-
1
-
-
0035899256
-
Clinical practice. Subclinical hyperthyroidism
-
Toft AD, (2001) Clinical practice. Subclinical hyperthyroidism. N Engl J Med 345: 512-516.
-
(2001)
N Engl J Med
, vol.345
, pp. 512-516
-
-
Toft, A.D.1
-
2
-
-
0035954660
-
Clinical practice. Subclinical hypothyroidism
-
Cooper DS, (2001) Clinical practice. Subclinical hypothyroidism. N Engl J Med 345: 260-265.
-
(2001)
N Engl J Med
, vol.345
, pp. 260-265
-
-
Cooper, D.S.1
-
3
-
-
33748749271
-
Thyroid function is intrinsically linked to insulin sensitivity and endothelium-dependent vasodilation in healthy euthyroid subjects
-
Fernandez-Real JM, Lopez-Bermejo A, Castro A, Casamitjana R, Ricart W, (2006) Thyroid function is intrinsically linked to insulin sensitivity and endothelium-dependent vasodilation in healthy euthyroid subjects. J Clin Endocrinol Metab 91: 3337-3343.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 3337-3343
-
-
Fernandez-Real, J.M.1
Lopez-Bermejo, A.2
Castro, A.3
Casamitjana, R.4
Ricart, W.5
-
4
-
-
39149116328
-
The clinical significance of subclinical thyroid dysfunction
-
Biondi B, Cooper DS, (2008) The clinical significance of subclinical thyroid dysfunction. Endocr Rev 29: 76-131.
-
(2008)
Endocr Rev
, vol.29
, pp. 76-131
-
-
Biondi, B.1
Cooper, D.S.2
-
5
-
-
67650233318
-
Minireview: Thyrotropin-releasing hormone and the thyroid hormone feedback mechanism
-
Chiamolera MI, Wondisford FE, (2009) Minireview: Thyrotropin-releasing hormone and the thyroid hormone feedback mechanism. Endocrinology 150: 1091-1096.
-
(2009)
Endocrinology
, vol.150
, pp. 1091-1096
-
-
Chiamolera, M.I.1
Wondisford, F.E.2
-
6
-
-
0036959745
-
Narrow individual variations in serum T(4) and T(3) in normal subjects: a clue to the understanding of subclinical thyroid disease
-
Andersen S, Pedersen KM, Bruun NH, Laurberg P, (2002) Narrow individual variations in serum T(4) and T(3) in normal subjects: a clue to the understanding of subclinical thyroid disease. J Clin Endocrinol Metab 87: 1068-1072.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 1068-1072
-
-
Andersen, S.1
Pedersen, K.M.2
Bruun, N.H.3
Laurberg, P.4
-
7
-
-
0036774549
-
Large differences in incidences of overt hyper- and hypothyroidism associated with a small difference in iodine intake: a prospective comparative register-based population survey
-
Bulow Pedersen I, Knudsen N, Jorgensen T, Perrild H, Ovesen L, et al. (2002) Large differences in incidences of overt hyper- and hypothyroidism associated with a small difference in iodine intake: a prospective comparative register-based population survey. J Clin Endocrinol Metab 87: 4462-4469.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 4462-4469
-
-
Bulow Pedersen, I.1
Knudsen, N.2
Jorgensen, T.3
Perrild, H.4
Ovesen, L.5
-
8
-
-
0022341972
-
The influence of age and sex on tests of thyroid function
-
Franklyn JA, Ramsden DB, Sheppard MC, (1985) The influence of age and sex on tests of thyroid function. Ann Clin Biochem 22 (Pt 5) (): 502-505.
-
(1985)
Ann Clin Biochem
, vol.22
, Issue.Pt 5
, pp. 502-505
-
-
Franklyn, J.A.1
Ramsden, D.B.2
Sheppard, M.C.3
-
9
-
-
0029872887
-
Measurement of serum free thyroid hormone concentrations: an essential tool for the diagnosis of thyroid dysfunction
-
Bartalena L, Bogazzi F, Brogioni S, Burelli A, Scarcello G, et al. (1996) Measurement of serum free thyroid hormone concentrations: an essential tool for the diagnosis of thyroid dysfunction. Horm Res 45: 142-147.
-
(1996)
Horm Res
, vol.45
, pp. 142-147
-
-
Bartalena, L.1
Bogazzi, F.2
Brogioni, S.3
Burelli, A.4
Scarcello, G.5
-
10
-
-
1642323634
-
Major genetic influence on the regulation of the pituitary-thyroid axis: a study of healthy Danish twins
-
Hansen PS, Brix TH, Sorensen TI, Kyvik KO, Hegedus L, (2004) Major genetic influence on the regulation of the pituitary-thyroid axis: a study of healthy Danish twins. J Clin Endocrinol Metab 89: 1181-1187.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 1181-1187
-
-
Hansen, P.S.1
Brix, T.H.2
Sorensen, T.I.3
Kyvik, K.O.4
Hegedus, L.5
-
11
-
-
3242662350
-
Genetic and environmental influences on thyroid hormone variation in Mexican Americans
-
Samollow PB, Perez G, Kammerer CM, Finegold D, Zwartjes PW, et al. (2004) Genetic and environmental influences on thyroid hormone variation in Mexican Americans. J Clin Endocrinol Metab 89: 3276-3284.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 3276-3284
-
-
Samollow, P.B.1
Perez, G.2
Kammerer, C.M.3
Finegold, D.4
Zwartjes, P.W.5
-
12
-
-
40749123615
-
Heritability of serum TSH, free T4 and free T3 concentrations: a study of a large UK twin cohort
-
Panicker V, Wilson SG, Spector TD, Brown SJ, Falchi M, et al. (2008) Heritability of serum TSH, free T4 and free T3 concentrations: a study of a large UK twin cohort. Clin Endocrinol (Oxf) 68: 652-659.
