-
1
-
-
0017845477
-
Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production
-
Allgrove, J., G. S. Clayden, D. B. Grant, and J. C. Macaulay. 1978. Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production. Lancet i:1284-1286.
-
(1978)
Lancet
, vol.1
, pp. 1284-1286
-
-
Allgrove, J.1
Clayden, G.S.2
Grant, D.B.3
Macaulay, J.C.4
-
2
-
-
20444370612
-
Disrupted compaction of CNS myelin in an OSP/Claudin-11 and PLP/DM20 double knockout mouse
-
Chow, E., J. Mottahedeh, M. Prins, W. Ridder, S. Nusinowitz, and J. M. Bronstein. 2005. Disrupted compaction of CNS myelin in an OSP/Claudin-11 and PLP/DM20 double knockout mouse. Mol. Cell. Neurosci. 29:405-413.
-
(2005)
Mol. Cell. Neurosci.
, vol.29
, pp. 405-413
-
-
Chow, E.1
Mottahedeh, J.2
Prins, M.3
Ridder, W.4
Nusinowitz, S.5
Bronstein, J.M.6
-
3
-
-
0032238826
-
Adrenocorticotropin insensitivity syndromes
-
Clark, A. J. L., and A. Weber. 1998. Adrenocorticotropin insensitivity syndromes. Endocr. Rev. 19:828-843.
-
(1998)
Endocr. Rev.
, vol.19
, pp. 828-843
-
-
Clark, A.J.L.1
Weber, A.2
-
4
-
-
0019199013
-
Preliminary report of a simple animal behavior model for the anxiolytic effects of benzodiazepines
-
Crawley, J., and F. K. Goodwin. 1980. Preliminary report of a simple animal behavior model for the anxiolytic effects of benzodiazepines. Pharmacol. Biochem. Behav. 13:167-170.
-
(1980)
Pharmacol. Biochem. Behav.
, vol.13
, pp. 167-170
-
-
Crawley, J.1
Goodwin, F.K.2
-
5
-
-
0037008997
-
Proteomic analysis of the mammalian nuclear pore complex
-
Cronshaw, J. M., A. N. Krutchinsky, W. Zhang, B. T. Chait, and M. J. Matunis. 2002. Proteomic analysis of the mammalian nuclear pore complex. J. Cell Biol. 158:915-927.
-
(2002)
J. Cell Biol.
, vol.158
, pp. 915-927
-
-
Cronshaw, J.M.1
Krutchinsky, A.N.2
Zhang, W.3
Chait, B.T.4
Matunis, M.J.5
-
6
-
-
0037947770
-
The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome
-
Cronshaw, J. M., and M. J. Matunis. 2003. The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome. Proc. Natl. Acad. Sci. USA 100:5823-5827.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 5823-5827
-
-
Cronshaw, J.M.1
Matunis, M.J.2
-
7
-
-
1842813943
-
The nuclear pore complex: A jack of all trades?
-
Fahrenkrog, B., J. Koser, and U. Aebi. 2004. The nuclear pore complex: a jack of all trades? Trends Biochem. Sci. 29:175-182.
-
(2004)
Trends Biochem. Sci.
, vol.29
, pp. 175-182
-
-
Fahrenkrog, B.1
Koser, J.2
Aebi, U.3
-
8
-
-
0033870093
-
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome
-
Hadj-Rabia, S., R. Salomon, A. Pelet, C. Penet, A. Rotschild, M. H. de Laet, B. Chaouachi, R. Hannachi, F. Bakiri, R. Brauner, J. L. Chaussain, A. Munnich, and S. Lyonnet. 2000. Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome. Eur. J. Hum. Genet. 8:613-620.
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 613-620
-
-
Hadj-Rabia, S.1
Salomon, R.2
Pelet, A.3
Penet, C.4
Rotschild, A.5
De Laet, M.H.6
Chaouachi, B.7
Hannachi, R.8
Bakiri, F.9
Brauner, R.10
Chaussain, J.L.11
Munnich, A.12
Lyonnet, S.13
-
9
-
-
0035253397
-
Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene
-
Handschug, K., S. Sperling, S. J. K. Yoon, S. Hennig, A. J. L. Clark, and A. Huebner. 2001. Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene. Hum. Mol. Genet. 10:283-290.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 283-290
-
-
Handschug, K.1
Sperling, S.2
Yoon, S.J.K.3
Hennig, S.4
Clark, A.J.L.5
Huebner, A.6
-
10
-
-
0345305849
-
Abnormal anxiety-related behavior in serotonin transporter null mutant mice: The influence of genetic background
-
Holmes, A., Q. Lit, D. L. Murphy, E. Gold, and J. N. Crawley. 2003. Abnormal anxiety-related behavior in serotonin transporter null mutant mice: the influence of genetic background. Genes Brain Behav. 2:365-380.
