-
1
-
-
78149259999
-
Correction of respiratory disorders in a mouse model of Rett syndrome
-
Abdala A.P., Dutschmann M., Bissonnette J.M., Paton J.F. Correction of respiratory disorders in a mouse model of Rett syndrome. Proc Natl Acad Sci U S A 2010, 107:18208-18213.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 18208-18213
-
-
Abdala, A.P.1
Dutschmann, M.2
Bissonnette, J.M.3
Paton, J.F.4
-
2
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir R.E., Van den Veyver I.B., Wan M., Tran C.Q., Francke U., Zoghbi H.Y. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 1999, 23:185-188.
-
(1999)
Nat Genet
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
Van den Veyver, I.B.2
Wan, M.3
Tran, C.Q.4
Francke, U.5
Zoghbi, H.Y.6
-
3
-
-
33847267187
-
Correlation between clinical severity in patients with Rett syndrome with a p. R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation
-
Archer H., Evans J., Leonard H., Colvin L., Ravine D., Christodoulou J., Williamson S., Charman T., Bailey M.E., Sampson J., de Klerk N., Clarke A. Correlation between clinical severity in patients with Rett syndrome with a p. R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation. J Med Genet 2007, 44:148-152.
-
(2007)
J Med Genet
, vol.44
, pp. 148-152
-
-
Archer, H.1
Evans, J.2
Leonard, H.3
Colvin, L.4
Ravine, D.5
Christodoulou, J.6
Williamson, S.7
Charman, T.8
Bailey, M.E.9
Sampson, J.10
de Klerk, N.11
Clarke, A.12
-
4
-
-
40549110266
-
Investigating genotype-phenotype relationships in Rett syndrome using an international data set
-
Bebbington A., Anderson A., Ravine D., Fyfe S., Pineda M., de Klerk N., Ben-Zeev B., Yatawara N., Percy A., Kaufmann W.E., Leonard H. Investigating genotype-phenotype relationships in Rett syndrome using an international data set. Neurology 2008, 70:868-875.
-
(2008)
Neurology
, vol.70
, pp. 868-875
-
-
Bebbington, A.1
Anderson, A.2
Ravine, D.3
Fyfe, S.4
Pineda, M.5
de Klerk, N.6
Ben-Zeev, B.7
Yatawara, N.8
Percy, A.9
Kaufmann, W.E.10
Leonard, H.11
-
5
-
-
33646893456
-
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
-
Bienvenu T., Chelly J. Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized. Nat Rev Genet 2006, 7:415-426.
-
(2006)
Nat Rev Genet
, vol.7
, pp. 415-426
-
-
Bienvenu, T.1
Chelly, J.2
-
6
-
-
33646688438
-
Separate respiratory phenotypes in methyl-CpG-binding protein 2 (Mecp2) deficient mice
-
Bissonnette J.M., Knopp S.J. Separate respiratory phenotypes in methyl-CpG-binding protein 2 (Mecp2) deficient mice. Pediatr Res 2006, 59:513-518.
-
(2006)
Pediatr Res
, vol.59
, pp. 513-518
-
-
Bissonnette, J.M.1
Knopp, S.J.2
-
7
-
-
3042775154
-
X-chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain
-
Braunschweig D., Simcox T., Samaco R.C., LaSalle J.M. X-chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain. Hum Mol Genet 2004, 13:1275-1286.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1275-1286
-
-
Braunschweig, D.1
Simcox, T.2
Samaco, R.C.3
LaSalle, J.M.4
-
8
-
-
79955748023
-
Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model
-
Brendel C., Belakhov V., Werner H., Wegener E., Gartner J., Nudelman I., Baasov T., Huppke P. Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model. J Mol Med (Berl) 2007, 89:389-398.
-
(2007)
J Mol Med (Berl)
, vol.89
, pp. 389-398
-
-
Brendel, C.1
Belakhov, V.2
Werner, H.3
Wegener, E.4
Gartner, J.5
Nudelman, I.6
Baasov, T.7
Huppke, P.8
-
9
-
-
1642482969
-
Refining the phenotype of common mutations in Rett syndrome
-
Colvin L., Leonard H., de Klerk N., Davis M., Weaving L., Williamson S., Christodoulou J. Refining the phenotype of common mutations in Rett syndrome. J Med Genet 2004, 41:25-30.
