Publications
Found 2 results
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“R620W functional polymorphism of protein tyrosine phosphatase non-receptor type 22 is not associated with pulmonary tuberculosis in Zahedan, southeast Iran”, vol. 11, pp. 1075-1081, 2012.
, Ban Y, Tozaki T, Taniyama M and Tomita M (2005). The codon 620 single nucleotide polymorphism of the protein tyrosine phosphatase-22 gene does not contribute to autoimmune thyroid disease susceptibility in the Japanese. Thyroid 15: 1115-1118.
http://dx.doi.org/10.1089/thy.2005.15.1115
PMid:16279843
Begovich AB, Carlton VE, Honigberg LA, Schrodi SJ, et al. (2004). A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. Am. J. Hum. Genet. 75: 330-337.
http://dx.doi.org/10.1086/422827
PMid:15208781
Bellamy R, Beyers N, McAdam KP, Ruwende C, et al. (2000). Genetic susceptibility to tuberculosis in Africans: a genome-wide scan. Proc. Natl. Acad. Sci. U. S. A. 97: 8005-8009.
http://dx.doi.org/10.1073/pnas.140201897
PMid:10859364
Bottini N, Musumeci L, Alonso A, Rahmouni S, et al. (2004). A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes. Nat. Genet. 36: 337-338.
http://dx.doi.org/10.1038/ng1323
PMid:15004560
Bravo MJ, Colmenero JD, Queipo-Ortuno MI, Morata P, et al. (2009). PTPN22 C1858T polymorphism and human brucellosis. Scand J. Infect. Dis. 41: 109-112.
http://dx.doi.org/10.1080/00365540802641864
PMid:19107641
Cervino AC, Lakiss S, Sow O, Bellamy R, et al. (2002). Fine mapping of a putative tuberculosis-susceptibility locus on chromosome 15q11-13 in African families. Hum. Mol. Genet. 11: 1599-1603.
http://dx.doi.org/10.1093/hmg/11.14.1599
PMid:12075004
Chabchoub G, Maalej A, Petit-Teixeira E, Glikmans E, et al. (2006). Polymorphisms in the protein tyrosine phosphatase (PTPN22) gene is not associated with autoimmune thyroid in a large affected Tunisian family. Clin. Immunol. 120: 235-236.
http://dx.doi.org/10.1016/j.clim.2006.04.565
PMid:16765647
Chabchoub G, Teixiera EP, Maalej A, Ben HM, et al. (2009). The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population. Ann. Hum. Biol. 36: 342-349.
http://dx.doi.org/10.1080/03014460902817968
PMid:19343596
Chelala C, Duchatelet S, Joffret ML, Bergholdt R, et al. (2007). PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits. Diabetes 56: 522-526.
http://dx.doi.org/10.2337/db06-0942
PMid:17259401
Cohen S, Dadi H, Shaoul E, Sharfe N, et al. (1999). Cloning and characterization of a lymphoid-specific, inducible human protein tyrosine phosphatase, Lyp. Blood 93: 2013-2024.
Comstock GW (1978). Tuberculosis in twins: a re-analysis of the Prophit survey. Am. Rev. Respir. Dis. 117: 621-624.
PMid:565607
Douroudis K, Prans E, Haller K, Nemvalts V, et al. (2008). Protein tyrosine phosphatase non-receptor type 22 gene variants at position 1858 are associated with type 1 and type 2 diabetes in Estonian population. Tissue Antigens 72: 425-430.
http://dx.doi.org/10.1111/j.1399-0039.2008.01115.x
PMid:18764813
Gomez LM, Anaya JM, Gonzalez CI, Pineda-Tamayo R, et al. (2005a). PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases. Genes Immun. 6: 628-631.
http://dx.doi.org/10.1038/sj.gene.6364261
PMid:16163373
Gomez LM, Anaya JM and Martin J (2005b). Genetic influence of PTPN22 R620W polymorphism in tuberculosis. Hum. Immunol. 66: 1242-1247.
http://dx.doi.org/10.1016/j.humimm.2005.11.008
PMid:16690411
Guide SV and Holland SM (2002). Host susceptibility factors in mycobacterial infection. Genetics and body morphotype. Infect. Dis. Clin. North Am. 16: 163-186.
http://dx.doi.org/10.1016/S0891-5520(03)00051-5
Hashemi M, Moazeni-Roodi AK, Fazaeli A, Sandoughi M, et al. (2010a). Lack of association between paraoxonase-1 Q192R polymorphism and rheumatoid arthritis in southeast Iran. Genet. Mol. Res. 9: 333-339.
