-
1
-
-
0036125773
-
Iodothyronine deiodinases
-
Kohrle J. Iodothyronine deiodinases. Methods Enzymol. 2002;347: 125–167.
-
(2002)
Methods Enzymol
, vol.347
, pp. 125-167
-
-
Kohrle, J.1
-
2
-
-
25144444814
-
Structure and function of the type 3 deiodinase gene
-
Hernandez A. Structure and function of the type 3 deiodinase gene. Thyroid. 2005;15:865–874.
-
(2005)
Thyroid
, vol.15
, pp. 865-874
-
-
Hernandez, A.1
-
3
-
-
0036191639
-
Biochemistry, cellular and molecular biology, and physiological roles of the iodothyronine selenodeiodinases
-
Bianco AC, Salvatore D, Gereben B, Berry MJ, Larsen PR. Biochemistry, cellular and molecular biology, and physiological roles of the iodothyronine selenodeiodinases. Endocr Rev. 2002; 23:38–89.
-
(2002)
Endocr Rev
, vol.23
, pp. 38-89
-
-
Bianco, A.C.1
Salvatore, D.2
Gereben, B.3
Berry, M.J.4
Larsen, P.R.5
-
4
-
-
0037338926
-
Type 3 iodothyronine deiodinase is highly expressed in the human uteroplacental unit and in fetal epithelium
-
Huang SA, Dorfman DM, Genest DR, Salvatore D, Larsen PR. Type 3 iodothyronine deiodinase is highly expressed in the human uteroplacental unit and in fetal epithelium. J Clin Endocrinol Metab. 2003;88:1384–1388.
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 1384-1388
-
-
Huang, S.A.1
Dorfman, D.M.2
Genest, D.R.3
Salvatore, D.4
Larsen, P.R.5
-
5
-
-
0032901159
-
Pregnant rat uterus expresses high levels of the type 3 iodothyronine deiodinase
-
Galton VA, Martinez E, Hernandez A, St Germain EA, Bates JM, St Germain D.. Pregnant rat uterus expresses high levels of the type 3 iodothyronine deiodinase. J Clin Invest. 1999;103:979–987.
-
(1999)
J Clin Invest
, vol.103
, pp. 979-987
-
-
Galton, V.A.1
Martinez, E.2
Hernandez, A.3
St Germain, E.A.4
Bates, J.M.5
St Germain, D.6
-
6
-
-
0018826826
-
Phenolic and tyrosyl ring deiodination of iodothyronines in rat brain homogenates
-
Kaplan MM, Yaskoski KA. Phenolic and tyrosyl ring deiodination of iodothyronines in rat brain homogenates. J Clin Invest. 1980;66: 551–562.
-
(1980)
J Clin Invest
, vol.66
, pp. 551-562
-
-
Kaplan, M.M.1
Yaskoski, K.A.2
-
7
-
-
0032941728
-
Regional expression of the type 3 iodothyronine deiodinase mes-senger ribonucleic acid in the rat central nervous system and its regulation by thyroid hormone
-
Tu HM, Legradi G, Bartha T, Salvatore D, Lechan R, Larsen PR. Regional expression of the type 3 iodothyronine deiodinase mes-senger ribonucleic acid in the rat central nervous system and its regulation by thyroid hormone. Endocrinology. 1999;140:784-790.
-
(1999)
Endocrinology
, vol.140
, pp. 784-790
-
-
Tu, H.M.1
Legradi, G.2
Bartha, T.3
Salvatore, D.4
Lechan, R.5
Larsen, P.R.6
-
8
-
-
32444438623
-
Type 3 deiodinase is critical for the maturation and function of the thyroid axis
-
Hernandez A, Martinez ME, Fiering S, Galton VA, St Germain D. Type 3 deiodinase is critical for the maturation and function of the thyroid axis. J Clin Invest. 2006;116:476-484.
-
(2006)
J Clin Invest
, vol.116
, pp. 476-484
-
-
Hernandez, A.1
Martinez, M.E.2
Fiering, S.3
Galton, V.A.4
St Germain, D.5
-
9
-
-
36348982798
-
Type 3 deiodinase deficiency results in functional abnormalities at multiple levels of the thyroid axis
-
Hernandez A, Martinez E, Liao X, et al Type 3 deiodinase deficiency results in functional abnormalities at multiple levels of the thyroid axis. Endocrinology. 2007;148:5680-5687.