-
(2008)
Clin Endocrinol (Oxf)
, vol.68
, pp. 652-659
-
-
Panicker, V.1
Wilson, S.G.2
Spector, T.D.3
Brown, S.J.4
Falchi, M.5
-
13
-
-
44449164338
-
Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function
-
Arnaud-Lopez L, Usala G, Ceresini G, Mitchell BD, Pilia MG, et al. (2008) Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function. Am J Hum Genet 82: 1270-1280.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 1270-1280
-
-
Arnaud-Lopez, L.1
Usala, G.2
Ceresini, G.3
Mitchell, B.D.4
Pilia, M.G.5
-
14
-
-
77956353609
-
A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study
-
Panicker V, Wilson SG, Walsh JP, Richards JB, Brown SJ, et al. (2010) A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study. Am J Hum Genet 87: 430-435.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 430-435
-
-
Panicker, V.1
Wilson, S.G.2
Walsh, J.P.3
Richards, J.B.4
Brown, S.J.5
-
15
-
-
84864035207
-
Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function
-
Rawal R, Teumer A, Volzke H, Wallaschofski H, Ittermann T, et al. (2012) Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function. Hum Mol Genet.
-
(2012)
Hum Mol Genet
-
-
Rawal, R.1
Teumer, A.2
Volzke, H.3
Wallaschofski, H.4
Ittermann, T.5
-
16
-
-
0037563907
-
Polymorphisms in thyroid hormone pathway genes are associated with plasma TSH and iodothyronine levels in healthy subjects
-
Peeters RP, van Toor H, Klootwijk W, de Rijke YB, Kuiper GG, et al. (2003) Polymorphisms in thyroid hormone pathway genes are associated with plasma TSH and iodothyronine levels in healthy subjects. J Clin Endocrinol Metab 88: 2880-2888.
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 2880-2888
-
-
Peeters, R.P.1
van Toor, H.2
Klootwijk, W.3
de Rijke, Y.B.4
Kuiper, G.G.5
-
17
-
-
49249115232
-
A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine
-
Panicker V, Cluett C, Shields B, Murray A, Parnell KS, et al. (2008) A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine. J Clin Endocrinol Metab 93: 3075-3081.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 3075-3081
-
-
Panicker, V.1
Cluett, C.2
Shields, B.3
Murray, A.4
Parnell, K.S.5
-
18
-
-
79955549824
-
A large-scale association analysis of 68 thyroid hormone pathway genes with serum TSH and FT4 levels
-
Medici M, van der Deure WM, Verbiest M, Vermeulen SH, Hansen PS, et al. (2011) A large-scale association analysis of 68 thyroid hormone pathway genes with serum TSH and FT4 levels. Eur J Endocrinol 164: 781-788.
-
(2011)
Eur J Endocrinol
, vol.164
, pp. 781-788
-
-
Medici, M.1
van der Deure, W.M.2
Verbiest, M.3
Vermeulen, S.H.4
Hansen, P.S.5
-
19
-
-
63449092713
-
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations
-
Gudmundsson J, Sulem P, Gudbjartsson DF, Jonasson JG, Sigurdsson A, et al. (2009) Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. Nat Genet 41: 460-464.
-
(2009)
Nat Genet
, vol.41
, pp. 460-464
-
-
Gudmundsson, J.1
Sulem, P.2
Gudbjartsson, D.F.3
Jonasson, J.G.4
Sigurdsson, A.5
-
20
-
-
80053896220
-
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies
-
Denny JC, Crawford DC, Ritchie MD, Bielinski SJ, Basford MA, et al. (2011) Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies. Am J Hum Genet 89: 529-542.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 529-542
-
-
Denny, J.C.1
Crawford, D.C.2
Ritchie, M.D.3
Bielinski, S.J.4
Basford, M.A.5
-
21
-
-
78651283161
-
An approach for development of age-, gender-, and ethnicity-specific thyrotropin reference limits
-
Boucai L, Hollowell JG, Surks MI, (2011) An approach for development of age-, gender-, and ethnicity-specific thyrotropin reference limits. Thyroid 21: 5-11.
-
(2011)
Thyroid
, vol.21
, pp. 5-11
-
-
Boucai, L.1
Hollowell, J.G.2
Surks, M.I.3
-
22
-
-
54049135312
-
The incidence of autoimmune thyroid disease: a systematic review of the literature
-
McGrogan A, Seaman HE, Wright JW, de Vries CS, (2008) The incidence of autoimmune thyroid disease: a systematic review of the literature. Clin Endocrinol (Oxf) 69: 687-696.
-
(2008)
Clin Endocrinol (Oxf)
, vol.69
, pp. 687-696
-
-
McGrogan, A.1
Seaman, H.E.2
Wright, J.W.3
de Vries, C.S.4
-
23
-
-
0036173697
-
Serum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III)
-
Hollowell JG, Staehling NW, Flanders WD, Hannon WH, Gunter EW, et al. (2002) Serum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III). J Clin Endocrinol Metab 87: 489-499.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 489-499
-
-
Hollowell, J.G.1
Staehling, N.W.2
Flanders, W.D.3
Hannon, W.H.4
Gunter, E.W.5
-
24
-
-
0001677717
-
Controlling the false discovery rate: a practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y, (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. Journal of the Royal Statistical Society Series B 57: 289-300.
