Search Results

Characterization of R132H Mutation-specific IDH1 Antibody Binding in Brain Tumors

Authors: Capper, David; Weißert, Susanne; Balss, Jörg; Habel, Antje; Meyer, Jochen; Jäger, Diana; Ackermann, Ulrike; Tessmer, Claudia; Korshunov, Andrey; Zentgraf, Hanswalter; Hartmann, Christian; von Deimling, Andreas

Source: Brain Pathology, Volume 20, Number 1, January 2010 , pp. 245-254(10)

Publisher: Blackwell Publishing

The Andalusian population from Huelva reveals a high diversification of Y-DNA paternal lineages from haplogroup E: Identifying human male movements within the Mediterranean space

Authors: Ambrosio, B.; Dugoujon, J. M.; Hernández, C.; De La Fuente, D.; González-Martín, A.; Fortes-Lima, C. A.; Novelletto, A.; Rodríguez, J. N.; Calderón, R.

Source: Annals of Human Biology, Volume 37, Number 1, February 2010 , pp. 86-107(22)

Publisher: Informa Healthcare

Insulin-independent promotion of chemically induced hepatocellular tumor development in genetically diabetic mice

Authors: Yamasaki, Kohtaro; Hayashi, Yoshihiro; Okamoto, Sumika; Osanai, Makoto; Lee, Gang-Hong

Source: Cancer Science, Volume 101, Number 1, January 2010 , pp. 65-72(8)

Publisher: Blackwell Publishing

Nightblindness-Associated Transient Tonic Downgaze (NATTD) in Infant Boys with Chin-Up Head Posture

Authors: Simonsz, H.J.; Florijn, R.J.; van Minderhout, H.M.; Bergen, A.A.B.; Kamermans, M.

Source: Strabismus, Volume 17, Number 4, December 2009 , pp. 158-164(7)

Publisher: Informa Healthcare

Polymorphism L26V in the Cathepsin B Gene may be Associated with a Risk of Prostate Cancer and Differentiation

Authors: Štiblar-Martinčič, D.; Hajdinjak, T.

Source: The Journal of International Medical Research, Volume 37, Number 5, September 2009 , pp. 1604-1610(7)

Publisher: Field House Publishing

Impact of polymorphisms of the major histocompatibility complex class II, interleukin-10, tumor necrosis factor-α and cytotoxic T-lymphocyte antigen-4 genes on inhibitor development in severe hemophilia A

Authors: PAVLOVA, A.; DELEV, D.; LACROIX-DESMAZES, S.; SCHWAAB, R.; MENDE, M.; FIMMERS, R.; ASTERMARK, J.; OLDENBURG, J.

Source: Journal of Thrombosis and Haemostasis, Volume 7, Number 12, December 2009 , pp. 2006-2015(10)

Publisher: Blackwell Publishing

Association of mannose-binding lectin gene polymorphisms with Kawasaki disease in the Japanese

Authors: SATO, Satoshi; KAWASHIMA, Hisashi; KASHIWAGI, Yasuyo; FUJIOKA, Tao; TAKEKUMA, Kouji; HOSHIKA, Akinori

Source: International Journal of Rheumatic Diseases, Volume 12, Number 4, December 2009 , pp. 307-310(4)

Publisher: Blackwell Publishing

Frequency and prognostic significance of murine double minute protein-2 overexpression and p53 gene mutations in childhood acute lymphoblastic leukemia

Authors: Hendy, Olfat M.; Elghannam, Doaa M.; El-Sharnouby, Jehan A.; Goda, Enas F.; El-Ashry, Rasha; Al-Tonbary, Youssef

Source: Hematology, Volume 14, Number 6, December 2009 , pp. 335-340(6)

Publisher: Maney Publishing

Genetic optimization of two-dimensional photonic crystals for large absolute band gaps under light line

Authors: Jiang, L. Y.; Li, H. P.; Zheng, G. G.; Li, X. Y.; Zhu, R. H.

Source: Journal of Modern Optics, Volume 56, Number 10, June 2009 , pp. 1220-1226(7)

Publisher: Taylor and Francis Ltd

Mutation frequency of NS5A in patients vertically infected with HCV genotype 1 predicts sustained virological response to peginterferon alfa-2b and ribavirin combination therapy

Authors: Jenke, A. C. W.; Moser, S.; Orth, V.; Zilbauer, M.; Gerner, P.; Wirth, S.

Source: Journal of Viral Hepatitis, Volume 16, Number 12, December 2009 , pp. 853-859(7)

Publisher: Blackwell Publishing

Genotyping Mutations in BmAChE3: A Survey of Organophosphate-Resistant and -Susceptible Strains of Rhipicephalus (Boophilus) microplus

Authors: Temeyer, Kevin B.; Olafson, Pia U.; Miller, Robert J.

