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2012
P. Liu, Wang, X., Hu, C. H., and Hu, T. H., Bioinformatics analysis with graph-based clustering to detect gastric cancer-related pathways, vol. 11, pp. 3497-3504, 2012.
Altaf-Ul-Amin M, Shinbo Y, Mihara K, Kurokawa K, et al. (2006). Development and implementation of an algorithm for detection of protein complexes in large interaction networks. BMC Bioinformatics 7: 207. http://dx.doi.org/10.1186/1471-2105-7-207 PMid:16613608 PMCid:1473204   Barbero S, Mielgo A, Torres V, Teitz T, et al. (2009). Caspase-8 association with the focal adhesion complex promotes tumor cell migration and metastasis. Cancer Res. 69: 3755-3763. http://dx.doi.org/10.1158/0008-5472.CAN-08-3937 PMid:19383910 PMCid:2684981   Begnami MD, Fregnani JH, Nonogaki S and Soares FA (2010). Evaluation of cell cycle protein expression in gastric cancer: cyclin B1 expression and its prognostic implication. Hum. Pathol. 41: 1120-1127. http://dx.doi.org/10.1016/j.humpath.2010.01.007 PMid:20334896   Calcagno DQ, Leal MF, Taken SS, Assumpcao PP, et al. (2005). Aneuploidy of chromosome 8 and C-MYC amplification in individuals from northern Brazil with gastric adenocarcinoma. Anticancer Res. 25: 4069-4074. PMid:16309200   Cao HX, Li SP, Wu JZ, Gao CM, et al. (2010). Alcohol dehydrogenase-2 and aldehyde dehydrogenase-2 genotypes, alcohol drinking and the risk for stomach cancer in Chinese males. Asian Pac. J. Cancer Prev. 11: 1073-1077. PMid:21133627   Cervantes A, Rodriguez BE, Perez FA and Chirivella G, I (2007). Molecular biology of gastric cancer. Clin. Transl. Oncol. 9: 208-215. http://dx.doi.org/10.1007/s12094-007-0041-4 PMid:17462972   Choi MG, Noh JH, An JY, Hong SK, et al. (2009). Expression levels of cyclin G2, but not cyclin E, correlate with gastric cancer progression. J. Surg. Res. 157: 168-174. http://dx.doi.org/10.1016/j.jss.2008.06.020 PMid:19559447   Crew KD and Neugut AI (2006). Epidemiology of gastric cancer. World J. Gastroenterol. 12: 354-362. PMid:16489633   Cui J, Chen Y, Chou WC, Sun L, et al. (2011a). An integrated transcriptomic and computational analysis for biomarker identification in gastric cancer. Nucleic Acids Res. 39: 1197-1207. http://dx.doi.org/10.1093/nar/gkq960 PMid:20965966 PMCid:3045610   Cui J, Li F, Wang G, Fang X, et al. (2011b). Gene-expression signatures can distinguish gastric cancer grades and stages. PLoS One 6: e17819. http://dx.doi.org/10.1371/journal.pone.0017819 PMid:21445269 PMCid:3060867   Feng L, Xie Y, Zhang H and Wu Y (2012). miR-107 targets cyclin-dependent kinase 6 expression, induces cell cycle G1 arrest and inhibits invasion in gastric cancer cells. Med. Oncol. 29: 856-863. http://dx.doi.org/10.1007/s12032-011-9823-1 PMid:21264532   Fukushima A, Kusano M, Redestig H, Arita M, et al. (2011). Metabolomic correlation-network modules in Arabidopsis based on a graph-clustering approach. BMC Syst. Biol. 5: 1. http://dx.doi.org/10.1186/1752-0509-5-1 PMid:21194489 PMCid:3030539   Hong F, Breitling R, McEntee CW, Wittner BS, et al. (2006). RankProd: a bioconductor package for detecting differentially expressed genes in meta-analysis. Bioinformatics 22: 2825-2827. http://dx.doi.org/10.1093/bioinformatics/btl476 PMid:16982708   Huang dW, Sherman BT and Lempicki RA (2009). Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat. Protoc. 4: 44-57.   Ii M, Yamamoto H, Adachi Y, Maruyama Y, et al. (2006). Role of matrix metalloproteinase-7 (matrilysin) in human cancer invasion, apoptosis, growth, and angiogenesis. Exp. Biol. Med. 231: 20-27.   