-
(1995)
Journal of the Royal Statistical Society Series B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
25
-
-
17444384218
-
The expression of calpain 1 and calpain 2 in spermatogenic cells and spermatozoa of the mouse
-
Ben-Aharon I, Brown PR, Etkovitz N, Eddy EM, Shalgi R, (2005) The expression of calpain 1 and calpain 2 in spermatogenic cells and spermatozoa of the mouse. Reproduction 129: 435-442.
-
(2005)
Reproduction
, vol.129
, pp. 435-442
-
-
Ben-Aharon, I.1
Brown, P.R.2
Etkovitz, N.3
Eddy, E.M.4
Shalgi, R.5
-
26
-
-
33748039452
-
Heritability of cardiovascular and personality traits in 6,148 Sardinians
-
doi: 10.1371/journal.pgen.0020132
-
Pilia G, Chen WM, Scuteri A, Orru M, Albai G, et al. (2006) Heritability of cardiovascular and personality traits in 6,148 Sardinians. PLoS Genet 2: e132 doi:10.1371/journal.pgen.0020132.
-
(2006)
PLoS Genet
, vol.2
-
-
Pilia, G.1
Chen, W.M.2
Scuteri, A.3
Orru, M.4
Albai, G.5
-
27
-
-
70449096468
-
Phosphodiesterase 8B gene polymorphism is associated with subclinical hypothyroidism in pregnancy
-
Shields BM, Freathy RM, Knight BA, Hill A, Weedon MN, et al. (2009) Phosphodiesterase 8B gene polymorphism is associated with subclinical hypothyroidism in pregnancy. J Clin Endocrinol Metab 94: 4608-4612.
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 4608-4612
-
-
Shields, B.M.1
Freathy, R.M.2
Knight, B.A.3
Hill, A.4
Weedon, M.N.5
-
28
-
-
80055041802
-
Adult-onset hypothyroidism enhances fear memory and upregulates mineralocorticoid and glucocorticoid receptors in the amygdala
-
doi: 10.1371/journal.pone.0026582
-
Montero-Pedrazuela A, Fernandez-Lamo I, Alieva M, Pereda-Perez I, Venero C, et al. (2011) Adult-onset hypothyroidism enhances fear memory and upregulates mineralocorticoid and glucocorticoid receptors in the amygdala. PLoS ONE 6: e26582 doi:10.1371/journal.pone.0026582.
-
(2011)
PLoS ONE
, vol.6
-
-
Montero-Pedrazuela, A.1
Fernandez-Lamo, I.2
Alieva, M.3
Pereda-Perez, I.4
Venero, C.5
-
29
-
-
84859506990
-
Novel Associations for Hypothyroidism Include Known Autoimmune Risk Loci
-
doi: 10.1371/journal.pone.0034442
-
Eriksson N, Tung JY, Kiefer AK, Hinds DA, Francke U, et al. (2012) Novel Associations for Hypothyroidism Include Known Autoimmune Risk Loci. PLoS ONE 7: e34442 doi:10.1371/journal.pone.0034442.
-
(2012)
PLoS ONE
, vol.7
-
-
Eriksson, N.1
Tung, J.Y.2
Kiefer, A.K.3
Hinds, D.A.4
Francke, U.5
-
30
-
-
9344229266
-
Specification of pituitary cell lineages by the LIM homeobox gene Lhx3
-
Sheng HZ, Zhadanov AB, Mosinger B Jr, Fujii T, Bertuzzi S, et al. (1996) Specification of pituitary cell lineages by the LIM homeobox gene Lhx3. Science 272: 1004-1007.
-
(1996)
Science
, vol.272
, pp. 1004-1007
-
-
Sheng, H.Z.1
Zhadanov, A.B.2
Mosinger Jr., B.3
Fujii, T.4
Bertuzzi, S.5
-
31
-
-
0034040904
-
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency
-
Netchine I, Sobrier ML, Krude H, Schnabel D, Maghnie M, et al. (2000) Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency. Nat Genet 25: 182-186.
-
(2000)
Nat Genet
, vol.25
, pp. 182-186
-
-
Netchine, I.1
Sobrier, M.L.2
Krude, H.3
Schnabel, D.4
Maghnie, M.5
-
32
-
-
84862777075
-
Discovery of common variants associated with low TSH levels and thyroid cancer risk
-
Gudmundsson J, Sulem P, Gudbjartsson DF, Jonasson JG, Masson G, et al. (2012) Discovery of common variants associated with low TSH levels and thyroid cancer risk. Nat Genet 44: 319-322.
-
(2012)
Nat Genet
, vol.44
, pp. 319-322
-
-
Gudmundsson, J.1
Sulem, P.2
Gudbjartsson, D.F.3
Jonasson, J.G.4
Masson, G.5
-
33
-
-
79955530386
-
A meta-analysis of the associations between common variation in the PDE8B gene and thyroid hormone parameters, including assessment of longitudinal stability of associations over time and effect of thyroid hormone replacement
-
Taylor PN, Panicker V, Sayers A, Shields B, Iqbal A, et al. (2011) A meta-analysis of the associations between common variation in the PDE8B gene and thyroid hormone parameters, including assessment of longitudinal stability of associations over time and effect of thyroid hormone replacement. Eur J Endocrinol 164: 773-780.
