-
2
-
-
0031758844
-
Is monoamine oxidase activity elevated in Prader-Willi syndrome?
-
Akefeldt A., and Mansson J.E. Is monoamine oxidase activity elevated in Prader-Willi syndrome?. Eur. Child Adolesc. Psychiatry 7 (1998) 163-165
-
(1998)
Eur. Child Adolesc. Psychiatry
, vol.7
, pp. 163-165
-
-
Akefeldt, A.1
Mansson, J.E.2
-
3
-
-
33751581604
-
Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death
-
Andrieu D., Meziane H., Marly F., Angelats C., Fernandez P.-A., and Muscatelli F. Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death. BMC Dev. Biol. 6 (2006) 56
-
(2006)
BMC Dev. Biol.
, vol.6
, pp. 56
-
-
Andrieu, D.1
Meziane, H.2
Marly, F.3
Angelats, C.4
Fernandez, P.-A.5
Muscatelli, F.6
-
4
-
-
0344876548
-
Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression
-
Andrieu D., Watrin F., Niinobe M., Yoshikawa K., Muscatelli F., and Fernandez P.A. Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression. Gene Expr. Patterns 3 (2003) 761-765
-
(2003)
Gene Expr. Patterns
, vol.3
, pp. 761-765
-
-
Andrieu, D.1
Watrin, F.2
Niinobe, M.3
Yoshikawa, K.4
Muscatelli, F.5
Fernandez, P.A.6
-
5
-
-
0028113590
-
Hypoxic and hypercapnic ventilatory responses in Prader-Willi syndrome
-
Arens R., Gozal D., Omlin K.J., Livingston F.R., Liu J., Keens T.G., and Ward S.L. Hypoxic and hypercapnic ventilatory responses in Prader-Willi syndrome. J. Appl. Physiol. 77 (1994) 2224-2230
-
(1994)
J. Appl. Physiol.
, vol.77
, pp. 2224-2230
-
-
Arens, R.1
Gozal, D.2
Omlin, K.J.3
Livingston, F.R.4
Liu, J.5
Keens, T.G.6
Ward, S.L.7
-
6
-
-
37249049731
-
Early diagnosis and multidisciplinary care reduce the hospitalization time and duration of tube feeding and prevent early obesity in PWS infants
-
Bachere N., Diene G., Delagnes V., Molinas C., Moulin P., and Tauber M. Early diagnosis and multidisciplinary care reduce the hospitalization time and duration of tube feeding and prevent early obesity in PWS infants. Horm. Res. 69 (2008) 45-52
-
(2008)
Horm. Res.
, vol.69
, pp. 45-52
-
-
Bachere, N.1
Diene, G.2
Delagnes, V.3
Molinas, C.4
Moulin, P.5
Tauber, M.6
-
7
-
-
38449092798
-
Brain nuclei controlling the spinal respiratory motoneurons in the newborn mouse
-
Bevengut M., Coulon P., and Hilaire G. Brain nuclei controlling the spinal respiratory motoneurons in the newborn mouse. Adv. Exp. Med. Biol. 605 (2008) 127-132
-
(2008)
Adv. Exp. Med. Biol.
, vol.605
, pp. 127-132
-
-
Bevengut, M.1
Coulon, P.2
Hilaire, G.3
-
8
-
-
0141765815
-
MafB deficiency causes defective respiratory rhythmogenesis and fatal central apnea at birth
-
Blanchi B., Kelly L.M., Viemari J.C., Lafon I., Burnet H., Bevengut M., Tillmanns S., Daniel L., Graf T., Hilaire G., and Sieweke M.H. MafB deficiency causes defective respiratory rhythmogenesis and fatal central apnea at birth. Nat. Neurosci. 6 (2003) 1091-1100
-
(2003)
Nat. Neurosci.
, vol.6
, pp. 1091-1100
-
-
Blanchi, B.1
Kelly, L.M.2
Viemari, J.C.3
Lafon, I.4
Burnet, H.5
Bevengut, M.6
Tillmanns, S.7
Daniel, L.8
Graf, T.9
Hilaire, G.10
Sieweke, M.H.11
-
9
-
-
51649093589
-
Prenatal activation of 5-HT2A receptor induces expression of 5-HT1B receptor in phrenic motoneurons and alters the organization of their premotor network in newborn mice
-
Bras H., Gaytan S.P., Portalier P., Zanella S., Pasaro R., Coulon P., and Hilaire G. Prenatal activation of 5-HT2A receptor induces expression of 5-HT1B receptor in phrenic motoneurons and alters the organization of their premotor network in newborn mice. Eur. J. Neurosci. 28 (2008) 1097-1107
-
(2008)
Eur. J. Neurosci.