Inoue T, Kataoka H, Goto K, Nagaike K, et al. (2004). Activation of c-Met (hepatocyte growth factor receptor) in human gastric cancer tissue. Cancer Sci. 95: 803-808. http://dx.doi.org/10.1111/j.1349-7006.2004.tb02185.x PMid:15504247   Kanehisa M (2002). The KEGG database. Novartis Found. Symp. 247: 91-101. http://dx.doi.org/10.1002/0470857897.ch8 PMid:12539951   Kang YH, Lee HS and Kim WH (2002). Promoter methylation and silencing of PTEN in gastric carcinoma. Lab. Invest. 82: 285-291. http://dx.doi.org/10.1038/labinvest.3780422 PMid:11896207   Kawashima A, Tsugawa S, Boku A, Kobayashi M, et al. (2003). Expression of alphav integrin family in gastric carcinomas: increased alphavbeta6 is associated with lymph node metastasis. Pathol. Res. Pract. 199: 57-64. http://dx.doi.org/10.1078/0344-0338-00355 PMid:12747466   Kim DH (2007). Prognostic implications of cyclin B1, p34cdc2, p27(Kip1) and p53 expression in gastric cancer. Yonsei Med. J. 48: 694-700. http://dx.doi.org/10.3349/ymj.2007.48.4.694 PMid:17722244 PMCid:2628048   Kim J, Kim C, Kim TS, Bang SI, et al. (2006). IL-18 enhances thrombospondin-1 production in human gastric cancer via JNK pathway. Biochem. Biophys. Res. Commun. 344: 1284-1289. http://dx.doi.org/10.1016/j.bbrc.2006.04.016 PMid:16650813   Kitoh T, Yanai H, Saitoh Y, Nakamura Y, et al. (2004). Increased expression of matrix metalloproteinase-7 in invasive early gastric cancer. J. Gastroenterol. 39: 434-440. http://dx.doi.org/10.1007/s00535-003-1316-3 PMid:15175941   Kurayoshi M, Oue N, Yamamoto H, Kishida M, et al. (2006). Expression of Wnt-5a is correlated with aggressiveness of gastric cancer by stimulating cell migration and invasion. Cancer Res. 66: 10439-10448. http://dx.doi.org/10.1158/0008-5472.CAN-06-2359 PMid:17079465   Lauren P (1965). The two histological main types of gastric carcinoma: diffuse and so-called intestinal-type carcinoma. An attempt at a histo-clinical classification. Acta Pathol. Microbiol. Scand. 64: 31-49. PMid:14320675   Nishigaki M, Aoyagi K, Danjoh I, Fukaya M, et al. (2005). Discovery of aberrant expression of R-RAS by cancer-linked DNA hypomethylation in gastric cancer using microarrays. Cancer Res. 65: 2115-2124. http://dx.doi.org/10.1158/0008-5472.CAN-04-3340 PMid:15781621   Park JH, Lee BL, Yoon J, Kim J, et al. (2010). Focal adhesion kinase (FAK) gene amplification and its clinical implications in gastric cancer. Hum. Pathol. 41: 1664-1673. http://dx.doi.org/10.1016/j.humpath.2010.06.004 PMid:20869748   Pavelic K, Kolak T, Kapitanovic S, Radosevic S, et al. (2003). Gastric cancer: the role of insulin-like growth factor 2 (IGF 2) and its receptors (IGF 1R and M6-P/IGF 2R). J. Pathol. 201: 430-438. http://dx.doi.org/10.1002/path.1465 PMid:14595755   Shin CM, Kim N, Cho SI, Kim JS, et al. (2011). Association between alcohol intake and risk for gastric cancer with regard to ALDH2 genotype in the Korean population. Int. J. Epidemiol. 40: 1047-1055. http://dx.doi.org/10.1093/ije/dyr067 PMid:21507992   Smith MG, Hold GL, Tahara E and El-Omar EM (2006). Cellular and molecular aspects of gastric cancer. World J. Gastroenterol. 12: 2979-2990. PMid:16718776   Song HS, Do YR, Kim IH, Sohn SS, et al. (2004). Prognostic significance of immunohistochemical expression of EGFR and C-erbB-2 oncoprotein in curatively resected gastric cancer. Cancer Res. Treat. 