-
1
-
-
0035807360
-
A forkhead-domain gene is mutated in a severe speech and language disorder
-
Lai, C. S., Fisher, S. E., Hurst, J. A., Vargha-Khadem, F. & Monaco, A. P. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413, 519-523 (2001).
-
(2001)
Nature
, vol.413
, pp. 519-523
-
-
Lai, C.S.1
Fisher, S.E.2
Hurst, J.A.3
Vargha-Khadem, F.4
Monaco, A.P.5
-
2
-
-
84880213877
-
Microfluidic affinity and ChIP-seq analyses converge on a conserved FOXP2-binding motif in chimp and human, which enables the detection of evolutionarily novel targets
-
Nelson, C. S. et al. Microfluidic affinity and ChIP-seq analyses converge on a conserved FOXP2-binding motif in chimp and human, which enables the detection of evolutionarily novel targets. Nucleic Acids Res 41, 5991-6004 (2013).
-
(2013)
Nucleic Acids Res
, vol.41
, pp. 5991-6004
-
-
Nelson, C.S.1
-
3
-
-
33749867547
-
Functional genetic analysis of mutations implicated in a human speech and language disorder
-
Vernes, S. C. et al. Functional genetic analysis of mutations implicated in a human speech and language disorder. Hum Mol Genet 15, 3154-3167 (2006).
-
(2006)
Hum Mol Genet
, vol.15
, pp. 3154-3167
-
-
Vernes, S.C.1
-
4
-
-
84881666129
-
Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria
-
Turner, S. J. et al. Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria. Am J Med Genet A 161A, 2321-2326 (2013).
-
(2013)
Am J Med Genet A
, vol.161 A
, pp. 2321-2326
-
-
Turner, S.J.1
-
5
-
-
84930651336
-
Monoallelic expression of the human FOXP2 speech gene
-
Adegbola, A. A. et al. Monoallelic expression of the human FOXP2 speech gene. Proc Natl Acad Sci USA 112, 6848-6854 (2015).
-
(2015)
Proc Natl Acad Sci USA
, vol.112
, pp. 6848-6854
-
-
Adegbola, A.A.1
-
6
-
-
84894305155
-
The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2
-
Nazaryan, L. et al. The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2. Eur J Hum Genet 22, 338-343 (2014).
-
(2014)
Eur J Hum Genet
, vol.22
, pp. 338-343
-
-
Nazaryan, L.1
-
7
-
-
84900333689
-
Etiological yield of SNP microarrays in idiopathic intellectual disability
-
Utine, G. E. et al. Etiological yield of SNP microarrays in idiopathic intellectual disability. Eur J Paediatr Neurol 18, 327-337 (2014).
-
(2014)
Eur J Paediatr Neurol
, vol.18
, pp. 327-337
-
-
Utine, G.E.1
-
8
-
-
79960955811
-
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain
-
Vernes, S. C. et al. Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS Genet 7, e1002145 (2011).
-
(2011)
PLoS Genet
, vol.7
, pp. e1002145
-
-
Vernes, S.C.1
-
9
-
-
40149112272
-
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits
-
Groszer, M. et al. Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Curr Biol 18, 354-362 (2008).
-
(2008)
Curr Biol
, vol.18
, pp. 354-362
-
-
Groszer, M.1
-
10
-
-
0037467540
-
Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain
-
Ferland, R. J., Cherry, T. J., Preware, P. O., Morrisey, E. E. & Walsh, C. A. Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. J Comp Neurol 460, 266-279 (2003).
-
(2003)
J Comp Neurol
, vol.460
, pp. 266-279
-
-
Ferland, R.J.1
Cherry, T.J.2
Preware, P.O.3
Morrisey, E.E.4
Walsh, C.A.5
-
11
-
-
0142153166
-
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
-
Lai, C. S., Gerrelli, D., Monaco, A. P., Fisher, S. E. & Copp, A. J. FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain 126, 2455-2462 (2003).
-
(2003)
Brain
, vol.126
, pp. 2455-2462
-
-
Lai, C.S.1
Gerrelli, D.2
Monaco, A.P.3
Fisher, S.E.4
Copp, A.J.5
-
12
-
-
63449102727
-
FOXP2 as a molecular window into speech and language
-
Fisher, S. E. & Scharff, C. FOXP2 as a molecular window into speech and language. Trends Genet 25, 166-177 (2009).
