 Sep 26:1-6.

  • Hereditary neuropathy with liability to pressure palsy (HNPP) in childhood: A case study emphasizing the relevance of detailed electrophysiological examination for suspected HNPP in the first decade.
    Bayrak AO, Battaloglu E, Turker H, Baris I, Oztas G.
    Brain Dev. 2008 Aug 28.

  • Factor 8 (F8) gene mutation profile of Turkish hemophilia A patients with inhibitors.
    Fidanci ID, Kavakl K, Uçar C, Timur C, Meral A, Kilinç Y, Sayilan H, Kazanci E, Cağlayan SH.
    Blood Coagul Fibrinolysis. 2008 Jul;19(5):383-8.

  • Iroquois complex genes induce co-expression of rhodopsins in Drosophila.
    Mazzoni EO, Celik A, Wernet MF, Vasiliauskas D, Johnston RJ, Cook TA, Pichaud F, Desplan C.
    PLoS Biol. 2008 Apr 22;6(4):e97.

  • Can you tBID on it?
    Yüksel S, Ozören N.
    Cancer Biol Ther. 2008 Nov 8;7(11).

  • Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation.
    Ugur SA, Tolun A.
    Hum Mol Genet. 2008 Sep 1;17(17):2644-53.

  • A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract.
    Ugur SA, Tolun A.
    Eur J Hum Genet. 2008 Feb;16(2):261-4.


2007

  • Spinocerebellar ataxia type 2 in a Turkish family.
    Dirik E, Yiş U, Başak N, Soydan E, Hüdaoğlu O, Ozgönül F.
    J Child Neurol. 2007 Jul;22(7):891-4.

  • The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN.
    Hemoglobin. 2007;31(2):233-41.

  • Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4.
    Stendel C, Roos A, Deconinck T, Pereira J, Castagner F, Niemann A, Kirschner J, Korinthenberg R, Ketelsen UP, Battaloglu E, Parman Y, Nicholson G, Ouvrier R, Seeger J, De Jonghe P, Weis J, Krüttgen A, Rudnik-Schöneborn S, Bergmann C, Suter U, Zerres K, Timmerman V, Relvas JB, Senderek J.
    Am J Hum Genet. 2007 Jul;81(1):158-64.

  • X-linked Charcot-Marie-Tooth disease and multiple sclerosis.
    Parman Y, Ciftci F, Poyraz M, Halefoglu AM, Oge AE, Eraksoy M, Saruhan-Direskeneli G, Deymeer F, Battaloglu E.
    J Neurol. 2007 Jul;254(7):953-5.

  • A novel missense mutation (N258S) in the KCNQ2 gene in a Turkish family afflicted with benign familial neonatal convulsions (BFNC).
    Yalçin O, Cağlayan SH, Saltik S, Cokar O, Ağan K, Dervent A, Steinlein OK.
    Turk J Pediatr. 2007 Oct-Dec;49(4):385-9.

  • Generation of uniform fly retinas.
    Wernet MF, Celik A, Mikeladze-Dvali T, Desplan C.
    Curr Biol. 2007 Dec 4;17(23):R1002-3.

  • Generating patterned arrays of photoreceptors.
    Morante J, Desplan C, Celik A.
    Curr Opin Genet Dev. 2007 Aug;17(4):314-9. Epub 2007 Jul 5.

  • Olfactory identity kicked up a NOTCH.
    Fuss S, Celik A, Desplan C.
    Nat Neurosci. 2007 Feb;10(2):138-40.

  • Local and cis effects of the H element on expression of odorant receptor genes in mouse.
    Fuss SH, Omura M, Mombaerts P.
    Cell. 2007 Jul 27;130(2):373-84.

  • Transfer of nisin gene cluster from Lactococcus lactis ATCC 11454 into the chromosome of Bacillus subtilis 168.
    Yuksel S, Hansen JN.
    Appl Microbiol Biotechnol. 2007 Mar;74(3):640-9.


2006

  • Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease.
    Metzger S, Bauer P, Tomiuk J, Laccone F, Didonato S, Gellera C, Mariotti C, Lange HW, Weirich-Schwaiger H, Wenning GK, Seppi K, Melegh B, Havasi V, Balikó L, Wieczorek S, Zaremba J, Hoffman-Zacharska D, Sulek A, Basak AN, Soydan E, Zidovska J, Kebrdlova V, Pandolfo M, Ribaï P, Kadasi L, Kvasnicova M, Weber BH, Kreuz F, Dose M, Stuhrmann M, Riess O.
    Hum Genet. 2006 Sep;120(2):285-92.