-
(2004)
J Med Genet
, vol.41
, pp. 25-30
-
-
Colvin, L.1
Leonard, H.2
de Klerk, N.3
Davis, M.4
Weaving, L.5
Williamson, S.6
Christodoulou, J.7
-
10
-
-
33749350208
-
Postnatal developmental changes in CO2 sensitivity in rats
-
Davis S.E., Solhied G., Castillo M., Dwinell M., Brozoski D., Forster H.V. Postnatal developmental changes in CO2 sensitivity in rats. J Appl Physiol 2006, 101:1097-1103.
-
(2006)
J Appl Physiol
, vol.101
, pp. 1097-1103
-
-
Davis, S.E.1
Solhied, G.2
Castillo, M.3
Dwinell, M.4
Brozoski, D.5
Forster, H.V.6
-
11
-
-
69749099201
-
Genotype-phenotype correlation in Brazillian Rett syndrome patients
-
de Lima F.T., Brunoni D., Schwartzman J.S., Pozzi M.C., Kok F., Juliano Y., Pereira L.V. Genotype-phenotype correlation in Brazillian Rett syndrome patients. Arq Neuropsiquiatr 2009, 67:577-584.
-
(2009)
Arq Neuropsiquiatr
, vol.67
, pp. 577-584
-
-
de Lima, F.T.1
Brunoni, D.2
Schwartzman, J.S.3
Pozzi, M.C.4
Kok, F.5
Juliano, Y.6
Pereira, L.V.7
-
12
-
-
0033837358
-
Ventrolateral pons mediates short-term depression of respiratory frequency after brief hypoxia
-
Dick T.E., Coles S.K. Ventrolateral pons mediates short-term depression of respiratory frequency after brief hypoxia. Respir Physiol 2000, 121:87-100.
-
(2000)
Respir Physiol
, vol.121
, pp. 87-100
-
-
Dick, T.E.1
Coles, S.K.2
-
13
-
-
84856270235
-
Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses
-
Goffin D., Allen M., Zhang L., Amorim M., Wang I.T., Reyes A.R., Mercado-Berton A., Ong C., Cohen S., Hu L., Blendy J.A., Carlson G.C., Siegel S.J., Greenberg M.E., Zhou Z. Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses. Nat Neurosci 2011, 15:274-283.
-
(2011)
Nat Neurosci
, vol.15
, pp. 274-283
-
-
Goffin, D.1
Allen, M.2
Zhang, L.3
Amorim, M.4
Wang, I.T.5
Reyes, A.R.6
Mercado-Berton, A.7
Ong, C.8
Cohen, S.9
Hu, L.10
Blendy, J.A.11
Carlson, G.C.12
Siegel, S.J.13
Greenberg, M.E.14
Zhou, Z.15
-
14
-
-
80054047383
-
The role of MeCP2 in the brain
-
Guy J., Cheval H., Selfridge J., Bird A. The role of MeCP2 in the brain. Annu Rev Cell Dev Biol 2011, 27:631-652.
-
(2011)
Annu Rev Cell Dev Biol
, vol.27
, pp. 631-652
-
-
Guy, J.1
Cheval, H.2
Selfridge, J.3
Bird, A.4
-
15
-
-
84856212881
-
Genotype-phenotype relationships as prognosticators in Rett syndrome should be handled with care in clinical practice
-
Halbach N.S., Smeets E.E., van den Braak N., van Roozendaal K.E., Blok R.M., Schrander-Stumpel C.T., Frijns J.P., Maaskant M.A., Curfs L.M. Genotype-phenotype relationships as prognosticators in Rett syndrome should be handled with care in clinical practice. Am J Med Genet A 2012, 158A:340-350.
-
(2012)
Am J Med Genet A
, vol.158 A
, pp. 340-350
-
-
Halbach, N.S.1
Smeets, E.E.2
van den Braak, N.3
van Roozendaal, K.E.4
Blok, R.M.5
Schrander-Stumpel, C.T.6
Frijns, J.P.7
Maaskant, M.A.8
Curfs, L.M.9
-
16
-
-
39549090166
-
MeCP2 binding to DNA depends upon hydration at methyl-CpG
-
Ho K.L., McNae I.W., Schmiedeberg L., Klose R.J., Bird A.P., Walkinshaw M.D. MeCP2 binding to DNA depends upon hydration at methyl-CpG. Mol Cell 2008, 29:525-531.