-
(2003)
Genes Brain Behav.
, vol.2
, pp. 365-380
-
-
Holmes, A.1
Lit, Q.2
Murphy, D.L.3
Gold, E.4
Crawley, J.N.5
-
12
-
-
0034519843
-
Triple A syndrome - Clinical aspects and molecular genetics
-
Huebner, A., S. J. Yoon, F. Ozkinay, C. Hilscher, H. Lee, A. J. Clark, and K. Handschug. 2000. Triple A syndrome-clinical aspects and molecular genetics. Endocr. Res. 26:751-759.
-
(2000)
Endocr. Res.
, vol.26
, pp. 751-759
-
-
Huebner, A.1
Yoon, S.J.2
Ozkinay, F.3
Hilscher, C.4
Lee, H.5
Clark, A.J.6
Handschug, K.7
-
13
-
-
11244262589
-
The triple a syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex
-
Huebner, A., A. M. Kaindl, K. P. Knobeloch, H. Petzold, P. Mann, and K. Koehler. 2004. The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex. Endocr. Res. 30:891-899.
-
(2004)
Endocr. Res.
, vol.30
, pp. 891-899
-
-
Huebner, A.1
Kaindl, A.M.2
Knobeloch, K.P.3
Petzold, H.4
Mann, P.5
Koehler, K.6
-
14
-
-
0014424692
-
Comprehensive observational assessment: Ia. A systematic, quantitative procedure for assessing the behavioral and physiologic state of the mouse
-
Irwin, S. 1968. Comprehensive observational assessment: Ia. A systematic, quantitative procedure for assessing the behavioral and physiologic state of the mouse. Psychopharmacologia 13:222-257.
-
(1968)
Psychopharmacologia
, vol.13
, pp. 222-257
-
-
Irwin, S.1
-
15
-
-
0026328818
-
Generation and analysis of interleukin-4 deficient mice
-
Kuhn, R., K. Rajewsky, and W. Muller. 1991. Generation and analysis of interleukin-4 deficient mice. Science 254:707-710.
-
(1991)
Science
, vol.254
, pp. 707-710
-
-
Kuhn, R.1
Rajewsky, K.2
Muller, W.3
-
16
-
-
0018866029
-
Glucocorticoid and partial mineralocorticoid deficiency associated with achalasia
-
Lanes, R., L. P. Plotnick, T. E. Bynum, P. A. Lee, J. F. Casella, C. E. Fox, A. A. Kowarski, and C. J. Migeon. 1980. Glucocorticoid and partial mineralocorticoid deficiency associated with achalasia. J. Clin. Endocrinol. Metab. 50:268-270.
-
(1980)
J. Clin. Endocrinol. Metab.
, vol.50
, pp. 268-270
-
-
Lanes, R.1
Plotnick, L.P.2
Bynum, T.E.3
Lee, P.A.4
Casella, J.F.5
Fox, C.E.6
Kowarski, A.A.7
Migeon, C.J.8
-
17
-
-
0034833344
-
The use of behavioral test batteries: Effects of training history
-
McIlwain, K. L., M. Y. Merriweather, L. A. Yuva-Paylor, and R. Paylor. 2001. The use of behavioral test batteries: effects of training history. Physiol. Behav. 73:705-717.
-
(2001)
Physiol. Behav.
, vol.73
, pp. 705-717
-
-
McIlwain, K.L.1
Merriweather, M.Y.2
Yuva-Paylor, L.A.3
Paylor, R.4
-
18
-
-
0028147078
-
Individual motor activity-relationships to dopaminergic responses
-
Schumacher, H. E., J. Oehler, and M. Jaehkel. 1994. Individual motor activity-relationships to dopaminergic responses. Pharmacol. Biochem. Behav. 48:839-844.
-
(1994)
Pharmacol. Biochem. Behav.
, vol.48
, pp. 839-844
-
-
Schumacher, H.E.1
Oehler, J.2
Jaehkel, M.3
-
19
-
-
0030769871
-
Segregation of Allgrove (triple-A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers
-
Stratakis, C. A., J. P. Lin, E. Pras, O. M. Rennert, C. J. Bourdony, and W. Y. Chan. 1997. Segregation of Allgrove (triple-A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers. Proc. Assoc. Am. Physicians 109:478-482.
