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Marcela Cohen Martelotte, Reinaldo Castro Souza and Eduardo Antônio Barros da Silva

.” Journal of the Royal Statistical Society: Series A (General) 143: 321-337. Doi: http://dx.doi.org/10.2307/2982132. Canova, F. and E. Ghysels. 1994. “Changes in Seasonal Patterns: Are They Cyclical?” Journal of Economic Dynamics and Control 18: 1143-1171. Available at: http://apps.eui.eu/Personal/Canova/Articles/chanseapat.pdf (accessed September 2015). Canova, F. and B.E. Hansen. 1995. “Are Seasonal Patterns Constant Over Time? A Test for Seasonal Stability.” Journal of Business & Economic Statistics 13: 237-252. Doi: http://dx.doi.org/10

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S Verma, R Shah, A Bhat, GR Bhat, R Dada and R Kumar

aneuploidies and autosomal structural abnormalities, respectively [ 3 ]. The frequency of autosomal reciprocal translocations is estimated to be 0.25% in the general population, 0.5% in azoospermia and 0.7% in oligozoospermia [ 4 , 5 ]. The incidence of these genetic abnormalities increases with decline in semen quality [ 6 ]. Kumar et al . [ 7 ] showed that Robertsonian translocations t(13;14) and t(13;13) are associated with extremely poor semen quality (low sperm count and abnormal sperm morphology). Guichaoua et al . [ 8 ] reported a sterile male with 14

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I Uzun, R Has, E Alici, M Ozdemir, C Inan and S Erzincan

Case Report A 35-year-old gravida 2, para 0 (G2P2A0) woman at 7-weeks gestation was admitted to our clinic for a routine prenatal check-up. Trans vaginal ultrasound revealed a pregnancy at 7 weeks of gestation. Amniocentesis had been performed for increased nuchal translucency (NT) (3.7 mm) in her first pregnancy 8 years ago and short arm satellite deletion of chromosome 13 (13p) had been found in the chromosomal analysis. Consequently, parental karyotyping was performed and polymorphisms in chromosome 13 were also found (46XX13p- and 46XY13ps-). The

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Artur Bryja, Marta Dyszkiewicz-Konwińska, Maurycy Jankowski, Piotr Celichowski, Katarzyna Stefańska, Agata Chamier-Gliszczyńska, Blanka Borowiec, Katarzyna Mehr, Dorota Bukowska, Paweł Antosik, Małgorzata Bruska, Maciej Zabel, Michał Nowicki and Bartosz Kempisty

mouse origin. Arch Oral Biol. 2008;53(11):1091–100; DOI:10.1016/j.archoralbio.2008.07.002. 11. Li Y, Yang J, Li S, Zhang J, Zheng J, Hou W, Zhao H, Guo Y, Liu X, Dou K, Situ Z, Yao L. N-myc downstream-regulated gene 2, a novel estrogen-targeted gene, is involved in the regulation of Na+/K+-ATPase. J Biol Chem. 2011;286(37):32289–99; DOI:10.1074/jbc.M111.247825. 12. Apell H-J, Hitzler T, Schreiber G. Modulation of the Na,K-ATPase by Magnesium Ions. Biochemistry. 2017;56(7):1005–16; DOI:10.1021/acs.biochem.6b01243. 13. Graf S, Haimel M, Bleda M

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Yangchun Xie, Xuefeng Han, Xu Zhou, Miaomiao Wang, Qingguo Zhang and Tun Liu

. 11. Hoffmann JF. Tissue expansion in the head and neck. Facial Plast Surg Clin North Am. 2005; 13:315-24, vii. 12. Fujinori R. Gate flap for the total reconstruction of the lower lip. Br J Plast Surg. 1980;33:340-5. 13. Aytekin A, Ay A, Aytekin O. Total upper lip reconstruction with bilateral Fujimori gate flaps. Plast Reconstr Surg. 2003; 111:797-800. 14. Rea JL, Davis WE, Rittenhouse LK. Reinnervation of an Abbe-Estlander and a Gillies fan flap of the lower lip: electromyographic comparison. Arch Otolaryngol. 1978

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Jakub Kenig, Piotr Richter, Beata Żychiewicz and Urszula Olszewska

Database Syst Rev 2011; 7: CD006211. 5. Saliba S, Elliott M, Rubenstein LA et al.: The Vulnerable Elders Survey (VES-13): A Tool for Identifying Vulnerable Elders in the Community. JA GS 2001; 49: 1691-99. 6. Min LC , Elliott MN , Wenger NS et al.: Higher vulnerable elders survey scores predict death and functional decline in vulnerable older people. J Am Geriatr Soc 2006; 54: 507-11. 7. Svensson O, Stromberg L, Ohlen G et al. Prediction of the outcome after hip fracture in elderly patients. J Bone Joint Surg Br 1996; 78

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S Yakut, E Mıhcı, Clark Altiok, Z Cetin, I Keser, S Berker and G Luleci

-Killian syndrome. Prenat Diagn. 1997; 17(3): 255-265. Vermeesch JR, Melotte C, Salden I, Riegel M, Trifnov V, Polityko A, Rumyantseva N, Naumchik I, Starke H, Matthijs G, Schinzel A, Fryns JP, Liehr T. Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype. Eur J Med Genet. 2005; 48(3): 319-327. Yeung A, Francis D, Giouzeppos O, Amor DJ. Pallister-Killian syndrome caused by mosaicism for a supernumerary ring chromosome 12p. Am J Med Genet A. 2009; 149A(3): 505

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P. Malakooti Rad, S. Yassemi, Sh. Ghalandarzadeh and P. Safari

, Divisibility conditions in commutative rings with zero divisors . Comm. Algebra 38 (2002) 40314047. [10] I. Beck, Coloring of commutative rings, J. Algebra 116 (1988) 208–226. [11] A. Cannon, K. Neuerburg, S.P. Redmond, Zero-divisor graphs of nearrings and semigroups. in, Kiechle, H. Kreuzer, A., Thomsen, M.J. (Eds.), Nearrings and Nearfields, Springer, Dordrecht, The Netherlands , (2005) 189–200. [12] R. Diestel, Graph Theory . Springer-Verlag, New York, (1997). [13] Z.A. El-Bast, P.F. Smith, Multiplication modules. comm. Algebra 16 (1988

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Małgorzata Kwaśnik, Wojciech Rożek and Jan F. Żmudziński

of Bcl-2 and Abl. J Exper Med 1995 , 182 , 1545-1556 . 12. Mohsin M.A., Morris S.J., Smith H., Sweet C.: Correlation between levels of apoptosis, levels of infection and haemagglutinin receptor binding interaction of various subtypes of influenza virus: does the viral neuraminidase have a role in these associations. Virus Res 2002, 10 , 123-131. 13. Mori I., Komatsu T., Takeuchi K., Nakakuki K., Sudo M., Kimura Y.: In vivo induction of apoptosis by influenza virus. J Gen Virol 1995, 76 , 2869-2873. 14. Morris S

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S Zachaki, E Kouvidi, A Mitrakos, L Lazaros, A Pantou, A Mavrou, M Tzetis and KN Manola

been interrupted at the breakpoints [ 3 - 5 ]. Paracentric inversions can only be detected by conventional cytogenetic analysis. However, submicroscopic chromosomal imbalances at breakpoint junctions of the inverted segment can be unveiled using molecular cytogenetic techniques, such as array comparative genomic hybridization (aCGH). In this report we present a novel de novo PAI on the long arm of chromosome 20 [inv(20)(q13.1q13.3)], detected by conventional karyotyping in a 14-year-old boy with mental retardation, which was further investigated for other