-
(2009)
Trends Genet
, vol.25
, pp. 166-177
-
-
Fisher, S.E.1
Scharff, C.2
-
13
-
-
84904470753
-
What can mice tell us about Foxp2 function?
-
French, C. A. & Fisher, S. E. What can mice tell us about Foxp2 function? Curr Opin Neurobiol 28, 72-79 (2014).
-
(2014)
Curr Opin Neurobiol
, vol.28
, pp. 72-79
-
-
French, C.A.1
Fisher, S.E.2
-
14
-
-
84867896115
-
An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
-
French, C. A. et al. An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning. Mol Psychiatry 17, 1077-1085 (2012).
-
(2012)
Mol Psychiatry
, vol.17
, pp. 1077-1085
-
-
French, C.A.1
-
15
-
-
84976287113
-
FoxP2 protein levels regulate cell morphology changes and migration patterns in the vertebrate developing telencephalon
-
Garcia-Calero, E., Botella-Lopez, A., Bahamonde, O., Perez-Balaguer, A. & Martinez, S. FoxP2 protein levels regulate cell morphology changes and migration patterns in the vertebrate developing telencephalon. Brain Struct Funct doi: 10.1007/s00429-015-1079-7 (2015).
-
(2015)
Brain Struct Funct
-
-
Garcia-Calero, E.1
Botella-Lopez, A.2
Bahamonde, O.3
Perez-Balaguer, A.4
Martinez, S.5
-
16
-
-
84871770267
-
FoxP2 regulates neurogenesis during embryonic cortical development
-
Tsui, D., Vessey, J. P., Tomita, H., Kaplan, D. R. & Miller, F. D. FoxP2 regulates neurogenesis during embryonic cortical development. J Neurosci 33, 244-258 (2013).
-
(2013)
J Neurosci
, vol.33
, pp. 244-258
-
-
Tsui, D.1
Vessey, J.P.2
Tomita, H.3
Kaplan, D.R.4
Miller, F.D.5
-
17
-
-
38549176222
-
Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X
-
Haesler, S. et al. Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. PLoS Biol 5, e321 (2007).
-
(2007)
PLoS Biol
, vol.5
, pp. e321
-
-
Haesler, S.1
-
18
-
-
84922985404
-
Behavior-linked FoxP2 regulation enables zebra finch vocal learning
-
Heston, J. B. & White, S. A. Behavior-linked FoxP2 regulation enables zebra finch vocal learning. J Neurosci 35, 2885-2894 (2015).
-
(2015)
J Neurosci
, vol.35
, pp. 2885-2894
-
-
Heston, J.B.1
White, S.A.2
-
19
-
-
1842454166
-
FoxP2 expression in avian vocal learners and non-learners
-
Haesler, S. et al. FoxP2 expression in avian vocal learners and non-learners. J Neurosci 24, 3164-3175 (2004).
-
(2004)
J Neurosci
, vol.24
, pp. 3164-3175
-
-
Haesler, S.1
-
20
-
-
34250896735
-
Recruitment of FoxP2-expressing neurons to area X varies during song development
-
Rochefort, C., He, X., Scotto-Lomassese, S. & Scharff, C. Recruitment of FoxP2-expressing neurons to area X varies during song development. Dev Neurobiol 67, 809-817 (2007).
-
(2007)
Dev Neurobiol
, vol.67
, pp. 809-817
-
-
Rochefort, C.1
He, X.2
Scotto-Lomassese, S.3
Scharff, C.4
-
21
-
-
84890493080
-
Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability
-
Murugan, M., Harward, S., Scharff, C. & Mooney, R. Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability. Neuron 80, 1464-1476 (2013).
-
(2013)
Neuron
, vol.80
, pp. 1464-1476
-
-
Murugan, M.1
Harward, S.2
Scharff, C.3
Mooney, R.4
-
22
-
-
33746083657
-
FoxP2 regulation during undirected singing in adult songbirds
-
Teramitsu, I. & White, S. A. FoxP2 regulation during undirected singing in adult songbirds. J Neurosci 26, 7390-7394 (2006).
-
(2006)
J Neurosci
, vol.26
, pp. 7390-7394
-
-
Teramitsu, I.1
White, S.A.2
-
23
-
-
57349177015
-
Birdsong decreases protein levels of FoxP2, a molecule required for human speech
-
Miller, J. E. et al. Birdsong decreases protein levels of FoxP2, a molecule required for human speech. J Neurophysiol 100, 2015-2025 (2008).