, vol.28
, pp. 1097-1107
-
-
Bras, H.1
Gaytan, S.P.2
Portalier, P.3
Zanella, S.4
Pasaro, R.5
Coulon, P.6
Hilaire, G.7
-
10
-
-
0035879181
-
Altered respiratory activity and respiratory regulations in adult monoamine oxidase A-deficient mice
-
Burnet H., Bevengut M., Chakri F., Bou-Flores C., Coulon P., Gaytan S., Pasaro R., and Hilaire G. Altered respiratory activity and respiratory regulations in adult monoamine oxidase A-deficient mice. J. Neurosci. 21 (2001) 5212-5221
-
(2001)
J. Neurosci.
, vol.21
, pp. 5212-5221
-
-
Burnet, H.1
Bevengut, M.2
Chakri, F.3
Bou-Flores, C.4
Coulon, P.5
Gaytan, S.6
Pasaro, R.7
Hilaire, G.8
-
11
-
-
0027017879
-
A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression
-
Cattanach B.M., Barr J.A., Evans E.P., Burtenshaw M., Beechey C.V., Leff S.E., Brannan C.I., Copeland N.G., Jenkins N.A., and Jones J. A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression. Nat. Genet. 2 (1992) 270-274
-
(1992)
Nat. Genet.
, vol.2
, pp. 270-274
-
-
Cattanach, B.M.1
Barr, J.A.2
Evans, E.P.3
Burtenshaw, M.4
Beechey, C.V.5
Leff, S.E.6
Brannan, C.I.7
Copeland, N.G.8
Jenkins, N.A.9
Jones, J.10
-
12
-
-
9744241653
-
Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice
-
Chamberlain S.J., Johnstone K.A., DuBose A.J., Simon T.A., Bartolomei M.S., Resnick J.L., and Brannan C.I. Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice. Hum. Mol. Genet. 13 (2004) 2971-2977
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2971-2977
-
-
Chamberlain, S.J.1
Johnstone, K.A.2
DuBose, A.J.3
Simon, T.A.4
Bartolomei, M.S.5
Resnick, J.L.6
Brannan, C.I.7
-
13
-
-
33845472885
-
Sleep-related breathing disorders in prepubertal children with Prader-Willi syndrome and effects of growth hormone treatment
-
Festen D.A., de Weerd A.W., van den Bossche R.A., Joosten K., Hoeve H., and Hokken-Koelega A.C. Sleep-related breathing disorders in prepubertal children with Prader-Willi syndrome and effects of growth hormone treatment. J. Clin. Endocrinol. Metab. 91 (2006) 4911-4915
-
(2006)
J. Clin. Endocrinol. Metab.
, vol.91
, pp. 4911-4915
-
-
Festen, D.A.1
de Weerd, A.W.2
van den Bossche, R.A.3
Joosten, K.4
Hoeve, H.5
Hokken-Koelega, A.C.6
-
14
-
-
34548031842
-
Thyroid hormone levels in children with Prader-Willi syndrome before and during growth hormone treatment
-
Festen D.A., Visser T.J., Otten B.J., Wit J.M., Duivenvoorden H.J., and Hokken-Koelega A.C. Thyroid hormone levels in children with Prader-Willi syndrome before and during growth hormone treatment. Clin. Endocrinol. (Oxf.) 67 (2007) 449-456
-
(2007)
Clin. Endocrinol. (Oxf.)
, vol.67
, pp. 449-456
-
-
Festen, D.A.1
Visser, T.J.2
Otten, B.J.3
Wit, J.M.4
Duivenvoorden, H.J.5
Hokken-Koelega, A.C.6
-
15
-
-
0033529801
-
A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes
-
Gabriel J.M., Merchant M., Ohta T., Ji Y., Caldwell R.G., Ramsey M.J., Tucker J.D., Longnecker R., and Nicholls R.D. A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes. Proc. Natl. Acad. Sci. U.S.A. 96 (1999) 9258-9263
-
(1999)
Proc. Natl. Acad. Sci. U.S.A.