http://dx.doi.org/10.4238/vol9-1gmr728
PMid:20198589
Hashemi M, Moazeni-Roodi AK, Fazaeli A, Sandoughi M, et al. (2010b). The L55M polymorphism of paraoxonase-1 is a risk factor for rheumatoid arthritis. Genet. Mol. Res. 9: 1735-1741.
http://dx.doi.org/10.4238/vol9-3gmr893
PMid:20812194
Hashemi M, Hoseini H, Yaghmaei P, Moazeni-Roodi A, et al. (2011a). Association of polymorphisms in glutamate-cysteine ligase catalytic subunit and microsomal triglyceride transfer protein genes with nonalcoholic fatty liver disease. DNA Cell Biol. 30: 569-575.
http://dx.doi.org/10.1089/dna.2010.1162
PMid:21438662
Hashemi M, Sharifi-Mood B, Nezamdoost M, Moazeni-Roodi A, et al. (2011b). Functional polymorphism of interferon-gamma (IFN-gamma) gene +874T/A polymorphism is associated with pulmonary tuberculosis in Zahedan, Southeast Iran. Prague Med. Rep. 112: 38-43.
PMid:21470497
Hermiston ML, Xu Z, Majeti R and Weiss A (2002). Reciprocal regulation of lymphocyte activation by tyrosine kinases and phosphatases. J. Clin. Invest. 109: 9-14.
PMid:11781344 PMCid:150828
Hill RJ, Zozulya S, Lu YL, Ward K, et al. (2002). The lymphoid protein tyrosine phosphatase Lyp interacts with the adaptor molecule Grb2 and functions as a negative regulator of T-cell activation. Exp. Hematol. 30: 237-244.
http://dx.doi.org/10.1016/S0301-472X(01)00794-9
Hinks A, Worthington J and Thomson W (2006). The association of PTPN22 with rheumatoid arthritis and juvenile idiopathic arthritis. Rheumatology 45: 365-368.
http://dx.doi.org/10.1093/rheumatology/kel005
PMid:16418195
Ikegami H, Kawabata Y, Noso S, Fujisawa T, et al. (2007). Genetics of type 1 diabetes in Asian and Caucasian populations. Diabetes Res. Clin. Pract. 77 (Suppl 1): S116-S121.
http://dx.doi.org/10.1016/j.diabres.2007.01.044
PMid:17452059
Jagiello P, Aries P, Arning L, Wagenleiter SE, et al. (2005). The PTPN22 620W allele is a risk factor for Wegener’s granulomatosis. Arthritis Rheum. 52: 4039-4043.
http://dx.doi.org/10.1002/art.21487
Lamsyah H, Rueda B, Baassi L, Elaouad R, et al. (2009). Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population. Tissue Antigens 74: 228-232.
http://dx.doi.org/10.1111/j.1399-0039.2009.01304.x
PMid:19563523
Lee YH, Rho YH, Choi SJ, Ji JD, et al. (2007). The PTPN22 C1858T functional polymorphism and autoimmune diseases - a meta-analysis. Rheumatology 46: 49-56.
http://dx.doi.org/10.1093/rheumatology/kel170
PMid:16760194
Mori M, Yamada R, Kobayashi K, Kawaida R, et al. (2005). Ethnic differences in allele frequency of autoimmune-disease-associated SNPs. J. Hum. Genet. 50: 264-266.
http://dx.doi.org/10.1007/s10038-005-0246-8
PMid:15883854
Mustelin T, Brockdorff J, Rudbeck L, Gjorloff-Wingren A, et al. (1999). The next wave: protein tyrosine phosphatases enter T cell antigen receptor signalling. Cell Signal. 11: 637-650.
http://dx.doi.org/10.1016/S0898-6568(99)00016-9
Mustelin T, Abraham RT, Rudd CE, Alonso A, et al. (2002). Protein tyrosine phosphorylation in T cell signaling. Front Biosci. 7: d918-d969.
http://dx.doi.org/10.2741/musteli1
PMid:11897562
Naderi M, Hashemi M, Kouhpayeh H and Ahmadi R (2009). The status of serum procalcitonin in pulmonary tuberculosis and nontuberculosis pulmonary disease. J. Pak. Med. Assoc. 59: 647-648.
PMid:19750868
Naderi M, Hashemi M, Mehdizadeh A and Mehrabifar H (2010). Serum adenosine deaminase activity and total antioxidant capacity of plasma in pulmonary tuberculosis and non-tuberculosis pulmonary disease. Turk. J. Med. Sci. 40: 701-706.