-
(2011)
Eur J Endocrinol
, vol.164
, pp. 773-780
-
-
Taylor, P.N.1
Panicker, V.2
Sayers, A.3
Shields, B.4
Iqbal, A.5
-
34
-
-
79961128283
-
Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27
-
Volpato CB, De Grandi A, Gogele M, Taliun D, Fuchsberger C, et al. (2011) Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27. J Med Genet 48: 549-556.
-
(2011)
J Med Genet
, vol.48
, pp. 549-556
-
-
Volpato, C.B.1
De Grandi, A.2
Gogele, M.3
Taliun, D.4
Fuchsberger, C.5
-
35
-
-
20244372135
-
Intracellular cAMP controls a physical association of V-1 with CapZ in cultured mammalian endocrine cells
-
Kitazawa M, Yamakuni T, Song SY, Kato C, Tsuchiya R, et al. (2005) Intracellular cAMP controls a physical association of V-1 with CapZ in cultured mammalian endocrine cells. Biochem Biophys Res Commun 331: 181-186.
-
(2005)
Biochem Biophys Res Commun
, vol.331
, pp. 181-186
-
-
Kitazawa, M.1
Yamakuni, T.2
Song, S.Y.3
Kato, C.4
Tsuchiya, R.5
-
36
-
-
79955860707
-
Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk
-
Teumer A, Rawal R, Homuth G, Ernst F, Heier M, et al. (2011) Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. Am J Hum Genet 88: 664-673.
-
(2011)
Am J Hum Genet
, vol.88
, pp. 664-673
-
-
Teumer, A.1
Rawal, R.2
Homuth, G.3
Ernst, F.4
Heier, M.5
-
37
-
-
0028851894
-
Transcription factor AP-2 regulates human insulin-like growth factor binding protein-5 gene expression
-
Duan C, Clemmons DR, (1995) Transcription factor AP-2 regulates human insulin-like growth factor binding protein-5 gene expression. J Biol Chem 270: 24844-24851.
-
(1995)
J Biol Chem
, vol.270
, pp. 24844-24851
-
-
Duan, C.1
Clemmons, D.R.2
-
38
-
-
33846965229
-
The association of polymorphisms in the type 1 and 2 deiodinase genes with circulating thyroid hormone parameters and atrophy of the medial temporal lobe
-
de Jong FJ, Peeters RP, den Heijer T, van der Deure WM, Hofman A, et al. (2007) The association of polymorphisms in the type 1 and 2 deiodinase genes with circulating thyroid hormone parameters and atrophy of the medial temporal lobe. J Clin Endocrinol Metab 92: 636-640.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 636-640
-
-
de Jong, F.J.1
Peeters, R.P.2
den Heijer, T.3
van der Deure, W.M.4
Hofman, A.5
-
39
-
-
57349119069
-
Cellular and molecular basis of deiodinase-regulated thyroid hormone signaling
-
Gereben B, Zavacki AM, Ribich S, Kim BW, Huang SA, et al. (2008) Cellular and molecular basis of deiodinase-regulated thyroid hormone signaling. Endocr Rev 29: 898-938.
-
(2008)
Endocr Rev
, vol.29
, pp. 898-938
-
-
Gereben, B.1
Zavacki, A.M.2
Ribich, S.3
Kim, B.W.4
Huang, S.A.5
-
40
-
-
17344366813
-
A mouse model for hereditary thyroid dysgenesis and cleft palate
-
De Felice M, Ovitt C, Biffali E, Rodriguez-Mallon A, Arra C, et al. (1998) A mouse model for hereditary thyroid dysgenesis and cleft palate. Nat Genet 19: 395-398.
-
(1998)
Nat Genet
, vol.19
, pp. 395-398
-
-
De Felice, M.1
Ovitt, C.2
Biffali, E.3
Rodriguez-Mallon, A.4
Arra, C.5
-
41
-
-
0031820442
-
Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia
-
Clifton-Bligh RJ, Wentworth JM, Heinz P, Crisp MS, John R, et al. (1998) Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia. Nat Genet 19: 399-401.
-
(1998)
Nat Genet
, vol.19
, pp. 399-401
-
-
Clifton-Bligh, R.J.1
Wentworth, J.M.2
Heinz, P.3
Crisp, M.S.4
John, R.5
-
42
-
-
34249855378
-
Four novel mutations of the LHX3 gene cause combined pituitary hormone deficiencies with or without limited neck rotation
-
Pfaeffle RW, Savage JJ, Hunter CS, Palme C, Ahlmann M, et al. (2007) Four novel mutations of the LHX3 gene cause combined pituitary hormone deficiencies with or without limited neck rotation. J Clin Endocrinol Metab 92: 1909-1919.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 1909-1919
-
-
Pfaeffle, R.W.1
Savage, J.J.2
Hunter, C.S.3
Palme, C.4
Ahlmann, M.5
-
43
-
-
46249099124
-
Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss
-
Rajab A, Kelberman D, de Castro SC, Biebermann H, Shaikh H, et al. (2008) Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss. Hum Mol Genet 17: 2150-2159.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 2150-2159
-
-
Rajab, A.1
Kelberman, D.2
de Castro, S.C.3
Biebermann, H.4
Shaikh, H.5
-
44
-
-
77953507639
-
A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci
-
Okada Y, Kamatani Y, Takahashi A, Matsuda K, Hosono N, et al. (2010) A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. Hum Mol Genet 19: 2303-2312.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 2303-2312
-
-
Okada, Y.1
Kamatani, Y.2
Takahashi, A.3
Matsuda, K.4
Hosono, N.5
-
45
-
-
23844459979
-
Relation between the hypothalamic-pituitary-thyroid (HPT) axis and the hypothalamic-pituitary-adrenal (HPA) axis during repeated stress
-
Helmreich DL, Parfitt DB, Lu XY, Akil H, Watson SJ, (2005) Relation between the hypothalamic-pituitary-thyroid (HPT) axis and the hypothalamic-pituitary-adrenal (HPA) axis during repeated stress. Neuroendocrinology 81: 183-192.