, vol.96
, pp. 9258-9263
-
-
Gabriel, J.M.1
Merchant, M.2
Ohta, T.3
Ji, Y.4
Caldwell, R.G.5
Ramsey, M.J.6
Tucker, J.D.7
Longnecker, R.8
Nicholls, R.D.9
-
16
-
-
0037012254
-
Identification of central nervous system neurons innervating the respiratory muscles of the mouse: a transneuronal tracing study
-
Gaytan S.P., Pasaro R., Coulon P., Bevengut M., and Hilaire G. Identification of central nervous system neurons innervating the respiratory muscles of the mouse: a transneuronal tracing study. Brain Res. Bull. 57 (2002) 335-339
-
(2002)
Brain Res. Bull.
, vol.57
, pp. 335-339
-
-
Gaytan, S.P.1
Pasaro, R.2
Coulon, P.3
Bevengut, M.4
Hilaire, G.5
-
17
-
-
0345062183
-
Disruption of the mouse necdin gene results in early post-natal lethality
-
Gerard M., Hernandez L., Wevrick R., and Stewart C.L. Disruption of the mouse necdin gene results in early post-natal lethality. Nat. Genet. 23 (1999) 199-202
-
(1999)
Nat. Genet.
, vol.23
, pp. 199-202
-
-
Gerard, M.1
Hernandez, L.2
Wevrick, R.3
Stewart, C.L.4
-
18
-
-
1042267409
-
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment
-
Goldstone A.P. Prader-Willi syndrome: advances in genetics, pathophysiology and treatment. Trends Endocrinol. Metab. 15 (2004) 12-20
-
(2004)
Trends Endocrinol. Metab.
, vol.15
, pp. 12-20
-
-
Goldstone, A.P.1
-
19
-
-
57349156874
-
Recommendations for the diagnosis and management of Prader-Willi syndrome
-
Goldstone A.P., Holland A.J., Hauffa B.P., Hokken-Koelega A.C., and Tauber M. Recommendations for the diagnosis and management of Prader-Willi syndrome. J. Clin. Endocrinol. Metab. 93 (2008) 4183-4197
-
(2008)
J. Clin. Endocrinol. Metab.
, vol.93
, pp. 4183-4197
-
-
Goldstone, A.P.1
Holland, A.J.2
Hauffa, B.P.3
Hokken-Koelega, A.C.4
Tauber, M.5
-
20
-
-
0028075517
-
Absent peripheral chemosensitivity in Prader-Willi syndrome
-
Gozal D., Arens R., Omlin K.J., Ward S.L., and Keens T.G. Absent peripheral chemosensitivity in Prader-Willi syndrome. J. Appl. Physiol. 77 (1994) 2231-2236
-
(1994)
J. Appl. Physiol.
, vol.77
, pp. 2231-2236
-
-
Gozal, D.1
Arens, R.2
Omlin, K.J.3
Ward, S.L.4
Keens, T.G.5
-
21
-
-
0038030751
-
Effects of growth hormone on pulmonary function, sleep quality, behavior, cognition, growth velocity, body composition, and resting energy expenditure in Prader-Willi syndrome
-
Haqq A.M., Stadler D.D., Jackson R.H., Rosenfeld R.G., Purnell J.Q., and LaFranchi S.H. Effects of growth hormone on pulmonary function, sleep quality, behavior, cognition, growth velocity, body composition, and resting energy expenditure in Prader-Willi syndrome. J. Clin. Endocrinol. Metab. 88 (2003) 2206-2212
-
(2003)
J. Clin. Endocrinol. Metab.
, vol.88
, pp. 2206-2212
-
-
Haqq, A.M.1
Stadler, D.D.2
Jackson, R.H.3
Rosenfeld, R.G.4
Purnell, J.Q.5
LaFranchi, S.H.6
-
22
-
-
68949171690
-
Developmental aspects of sleep in Prader-Willi syndrome
-
Heussler H., Suresh S., Harris M., Cooper D., Dakin C., Williams G., and Wilson S. Developmental aspects of sleep in Prader-Willi syndrome. J. Intellect. Disabil. Res. 52 (2008) 815-1815
-
(2008)