North RJ and Jung YJ (2004). Immunity to tuberculosis. Annu. Rev. Immunol. 22: 599-623.
http://dx.doi.org/10.1146/annurev.immunol.22.012703.104635
PMid:15032590
Orozco G, Sanchez E, Gonzalez-Gay MA, Lopez-Nevot MA, et al. (2005). Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus. Arthritis Rheum. 52: 219-224.
http://dx.doi.org/10.1002/art.20771
Porter JD and McAdam KP (1994). The re-emergence of tuberculosis. Annu. Rev. Public Health 15: 303-323.
http://dx.doi.org/10.1146/annurev.pu.15.050194.001511
PMid:8054087
Qu HQ, Fisher-Hoch SP and McCormick JB (2011). Molecular immunity to mycobacteria: knowledge from the mutation and phenotype spectrum analysis of Mendelian susceptibility to mycobacterial diseases. Int. J. Infect. Dis. 15: e305-e313.
http://dx.doi.org/10.1016/j.ijid.2011.01.004
PMid:21330176 PMCid:3078969
Reddy MV, Johansson M, Sturfelt G, Jonsen A, et al. (2005). The R620W C/T polymorphism of the gene PTPN22 is associated with SLE independently of the association of PDCD1. Genes Immun. 6: 658-662.
PMid:16052172
Seldin MF, Shigeta R, Laiho K, Li H, et al. (2005). Finnish case-control and family studies support PTPN22 R620W polymorphism as a risk factor in rheumatoid arthritis, but suggest only minimal or no effect in juvenile idiopathic arthritis. Genes Immun. 6: 720-722.
PMid:16107870
Veillette A, Latour S and Davidson D (2002). Negative regulation of immunoreceptor signaling. Annu. Rev. Immunol. 20: 669-707.
http://dx.doi.org/10.1146/annurev.immunol.20.081501.130710
PMid:11861615
Wipff J, Allanore Y, Kahan A, Meyer O, et al. (2006). Lack of association between the protein tyrosine phosphatase non-receptor 22 (PTPN22)*620W allele and systemic sclerosis in the French Caucasian population. Ann. Rheum. Dis. 65: 1230-1232.
http://dx.doi.org/10.1136/ard.2005.048181
PMid:16464986 PMCid:1798267
Zhang ZH, Chen F, Zhang XL, Jin Y, et al. (2008). PTPN22 allele polymorphisms in 15 Chinese populations. Int. J. Immunogenet. 35: 433-437.
http://dx.doi.org/10.1111/j.1744-313X.2008.00803.x
PMid:19046301
“mtDNA variation of the critically endangered hawksbill turtle (Eretmochelys imbricata) nesting on Iranian islands of the Persian Gulf”, vol. 10, pp. 1499-1503, 2011.
, Baillie J and Groombridge B (1996). IUCN Red List of Threatened Animals. IUCN, Gland, Switzerland and Cambridge.
Bass AL (1996). Application of Isolation by Distance Models to Hawksbill Turtle (Eretmochelys imbricata) Nesting Sites in the Caribbean. In: Proceedings of the International Symposium on Sea Turtle Conservation Genetics (Bowen BW and Witzell WN, eds.). NOAA Technical Memorandum. National Marine Fisheries Service, Southeast Fisheries Science Center, 396, Miami, 41-46.
Bourjea J, Lapegue S, Gagnevin L, Broderick D, et al. (2007). Phylogeography of the green turtle, Chelonia mydas, in the Southwest Indian Ocean. Mol. Ecol. 16: 175-186.
doi:10.1111/j.1365-294X.2006.03122.x
PMid:17181729
Bowen BW (2003). What is a Loggerhead Turtle? The Genetic Perspective. In: Loggerhead Sea Turtles (Bolten AB and Witherington BE, eds.). Smithsonian Institution Press, Washington, 7-27.
Bowen BW and Karl SA (2007). Population genetics and phylogeography of sea turtles. Mol. Ecol. 16: 4886-4907.
doi:10.1111/j.1365-294X.2007.03542.x
PMid:17944856
Bowen BW, Avise JC, Richardson JI, Meylan AB, et al. (1993). Population structure of loggerhead turtles (Caretta caretta) in the northwestern Atlantic Ocean and Mediterranean Sea. Conserv. Biol. 7: 834-844.
doi:10.1046/j.1523-1739.1993.740834.x
Bowen BW, Bass AL, Garcia-Rodriguez A, Diez CE, et al. (1996). Origin of hawksbill turtles in a Caribbean feeding area as indicated by genetic markers. Ecol. Appl. 6: 566-572.
doi:10.2307/2269392
Broderick D and Moritz C (1996). Hawksbill Breeding and Foraging Populations in the Indo-Pacific Region. In: Proceedings of the International Symposium on Sea Turtle Conservation Genetics (Bowen BW and Witzell WN, eds.). NOAA Technical Memorandum. National Marine Fisheries Service, Southeast Fisheries Science Center, 396, Miami, 119-128.