  • The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease.
    Metzger S, Bauer P, Tomiuk J, Laccone F, Didonato S, Gellera C, Soliveri P, Lange HW, Weirich-Schwaiger H, Wenning GK, Melegh B, Havasi V, Balikó L, Wieczorek S, Arning L, Zaremba J, Sulek A, Hoffman-Zacharska D, Basak AN, Ersoy N, Zidovska J, Kebrdlova V, Pandolfo M, Ribaï P, Kadasi L, Kvasnicova M, Weber BH, Kreuz F, Dose M, Stuhrmann M, Riess O.
    Neurogenetics. 2006 Mar;7(1):27-30.

  • A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis.
    Baris I, Arisoy AE, Smith A, Agostini M, Mitchell CS, Park SM, Halefoglu AM, Zengin E, Chatterjee VK, Battaloglu E.
    J Clin Endocrinol Metab. 2006 Oct;91(10):4183-7.

  • A large family with Charcot-Marie-Tooth Type 1a and Type 2 diabetes mellitus.
    Koç F, Sarica Y, Yerdelen D, Baris I, Battaloglu E, Sert M.
    Int J Neurosci. 2006 Feb;116(2):103-14.

  • Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N.
    Berber E, Fidanci ID, Un C, El-Maarri O, Aktuglu G, Gurgey A, Celkan T, Meral A, Oldenburg J, Graw J, Akar N, Caglayan H.
    Haemophilia. 2006 Jul;12(4):398-400.

  • The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleus.
    Laser H, Conforti L, Morreale G, Mack TG, Heyer M, Haley JE, Wishart TM, Beirowski B, Walker SA, Haase G, Celik A, Adalbert R, Wagner D, Grumme D, Ribchester RR, Plomann M, Coleman MP.
    Mol Biol Cell. 2006 Mar;17(3):1075-84.

  • Stochastic spineless expression creates the retinal mosaic for colour vision.
    Wernet MF, Mazzoni EO, Celik A, Duncan DM, Duncan I, Desplan C.
    Nature. 2006 Mar 9;440(7081):174-80.

  • Regulation of Legionella phagosome maturation and infection through flagellin and host Ipaf.
    Amer A, Franchi L, Kanneganti TD, Body-Malapel M, Ozören N, Brady G, Meshinchi S, Jagirdar R, Gewirtz A, Akira S, Núñez G.
    J Biol Chem. 2006 Nov 17;281(46):35217-23.

  • Cytosolic flagellin requires Ipaf for activation of caspase-1 and interleukin 1beta in salmonella-infected macrophages.
    Franchi L, Amer A, Body-Malapel M, Kanneganti TD, Ozören N, Jagirdar R, Inohara N, Vandenabeele P, Bertin J, Coyle A, Grant EP, Núñez G.
    Nat Immunol. 2006 Jun;7(6):576-82.

  • Distinct roles of TLR2 and the adaptor ASC in IL-1beta/IL-18 secretion in response to Listeria monocytogenes.
    Ozören N, Masumoto J, Franchi L, Kanneganti TD, Body-Malapel M, Ertürk I, Jagirdar R, Zhu L, Inohara N, Bertin J, Coyle A, Grant EP, Núñez G.
    J Immunol. 2006 Apr 1;176(7):4337-42.

  • Bacterial RNA and small antiviral compounds activate caspase-1 through cryopyrin/Nalp3.
    Kanneganti TD, Ozören N, Body-Malapel M, Amer A, Park JH, Franchi L, Whitfield J, Barchet W, Colonna M, Vandenabeele P, Bertin J, Coyle A, Grant EP, Akira S, Núñez G.
    Nature. 2006 Mar 9;440(7081):233-6.

  • Mutations in SLC34A2 cause pulmonary alveolar microlithiasis and are possibly associated with testicular microlithiasis.
    Corut A, Senyigit A, Ugur SA, Altin S, Ozcelik U, Calisir H, Yildirim Z, Gocmen A, Tolun A.
    Am J Hum Genet. 2006 Oct;79(4):650-6.

  • Severe form of Cockayne syndrome with varying clinical presentation and no photosensitivity in a family.
    Sonmez FM, Celep F, Ugur SA, Tolun A.
    J Child Neurol. 2006 Apr;21(4):333-7.


2005

  • Voltage-gated sodium channel expression and potentiation of human breast cancer metastasis.
    Fraser SP, Diss JK, Chioni AM, Mycielska ME, Pan H, Yamaci RF, Pani F, Siwy Z, Krasowska M, Grzywna Z, Brackenbury WJ, Theodorou D, Koyutürk M, Kaya H, Battaloglu E, De Bella MT, Slade MJ, Tolhurst R, Palmieri C, Jiang J, Latchman DS, Coombes RC, Djamgoz MB.
    Clin Cancer Res. 2005 Aug 1;11(15):5381-9.

  • Acidic fibroblast growth factor (FGF-1) and FGF receptor 1 signaling in human Y79 retinoblastoma.
    Siffroi-Fernandez S, Cinaroglu A, Fuhrmann-Panfalone V, Normand G, Bugra K, Sahel J, Hicks D.
    Arch Ophthalmol. 2005 Mar;123(3):368-76.