J. Intellect. Disabil. Res.
, vol.52
, pp. 815-1815
-
-
Heussler, H.1
Suresh, S.2
Harris, M.3
Cooper, D.4
Dakin, C.5
Williams, G.6
Wilson, S.7
-
23
-
-
0030926434
-
Serotonergic modulation of central respiratory activity in the neonatal mouse: an in vitro study
-
Hilaire G., Bou C., and Monteau R. Serotonergic modulation of central respiratory activity in the neonatal mouse: an in vitro study. Eur. J. Pharmacol. 329 (1997) 115-120
-
(1997)
Eur. J. Pharmacol.
, vol.329
, pp. 115-120
-
-
Hilaire, G.1
Bou, C.2
Monteau, R.3
-
24
-
-
16944363776
-
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region
-
Jay P., Rougeulle C., Massacrier A., Moncla A., Mattei M.G., Malzac P., Roeckel N., Taviaux S., Lefranc J.L., Cau P., Berta P., Lalande M., and Muscatelli F. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nat. Genet. 17 (1997) 357-361
-
(1997)
Nat. Genet.
, vol.17
, pp. 357-361
-
-
Jay, P.1
Rougeulle, C.2
Massacrier, A.3
Moncla, A.4
Mattei, M.G.5
Malzac, P.6
Roeckel, N.7
Taviaux, S.8
Lefranc, J.L.9
Cau, P.10
Berta, P.11
Lalande, M.12
Muscatelli, F.13
-
25
-
-
33744996959
-
Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins
-
Kuwajima T., Nishimura I., and Yoshikawa K. Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins. J. Neurosci. 26 (2006) 5383-5392
-
(2006)
J. Neurosci.
, vol.26
, pp. 5383-5392
-
-
Kuwajima, T.1
Nishimura, I.2
Yoshikawa, K.3
-
26
-
-
23044445639
-
Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival
-
Kuwako K., Hosokawa A., Nishimura I., Uetsuki T., Yamada M., Nada S., Okada M., and Yoshikawa K. Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival. J. Neurosci. 25 (2005) 7090-7099
-
(2005)
J. Neurosci.
, vol.25
, pp. 7090-7099
-
-
Kuwako, K.1
Hosokawa, A.2
Nishimura, I.3
Uetsuki, T.4
Yamada, M.5
Nada, S.6
Okada, M.7
Yoshikawa, K.8
-
27
-
-
14644391578
-
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
-
Lee S., Walker C.L., Karten B., Kuny S.L., Tennese A.A., O'Neill M.A., and Wevrick R. Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth. Hum. Mol. Genet. 14 (2005) 627-637
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 627-637
-
-
Lee, S.1
Walker, C.L.2
Karten, B.3
Kuny, S.L.4
Tennese, A.A.5
O'Neill, M.A.6
Wevrick, R.7
-
28
-
-
0042786856
-
Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain
-
Lee S., Walker C.L., and Wevrick R. Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain. Gene Expr. Patterns 3 (2003) 599-609
-
(2003)
Gene Expr. Patterns
, vol.3
, pp. 599-609
-
-
Lee, S.1
Walker, C.L.2
Wevrick, R.3
-
29
-
-
0032871118
-
Growth hormone treatment increases CO(2) response, ventilation and central inspiratory drive in children with Prader-Willi syndrome
-
Lindgren A.C., Hellstrom L.G., Ritzen E.M., and Milerad J. Growth hormone treatment increases CO(2) response, ventilation and central inspiratory drive in children with Prader-Willi syndrome. Eur. J. Pediatr. 158 (1999) 936-940
-
(1999)
Eur. J. Pediatr.
, vol.158
, pp. 936-940
-
-
Lindgren, A.C.1
Hellstrom, L.G.2
Ritzen, E.M.3
Milerad, J.4
-
30
-
-
0032821127
-
Abnormal ventilatory responses in patients with Prader-Willi syndrome
-
Menendez A.A. Abnormal ventilatory responses in patients with Prader-Willi syndrome. Eur. J. Pediatr. 158 (1999) 941-942
-
(1999)
Eur. J. Pediatr.