Broderick D, Moritz C, Miller JD, Guine M, et al. (1994). Genetic studies of the Hawksbill turtle (Eretmochelys imbricate): evidence for multiple stocks in Australian waters. Pacific Conserv. Biol. 1: 123-131.
Encalada SE, Bjorndal KA, Bolten AB, Zurita JC, et al. (1998). Population structure of loggerhead turtle (Caretta caretta) nesting colonies in the Atlantic and Mediterranean as inferred from mitochondrial DNA control region sequences. Mar. Biol. 130: 567-575.
doi:10.1007/s002270050278
Groombridge B and Luxmoore R (1989). The Green Turtle and Hawksbill (Reptilia: Cheloniidae): World Status, Exploitation, and Trade. CITES Secretatiat, Lausanne.
Hillis DM and Moritz C (1990). Molecular Taxonomy. Sinauer Associates Inc. Publishers, Sanderland.
Hirayama R (1998). Oldest known sea turtle. Nature 392: 705-708.
doi:10.1038/33669
IUCN (1968). Classifications of Rare and Endangered Forms. In: Survival Service Commission Red Data Book. IUCN, Morges.
IUCN (2009). The IUCN Red List of Threatened Species. Available at [http://www.iucnredlist.org]. Accessed July 2011.
Kinunen W and Walczak PS (1971). Persian Gulf Sea Turtle Nesting Surveys. Job Completion Rept., Division of Research Development, F7-F50.
Koike H, Okayama T, Baba Y, Diaz R, et al. (1996). Conservation Genetics for the CITES-Listed Animals - Mitochondrial DNA Analysis Using the Scutes of Hawksbill Turtles. International Symposium on Network and Evolution of Molecular Information, Tokyo.
Lara-Ruiz P, Lopez GG, Santos FR and Soares LS (2006). Extensive hybridization in hawksbill turtles (Eretmochelys imbricata) nesting in Brazil revealed by mtDNA analyses. Conserv. Genet. 7: 773-781.
doi:10.1007/s10592-005-9102-9
Laurent L, Casale P, Bradai MN, Godley BJ, et al. (1998). Molecular resolution of marine turtle stock composition in fishery bycatch: a case study in the Mediterranean. Mol. Ecol. 7: 1529-1542.
doi:10.1046/j.1365-294x.1998.00471.x
PMid:9819906
Maffucci F, Kooistra WHCF and Bentivegna F (2006). Natal origin of loggerhead turtles, Caretta caretta, in the neritic habitat off the Italian coasts, Central Mediterranean. Biol. Conserv. 127: 183-189.
doi:10.1016/j.biocon.2005.08.009
Mobaraki A (2004). Nesting of the hawksbill turtle in Shidvar Island, Hormozgan Province, Iran. Mar. Turtle Newsl. 103: 13.
Okayama T, Diaz R, Koike H, Diez CE, et al. (1996). Mitochondrial DNA Analysis of the Hawksbill Turtle. I. Haplotype Detection Among Samples in the Pacific and Atlantic Oceans. International Symposium on Network and Evolution of Molecular Information, Tokyo.
Okayama T, Diaz-Fernandez R, Baba Y, Halim M, et al. (1999). Genetic diversity of the hawksbill turtle in the Indo- Pacific and Caribbean regions. Chelonian Conserv. Biol. 3: 362-367.
Pritchard PCH (1996). Evolution, Phylogeny and Current Status. In: The Biology of Sea Turtles (Lutz PL and Musick JA, eds.). CRC Press, Florida, 1-28.
Schroth W, Streit B and Schierwater B (1996). Evolutionary handicap for turtles. Nature 384: 521-522.
doi:10.1038/384521a0
Thompson JD, Higgins DG and Gibson TJ (1994). CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 22: 4673-4680.
doi:10.1093/nar/22.22.4673
PMid:7984417 PMCid:308517
Velez-Zuazo X, Ramos WD, van Dam RP, Diez CE, et al. (2008). Dispersal, recruitment and migratory behaviour in a hawksbill sea turtle aggregation. Mol. Ecol. 17: 839-853.
doi:10.1111/j.1365-294X.2007.03635.x
PMid:18208487