36: 240-245. http://dx.doi.org/10.4143/crt.2004.36.4.240 PMid:20368841 PMCid:2843891   Stock M and Otto F (2005). Gene deregulation in gastric cancer. Gene 360: 1-19. http://dx.doi.org/10.1016/j.gene.2005.06.026 PMid:16154715   Toyokawa T, Yashiro M and Hirakawa K (2009). Co-expression of keratinocyte growth factor and K-sam is an independent prognostic factor in gastric carcinoma. Oncol. Rep. 21: 875-880. PMid:19287982   Yasui W, Oue N, Aung PP, Matsumura S, et al. (2005). Molecular-pathological prognostic factors of gastric cancer: a review. Gastric. Cancer 8: 86-94. http://dx.doi.org/10.1007/s10120-005-0320-0 PMid:15864715   Yokozaki H, Yasui W and Tahara E (2001). Genetic and epigenetic changes in stomach cancer. Int. Rev. Cytol. 204: 49-95. http://dx.doi.org/10.1016/S0074-7696(01)04003-7   Zheng L, Wang L, Ajani J and Xie K (2004). Molecular basis of gastric cancer development and progression. Gastric Cancer 7: 61-77. http://dx.doi.org/10.1007/s10120-004-0277-4 PMid:15224192
C. - L. Zhao, Wu, R., Liu, L., Li, F. - D., Zhang, X. - L., Wang, C., Wang, F., Diao, X. - L., Guan, H. - W., Wang, X., and Zhou, L., Ovine prion protein genotype frequencies in northwestern China, vol. 11, pp. 1671-1681, 2012.
Andreoletti O, Morel N, Lacroux C, Rouillon V, et al. (2006). Bovine spongiform encephalopathy agent in spleen from an ARR/ARR orally exposed sheep. J. Gen. Virol. 87: 1043-1046. http://dx.doi.org/10.1099/vir.0.81318-0 PMid:16528056 Babar ME, Abdullah M, Nadeem A and Haq AU (2009). Prion protein gene polymorphisms in four goat breeds of Pakistan. Mol. Biol. Rep. 36: 141-144. http://dx.doi.org/10.1007/s11033-007-9162-7 PMid:17934795 Baylis M, Goldmann W, Houston F, Cairns D, et al. (2002). Scrapie epidemic in a fully PrP-genotyped sheep flock. J. Gen. Virol. 83: 2907-2914. PMid:12388827 Belt PB, Muileman IH, Schreuder BE, Bos-de Ruijter J, et al. (1995). Identification of five allelic variants of the sheep PrP gene and their association with natural scrapie. J. Gen. Virol. 76: 509-517. http://dx.doi.org/10.1099/0022-1317-76-3-509 PMid:7897344 Buitkamp J and Semmer J (2004). A robust, low- to medium-throughput prnp genotyping system in sheep. BMC Infect. Dis. 4: 30. http://dx.doi.org/10.1186/1471-2334-4-30 PMid:15345029 PMCid:517712 De Vries F, Borchers N, Hamann H, Drogemuller C, et al. (2004). Associations between the prion protein genotype and performance traits of meat breeds of sheep. Vet. Rec. 155: 140-143. http://dx.doi.org/10.1136/vr.155.5.140 PMid:15338706 Goldmann W, Houston F, Stewart P, Perucchini M, et al. (2006). Ovine prion protein variant A136 R154 L168 Q171 increases resistance to experimental challenge with bovine spongiform encephalopathy agent. J. Gen. Virol. 87: 3741-3745. http://dx.doi.org/10.1099/vir.0.82083-0 PMid:17098993 Hagenaars TJ, Donnelly CA and Ferguson NM (2006). Epidemiological analysis of data for scrapie in Great Britain. Epidemiol. Infect. 134: 359-367. http://dx.doi.org/10.1017/S0950268805004966 PMid:16490141 PMCid:2870388 Humeny A, Schiebel K, Seeber S and Becker CM (2002). Identification of polymorphisms within the bovine prion protein gene (Prnp) by DNA sequencing and genotyping by MALDI-TOF-MS. Neurogenetics 4: 59-60. http://dx.doi.org/10.1007/s10048-001-0126-0 PMid:12030333 Hunter N (1997). Molecular Biology and Genetics of Scrapie in Sheep. In: The Genetics of Sheep. (Piper L and Ruvinsky A, eds.). CAB International, Wallingford, 225-240. PMid:9223132 Hunter N, Foster JD, Benson G and Hope J (1991). Restriction fragment length polymorphisms of the scrapie-associated fibril protein (PrP) gene and their association with susceptibility to natural scrapie in British sheep. J. Gen. Virol. 