-
(2005)
Neuroendocrinology
, vol.81
, pp. 183-192
-
-
Helmreich, D.L.1
Parfitt, D.B.2
Lu, X.Y.3
Akil, H.4
Watson, S.J.5
-
46
-
-
67650178847
-
The role of kynurenines in disorders of the central nervous system: possibilities for neuroprotection
-
Vamos E, Pardutz A, Klivenyi P, Toldi J, Vecsei L, (2009) The role of kynurenines in disorders of the central nervous system: possibilities for neuroprotection. J Neurol Sci 283: 21-27.
-
(2009)
J Neurol Sci
, vol.283
, pp. 21-27
-
-
Vamos, E.1
Pardutz, A.2
Klivenyi, P.3
Toldi, J.4
Vecsei, L.5
-
47
-
-
0036377837
-
Characterization of the human gene encoding alpha-aminoadipate aminotransferase (AADAT)
-
Goh DL, Patel A, Thomas GH, Salomons GS, Schor DS, et al. (2002) Characterization of the human gene encoding alpha-aminoadipate aminotransferase (AADAT). Mol Genet Metab 76: 172-180.
-
(2002)
Mol Genet Metab
, vol.76
, pp. 172-180
-
-
Goh, D.L.1
Patel, A.2
Thomas, G.H.3
Salomons, G.S.4
Schor, D.S.5
-
48
-
-
79955471215
-
Association of kynurenine aminotransferase II gene C401T polymorphism with immune response in patients with meningitis
-
de Souza FR, Fontes FL, da Silva TA, Coutinho LG, Leib SL, et al. (2010) Association of kynurenine aminotransferase II gene C401T polymorphism with immune response in patients with meningitis. BMC Med Genet 12: 51.
-
(2010)
BMC Med Genet
, vol.12
, pp. 51
-
-
de Souza, F.R.1
Fontes, F.L.2
da Silva, T.A.3
Coutinho, L.G.4
Leib, S.L.5
-
49
-
-
75849150001
-
Structure, expression, and function of kynurenine aminotransferases in human and rodent brains
-
Han Q, Cai T, Tagle DA, Li J, (2009) Structure, expression, and function of kynurenine aminotransferases in human and rodent brains. Cell Mol Life Sci 67: 353-368.
-
(2009)
Cell Mol Life Sci
, vol.67
, pp. 353-368
-
-
Han, Q.1
Cai, T.2
Tagle, D.A.3
Li, J.4
-
50
-
-
77957342306
-
Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits
-
doi: 10.1371/journal.pgen.1001058
-
Segrè AV, Groop L, Mootha VK, Daly MJ, Altshuler D, (2010) Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits. PLoS Genet 6: e1001058 doi:10.1371/journal.pgen.1001058.
-
(2010)
PLoS Genet
, vol.6
-
-
Segrè, A.V.1
Groop, L.2
Mootha, V.K.3
Daly, M.J.4
Altshuler, D.5
-
51
-
-
67651205715
-
Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions
-
doi: 10.1371/journal.pgen.1000534
-
Raychaudhuri S, Plenge RM, Rossin EJ, Ng AC, Purcell SM, et al. (2009) Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions. PLoS Genet 5: e1000534 doi:10.1371/journal.pgen.1000534.
-
(2009)
PLoS Genet
, vol.5
-
-
Raychaudhuri, S.1
Plenge, R.M.2
Rossin, E.J.3
Ng, A.C.4
Purcell, S.M.5
-
52
-
-
33745268851
-
Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism
-
Senee V, Chelala C, Duchatelet S, Feng D, Blanc H, et al. (2006) Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism. Nat Genet 38: 682-687.
-
(2006)
Nat Genet
, vol.38
, pp. 682-687
-
-
Senee, V.1
Chelala, C.2
Duchatelet, S.3
Feng, D.4
Blanc, H.5
-
53
-
-
78650257143
-
Single nucleotide polymorphisms and mRNA expression of VEGF-A in papillary thyroid carcinoma: potential markers for aggressive phenotypes
-
Salajegheh A, Smith RA, Kasem K, Gopalan V, Nassiri MR, et al. (2011) Single nucleotide polymorphisms and mRNA expression of VEGF-A in papillary thyroid carcinoma: potential markers for aggressive phenotypes. Eur J Surg Oncol 37: 93-99.
-
(2011)
Eur J Surg Oncol
, vol.37
, pp. 93-99
-
-
Salajegheh, A.1
Smith, R.A.2
Kasem, K.3
Gopalan, V.4
Nassiri, M.R.5
-
54
-
-
0037430644
-
Differential expression of IGFBP-5 and two human ESTs in thyroid glands with goiter, adenoma and papillary or follicular carcinomas
-
Stolf BS, Carvalho AF, Martins WK, Runza FB, Brun M, et al. (2003) Differential expression of IGFBP-5 and two human ESTs in thyroid glands with goiter, adenoma and papillary or follicular carcinomas. Cancer Lett 191: 193-202.