-
(2008)
J Neurophysiol
, vol.100
, pp. 2015-2025
-
-
Miller, J.E.1
-
24
-
-
84873712764
-
Young and intense: FoxP2 immunoreactivity in Area X varies with age, song stereotypy, and singing in male zebra finches
-
Thompson, C. K. et al. Young and intense: FoxP2 immunoreactivity in Area X varies with age, song stereotypy, and singing in male zebra finches. Front Neural Circuits 7, 24 (2013).
-
(2013)
Front Neural Circuits
, vol.7
, pp. 24
-
-
Thompson, C.K.1
-
25
-
-
84928288385
-
Differential coexpression of FoxP1, FoxP2, and FoxP4 in the Zebra Finch (Taeniopygia guttata) song system
-
Mendoza, E. et al. Differential coexpression of FoxP1, FoxP2, and FoxP4 in the Zebra Finch (Taeniopygia guttata) song system. J Comp Neurol 523, 1318-1340 (2015).
-
(2015)
J Comp Neurol
, vol.523
, pp. 1318-1340
-
-
Mendoza, E.1
-
26
-
-
84908096053
-
Multiple microRNAs regulate human FOXP2 gene expression by targeting sequences in its 3′ untranslated region
-
Fu, L. et al. Multiple microRNAs regulate human FOXP2 gene expression by targeting sequences in its 3′ untranslated region. Mol Brain 7, 71 (2014).
-
(2014)
Mol Brain
, vol.7
, pp. 71
-
-
Fu, L.1
-
27
-
-
84948710248
-
A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment
-
Lozano, R., Vino, A., Lozano, C., Fisher, S. E. & Deriziotis, P. A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment. Eur J Hum Genet 23, 1702-1707 (2015).
-
(2015)
Eur J Hum Genet
, vol.23
, pp. 1702-1707
-
-
Lozano, R.1
Vino, A.2
Lozano, C.3
Fisher, S.E.4
Deriziotis, P.5
-
28
-
-
84923327027
-
De novo TBR1 mutations in sporadic autism disrupt protein functions
-
Deriziotis, P. et al. De novo TBR1 mutations in sporadic autism disrupt protein functions. Nat Commun 5, 4954 (2014).
-
(2014)
Nat Commun
, vol.5
, pp. 4954
-
-
Deriziotis, P.1
-
29
-
-
84901419964
-
Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer
-
Deriziotis, P., Graham, S. A., Estruch, S. B. & Fisher, S. E. Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer. J Vis Exp doi: 10.3791/51438 (2014).
-
(2014)
J Vis Exp
-
-
Deriziotis, P.1
Graham, S.A.2
Estruch, S.B.3
Fisher, S.E.4
-
30
-
-
0347986673
-
Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions
-
Li, S., Weidenfeld, J. & Morrisey, E. E. Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions. Mol Cell Biol 24, 809-822 (2004).
-
(2004)
Mol Cell Biol
, vol.24
, pp. 809-822
-
-
Li, S.1
Weidenfeld, J.2
Morrisey, E.E.3
-
31
-
-
42049108221
-
Cell biology: SUMO
-
Meulmeester, E. & Melchior, F. Cell biology: SUMO. Nature 452, 709-711 (2008).
-
(2008)
Nature
, vol.452
, pp. 709-711
-
-
Meulmeester, E.1
Melchior, F.2
-
32
-
-
73649111322
-
PIAS proteins: Pleiotropic interactors associated with SUMO
-
Rytinki, M. M., Kaikkonen, S., Pehkonen, P., Jaaskelainen, T. & Palvimo, J. J. PIAS proteins: pleiotropic interactors associated with SUMO. Cell Mol Life Sci 66, 3029-3041 (2009).
-
(2009)
Cell Mol Life Sci
, vol.66
, pp. 3029-3041
-
-
Rytinki, M.M.1
Kaikkonen, S.2
Pehkonen, P.3
Jaaskelainen, T.4
Palvimo, J.J.5
-
33
-
-
79958204980
-
Protein interactome reveals converging molecular pathways among autism disorders
-
Sakai, Y. et al. Protein interactome reveals converging molecular pathways among autism disorders. Sci Transl Med 3, 86ra49 (2011).
-
(2011)
Sci Transl Med
, vol.3
, pp. 86ra49
-
-
Sakai, Y.1
-
34
-
-
0036291475
-
PIAS proteins modulate transcription factors by functioning as SUMO-1 ligases
-
Kotaja, N., Karvonen, U., Janne, O. A. & Palvimo, J. J. PIAS proteins modulate transcription factors by functioning as SUMO-1 ligases. Mol Cell Biol 22, 5222-5234 (2002).