, vol.158
, pp. 941-942
-
-
Menendez, A.A.1
-
31
-
-
32544436250
-
Short-term effects of growth hormone on sleep abnormalities in Prader-Willi syndrome
-
Miller J., Silverstein J., Shuster J., Driscoll D.J., and Wagner M. Short-term effects of growth hormone on sleep abnormalities in Prader-Willi syndrome. J. Clin. Endocrinol. Metab. 91 (2006) 413-417
-
(2006)
J. Clin. Endocrinol. Metab.
, vol.91
, pp. 413-417
-
-
Miller, J.1
Silverstein, J.2
Shuster, J.3
Driscoll, D.J.4
Wagner, M.5
-
32
-
-
43049125542
-
Pituitary abnormalities in Prader-Willi syndrome and early onset morbid obesity
-
Miller J.L., Goldstone A.P., Couch J.A., Shuster J., He G., Driscoll D.J., Liu Y., and Schmalfuss I.M. Pituitary abnormalities in Prader-Willi syndrome and early onset morbid obesity. Am. J. Med. Genet. A 146A (2008) 570-577
-
(2008)
Am. J. Med. Genet. A
, vol.146 A
, pp. 570-577
-
-
Miller, J.L.1
Goldstone, A.P.2
Couch, J.A.3
Shuster, J.4
He, G.5
Driscoll, D.J.6
Liu, Y.7
Schmalfuss, I.M.8
-
33
-
-
21244488269
-
Negative regulation of hypoxia inducible factor-1alpha by necdin
-
Moon H.E., Ahn M.Y., Park J.A., Min K.J., Kwon Y.W., and Kim K.W. Negative regulation of hypoxia inducible factor-1alpha by necdin. FEBS Lett. 579 (2005) 3797-3801
-
(2005)
FEBS Lett.
, vol.579
, pp. 3797-3801
-
-
Moon, H.E.1
Ahn, M.Y.2
Park, J.A.3
Min, K.J.4
Kwon, Y.W.5
Kim, K.W.6
-
34
-
-
0034642301
-
Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome
-
Muscatelli F., Abrous D.N., Massacrier A., Boccaccio I., Le Moal M., Cau P., and Cremer H. Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome. Hum. Mol. Genet. 9 (2000) 3101-3110
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 3101-3110
-
-
Muscatelli, F.1
Abrous, D.N.2
Massacrier, A.3
Boccaccio, I.4
Le Moal, M.5
Cau, P.6
Cremer, H.7
-
35
-
-
0035777024
-
Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes
-
Nicholls R.D., and Knepper J.L. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes. Annu. Rev. Genomics Hum. Genet. 2 (2001) 153-175
-
(2001)
Annu. Rev. Genomics Hum. Genet.
, vol.2
, pp. 153-175
-
-
Nicholls, R.D.1
Knepper, J.L.2
-
36
-
-
0033798523
-
Cellular and subcellular localization of necdin in fetal and adult mouse brain
-
Niinobe M., Koyama K., and Yoshikawa K. Cellular and subcellular localization of necdin in fetal and adult mouse brain. Dev. Neurosci. 22 (2000) 310-319
-
(2000)
Dev. Neurosci.
, vol.22
, pp. 310-319
-
-
Niinobe, M.1
Koyama, K.2
Yoshikawa, K.3
-
37
-
-
0036708197
-
Sleep and breathing in Prader-Willi syndrome
-
Nixon G.M., and Brouillette R.T. Sleep and breathing in Prader-Willi syndrome. Pediatr. Pulmonol. 34 (2002) 209-217
-
(2002)
Pediatr. Pulmonol.
, vol.34
, pp. 209-217
-
-
Nixon, G.M.1
Brouillette, R.T.2
-
38
-
-
21244450398
-
Developmental abnormalities of neuronal structure and function in prenatal mice lacking the Prader-Willi syndrome gene necdin
-
Pagliardini S., Ren J., Wevrick R., and Greer J.J. Developmental abnormalities of neuronal structure and function in prenatal mice lacking the Prader-Willi syndrome gene necdin. Am. J. Pathol. 167 (2005) 175-191
-
(2005)
Am. J. Pathol.