-
(2003)
Cancer Lett
, vol.191
, pp. 193-202
-
-
Stolf, B.S.1
Carvalho, A.F.2
Martins, W.K.3
Runza, F.B.4
Brun, M.5
-
55
-
-
0036148531
-
A novel autocrine loop involving IGF-II and the insulin receptor isoform-A stimulates growth of thyroid cancer
-
Vella V, Pandini G, Sciacca L, Mineo R, Vigneri R, et al. (2002) A novel autocrine loop involving IGF-II and the insulin receptor isoform-A stimulates growth of thyroid cancer. J Clin Endocrinol Metab 87: 245-254.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 245-254
-
-
Vella, V.1
Pandini, G.2
Sciacca, L.3
Mineo, R.4
Vigneri, R.5
-
56
-
-
34548564313
-
Proteomic expression profiling of thyroid neoplasms
-
Braunschweig T, Kaserer K, Chung JY, Bilke S, Krizman D, et al. (2007) Proteomic expression profiling of thyroid neoplasms. Proteomics Clin Appl 1: 264-271.
-
(2007)
Proteomics Clin Appl
, vol.1
, pp. 264-271
-
-
Braunschweig, T.1
Kaserer, K.2
Chung, J.Y.3
Bilke, S.4
Krizman, D.5
-
57
-
-
77955894071
-
METAL: fast and efficient meta-analysis of genomewide association scans
-
Willer CJ, Li Y, Abecasis GR, (2010) METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 26: 2190-2191.
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
58
-
-
78649508578
-
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
-
Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR, (2010) MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol 34: 816-834.
-
(2010)
Genet Epidemiol
, vol.34
, pp. 816-834
-
-
Li, Y.1
Willer, C.J.2
Ding, J.3
Scheet, P.4
Abecasis, G.R.5
-
59
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini J, Howie B, Myers S, McVean G, Donnelly P, (2007) A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet 39: 906-913.
-
(2007)
Nat Genet
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
60
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
doi: 10.1371/journal.pgen.1000529
-
Howie BN, Donnelly P, Marchini J, (2009) A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 5: e1000529 doi:10.1371/journal.pgen.1000529.
-
(2009)
PLoS Genet
, vol.5
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
61
-
-
77956586071
-
LocusZoom: regional visualization of genome-wide association scan results
-
Pruim RJ, Welch RP, Sanna S, Teslovich TM, Chines PS, et al. (2010) LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics 26: 2336-2337.
-
(2010)
Bioinformatics
, vol.26
, pp. 2336-2337
-
-
Pruim, R.J.1
Welch, R.P.2
Sanna, S.3
Teslovich, T.M.4
Chines, P.S.5
-
62
-
-
36549072418
-
VEGF in physiological process and thyroid disease
-
Klein M, Catargi B, (2007) VEGF in physiological process and thyroid disease. Ann Endocrinol (Paris) 68: 438-448.
-
(2007)
Ann Endocrinol (Paris)
, vol.68
, pp. 438-448
-
-
Klein, M.1
Catargi, B.2
-
63
-
-
40449103287
-
Iodine deficiency induces a thyroid stimulating hormone-independent early phase of microvascular reshaping in the thyroid
-
Gerard AC, Poncin S, Caetano B, Sonveaux P, Audinot JN, et al. (2008) Iodine deficiency induces a thyroid stimulating hormone-independent early phase of microvascular reshaping in the thyroid. Am J Pathol 172: 748-760.
-
(2008)
Am J Pathol
, vol.172
, pp. 748-760
-
-
Gerard, A.C.1
Poncin, S.2
Caetano, B.3
Sonveaux, P.4
Audinot, J.N.5
-
64
-
-
33745982267
-
Iodide inhibits vascular endothelial growth factor-A expression in cultured human thyroid follicles: a microarray search for effects of thyrotropin and iodide on angiogenesis factors
-
Yamada E, Yamazaki K, Takano K, Obara T, Sato K, (2006) Iodide inhibits vascular endothelial growth factor-A expression in cultured human thyroid follicles: a microarray search for effects of thyrotropin and iodide on angiogenesis factors. Thyroid 16: 545-554.
-
(2006)
Thyroid
, vol.16
, pp. 545-554
-
-
Yamada, E.1
Yamazaki, K.2
Takano, K.3
Obara, T.4
Sato, K.5
-
65
-
-
76349089321
-
Stimulatory effects of thyroid hormone on brain angiogenesis in vivo and in vitro
-
Zhang L, Cooper-Kuhn CM, Nannmark U, Blomgren K, Kuhn HG, (2010) Stimulatory effects of thyroid hormone on brain angiogenesis in vivo and in vitro. J Cereb Blood Flow Metab 30: 323-335.
-
(2010)
J Cereb Blood Flow Metab
, vol.30
, pp. 323-335
-
-
Zhang, L.1
Cooper-Kuhn, C.M.2
Nannmark, U.3
Blomgren, K.4
Kuhn, H.G.5
-
66
-
-
0034692430
-
Role of the insulin-like growth factor family in cancer development and progression
-
Yu H, Rohan T, (2000) Role of the insulin-like growth factor family in cancer development and progression. J Natl Cancer Inst 92: 1472-1489.