Source: Journal of Medical Entomology, Volume 46, Number 6, November 2009 , pp. 1355-1360(6)

Publisher: Entomological Society of America

Permethrin Resistance and Target Site Insensitivity in the Mosquito Culex quinquefasciatus in Alabama

Authors: Liu, Nannan; Xu, Qiang; Li, Ting; He, Lin; Zhang, Lee

Source: Journal of Medical Entomology, Volume 46, Number 6, November 2009 , pp. 1424-1429(6)

Publisher: Entomological Society of America

Fine mapping of an epilepsy modifier gene on mouse Chromosome 19

Authors: Bergren, Sarah; Rutter, Elizabeth; Kearney, Jennifer

Source: Mammalian Genome, Volume 20, Number 6, June 2009 , pp. 359-366(8)

Publisher: Springer

Frequency of Val1016Ile mutation in the voltage-gated sodium channel gene of Aedes aegypti Brazilian populations

Authors: Martins, Ademir Jesus; Lima, José Bento Pereira; Peixoto, Alexandre Afranio; Valle, Denise

Source: Tropical Medicine & International Health, Volume 14, Number 11, November 2009 , pp. 1351-1355(5)

Publisher: Blackwell Publishing

Evolution of raltegravir resistance during therapy

Authors: Sichtig, Nadine; Sierra, Saleta; Kaiser, Rolf; Dumer, Martin; Reuter, Stefan; Schlter, Eugen; Altmann, Andre; Ftkenheuer, Gerd; Dittmer, Ulf; Pfister, Herbert; Esser, Stefan

Source: Journal of Antimicrobial Chemotherapy, Volume 64, Number 1, 14 July 2009 , pp. 25-32(8)

Publisher: Oxford University Press

Inferring Population Mutation Rate and Sequencing Error Rate Using the SNP Frequency Spectrum in a Sample of DNA Sequences

Authors: Liu, Xiaoming; Maxwell, Taylor J.; Boerwinkle, Eric; Fu, Yun-Xin

Source: Molecular Biology and Evolution, Volume 26, Number 7, 6 July 2009 , pp. 1479-1490(12)

Publisher: Oxford University Press

PIK3CA amplification is predictive of poor prognosis in Tunisian patients with nasopharyngeal carcinoma

Authors: Fendri, Ali; Khabir, Abdelmajid; Mnejja, Wafa; Sellami-Boudawara, Tahia; Daoud, Jamel; Frikha, Mounir; Ghorbel, Abdelmonem; Gargouri, Ali; Mokdad-Gargouri, Raja

Source: Cancer Science, Volume 100, Number 11, November 2009 , pp. 2034-2039(6)

Publisher: Blackwell Publishing

Further genetic evidence implicates the vasopressin system in childhood-onset mood disorders

Authors: Dempster, Emma L.; Burcescu, Irina; Wigg, Karen; Kiss, Eniko; Baji, Ildiko; Gadoros, Julia; Tamás, Zsuzsanna; Kapornai, Krisztina; Daróczy, Gabriella; Kennedy, James L.; Vetró, Agnes; Kovacs, Maria; Barr, Cathy L.

Source: European Journal of Neuroscience, Volume 30, Number 8, October 2009 , pp. 1615-1619(5)

Publisher: Blackwell Publishing

Forty-two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large European dystrophic epidermolysis bullosa cohort

Authors: Kern, J.S.; Grüninger, G.; Imsak, R.; Müller, M.L.; Schumann, H.; Kiritsi, D.; Emmert, S.; Borozdin, W.; Kohlhase, J.; Bruckner-Tuderman, L.; Has, C.

Source: British Journal of Dermatology, Volume 161, Number 5, November 2009 , pp. 1089-1097(9)

Publisher: Blackwell Publishing

Drug resistant ADLTE and recurrent partial status epilepticus with dysphasic features in a family with a novel LGI1mutation: electroclinical, genetic, and EEG/fMRI findings

Authors: Bonaventura, Carlo Di; Carni, Marco; Diani, Erica; Fattouch, Jinane; Vaudano, Elisabetta A.; Egeo, Gabriella; Pantano, Patrizia; Maraviglia, Bruno; Bozzao, Luigi; Manfredi, Mario; Prencipe, Massimiliano; Giallonardo, Teresa A.; Nobile, Carlo

Source: Epilepsia, Volume 50, Number 11, November 2009 , pp. 2481-2486(6)

Publisher: Blackwell Publishing