72: 1287-1292. http://dx.doi.org/10.1099/0022-1317-72-6-1287 PMid:1675248 Hunter N, Goldmann W, Benson G, Foster JD, et al. (1993). Swaledale sheep affected by natural scrapie differ significantly in PrP genotype frequencies from healthy sheep and those selected for reduced incidence of scrapie. J. Gen. Virol. 74: 1025-1031. http://dx.doi.org/10.1099/0022-1317-74-6-1025 PMid:8099602 Hunter N, Moore L, Hosie BD, Dingwall WS, et al. (1997). Association between natural scrapie and PrP genotype in a flock of Suffolk sheep in Scotland. Vet. Rec. 140: 59-63. http://dx.doi.org/10.1136/vr.140.3.59 PMid:9023905 Ishiguro N, Shinagawa M, Onoe S, Yamanouchi K, et al. (1998). Rapid analysis of allelic variants of the sheep PrP gene by oligonucleotide probes. Microbiol. Immunol. 42: 579-582. PMid:9776400 Lan Z, Wang ZL, Liu Y and Zhang X (2006). Prion protein gene (PRNP) polymorphisms in Xinjiang local sheep breeds in China. Arch. Virol. 151: 2095-2101. http://dx.doi.org/10.1007/s00705-006-0758-3 PMid:16622593 Langeveld JP, Jacobs JG, Erkens JH, Bossers A, et al. (2006). Rapid and discriminatory diagnosis of scrapie and BSE in retro-pharyngeal lymph nodes of sheep. BMC Vet. Res. 2: 19. http://dx.doi.org/10.1186/1746-6148-2-19 PMid:16764717 PMCid:1544330 Lee MA, Manley TR, Glass BC, Anderson RM, et al. (2007). Distribution of prion protein genotypes in breeds of sheep in New Zealand. N. Z. Vet. J. 55: 222-227. http://dx.doi.org/10.1080/00480169.2007.36772 PMid:17928898 Lezmi S, Ronzon F, Bencsik A, Bedin A, et al. (2006). PrP(d) accumulation in organs of ARQ/ARQ sheep experimentally infected with BSE by peripheral routes. Acta Biochim. Pol. 53: 399-405. PMid:16770445 Li YM and Tian B (2002). Chinese little-fat-tail sheep prion protein gene belongs to PrPARH genotype. Sheng Wu Hua Xue. Yu Sheng Wu Wu Li Xue Bao 34: 62-66. Lipsky S, Brandt H, Luhken G and Erhardt G (2008). Analysis of prion protein genotypes in relation to reproduction traits in local and cosmopolitan German sheep breeds. Anim. Reprod. Sci. 103: 69-77. http://dx.doi.org/10.1016/j.anireprosci.2006.12.005 PMid:17204379 Marcos-Carcavilla A, Moreno C, Serrano M, Laurent P, et al. (2010). Polymorphisms in the HSP90AA1 5' flanking region are associated with scrapie incubation period in sheep. Cell Stress Chaperones 15: 343-349. http://dx.doi.org/10.1007/s12192-009-0149-2 PMid:19838832 PMCid:3082647 Melchior MB, Windig JJ, Hagenaars TJ, Bossers A, et al. (2010). Eradication of scrapie with selective breeding: are we nearly there? BMC Vet. Res. 6: 24. http://dx.doi.org/10.1186/1746-6148-6-24 PMid:20441587 PMCid:2873516 Sanguinetti CJ, Dias NE and Simpson AJ (1994). Rapid silver staining and recovery of PCR products separated on polyacrylamide gels. Biotechniques 17: 914-921. PMid:7840973 Sawalha RM, Brotherstone S, Man WY, Conington J, et al. (2007). Associations of polymorphisms of the ovine prion protein gene with growth, carcass, and computerized tomography traits in Scottish Blackface lambs. J. Anim. Sci. 85: 632-640. http://dx.doi.org/10.2527/jas.2006-372 PMid:17040947 Sweeney T, Hanrahan JP and O'Doherty E (2007). Is there a relationship between prion protein genotype and ovulation rate and litter size in sheep? Anim. Reprod. Sci. 101: 153-157. http://dx.doi.org/10.1016/j.anireprosci.2006.12.004 PMid:17204381 Tongue SC, Pfeiffer DU, Warner R, Elliott H, et al. (2006). Estimation of the relative risk of developing clinical scrapie: the role of prion protein (PrP) genotype and selection bias. Vet. Rec. 158: 43-50. http://dx.doi.org/10.1136/vr.158.2.43 PMid:16415231 Tranulis MA, Osland A, Bratberg B and Ulvund MJ (1999). Prion protein gene polymorphisms in sheep with natural scrapie and healthy controls in Norway. J. Gen. Virol. 