-
(2008)
Mol Cell
, vol.29
, pp. 525-531
-
-
Ho, K.L.1
McNae, I.W.2
Schmiedeberg, L.3
Klose, R.J.4
Bird, A.P.5
Walkinshaw, M.D.6
-
17
-
-
0035409467
-
Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder
-
Julu P.O., Kerr A.M., Apartopoulos F., Al-Rawas S., Engerstrom I.W., Engerstrom L., Jamal G.A., Hansen S. Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder. Arch Dis Child 2001, 85:29-37.
-
(2001)
Arch Dis Child
, vol.85
, pp. 29-37
-
-
Julu, P.O.1
Kerr, A.M.2
Apartopoulos, F.3
Al-Rawas, S.4
Engerstrom, I.W.5
Engerstrom, L.6
Jamal, G.A.7
Hansen, S.8
-
18
-
-
69249232208
-
Breathing disorders in Rett syndrome: progressive neurochemical dysfunction in the respiratory network after birth
-
Katz D.M., Dutschmann M., Ramirez J.M., Hilaire G. Breathing disorders in Rett syndrome: progressive neurochemical dysfunction in the respiratory network after birth. Respir Physiol Neurobiol 2009, 168:101-108.
-
(2009)
Respir Physiol Neurobiol
, vol.168
, pp. 101-108
-
-
Katz, D.M.1
Dutschmann, M.2
Ramirez, J.M.3
Hilaire, G.4
-
19
-
-
84870018625
-
Preclinical research in Rett syndrome: setting the foundation for translational success
-
Katz D.M., Berger-Sweeney J.E., Eubanks J.H., Justice M.J., Neul J.L., Pozzo-Miller L., Blue M.E., Christian D., Crawley J.N., Giustetto M., Guy J., Howell C.J., Kron M., Nelson S.B., Samaco R.C., Schaevitz L.R., St Hillaire-Clarke C., Young J.L., Zoghbi H.Y., Mamounas L.A. Preclinical research in Rett syndrome: setting the foundation for translational success. Dis Model Mech 2012, 5:733-745.
-
(2012)
Dis Model Mech
, vol.5
, pp. 733-745
-
-
Katz, D.M.1
Berger-Sweeney, J.E.2
Eubanks, J.H.3
Justice, M.J.4
Neul, J.L.5
Pozzo-Miller, L.6
Blue, M.E.7
Christian, D.8
Crawley, J.N.9
Giustetto, M.10
Guy, J.11
Howell, C.J.12
Kron, M.13
Nelson, S.B.14
Samaco, R.C.15
Schaevitz, L.R.16
St Hillaire-Clarke, C.17
Young, J.L.18
Zoghbi, H.Y.19
Mamounas, L.A.20
more..
-
20
-
-
77951014800
-
Katz DM (Exogenous brain-derived neurotrophic factor rescues synaptic dysfunction in Mecp2-null mice
-
Kline D.D., Ogier M., Kunze D.L. Katz DM (Exogenous brain-derived neurotrophic factor rescues synaptic dysfunction in Mecp2-null mice. J Neurosci 2010, 30:5303-5310.
-
(2010)
J Neurosci
, vol.30
, pp. 5303-5310
-
-
Kline, D.D.1
Ogier, M.2
Kunze, D.L.3
-
21
-
-
43149121772
-
Analysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivo
-
Kumar A., Kamboj S., Malone B.M., Kudo S., Twiss J.L., Czymmek K.J., LaSalle J.M., Schanen N.C. Analysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivo. J Cell Sci 2008, 121:1128-1137.
-
(2008)
J Cell Sci
, vol.121
, pp. 1128-1137
-
-
Kumar, A.1
Kamboj, S.2
Malone, B.M.3
Kudo, S.4
Twiss, J.L.5
Czymmek, K.J.6
LaSalle, J.M.7
Schanen, N.C.8
-
22
-
-
35548983001
-
Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant mice
-
Lawson-Yuen A., Liu D., Han L., Jiang Z.I., Tsai G.E., Basu A.C., Picker J., Feng J., Coyle J.T. Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant mice. Brain Res 2007, 1180:1-6.