-
(2007)
Endocrinology
, vol.148
, pp. 5680-5687
-
-
Hernandez, A.1
Martinez, E.2
Liao, X.3
-
10
-
-
84860331721
-
Absence of myocardial thyroid hormone inactivating deiodinase results in restrictive cardiomyopathy in mice
-
Ueta CB, Oskouei BN, Pinto JR, et al. Absence of myocardial thyroid hormone inactivating deiodinase results in restrictive cardiomyopathy in mice. Mol Endocrinol. 2012;26:809-818.
-
(2012)
Mol Endocrinol
, vol.26
, pp. 809-818
-
-
Ueta, C.B.1
Oskouei, B.N.2
Pinto, J.R.3
-
11
-
-
63849159901
-
A protective role for type 3 deiodinase, a thyroid hormone-inactivating enzyme, in cochlear development and auditory function
-
Ng L, Hernandez A, He W, et al. A protective role for type 3 deiodinase, a thyroid hormone-inactivating enzyme, in cochlear development and auditory function. Endocrinology. 2009;150: 1952-1960.
-
(2009)
Endocrinology
, vol.150
, pp. 1952-1960
-
-
Ng, L.1
Hernandez, A.2
He, W.3
-
12
-
-
77749343305
-
Type 3 deiodinase, a thyroid-hormone inactivating enzyme, controls survival and maturation of cone photoreceptors
-
Ng L, Lyubarsky A, Nikonov SS, et al. Type 3 deiodinase, a thyroid-hormone inactivating enzyme, controls survival and maturation of cone photoreceptors. J Neuroscience. 2010;30:3347-3357.
-
(2010)
J Neuroscience
, vol.30
, pp. 3347-3357
-
-
Ng, L.1
Lyubarsky, A.2
Nikonov, S.S.3
-
13
-
-
80053152577
-
The thyroid hormone-inactivating type III deiodinase is expressed in mouse and human β-cells and its targeted inactivation impairs insulin secretion
-
Medina MC, Molina J, Gadea Y, et al. The thyroid hormone-inactivating type III deiodinase is expressed in mouse and human β-cells and its targeted inactivation impairs insulin secretion. Endocrinology. 2011;152:3717-3727.
-
(2011)
Endocrinology
, vol.152
, pp. 3717-3727
-
-
Medina, M.C.1
Molina, J.2
Gadea, Y.3
-
14
-
-
78049517201
-
Type 3 deiodinase deficiency causes spatial and temporal alterations in brain T3 signaling that are dissociated from serum thyroid hormone levels
-
Hernandez A, Quignodon L, Martinez ME, Flamant F, St Germain DL. Type 3 deiodinase deficiency causes spatial and temporal alterations in brain T3 signaling that are dissociated from serum thyroid hormone levels. Endocrinology. 2010;151:5550-5558.
-
(2010)
Endocrinology
, vol.151
, pp. 5550-5558
-
-
Hernandez, A.1
Quignodon, L.2
Martinez, M.E.3
Flamant, F.4
St Germain, D.L.5
-
15
-
-
84861313021
-
Critical role of type 2 and 3 deiodinases in negative regulation of gene expression by T3 in the brain
-
Hernandez A, Morte B, Belinchon MM, Ceballos A, Bernal J. Critical role of type 2 and 3 deiodinases in negative regulation of gene expression by T3 in the brain. Endocrinology. 2012;153(6):2919-2928.
-
(2012)
Endocrinology
, vol.153
, Issue.6
, pp. 2919-2928
-
-
Hernandez, A.1
Morte, B.2
Belinchon, M.M.3
Ceballos, A.4
Bernal, J.5
-
16
-
-
0037162286
-
Genomic Imprinting contributes to thyroid hormone metabolism in the mouse embryo
-
Tsai C, Lin SP, Ito M, Takagi N, Takada S, Ferguson-Smith AC. Genomic Imprinting contributes to thyroid hormone metabolism in the mouse embryo. Curr Biol. 2002;12:1221-1226.