, vol.167
, pp. 175-191
-
-
Pagliardini, S.1
Ren, J.2
Wevrick, R.3
Greer, J.J.4
-
39
-
-
33750518186
-
Multiple serotonergic brainstem abnormalities in sudden infant death syndrome
-
Paterson D.S., Trachtenberg F.L., Thompson E.G., Belliveau R.A., Beggs A.H., Darnall R., Chadwick A.E., Krous H.F., and Kinney H.C. Multiple serotonergic brainstem abnormalities in sudden infant death syndrome. JAMA 296 (2006) 2124-2132
-
(2006)
JAMA
, vol.296
, pp. 2124-2132
-
-
Paterson, D.S.1
Trachtenberg, F.L.2
Thompson, E.G.3
Belliveau, R.A.4
Beggs, A.H.5
Darnall, R.6
Chadwick, A.E.7
Krous, H.F.8
Kinney, H.C.9
-
40
-
-
0037114964
-
Endogenous activation of serotonin-2A receptors is required for respiratory rhythm generation in vitro
-
Pena F., and Ramirez J.M. Endogenous activation of serotonin-2A receptors is required for respiratory rhythm generation in vitro. J. Neurosci. 22 (2002) 11055-11064
-
(2002)
J. Neurosci.
, vol.22
, pp. 11055-11064
-
-
Pena, F.1
Ramirez, J.M.2
-
41
-
-
30544435620
-
Contribution of 5-HT2 receptor subtypes to sleep-wakefulness and respiratory control, and functional adaptations in knock-out mice lacking 5-HT2A receptors
-
Popa D., Lena C., Fabre V., Prenat C., Gingrich J., Escourrou P., Hamon M., and Adrien J. Contribution of 5-HT2 receptor subtypes to sleep-wakefulness and respiratory control, and functional adaptations in knock-out mice lacking 5-HT2A receptors. J. Neurosci. 25 (2005) 11231-11238
-
(2005)
J. Neurosci.
, vol.25
, pp. 11231-11238
-
-
Popa, D.1
Lena, C.2
Fabre, V.3
Prenat, C.4
Gingrich, J.5
Escourrou, P.6
Hamon, M.7
Adrien, J.8
-
42
-
-
0037335439
-
Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice
-
Ren J., Lee S., Pagliardini S., Gerard M., Stewart C.L., Greer J.J., and Wevrick R. Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice. J. Neurosci. 23 (2003) 1569-1573
-
(2003)
J. Neurosci.
, vol.23
, pp. 1569-1573
-
-
Ren, J.1
Lee, S.2
Pagliardini, S.3
Gerard, M.4
Stewart, C.L.5
Greer, J.J.6
Wevrick, R.7
-
43
-
-
44349191455
-
Prader-Willi phenotype caused by paternal deficiency for the HBII-85C/D box small nucleolar RNA cluster
-
Sahoo T., del Gaudio D., German J.R., Shinawi M., Peters S.U., Person R.E., Garnica A., Cheung S.W., and Beaudet A.L. Prader-Willi phenotype caused by paternal deficiency for the HBII-85C/D box small nucleolar RNA cluster. Nat. Genet. 40 (2008) 719-721
-
(2008)
Nat. Genet.
, vol.40
, pp. 719-721
-
-
Sahoo, T.1
del Gaudio, D.2
German, J.R.3
Shinawi, M.4
Peters, S.U.5
Person, R.E.6
Garnica, A.7
Cheung, S.W.8
Beaudet, A.L.9
-
45
-
-
36749082384
-
Spontaneous central apneas occur in the C57BL/6J mouse strain
-
Stettner G.M., Zanella S., Huppke P., Gartner J., Hilaire G., and Dutschmann M. Spontaneous central apneas occur in the C57BL/6J mouse strain. Respir. Physiol. Neurobiol. 160 (2008) 21-27
-
(2008)
Respir. Physiol. Neurobiol.
, vol.160
, pp. 21-27
-
-
Stettner, G.M.1
Zanella, S.2
Huppke, P.3
Gartner, J.4
Hilaire, G.5
Dutschmann, M.6
-
46
-
-
41849091898
-
Review of 64 cases of death in children with Prader-Willi syndrome (PWS)
-
Tauber M., Diene G., Molinas C., and Hebert M. Review of 64 cases of death in children with Prader-Willi syndrome (PWS). Am. J. Med. Genet. A 146 (2008) 881-887
-
(2008)
Am. J. Med. Genet. A
, vol.146
, pp. 881-887
-
-
Tauber, M.1
Diene, G.2
Molinas, C.3
Hebert, M.4
-
47
-
-
0032963667
-
Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome
-
Tsai T.F., Armstrong D., and Beaudet A.L. Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome. Nat. Genet. 22 (1999) 15-16
-
(1999)
Nat. Genet.