-
(2002)
Mol Cell Biol
, vol.22
, pp. 5222-5234
-
-
Kotaja, N.1
Karvonen, U.2
Janne, O.A.3
Palvimo, J.J.4
-
35
-
-
33847649960
-
Ubc9 fusion-directed SUMOylation (UFDS): A method to analyze function of protein SUMOylation
-
Jakobs, A. et al. Ubc9 fusion-directed SUMOylation (UFDS): a method to analyze function of protein SUMOylation. Nat Methods 4, 245-250 (2007).
-
(2007)
Nat Methods
, vol.4
, pp. 245-250
-
-
Jakobs, A.1
-
36
-
-
0034789730
-
Involvement of PIAS1 in the sumoylation of tumor suppressor p53
-
Kahyo, T., Nishida, T. & Yasuda, H. Involvement of PIAS1 in the sumoylation of tumor suppressor p53. Mol Cell 8, 713-718 (2001).
-
(2001)
Mol Cell
, vol.8
, pp. 713-718
-
-
Kahyo, T.1
Nishida, T.2
Yasuda, H.3
-
38
-
-
84904804885
-
GPS-SUMO: A tool for the prediction of sumoylation sites and SUMO-interaction motifs
-
Zhao, Q. et al. GPS-SUMO: a tool for the prediction of sumoylation sites and SUMO-interaction motifs. Nucleic Acids Res 42, W325-330 (2014).
-
(2014)
Nucleic Acids Res
, vol.42
, pp. W325-330
-
-
Zhao, Q.1
-
39
-
-
84947557944
-
JASSA: A comprehensive tool for prediction of SUMOylation sites and SIMs
-
Beauclair, G., Bridier-Nahmias, A., Zagury, J. F., Saib, A. & Zamborlini, A. JASSA: a comprehensive tool for prediction of SUMOylation sites and SIMs. Bioinformatics 31, 3483-3491 (2015).
-
(2015)
Bioinformatics
, vol.31
, pp. 3483-3491
-
-
Beauclair, G.1
Bridier-Nahmias, A.2
Zagury, J.F.3
Saib, A.4
Zamborlini, A.5
-
40
-
-
49549122501
-
Understanding eukaryotic linear motifs and their role in cell signaling and regulation
-
Diella, F. et al. Understanding eukaryotic linear motifs and their role in cell signaling and regulation. Front Biosci 13, 6580-6603 (2008).
-
(2008)
Front Biosci
, vol.13
, pp. 6580-6603
-
-
Diella, F.1
-
41
-
-
58149163609
-
KEPE-A motif frequently superimposed on sumoylation sites in metazoan chromatin proteins and transcription factors
-
Diella, F. et al. KEPE-a motif frequently superimposed on sumoylation sites in metazoan chromatin proteins and transcription factors. Bioinformatics 25, 1-5 (2009).
-
(2009)
Bioinformatics
, vol.25
, pp. 1-5
-
-
Diella, F.1
-
42
-
-
70249111471
-
Detection of protein SUMOylation in vivo
-
Tatham, M. H., Rodriguez, M. S., Xirodimas, D. P. & Hay, R. T. Detection of protein SUMOylation in vivo. Nat Protoc 4, 1363-1371 (2009).
-
(2009)
Nat Protoc
, vol.4
, pp. 1363-1371
-
-
Tatham, M.H.1
Rodriguez, M.S.2
Xirodimas, D.P.3
Hay, R.T.4
-
43
-
-
78649477258
-
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex
-
Roll, P. et al. Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. Hum Mol Genet 19, 4848-4860 (2010).
-
(2010)
Hum Mol Genet
, vol.19
, pp. 4848-4860
-
-
Roll, P.1
-
44
-
-
33644800026
-
Structure of the forkhead domain of FOXP2 bound to DNA
-
Stroud, J. C. et al. Structure of the forkhead domain of FOXP2 bound to DNA. Structure 14, 159-166 (2006).
-
(2006)
Structure
, vol.14
, pp. 159-166
-
-
Stroud, J.C.1
-
45
-
-
4644340117
-
Foxp4: A novel member of the Foxp subfamily of winged-helix genes co-expressed with Foxp1 and Foxp2 in pulmonary and gut tissues
-
Lu, M. M., Li, S., Yang, H. & Morrisey, E. E. Foxp4: a novel member of the Foxp subfamily of winged-helix genes co-expressed with Foxp1 and Foxp2 in pulmonary and gut tissues. Mech Dev 119 Suppl 1, S197-202 (2002).