-
(2007)
Brain Res
, vol.1180
, pp. 1-6
-
-
Lawson-Yuen, A.1
Liu, D.2
Han, L.3
Jiang, Z.I.4
Tsai, G.E.5
Basu, A.C.6
Picker, J.7
Feng, J.8
Coyle, J.T.9
-
24
-
-
84883462358
-
Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor
-
Lyst M.J., Ekiert R., Ebert D.H., Merusi C., Nowak J., Selfridge J., Guy J., Kastan N.R., Robinson N.D., de Lima Alves F., Rappsilber J., Greenberg M.E., Bird A. Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor. Nat Neurosci 2013, 16:898-902.
-
(2013)
Nat Neurosci
, vol.16
, pp. 898-902
-
-
Lyst, M.J.1
Ekiert, R.2
Ebert, D.H.3
Merusi, C.4
Nowak, J.5
Selfridge, J.6
Guy, J.7
Kastan, N.R.8
Robinson, N.D.9
de Lima Alves, F.10
Rappsilber, J.11
Greenberg, M.E.12
Bird, A.13
-
25
-
-
0020597235
-
Two-sidearm tracheal cannula for respiratory airflow measurements in small animals
-
Mortola J.P., Noworaj A. Two-sidearm tracheal cannula for respiratory airflow measurements in small animals. J Appl Physiol 1983, 55:250-253.
-
(1983)
J Appl Physiol
, vol.55
, pp. 250-253
-
-
Mortola, J.P.1
Noworaj, A.2
-
26
-
-
42249095974
-
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome
-
Neul J.L., Fang P., Barrish J., Lane J., Caeg E.B., Smith E.O., Zoghbi H., Percy A., Glaze D.G. Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome. Neurology 2008, 70:1313-1321.
-
(2008)
Neurology
, vol.70
, pp. 1313-1321
-
-
Neul, J.L.1
Fang, P.2
Barrish, J.3
Lane, J.4
Caeg, E.B.5
Smith, E.O.6
Zoghbi, H.7
Percy, A.8
Glaze, D.G.9
-
27
-
-
84886239167
-
Breathing challenges in Rett syndrome: lessons learned from humans and animal models
-
Ramirez J.M., Ward C.S., Neul J.L. Breathing challenges in Rett syndrome: lessons learned from humans and animal models. Respir Physiol Neurobiol 2013, 189:280-287.
-
(2013)
Respir Physiol Neurobiol
, vol.189
, pp. 280-287
-
-
Ramirez, J.M.1
Ward, C.S.2
Neul, J.L.3
-
28
-
-
84870213306
-
Anxiety-related mechanisms of respiratory dysfunction in a mouse model of Rett syndrome
-
Ren J., Ding X., Funk G.D., Greer J.J. Anxiety-related mechanisms of respiratory dysfunction in a mouse model of Rett syndrome. J Neurosci 2012, 32:17230-17240.
-
(2012)
J Neurosci
, vol.32
, pp. 17230-17240
-
-
Ren, J.1
Ding, X.2
Funk, G.D.3
Greer, J.J.4
-
29
-
-
84870016257
-
Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies
-
Samaco R.C., McGraw C.M., Ward C.S., Sun Y., Neul J.L., Zoghbi H.Y. Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies. Hum Mol Genet 2013, 22:96-109.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 96-109
-
-
Samaco, R.C.1
McGraw, C.M.2
Ward, C.S.3
Sun, Y.4
Neul, J.L.5
Zoghbi, H.Y.6
-
30
-
-
84884980237
-
MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits
-
Schaevitz L.R., Gomez N.B., Zhen D.P., Berger-Sweeney J.E. MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits. Genes Brain Behav 2013, 12:732-740.