-
(1997)
Proc. Assoc. Am. Physicians
, vol.109
, pp. 478-482
-
-
Stratakis, C.A.1
Lin, J.P.2
Pras, E.3
Rennert, O.M.4
Bourdony, C.J.5
Chan, W.Y.6
-
20
-
-
0033763096
-
Mutant WD-repeat protein in triple-A syndrome
-
Tullio-Pelet, A., R. Salomon, S. Hadj-Rabia, C. Mugnier, M. H. de Laet, B. Chaouachi, F. Bakiri, P. Brottier, L. Cattolico, C. Penet, M. Begeot, D. Naville, M. Nicolino, J. L. Chaussain, J. Weissenbach, A. Munnich, and S. Lyonnet. 2000. Mutant WD-repeat protein in triple-A syndrome. Nat. Genet. 26:332-335.
-
(2000)
Nat. Genet.
, vol.26
, pp. 332-335
-
-
Tullio-Pelet, A.1
Salomon, R.2
Hadj-Rabia, S.3
Mugnier, C.4
De Laet, M.H.5
Chaouachi, B.6
Bakiri, F.7
Brottier, P.8
Cattolico, L.9
Penet, C.10
Begeot, M.11
Naville, D.12
Nicolino, M.13
Chaussain, J.L.14
Weissenbach, J.15
Munnich, A.16
Lyonnet, S.17
-
21
-
-
0025780879
-
Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene
-
Tybulewicz, V. L., C. E. Crawford, P. K. Jackson, R. T. Bronson, and R. C. Mulligan. 1991. Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene. Cell 65:1153-1163.
-
(1991)
Cell
, vol.65
, pp. 1153-1163
-
-
Tybulewicz, V.L.1
Crawford, C.E.2
Jackson, P.K.3
Bronson, R.T.4
Mulligan, R.C.5
-
22
-
-
0029903414
-
G2 arrest and impaired nucleocytoplasmic transport in mouse embryos lacking the protooncogene CAN/Nup214
-
van Deursen, J., J. Boer, L. Kasper, and G. Grosveld. 1996. G2 arrest and impaired nucleocytoplasmic transport in mouse embryos lacking the protooncogene CAN/Nup214. EMBO J. 15:5574-5583.
-
(1996)
EMBO J.
, vol.15
, pp. 5574-5583
-
-
Van Deursen, J.1
Boer, J.2
Kasper, L.3
Grosveld, G.4
-
23
-
-
0037043339
-
The cytoplasmic filaments of the nuclear pore complex are dispensable for selective nuclear protein import
-
Walther, T. C., H. S. Pickersgill, V. C. Cordes, M. W. Goldberg, T. D. Allen, I. W. Mattaj, and M. Fornerod. 2002, The cytoplasmic filaments of the nuclear pore complex are dispensable for selective nuclear protein import. J. Cell Biol. 158:63-77.
-
(2002)
J. Cell Biol.
, vol.158
, pp. 63-77
-
-
Walther, T.C.1
Pickersgill, H.S.2
Cordes, V.C.3
Goldberg, M.W.4
Allen, T.D.5
Mattaj, I.W.6
Fornerod, M.7
-
24
-
-
0014375987
-
Drug effects on motor coordination
-
Watzman, N., and H. Berry III. 1968. Drug effects on motor coordination. Psychopharmacologia 12:414-423.
-
(1968)
Psychopharmacologia
, vol.12
, pp. 414-423
-
-
Watzman, N.1
Berry III, H.2
-
25
-
-
0029827345
-
Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster
-
Weber, A., T. F. Wienker, M. Jung, D. Easton, H. J. Dean, C. Heinrichs, A. Reis, and A. J. Clark. 1996. Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster. Hum. Mol. Genet. 5:2061-2066.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 2061-2066
-
-
Weber, A.1
Wienker, T.F.2
Jung, M.3
Easton, D.4
Dean, H.J.5
Heinrichs, C.6
Reis, A.7
Clark, A.J.8
-
26
-
-
0035853083
-
Disruption of the FG nucleoporin NUP98 causes selective changes in nuclear pore complex stoichiometry and function
-
Wu, X., L. H. Kasper, R. T. Mantcheva, G. T. Mantchev, M. J. Springett, and J. M. van Deursen. 2001. Disruption of the FG nucleoporin NUP98 causes selective changes in nuclear pore complex stoichiometry and function. Proc. Natl. Acad. Sci. USA 98:3191-3196.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 3191-3196
-
-
Wu, X.1
Kasper, L.H.2
Mantcheva, R.T.3
Mantchev, G.T.4
Springett, M.J.5
Van Deursen, J.M.6
|