80: 1073-1077. PMid:10211978 Vaccari G, Conte M, Morelli L, Di Guardo G, et al. (2004). Primer extension assay for prion protein genotype determination in sheep. Mol. Cell Probes 18: 33-37. http://dx.doi.org/10.1016/j.mcp.2003.06.001 PMid:15036367 Vitezica ZG, Moreno CR, Lantier F, Lantier I, et al. (2007). Quantitative trait loci linked to PRNP gene controlling health and production traits in INRA 401 sheep. Genet. Sel. Evol. 39: 421-430. http://dx.doi.org/10.1186/1297-9686-39-4-421 PMid:17612481 PMCid:2682820 Vollmert C, Windl O, Xiang W, Rosenberger A, et al. (2006). Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study. J. Med. Genet. 43: e53. http://dx.doi.org/10.1136/jmg.2006.040931 PMid:17047093 PMCid:2563174 Zhang L, Li N, Fan B, Fang M, et al. (2004). PRNP polymorphisms in Chinese ovine, caprine and bovine breeds. Anim. Genet. 35: 457-461. http://dx.doi.org/10.1111/j.1365-2052.2004.01204.x PMid:15566469 Zhou H, Hickford JG and Fang Q (2005). Technical note: determination of alleles of the ovine PRNP gene using PCR-single-strand conformational polymorphism analysis. J. Anim. Sci. 83: 745-749. PMid:15753327 Zsolnai A, Anton I, Kuhn C and Fesus L (2003). Detection of single-nucleotide polymorphisms coding for three ovine prion protein variants by primer extension assay and capillary electrophoresis. Electrophoresis 24: 634-638. http://dx.doi.org/10.1002/elps.200390074 PMid:12601731
2011
B. K. Li, Ding, Q., Wan, X. D., and Wang, X., Clinical and genetic characterization of complete androgen insensitivity syndrome in a Chinese family, vol. 10, pp. 1022-1031, 2011.
Ahmed SF, Cheng A, Dovey L, Hawkins JR, et al. (2000). Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome. J. Clin. Endocrinol. Metab. 85: 658-665. doi:10.1210/jc.85.2.658 Alvarez NR, Lee TM and Solorzano CC (2005). Complete androgen insensitivity syndrome: the role of the endocrine surgeon. Am. Surg. 71: 241-243. PMid:15869141 Avila DM, Wilson CM, Nandi N, Griffin JE, et al. (2002). Immunoreactive AR and genetic alterations in subjects with androgen resistance and undetectable AR levels in genital skin fibroblast ligand-binding assays. J. Clin. Endocrinol. Metab. 87: 182-188. doi:10.1210/jc.87.1.182 Beitel LK, Prior L, Vasiliou DM, Gottlieb B, et al. (1994). Complete androgen insensitivity due to mutations in the probable alpha-helical segments of the DNA-binding domain in the human androgen receptor. Hum. Mol. Genet. 3: 21-27. doi:10.1093/hmg/3.1.21 PMid:8162033 Brinkmann AO (2001). Molecular basis of androgen insensitivity. Mol. Cell. Endocrinol. 179: 105-109. doi:10.1016/S0303-7207(01)00466-X Cheikhelard A, Morel Y, Thibaud E, Lortat-Jacob S, et al. (2008). Long-term followup and comparison between genotype and phenotype in 29 cases of complete androgen insensitivity syndrome. J. Urol. 180: 1496-1501. doi:10.1016/j.juro.2008.06.045 PMid:18710728 Cools M, Looijenga LH, Wolffenbuttel KP and Drop SL (2009). Disorders of sex development: update on the genetic background, terminology and risk for the development of germ cell tumors. World J. Pediatr. 5: 93-102. doi:10.1007/s12519-009-0020-7 PMid:19718530 Fogu G, Bertini V, Dessole S, Bandiera P, et al. (2003). Identification of a mutant allele of the androgen receptor gene in a family with androgen insensitivity syndrome: detection of carriers and prenatal diagnosis. Arch. Gynecol. Obstet. 