-
(2002)
Curr Biol
, vol.12
, pp. 1221-1226
-
-
Tsai, C.1
Lin, S.P.2
Ito, M.3
Takagi, N.4
Takada, S.5
Ferguson-Smith, A.C.6
-
17
-
-
0036827952
-
The gene locus encoding iodothyronine deiodinase type 3 (Dio3) is imprinted in the fetus and expresses antisense transcripts
-
Hernandez A, Fiering S, Martinez E, Galton VA, St Germain D. The gene locus encoding iodothyronine deiodinase type 3 (Dio3) is imprinted in the fetus and expresses antisense transcripts. Endocrinology. 2002;143:4483-4486.
-
(2002)
Endocrinology
, vol.143
, pp. 4483-4486
-
-
Hernandez, A.1
Fiering, S.2
Martinez, E.3
Galton, V.A.4
St Germain, D.5
-
18
-
-
0035234557
-
Genomic imprinting: Parental influence on the genome
-
Reik W, Walter J. Genomic imprinting: parental influence on the genome. Nat Rev Genet. 2001;2:21-32.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 21-32
-
-
Reik, W.1
Walter, J.2
-
19
-
-
79960530899
-
Genomic imprinting: The emergence of an epi-gentic paradigm
-
Ferguson-Smith AC. Genomic imprinting: the emergence of an epi-gentic paradigm. Nat Rev Genet. 2011;12(8):565-575.
-
(2011)
Nat Rev Genet
, vol.12
, Issue.8
, pp. 565-575
-
-
Ferguson-Smith, A.C.1
-
21
-
-
0033694804
-
Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12
-
Georgiades P, Watkins M, Surani MA, Ferguson-Smith AC. Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12. Development. 2000;127(21):4719-4728.
-
(2000)
Development
, vol.127
, Issue.21
, pp. 4719-4728
-
-
Georgiades, P.1
Watkins, M.2
Surani, M.A.3
Ferguson-Smith, A.C.4
-
22
-
-
84906858353
-
Phenotypic outcomes of imprinted gene models in mice: elucidation of pre- and postnatal functions of imprinted genes
-
Cleaton MAM, Edwards CA, Ferguson-Smith AC. Phenotypic outcomes of imprinted gene models in mice: elucidation of pre- and postnatal functions of imprinted genes. Annu Rev Genom Hum Genet. 2014;15:93-126.
-
(2014)
Annu Rev Genom Hum Genet
, vol.15
, pp. 93-126
-
-
Cleaton, M.A.M.1
Edwards, C.A.2
Ferguson-Smith, A.C.3
-
24
-
-
0033073395
-
Imprinting-mutation mechanisms in Prader-Willi syndrome
-
Ohta T, Gray TA, Rogan PK, et al. Imprinting-mutation mechanisms in Prader-Willi syndrome. Am J Hum Genet. 1999;64:397-413.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 397-413
-
-
Ohta, T.1
Gray, T.A.2
Rogan, P.K.3
-
25
-
-
0032939631
-
The spectrum of mutations in UBE3A causing Angelman syndrome
-
Fang P, Lev-Lehman E, Tsai TF, et al. The spectrum of mutations in UBE3A causing Angelman syndrome. Hum Mol Genet. 1999;8: 129-135.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 129-135
-
-
Fang, P.1
Lev-Lehman, E.2
Tsai, T.F.3
-
26
-
-
0033975096
-
Beckwith-Wiedemann syndrome: Imprinting in clusters revisited
-
Maher ER, Reik W. Beckwith-Wiedemann syndrome: imprinting in clusters revisited. J Clin Invest. 2000;105:247-252.
-
(2000)
J Clin Invest
, vol.105
, pp. 247-252
-
-
Maher, E.R.1
Reik, W.2
-
27
-
-
0025866731
-
Maternal uniparental disomy for chromosome 14
-
Temple IK, Cockwell A, Hassold T, Pettay D, Jacobs P. Maternal uniparental disomy for chromosome 14. J Med Genet. 1991;28: 511-514.