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 1472-1489
-
-
Yu, H.1
Rohan, T.2
-
67
-
-
0029810375
-
Functional human thyroid cells and their insulin-like growth factor-binding proteins: regulation by thyrotropin, cyclic 3′,5′ adenosine monophosphate, and growth factors
-
Eggo MC, King WJ, Black EG, Sheppard MC, (1996) Functional human thyroid cells and their insulin-like growth factor-binding proteins: regulation by thyrotropin, cyclic 3′,5′ adenosine monophosphate, and growth factors. J Clin Endocrinol Metab 81: 3056-3062.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 3056-3062
-
-
Eggo, M.C.1
King, W.J.2
Black, E.G.3
Sheppard, M.C.4
-
68
-
-
0027467505
-
Synthesis and regulation of insulin-like growth factor binding protein-5 in FRTL-5 cells
-
Backeljauw PF, Dai Z, Clemmons DR, D'Ercole AJ, (1993) Synthesis and regulation of insulin-like growth factor binding protein-5 in FRTL-5 cells. Endocrinology 132: 1677-1681.
-
(1993)
Endocrinology
, vol.132
, pp. 1677-1681
-
-
Backeljauw, P.F.1
Dai, Z.2
Clemmons, D.R.3
D'Ercole, A.J.4
-
69
-
-
0035212787
-
Effects of triiodothyronine on the insulin-like growth factor system in primary human osteoblastic cells in vitro
-
Pepene CE, Kasperk CH, Pfeilschifter J, Borcsok I, Gozariu L, et al. (2001) Effects of triiodothyronine on the insulin-like growth factor system in primary human osteoblastic cells in vitro. Bone 29: 540-546.
-
(2001)
Bone
, vol.29
, pp. 540-546
-
-
Pepene, C.E.1
Kasperk, C.H.2
Pfeilschifter, J.3
Borcsok, I.4
Gozariu, L.5
-
70
-
-
18444401112
-
SOX9 interacts with a component of the human thyroid hormone receptor-associated protein complex
-
Zhou R, Bonneaud N, Yuan CX, de Santa Barbara P, Boizet B, et al. (2002) SOX9 interacts with a component of the human thyroid hormone receptor-associated protein complex. Nucleic Acids Res 30: 3245-3252.
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 3245-3252
-
-
Zhou, R.1
Bonneaud, N.2
Yuan, C.X.3
de Santa Barbara, P.4
Boizet, B.5
-
71
-
-
0032692783
-
Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum
-
das Neves L, Duchala CS, Tolentino-Silva F, Haxhiu MA, Colmenares C, et al. (1999) Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum. Proc Natl Acad Sci U S A 96: 11946-11951.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 11946-11951
-
-
das Neves, L.1
Duchala, C.S.2
Tolentino-Silva, F.3
Haxhiu, M.A.4
Colmenares, C.5
-
72
-
-
0033756193
-
Thyroglobulin repression of thyroid transcription factor 1 (TTF-1) gene expression is mediated by decreased DNA binding of nuclear factor I proteins which control constitutive TTF-1 expression
-
Nakazato M, Chung HK, Ulianich L, Grassadonia A, Suzuki K, et al. (2000) Thyroglobulin repression of thyroid transcription factor 1 (TTF-1) gene expression is mediated by decreased DNA binding of nuclear factor I proteins which control constitutive TTF-1 expression. Mol Cell Biol 20: 8499-8512.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 8499-8512
-
-
Nakazato, M.1
Chung, H.K.2
Ulianich, L.3
Grassadonia, A.4
Suzuki, K.5
-
73
-
-
0242267051
-
Hypothyroidism in thyroid transcription factor 1 haploinsufficiency is caused by reduced expression of the thyroid-stimulating hormone receptor
-
Moeller LC, Kimura S, Kusakabe T, Liao XH, Van Sande J, et al. (2003) Hypothyroidism in thyroid transcription factor 1 haploinsufficiency is caused by reduced expression of the thyroid-stimulating hormone receptor. Mol Endocrinol 17: 2295-2302.
-
(2003)
Mol Endocrinol
, vol.17
, pp. 2295-2302
-
-
Moeller, L.C.1
Kimura, S.2
Kusakabe, T.3
Liao, X.H.4
Van Sande, J.5
-
74
-
-
0035281514
-
Fibroblast growth factor receptor 2-IIIb acts upstream of Shh and Fgf4 and is required for limb bud maintenance but not for the induction of Fgf8, Fgf10, Msx1, or Bmp4
-
Revest JM, Spencer-Dene B, Kerr K, De Moerlooze L, Rosewell I, et al. (2001) Fibroblast growth factor receptor 2-IIIb acts upstream of Shh and Fgf4 and is required for limb bud maintenance but not for the induction of Fgf8, Fgf10, Msx1, or Bmp4. Dev Biol 231: 47-62.
-
(2001)
Dev Biol
, vol.231
, pp. 47-62
-
-
Revest, J.M.1
Spencer-Dene, B.2
Kerr, K.3
De Moerlooze, L.4
Rosewell, I.5
-
75
-
-
0033967477
-
The yin-yang of PR-domain family genes in tumorigenesis
-
Jiang GL, Huang S, (2000) The yin-yang of PR-domain family genes in tumorigenesis. Histol Histopathol 15: 109-117.
-
(2000)
Histol Histopathol
, vol.15
, pp. 109-117
-
-
Jiang, G.L.1
Huang, S.2
-
76
-
-
84857467976
-
A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation
-
doi: 10.1371/journal.pgen.1002480
-
Naitza S, Porcu E, Steri M, Taub DD, Mulas A, et al. (2012) A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation. PLoS Genet 8: e1002480 doi:10.1371/journal.pgen.1002480.