269: 25-29. doi:10.1007/s00404-002-0386-4 PMid:14605819 Gottlieb B, Beitel LK, Wu JH and Trifiro M (2004). The androgen receptor gene mutations database (ARDB): 2004 update. Hum. Mutat. 23: 527-533. doi:10.1002/humu.20044 PMid:15146455 Hashmi A, Hanif F, Hanif SM, Abdullah FE, et al. (2008). Complete androgen insensitivity syndrome. J. Coll. Phys. Surg. Pak. 18: 442-444. PMid:18760072 Jaaskelainen J, Mongan NP, Harland S and Hughes IA (2006). Five novel androgen receptor gene mutations associated with complete androgen insensitivity syndrome. Hum. Mutat. 27: 291. doi:10.1002/humu.9405 PMid:16470553 MacLean HE, Ball EM, Rekaris G, Warne GL, et al. (2004). Novel androgen receptor gene mutations in Australian patients with complete androgen insensitivity syndrome. Hum. Mutat. 23: 287. doi:10.1002/humu.9221 PMid:14974091 MacLean HE, Favaloro JM, Warne GL and Zajac JD (2006). Double-strand DNA break repair with replication slippage on two strands: a novel mechanism of deletion formation. Hum. Mutat. 27: 483-489. doi:10.1002/humu.20327 PMid:16619235 McPhaul MJ, Marcelli M, Zoppi S, Griffin JE, et al. (1993). Genetic basis of endocrine disease. 4. The spectrum of mutations in the androgen receptor gene that causes androgen resistance. J. Clin. Endocrinol. Metab. 76: 17-23. doi:10.1210/jc.76.1.17 Melo KF, Mendonca BB, Billerbeck AE, Costa EM, et al. (2003). Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitivity syndrome in a Brazilian cohort: five novel mutations in the androgen receptor gene. J. Clin. Endocrinol. Metab. 88: 3241-3250. doi:10.1210/jc.2002-021658 Nitsche EM and Hiort O (2000). The molecular basis of androgen insensitivity. Horm. Res. 54: 327-333. doi:10.1159/000053282 PMid:11595828 Oakes MB, Eyvazzadeh AD, Quint E and Smith YR (2008). Complete androgen insensitivity syndrome--a review. J. Pediatr. Adolesc. Gynecol. 21: 305-310. doi:10.1016/j.jpag.2007.09.006 PMid:19064222 Quigley CA, De Bellis A, Marschke KB, el-Awady MK, et al. (1995). Androgen receptor defects: historical, clinical, and molecular perspectives. Endocr. Rev. 16: 271-321. PMid:7671849 Quigley CA, Tan JA, He B, Zhou ZX, et al. (2004). Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH(2)- and carboxyl-terminal interaction. Mech. Ageing Dev. 125: 683-695. doi:10.1016/j.mad.2004.08.007 PMid:15541764 Ris-Stalpers C, Verleun-Mooijman MC, de Blaeij TJ, Degenhart HJ, et al. (1994). Differential splicing of human androgen receptor pre-mRNA in X-linked Reifenstein syndrome, because of a deletion involving a putative branch site. Am. J. Hum. Genet. 54: 609-617. PMid:8128958    PMCid:1918097 Ross GT (1985). Disorders of the Ovary and Female Reproductive Tract. 7th edn. In: William Textbook of Endocrinology (Wilson JD and Foster DW, eds.). Saunders WB, Philadelphia, 206-258. Tian QJ, Dai ZQ, Yu W, Tian JP, et al. (2005). Study of bone mineral density in complete androgen insensitivity syndrome patients. Zhonghua Fu Chan Ke Za Zhi 40: 799-802. PMid:16412322 Ulloa-Aguirre A, Carranza-Lira S, Mendez JP, Angeles A, et al. (1990). Incomplete regression of mullerian ducts in the androgen insensitivity syndrome. Fertil. Steril. 53: 1024-1028. PMid:2112490 Wilson JD, Leihy MW, Shaw G and Renfree MB (2002). Androgen physiology: unsolved problems at the millennium. Mol. Cell. Endocrinol. 198: 1-5. doi:10.1016/S0303-7207(02)00362-3

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