-
(1991)
J Med Genet
, vol.28
, pp. 511-514
-
-
Temple, I.K.1
Cockwell, A.2
Hassold, T.3
Pettay, D.4
Jacobs, P.5
-
28
-
-
44149101388
-
Genomic imprinting at the mammalian Dlk1-Dio3 domain. (Review, 85 references)
-
da Rocha ST, Edwards CA, Ito M, Ogata T, Ferguson-Smith AC. Genomic imprinting at the mammalian Dlk1-Dio3 domain. (Review, 85 references). Trends Genet. 2008;24(6):306-316.
-
(2008)
Trends Genet
, vol.24
, Issue.6
, pp. 306-316
-
-
Da Rocha, S.T.1
Edwards, C.A.2
Ito, M.3
Ogata, T.4
Ferguson-Smith, A.C.5
-
29
-
-
33846977748
-
Differential regulation of imprinting in the murine embryo and placenta by the Dlk1-Dio3 imprinting control region
-
Lin SP, Coan P, da Rocha ST, et al. Differential regulation of imprinting in the murine embryo and placenta by the Dlk1-Dio3 imprinting control region. Development. 2007;134(2):417-426.
-
(2007)
Development
, vol.134
, Issue.2
, pp. 417-426
-
-
Lin, S.P.1
Coan, P.2
Da Rocha, S.T.3
-
31
-
-
0027321548
-
Derivation of completely cell culture-derived mice from early passage embryonic stem cells
-
Nagy A, Rossant J, Nagy R, Abramow-Newerly W, Roder JC. Derivation of completely cell culture-derived mice from early passage embryonic stem cells. ProcNatlAcad Sci USA. 1993;90:8424-8428.
-
(1993)
ProcNatlAcad Sci USA
, vol.90
, pp. 8424-8428
-
-
Nagy, A.1
Rossant, J.2
Nagy, R.3
Abramow-Newerly, W.4
Roder, J.C.5
-
32
-
-
0023269862
-
Hepatic iodothyronine 5-deiodinase activity in Rana catesbeiana tadpoles at different stages of the life cycle
-
Galton VA, Hiebert A. Hepatic iodothyronine 5-deiodinase activity in Rana catesbeiana tadpoles at different stages of the life cycle. Endocrinology. 1987;121:42-47.
-
(1987)
Endocrinology
, vol.121
, pp. 42-47
-
-
Galton, V.A.1
Hiebert, A.2
-
33
-
-
0036151866
-
Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: Implications for imprinting control from comparison with Igf2-H19
-
Takada S, Paulsen M, Tevendale M, et al. Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19. Hum Mol Genet. 2002;11:77-86.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 77-86
-
-
Takada, S.1
Paulsen, M.2
Tevendale, M.3
-
34
-
-
84856097156
-
Status of genomic imprinting in epigenetically distinct pluripotent stem cells
-
Sun B, Ito M, Brions IG, et al. Status of genomic imprinting in epigenetically distinct pluripotent stem cells. Stem Cells. 2012;30: 161-168.
-
(2012)
Stem Cells
, vol.30
, pp. 161-168
-
-
Sun, B.1
Ito, M.2
Brions, I.G.3
-
35
-
-
0037508742
-
Substitution of cysteine for selenocysteine in the catalytic center of type III iodothyronine deiodinase reduces catalytic efficiency and alters substrate preference
-
Kuiper GG, Klootwijk W, Visser TJ. Substitution of cysteine for selenocysteine in the catalytic center of type III iodothyronine deiodinase reduces catalytic efficiency and alters substrate preference. Endocrinology. 2003;144:2505-2513.
-
(2003)
Endocrinology
, vol.144
, pp. 2505-2513
-
-
Kuiper, G.G.1
Klootwijk, W.2
Visser, T.J.3
-
36
-
-
0042856381
-
Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12
-
Lin SP, Youngson N, Takada S, et al. Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12. Nat Genet. 2003; 35:97-102.
-
(2003)
Nat Genet
, vol.35
, pp. 97-102
-
-
Lin, S.P.1
Youngson, N.2
Takada, S.3
-
37
-
-
18944371032
-
Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors
-
Croteau S, Roquis D, Charron MC, et al. Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors. Mamm Genome. 2005;16:127-135.