-
(2013)
Genes Brain Behav
, vol.12
, pp. 732-740
-
-
Schaevitz, L.R.1
Gomez, N.B.2
Zhen, D.P.3
Berger-Sweeney, J.E.4
-
31
-
-
84863025204
-
A TrkB small molecule partial agonist rescues TrkB phosphorylation deficits and improves respiratory function in a mouse model of Rett syndrome
-
Schmid D.A., Yang T., Ogier M., Adams I., Mirakhur Y., Wang Q., Massa S.M., Longo F.M., Katz D.M. A TrkB small molecule partial agonist rescues TrkB phosphorylation deficits and improves respiratory function in a mouse model of Rett syndrome. J Neurosci 2012, 32:1803-1810.
-
(2012)
J Neurosci
, vol.32
, pp. 1803-1810
-
-
Schmid, D.A.1
Yang, T.2
Ogier, M.3
Adams, I.4
Mirakhur, Y.5
Wang, Q.6
Massa, S.M.7
Longo, F.M.8
Katz, D.M.9
-
32
-
-
33749251447
-
Management of a severe forceful breather with Rett syndrome using carbogen
-
Smeets E.E., Julu P.O., van Waardenburg D., Engerstrom I.W., Hansen S., Apartopoulos F., Curfs L.M., Schrander-Stumpel C.T. Management of a severe forceful breather with Rett syndrome using carbogen. Brain Dev 2006, 28:625-632.
-
(2006)
Brain Dev
, vol.28
, pp. 625-632
-
-
Smeets, E.E.1
Julu, P.O.2
van Waardenburg, D.3
Engerstrom, I.W.4
Hansen, S.5
Apartopoulos, F.6
Curfs, L.M.7
Schrander-Stumpel, C.T.8
-
33
-
-
57749109849
-
Lateral parabrachial nucleus mediates shortening of expiration during hypoxia
-
Song G., Poon C.S. Lateral parabrachial nucleus mediates shortening of expiration during hypoxia. Respir Physiol Neurobiol 2009, 165:1-8.
-
(2009)
Respir Physiol Neurobiol
, vol.165
, pp. 1-8
-
-
Song, G.1
Poon, C.S.2
-
34
-
-
82255177125
-
Habituation without NMDA receptor-dependent desensitization of Hering-Breuer apnea reflex in a Mecp2 mutant mouse model of Rett syndrome
-
Song G., Tin C., Giacometti E., Poon C.S. Habituation without NMDA receptor-dependent desensitization of Hering-Breuer apnea reflex in a Mecp2 mutant mouse model of Rett syndrome. Front Integr Neurosci 2011, 5:6.
-
(2011)
Front Integr Neurosci
, vol.5
, pp. 6
-
-
Song, G.1
Tin, C.2
Giacometti, E.3
Poon, C.S.4
-
35
-
-
0023718501
-
Hyperventilation in the awake state: potentially treatable component of Rett syndrome
-
Southall D.P., Kerr A.M., Tirosh E., Amos P., Lang M.H., Stephenson J.B. Hyperventilation in the awake state: potentially treatable component of Rett syndrome. Arch Dis Child 1988, 63:1039-1048.
-
(1988)
Arch Dis Child
, vol.63
, pp. 1039-1048
-
-
Southall, D.P.1
Kerr, A.M.2
Tirosh, E.3
Amos, P.4
Lang, M.H.5
Stephenson, J.B.6
-
36
-
-
0043178993
-
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos
-
Stancheva I., Collins A.L., Van den Veyver I.B., Zoghbi H., Meehan R.R. A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos. Mol Cell 2003, 12:425-435.
-
(2003)
Mol Cell
, vol.12
, pp. 425-435
-
-
Stancheva, I.1
Collins, A.L.2
Van den Veyver, I.B.3
Zoghbi, H.4
Meehan, R.R.5
-
37
-
-
38449113272
-
Disturbances of breathing in Rett syndrome: results from patients and animal models
-
Stettner G.M., Huppke P., Gartner J., Richter D.W., Dutschmann M. Disturbances of breathing in Rett syndrome: results from patients and animal models. Adv Exp Med Biol 2008, 605:503-507.
-
(2008)
Adv Exp Med Biol
, vol.605
, pp. 503-507
-
-
Stettner, G.M.1
Huppke, P.2
Gartner, J.3
Richter, D.W.4
Dutschmann, M.5
-
38
-
-
84874076142
-
Increasing brain serotonin corrects CO2 chemosensitivity in methyl-CpG-binding protein 2 (Mecp2) deficient mice
-
Toward M., Abdala A.P., Knopp S.J., Paton J.F.R., Bissonnette J.M. Increasing brain serotonin corrects CO2 chemosensitivity in methyl-CpG-binding protein 2 (Mecp2) deficient mice. Exp Physiol 2013, 98:842-849.