  • Expression and possible function of fibroblast growth factor 9 (FGF9) and its cognate receptors FGFR2 and FGFR3 in postnatal and adult retina.
    Cinaroglu A, Ozmen Y, Ozdemir A, Ozcan F, Ergorul C, Cayirlioglu P, Hicks D, Bugra K.
    J Neurosci Res. 2005 Feb 1;79(3):329-39.

  • A rat model of slow Wallerian degeneration (WldS) with improved preservation of neuromuscular synapses.
    Adalbert R, Gillingwater TH, Haley JE, Bridge K, Beirowski B, Berek L, Wagner D, Grumme D, Thomson D, Celik A, Addicks K, Ribchester RR, Coleman MP.
    Eur J Neurosci. 2005 Jan;21(1):271-7.

  • The Grueneberg ganglion of the mouse projects axons to glomeruli in the olfactory bulb.
    Fuss SH, Omura M, Mombaerts P.
    Eur J Neurosci. 2005 Nov;22(10):2649-54.


2004

  • Clinicopathological and genetic study of early-onset demyelinating neuropathy.
    Parman Y, Battaloglu E, Baris I, Bilir B, Poyraz M, Bissar-Tadmouri N, Williams A, Ammar N, Nelis E, Timmerman V, De Jonghe P, Najafov A, Deymeer F, Serdaroglu P, Brophy PJ, Said G.
    Brain. 2004 Nov;127(Pt 11):2540-50.

  • Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene.
    Bissar-Tadmouri N, Nelis E, Züchner S, Parman Y, Deymeer F, Serdaroglu P, De Jonghe P, Van Gerwen V, Timmerman V, Schröder JM, Battaloglu E.
    Neurology. 2004 May 11;62(9):1522-5.

  • Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
    Züchner S, Mersiyanova IV, Muglia M, Bissar-Tadmouri N, Rochelle J, Dadali EL, Zappia M, Nelis E, Patitucci A, Senderek J, Parman Y, Evgrafov O, Jonghe PD, Takahashi Y, Tsuji S, Pericak-Vance MA, Quattrone A, Battaloglu E, Polyakov AV, Timmerman V, Schröder JM, Vance JM.
    Nat Genet. 2004 May;36(5):449-51.

  • 'One receptor' rules in sensory neurons.
    Mazzoni EO, Desplan C, Celik A.
    Dev Neurosci. 2004;26(5-6):388-95.

  • Identification of a locus for an autosomal recessive hyaline body myopathy at chromosome 3p22.2-p21.32.
    Onengüt S, Uğur SA, Karasoy H, Yüceyar N, Tolun A.
    Neuromuscul Disord. 2004 Jan;14(1):4-9.

  • Formation of wheat (Triticum aestivum L.) embryogenic callus involves peroxide-generating germin-like oxalate oxidase.
    Caliskan M, Turet M, Cuming AC.
    Planta. 2004 May;219(1):132-40.


2003

  • Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy.
    Senderek J, Bergmann C, Stendel C, Kirfel J, Verpoorten N, De Jonghe P, Timmerman V, Chrast R, Verheijen MH, Lemke G, Battaloglu E, Parman Y, Erdem S, Tan E, Topaloglu H, Hahn A, Müller-Felber W, Rizzuto N, Fabrizi GM, Stuhrmann M, Rudnik-Schöneborn S, Züchner S, Michael Schröder J, Buchheim E, Straub V, Klepper J, Huehne K, Rautenstrauss B, Büttner R, Nelis E, Zerres K.
    Am J Hum Genet. 2003 Nov;73(5):1106-19.

  • Retinal pigment epithelium cell culture on surface modified poly(hydroxybutyrate-co-hydroxyvalerate) thin films.
    Tezcaner A, Bugra K, Hasirci V.
    Biomaterials. 2003 Nov;24(25):4573-83.

  • Molecular pathology of haemophilia B in Turkish patients: identification of a large deletion and 33 independent point mutations.
    Onay UV, Kavakli K, Kilinç Y, Gürgey A, Aktuğlu G, Kemahli S, Ozbek U, Cağlayan SH.
    Br J Haematol. 2003 Feb;120(4):656-9.

  • Cell surface Death Receptor signaling in normal and cancer cells.
    Ozören N, El-Deiry WS.
    Semin Cancer Biol. 2003 Apr;13(2):135-47.

  • Is the novel SCKL3 at 14q23 the predominant Seckel locus?
    Kilinç MO, Ninis VN, Ugur SA, Tüysüz B, Seven M, Balci S, Goodship J, Tolun A.
    Eur J Hum Genet. 2003 Nov;11(11):851-7.

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