-
(2005)
Mamm Genome
, vol.16
, pp. 127-135
-
-
Croteau, S.1
Roquis, D.2
Charron, M.C.3
-
38
-
-
84901407054
-
Ground-state conditions promote robust Prdm14 reactivation and maintain and active Dlk1-Dio3 region during reprogramming
-
Habib O, Habib G, Moon SH, et al. Ground-state conditions promote robust Prdm14 reactivation and maintain and active Dlk1-Dio3 region during reprogramming. Mol Cells. 2014;37:31-35.
-
(2014)
Mol Cells
, vol.37
, pp. 31-35
-
-
Habib, O.1
Habib, G.2
Moon, S.H.3
-
39
-
-
0034664768
-
Pausing for thought on the boundaries of imprinting
-
Allshire R, Bickmore W. Pausing for thought on the boundaries of imprinting. Cell. 2000;102:705-708.
-
(2000)
Cell
, vol.102
, pp. 705-708
-
-
Allshire, R.1
Bickmore, W.2
-
40
-
-
0038364061
-
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark
-
Arnaud P, Monk D, Hitchins M, et al. Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark. Hum Mol Genet. 2003;12:1005-1019.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1005-1019
-
-
Arnaud, P.1
Monk, D.2
Hitchins, M.3
-
42
-
-
62749151020
-
Retarded developmental expression and patterning of retinal cone opsins in hypothyroid mice
-
Lu A, Ng L, Ma M, et al. Retarded developmental expression and patterning of retinal cone opsins in hypothyroid mice. Endocrinology. 2009;150:1536-1544.
-
(2009)
Endocrinology
, vol.150
, pp. 1536-1544
-
-
Lu, A.1
Ng, L.2
Ma, M.3
-
43
-
-
79960631454
-
Postnatal loss of Dlk1 imprinting in stem cells and niche astrocytes regulates neurogenesis
-
Ferron SR, Charalambous M, Radford E, et al. Postnatal loss of Dlk1 imprinting in stem cells and niche astrocytes regulates neurogenesis. Nature. 2011;475:381-385.
-
(2011)
Nature
, vol.475
, pp. 381-385
-
-
Ferron, S.R.1
Charalambous, M.2
Radford, E.3
-
44
-
-
35448945645
-
Sonic hedgehog-induced type 3 deiodinase blocks thyroid hormone action enhancing proliferation of normal and malignant keratinocytes
-
Dentice M, Luongo C, Huang S, et al. Sonic hedgehog-induced type 3 deiodinase blocks thyroid hormone action enhancing proliferation of normal and malignant keratinocytes. Proc Nat Acad Sci USA. 2007;104:14466-14471.
-
(2007)
Proc Nat Acad Sci USA
, vol.104
, pp. 14466-14471
-
-
Dentice, M.1
Luongo, C.2
Huang, S.3
-
45
-
-
79960169426
-
Strain-specific vulnerability to alcohol exposure in utero via hippocampal parent-of-origin expression of deiodinase-III
-
Sittig LJ, Shukla PK, Herzing LB, Redei EE. Strain-specific vulnerability to alcohol exposure in utero via hippocampal parent-of-origin expression of deiodinase-III. FASEB J. 2011;25:2313-2324.
-
(2011)
FASEB J
, vol.25
, pp. 2313-2324
-
-
Sittig, L.J.1
Shukla, P.K.2
Herzing, L.B.3
Redei, E.E.4
-
46
-
-
84904966116
-
Maternal inheritance of an inactive type III deiodinase gene affects mouse pancreatic β-cells and disrupts glucose homeostasis
-
Correa MC, Fonseca T, Molina J, et al. Maternal inheritance of an inactive type III deiodinase gene affects mouse pancreatic β-cells and disrupts glucose homeostasis. Endocrinology. 2014; 155: 3160-3171.
-
(2014)
Endocrinology
, vol.155
, pp. 3160-3171
-
-
Correa, M.C.1
Fonseca, T.2
Molina, J.3
|