-
(2002)
Mech Dev
, vol.119
, pp. S197-202
-
-
Lu, M.M.1
Li, S.2
Yang, H.3
Morrisey, E.E.4
-
46
-
-
0037385330
-
Foxp3 programs the development and function of CD4 + CD25 + regulatory T cells
-
Fontenot, J. D., Gavin, M. A. & Rudensky, A. Y. Foxp3 programs the development and function of CD4 + CD25 + regulatory T cells. Nat Immunol 4, 330-336 (2003).
-
(2003)
Nat Immunol
, vol.4
, pp. 330-336
-
-
Fontenot, J.D.1
Gavin, M.A.2
Rudensky, A.Y.3
-
47
-
-
84888066687
-
FOXP1 mutations cause intellectual disability and a recognizable phenotype
-
Le Fevre, A. K. et al. FOXP1 mutations cause intellectual disability and a recognizable phenotype. Am J Med Genet A 161A, 3166-3175 (2013).
-
(2013)
Am J Med Genet A
, vol.161 A
, pp. 3166-3175
-
-
Le Fevre, A.K.1
-
48
-
-
77957896206
-
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
-
Horn, D. et al. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Hum Mutat 31, E1851-1860 (2010).
-
(2010)
Hum Mutat
, vol.31
, pp. E1851-1860
-
-
Horn, D.1
-
49
-
-
78249268820
-
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment
-
Hamdan, F. F. et al. De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. Am J Hum Genet 87, 671-678 (2010).
-
(2010)
Am J Hum Genet
, vol.87
, pp. 671-678
-
-
Hamdan, F.F.1
-
50
-
-
79957589237
-
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
-
O'Roak, B. J. et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nat Genet 43, 585-589 (2011).
-
(2011)
Nat Genet
, vol.43
, pp. 585-589
-
-
O'Roak, B.J.1
-
51
-
-
84867581362
-
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
-
Bacon, C. & Rappold, G. A. The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders. Hum Genet 131, 1687-1698 (2012).
-
(2012)
Hum Genet
, vol.131
, pp. 1687-1698
-
-
Bacon, C.1
Rappold, G.A.2
-
52
-
-
67649173012
-
System-wide changes to SUMO modifications in response to heat shock
-
Golebiowski, F. et al. System-wide changes to SUMO modifications in response to heat shock. Sci Signal 2, ra24 (2009).
-
(2009)
Sci Signal
, vol.2
, pp. ra24
-
-
Golebiowski, F.1
-
53
-
-
79959381925
-
Comparative proteomic analysis identifies a role for SUMO in protein quality control
-
Tatham, M. H., Matic, I., Mann, M. & Hay, R. T. Comparative proteomic analysis identifies a role for SUMO in protein quality control. Sci Signal 4, rs4 (2011).
-
(2011)
Sci Signal
, vol.4
, pp. rs4
-
-
Tatham, M.H.1
Matic, I.2
Mann, M.3
Hay, R.T.4
-
54
-
-
84905368957
-
Important role of SUMOylation of Spliceosome factors in prostate cancer cells
-
Wen, D. et al. Important role of SUMOylation of Spliceosome factors in prostate cancer cells. J Proteome Res 13, 3571-3582 (2014).
-
(2014)
J Proteome Res
, vol.13
, pp. 3571-3582
-
-
Wen, D.1
-
55
-
-
28444448039
-
The SUMO pathway is essential for nuclear integrity and chromosome segregation in mice
-
Nacerddine, K. et al. The SUMO pathway is essential for nuclear integrity and chromosome segregation in mice. Dev Cell 9, 769-779 (2005).
-
(2005)
Dev Cell
, vol.9
, pp. 769-779
-
-
Nacerddine, K.1
-
56
-
-
84858388660
-
Developmental regulation and spatiotemporal redistribution of the sumoylation machinery in the rat central nervous system
-
Loriol, C., Parisot, J., Poupon, G., Gwizdek, C. & Martin, S. Developmental regulation and spatiotemporal redistribution of the sumoylation machinery in the rat central nervous system. PLoS One 7, e33757 (2012).