-
(2012)
PLoS Genet
, vol.8
-
-
Naitza, S.1
Porcu, E.2
Steri, M.3
Taub, D.D.4
Mulas, A.5
-
77
-
-
0019945295
-
Clinical and subclinical thyroid disorders associated with pernicious anemia. Observations on abnormal thyroid-stimulating hormone levels and on a possible association of blood group O with hyperthyroidism
-
Carmel R, Spencer CA, (1982) Clinical and subclinical thyroid disorders associated with pernicious anemia. Observations on abnormal thyroid-stimulating hormone levels and on a possible association of blood group O with hyperthyroidism. Arch Intern Med 142: 1465-1469.
-
(1982)
Arch Intern Med
, vol.142
, pp. 1465-1469
-
-
Carmel, R.1
Spencer, C.A.2
-
78
-
-
77955286905
-
Expression of inositol 1,3,4-trisphosphate 5/6-kinase (ITPK1) and its role in neural tube defects
-
Majerus PW, Wilson DB, Zhang C, Nicholas PJ, Wilson MP, (2010) Expression of inositol 1,3,4-trisphosphate 5/6-kinase (ITPK1) and its role in neural tube defects. Adv Enzyme Regul 50: 365-372.
-
(2010)
Adv Enzyme Regul
, vol.50
, pp. 365-372
-
-
Majerus, P.W.1
Wilson, D.B.2
Zhang, C.3
Nicholas, P.J.4
Wilson, M.P.5
-
79
-
-
34447134181
-
A familial thyrotropin (TSH) receptor mutation provides in vivo evidence that the inositol phosphates/Ca2+ cascade mediates TSH action on thyroid hormone synthesis
-
Grasberger H, Van Sande J, Hag-Dahood Mahameed A, Tenenbaum-Rakover Y, Refetoff S, (2007) A familial thyrotropin (TSH) receptor mutation provides in vivo evidence that the inositol phosphates/Ca2+ cascade mediates TSH action on thyroid hormone synthesis. J Clin Endocrinol Metab 92: 2816-2820.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 2816-2820
-
-
Grasberger, H.1
Van Sande, J.2
Hag-Dahood Mahameed, A.3
Tenenbaum-Rakover, Y.4
Refetoff, S.5
-
80
-
-
0034647552
-
MAPK upstream kinase (MUK)-binding inhibitory protein, a negative regulator of MUK/dual leucine zipper-bearing kinase/leucine zipper protein kinase
-
Fukuyama K, Yoshida M, Yamashita A, Deyama T, Baba M, et al. (2000) MAPK upstream kinase (MUK)-binding inhibitory protein, a negative regulator of MUK/dual leucine zipper-bearing kinase/leucine zipper protein kinase. J Biol Chem 275: 21247-21254.
-
(2000)
J Biol Chem
, vol.275
, pp. 21247-21254
-
-
Fukuyama, K.1
Yoshida, M.2
Yamashita, A.3
Deyama, T.4
Baba, M.5
-
81
-
-
84861862859
-
The polymorphism rs944289 predisposes to papillary thyroid carcinoma through a large intergenic noncoding RNA gene of tumor suppressor type
-
Jendrzejewski J, He H, Radomska HS, Li W, Tomsic J, et al. (2012) The polymorphism rs944289 predisposes to papillary thyroid carcinoma through a large intergenic noncoding RNA gene of tumor suppressor type. Proc Natl Acad Sci U S A 109: 8646-8651.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, pp. 8646-8651
-
-
Jendrzejewski, J.1
He, H.2
Radomska, H.S.3
Li, W.4
Tomsic, J.5
-
82
-
-
72149099120
-
Differential 14-3-3 affinity capture reveals new downstream targets of phosphatidylinositol 3-kinase signaling
-
Dubois F, Vandermoere F, Gernez A, Murphy J, Toth R, et al. (2009) Differential 14-3-3 affinity capture reveals new downstream targets of phosphatidylinositol 3-kinase signaling. Mol Cell Proteomics 8: 2487-2499.
-
(2009)
Mol Cell Proteomics
, vol.8
, pp. 2487-2499
-
-
Dubois, F.1
Vandermoere, F.2
Gernez, A.3
Murphy, J.4
Toth, R.5
-
83
-
-
77955301455
-
The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl
-
Takahashi M, Saenko VA, Rogounovitch TI, Kawaguchi T, Drozd VM, et al. The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl. Hum Mol Genet 19: 2516-2523.
-
Hum Mol Genet
, vol.19
, pp. 2516-2523
-
-
Takahashi, M.1
Saenko, V.A.2
Rogounovitch, T.I.3
Kawaguchi, T.4
Drozd, V.M.5
-
84
-
-
70349690194
-
The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors
-
doi: 10.1371/journal.pgen.1000637
-
Landa I, Ruiz-Llorente S, Montero-Conde C, Inglada-Perez L, Schiavi F, et al. (2009) The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors. PLoS Genet 5: e1000637 doi:10.1371/journal.pgen.1000637.
-
(2009)
PLoS Genet
, vol.5
-
-
Landa, I.1
Ruiz-Llorente, S.2
Montero-Conde, C.3
Inglada-Perez, L.4
Schiavi, F.5
-
85
-
-
77955301455
-
The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl
-
Takahashi M, Saenko VA, Rogounovitch TI, Kawaguchi T, Drozd VM, et al. (2010) The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl. Hum Mol Genet 19: 2516-2523.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 2516-2523
-
-
Takahashi, M.1
Saenko, V.A.2
Rogounovitch, T.I.3
Kawaguchi, T.4
Drozd, V.M.5
|