, vol.22
, pp. 15-16
-
-
Tsai, T.F.1
Armstrong, D.2
Beaudet, A.L.3
-
48
-
-
0032837539
-
Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome
-
Tsai T.F., Jiang Y.H., Bressler J., Armstrong D., and Beaudet A.L. Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome. Hum. Mol. Genet. 8 (1999) 1357-1364
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1357-1364
-
-
Tsai, T.F.1
Jiang, Y.H.2
Bressler, J.3
Armstrong, D.4
Beaudet, A.L.5
-
49
-
-
68949167065
-
Analysis of NREM sleep in children with Prader-Willi syndrome and the effect of growth hormone treatment
-
Verrillo E., Bruni O., Franco P., Ferri R., Thiriez G., Pavone M., Petrone A., Paglietti M.G., Crino A., and Cutrera R. Analysis of NREM sleep in children with Prader-Willi syndrome and the effect of growth hormone treatment. Sleep Med. (2008)
-
(2008)
Sleep Med.
-
-
Verrillo, E.1
Bruni, O.2
Franco, P.3
Ferri, R.4
Thiriez, G.5
Pavone, M.6
Petrone, A.7
Paglietti, M.G.8
Crino, A.9
Cutrera, R.10
-
50
-
-
47849086593
-
Sleepiness and sleep disordered breathing in Prader-Willi syndrome: relationship to genotype, growth hormone therapy, and body composition
-
Williams K., Scheimann A., Sutton V., Hayslett E., and Glaze D.G. Sleepiness and sleep disordered breathing in Prader-Willi syndrome: relationship to genotype, growth hormone therapy, and body composition. J. Clin. Sleep Med. 4 (2008) 111-118
-
(2008)
J. Clin. Sleep Med.
, vol.4
, pp. 111-118
-
-
Williams, K.1
Scheimann, A.2
Sutton, V.3
Hayslett, E.4
Glaze, D.G.5
-
51
-
-
47249115193
-
Post-sigh breathing behavior and spontaneous pauses in the C57BL/6J (B6) mouse
-
Yamauchi M., Ocak H., Dostal J., Jacono F.J., Loparo K.A., and Strohl K.P. Post-sigh breathing behavior and spontaneous pauses in the C57BL/6J (B6) mouse. Respir. Physiol. Neurobiol. 162 (2008) 117-125
-
(2008)
Respir. Physiol. Neurobiol.
, vol.162
, pp. 117-125
-
-
Yamauchi, M.1
Ocak, H.2
Dostal, J.3
Jacono, F.J.4
Loparo, K.A.5
Strohl, K.P.6
-
52
-
-
0031747932
-
A mouse model for Prader-Willi syndrome imprinting-centre mutations
-
Yang T., Adamson T.E., Resnick J.L., Leff S., Wevrick R., Francke U., Jenkins N.A., Copeland N.G., and Brannan C.I. A mouse model for Prader-Willi syndrome imprinting-centre mutations. Nat. Genet. 19 (1998) 25-31
-
(1998)
Nat. Genet.
, vol.19
, pp. 25-31
-
-
Yang, T.1
Adamson, T.E.2
Resnick, J.L.3
Leff, S.4
Wevrick, R.5
Francke, U.6
Jenkins, N.A.7
Copeland, N.G.8
Brannan, C.I.9
-
53
-
-
39549109269
-
Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome
-
Zanella S., Watrin F., Mebarek S., Marly F., Roussel M., Gire C., Diene G., Tauber M., Muscatelli F., and Hilaire G. Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome. J. Neurosci. 28 (2008) 1745-1755
-
(2008)
J. Neurosci.
, vol.28
, pp. 1745-1755
-
-
Zanella, S.1
Watrin, F.2
Mebarek, S.3
Marly, F.4
Roussel, M.5
Gire, C.6
Diene, G.7
Tauber, M.8
Muscatelli, F.9
Hilaire, G.10
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