-
(2012)
PLoS One
, vol.7
, pp. e33757
-
-
Loriol, C.1
Parisot, J.2
Poupon, G.3
Gwizdek, C.4
Martin, S.5
-
57
-
-
84903973595
-
Spatiotemporal distribution of SUMOylation components during mouse brain development
-
Hasegawa, Y., Yoshida, D., Nakamura, Y. & Sakakibara, S. Spatiotemporal distribution of SUMOylation components during mouse brain development. J Comp Neurol 522, 3020-3036 (2014).
-
(2014)
J Comp Neurol
, vol.522
, pp. 3020-3036
-
-
Hasegawa, Y.1
Yoshida, D.2
Nakamura, Y.3
Sakakibara, S.4
-
58
-
-
84888197260
-
Protein sumoylation in brain development, neuronal morphology and spinogenesis
-
Gwizdek, C., Casse, F. & Martin, S. Protein sumoylation in brain development, neuronal morphology and spinogenesis. Neuromolecular Med 15, 677-691 (2013).
-
(2013)
Neuromolecular Med
, vol.15
, pp. 677-691
-
-
Gwizdek, C.1
Casse, F.2
Martin, S.3
-
59
-
-
79961242786
-
Eliminating SF-1 (NR5A1) sumoylation in vivo results in ectopic hedgehog signaling and disruption of endocrine development
-
Lee, F. Y. et al. Eliminating SF-1 (NR5A1) sumoylation in vivo results in ectopic hedgehog signaling and disruption of endocrine development. Dev Cell 21, 315-327 (2011).
-
(2011)
Dev Cell
, vol.21
, pp. 315-327
-
-
Lee, F.Y.1
-
60
-
-
4644367257
-
PIAS1 selectively inhibits interferon-inducible genes and is important in innate immunity
-
Liu, B. et al. PIAS1 selectively inhibits interferon-inducible genes and is important in innate immunity. Nat Immunol 5, 891-898 (2004).
-
(2004)
Nat Immunol
, vol.5
, pp. 891-898
-
-
Liu, B.1
-
61
-
-
21344432585
-
Disruption of the murine PIASx gene results in reduced testis weight
-
Santti, H. et al. Disruption of the murine PIASx gene results in reduced testis weight. J Mol Endocrinol 34, 645-654 (2005).
-
(2005)
J Mol Endocrinol
, vol.34
, pp. 645-654
-
-
Santti, H.1
-
62
-
-
2942557397
-
Protein inhibitor of activated STAT y (PIASy) and a splice variant lacking exon 6 enhance sumoylation but are not essential for embryogenesis and adult life
-
Wong, K. A. et al. Protein inhibitor of activated STAT Y (PIASy) and a splice variant lacking exon 6 enhance sumoylation but are not essential for embryogenesis and adult life. Mol Cell Biol 24, 5577-5586 (2004).
-
(2004)
Mol Cell Biol
, vol.24
, pp. 5577-5586
-
-
Wong, K.A.1
-
63
-
-
77949720991
-
The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: Sumoylation affects its stability, localization, and activity
-
Marongiu, M. et al. The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity. PLoS One 5, e9477 (2010).
-
(2010)
PLoS One
, vol.5
, pp. e9477
-
-
Marongiu, M.1
-
64
-
-
84868295291
-
Forkhead box protein A2 (FOXA2) protein stability and activity are regulated by sumoylation
-
Belaguli, N. S., Zhang, M., Brunicardi, F. C. & Berger, D. H. Forkhead box protein A2 (FOXA2) protein stability and activity are regulated by sumoylation. PLoS One 7, e48019 (2012).
-
(2012)
PLoS One
, vol.7
, pp. e48019
-
-
Belaguli, N.S.1
Zhang, M.2
Brunicardi, F.C.3
Berger, D.H.4
-
65
-
-
79956294799
-
Forkhead transcription factors: Key players in health and disease
-
Benayoun, B. A., Caburet, S. & Veitia, R. A. Forkhead transcription factors: key players in health and disease. Trends Genet 27, 224-232 (2011).
-
(2011)
Trends Genet
, vol.27
, pp. 224-232
-
-
Benayoun, B.A.1
Caburet, S.2
Veitia, R.A.3
-
66
-
-
84957309430
-
The key regulator for language and speech development, FOXP2, is a novel substrate for SUMOylation
-
Meredith, L. J. et al. The key regulator for language and speech development, FOXP2, is a novel substrate for SUMOylation. J Cell Biochem doi: 10.1002/jcb.25288 (2015).
-
(2015)
J Cell Biochem
-
-
Meredith, L.J.1
|