-
(2013)
Exp Physiol
, vol.98
, pp. 842-849
-
-
Toward, M.1
Abdala, A.P.2
Knopp, S.J.3
Paton, J.F.R.4
Bissonnette, J.M.5
-
39
-
-
0035192456
-
Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome
-
Van den Veyver I.B., Zoghbi H.Y. Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome. Brain Dev 2001, 23(Suppl. 1):S147-S151.
-
(2001)
Brain Dev
, vol.23
, Issue.SUPPL. 1
-
-
Van den Veyver, I.B.1
Zoghbi, H.Y.2
-
40
-
-
30144441211
-
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
-
Viemari J.C., Roux J.C., Tryba A.K., Saywell V., Burnet H., Pena F., Zanella S., Bevengut M., Barthelemy-Requin M., Herzing L.B., Moncla A., Mancini J., Ramirez J.M., Villard L., Hilaire G. Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice. J Neurosci 2005, 25:11521-11530.
-
(2005)
J Neurosci
, vol.25
, pp. 11521-11530
-
-
Viemari, J.C.1
Roux, J.C.2
Tryba, A.K.3
Saywell, V.4
Burnet, H.5
Pena, F.6
Zanella, S.7
Bevengut, M.8
Barthelemy-Requin, M.9
Herzing, L.B.10
Moncla, A.11
Mancini, J.12
Ramirez, J.M.13
Villard, L.14
Hilaire, G.15
-
41
-
-
69249208529
-
Early breathing defects after moderate hypoxia or hypercapnia in a mouse model of Rett syndrome
-
Voituron N., Zanella S., Menuet C., Dutschmann M., Hilaire G. Early breathing defects after moderate hypoxia or hypercapnia in a mouse model of Rett syndrome. Respir Physiol Neurobiol 2009, 168:109-118.
-
(2009)
Respir Physiol Neurobiol
, vol.168
, pp. 109-118
-
-
Voituron, N.1
Zanella, S.2
Menuet, C.3
Dutschmann, M.4
Hilaire, G.5
-
42
-
-
79960416688
-
MeCP2 is critical within HoxB1-derived tissues of mice for normal lifespan
-
Ward C.S., Arvide E.M., Huang T.W., Yoo J., Noebels J.L., Neul J.L. MeCP2 is critical within HoxB1-derived tissues of mice for normal lifespan. J Neurosci 2011, 31:10359-10370.
-
(2011)
J Neurosci
, vol.31
, pp. 10359-10370
-
-
Ward, C.S.1
Arvide, E.M.2
Huang, T.W.3
Yoo, J.4
Noebels, J.L.5
Neul, J.L.6
-
43
-
-
33748899822
-
Autonomic nervous system dysregulation: breathing and heart rate perturbation during wakefulness in young girls with Rett syndrome
-
Weese-Mayer D.E., Lieske S.P., Boothby C.M., Kenny A.S., Bennett H.L., Silvestri J.M., Ramirez J.M. Autonomic nervous system dysregulation: breathing and heart rate perturbation during wakefulness in young girls with Rett syndrome. Pediatr Res 2006, 60:443-449.
-
(2006)
Pediatr Res
, vol.60
, pp. 443-449
-
-
Weese-Mayer, D.E.1
Lieske, S.P.2
Boothby, C.M.3
Kenny, A.S.4
Bennett, H.L.5
Silvestri, J.M.6
Ramirez, J.M.7
-
44
-
-
80052242765
-
The disruption of central CO2 chemosensitivity in a mouse model of Rett syndrome
-
Zhang X., Su J., Cui N., Gai H., Wu Z., Jiang C. The disruption of central CO2 chemosensitivity in a mouse model of Rett syndrome. Am J Physiol Cell Physiol 2011, 301:C729-C738.
-
(2011)
Am J Physiol Cell Physiol
, vol.301
-
-
Zhang, X.1
Su, J.2
Cui, N.3
Gai, H.4
Wu, Z.5
Jiang, C.6
|