-
1
-
-
0041595736
-
Human metabolic diseases
-
Chalmers RA, Lawson AM (1975) Human metabolic diseases. Chem Br 11:290-295
-
(1975)
Chem Br
, vol.11
, pp. 290-295
-
-
Chalmers, R.A.1
Lawson, A.M.2
-
2
-
-
0027203048
-
Human Aminoacylase-1: Cloning, sequence and expression analysis of a chromosome 3p21 gene inactivated in small cell lung cancer
-
Cook RM, Burke BJ, Buchhagen DL, Minna JD, Miller YE (1993) Human Aminoacylase-1: Cloning, sequence and expression analysis of a chromosome 3p21 gene inactivated in small cell lung cancer. J Biol Chem 268:17010-17017
-
(1993)
J Biol Chem
, vol.268
, pp. 17010-17017
-
-
Cook, R.M.1
Burke, B.J.2
Buchhagen, D.L.3
Minna, J.D.4
Miller, Y.E.5
-
3
-
-
0038601952
-
Evidence of brain overgrowth in the first year of life in autism
-
Courchesne E, Carper R, Akshoomoff N (2003) Evidence of brain overgrowth in the first year of life in autism. JAMA 290:337-344
-
(2003)
JAMA
, vol.290
, pp. 337-344
-
-
Courchesne, E.1
Carper, R.2
Akshoomoff, N.3
-
4
-
-
40449129783
-
NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolism
-
Engelke UF, Sass JO, Van Coster R, Gerlo E, Olbrich H, Krwawych S et al. (2008) NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolism. NMR Biomed 21:138-147
-
(2008)
NMR Biomed
, vol.21
, pp. 138-147
-
-
Engelke, U.F.1
Sass, J.O.2
Van Coster, R.3
Gerlo, E.4
Olbrich, H.5
Krwawych, S.6
-
5
-
-
51449107119
-
Syndromes and epistemology II: Is autism a polygenic disorder?
-
Fisch GS (2008) Syndromes and epistemology II: is autism a polygenic disorder? Am J Med Genet 146A:2203-2212
-
(2008)
Am J Med Genet
, vol.146 A
, pp. 2203-2212
-
-
Fisch, G.S.1
-
6
-
-
33745241644
-
Gas chromatographic-mass spectrometric analysis of N-Acetylated amino acids: The first case of aminoacylase 1 deficiency
-
Gerlo E, Van Coster R, Lissens W, Winckelmans G, De Meirleir L, Wevers R (2006) Gas chromatographic-mass spectrometric analysis of N-Acetylated amino acids: the first case of aminoacylase 1 deficiency. Anal Chim Acta 571:191-199
-
(2006)
Anal Chim Acta
, vol.571
, pp. 191-199
-
-
Gerlo, E.1
Van Coster, R.2
Lissens, W.3
Winckelmans, G.4
De Meirleir, L.5
Wevers, R.6
-
7
-
-
12744278201
-
Cumulative incidence of childhood autism: A total population study of better accuracy and precision
-
Honda H, Shimizu Y, Imai M, Nitto Y (2005) Cumulative incidence of childhood autism: a total population study of better accuracy and precision. Dev Med Child Neurol 47:10-18
-
(2005)
Dev Med Child Neurol
, vol.47
, pp. 10-18
-
-
Honda, H.1
Shimizu, Y.2
Imai, M.3
Nitto, Y.4
-
8
-
-
0028301596
-
Long-term results of selective screening for inborn errors of metabolism
-
Lehnert W (1994) Long-term results of selective screening for inborn errors of metabolism. Eur J Pediatr 153(7 Suppl 1):S9-S13
-
(1994)
Eur J Pediatr
, vol.153
, Issue.7 SUPPL. 1
-
-
Lehnert, W.1
-
9
-
-
2942527522
-
Aminoacylase 1 is a sphingosine kinase 1-interacting protein
-
Maceyka M, Nava VE, Milstien S, Spiegel S (2004) Aminoacylase 1 is a sphingosine kinase 1-interacting protein. FEBS Lett 568:30-34
-
(2004)
FEBS Lett
, vol.568
, pp. 30-34
-
-
Maceyka, M.1
Nava, V.E.2
Milstien, S.3
Spiegel, S.4
-
10
-
-
0024516282
-
Monoclonal antibody based immunoassay for human aminoacylase-1
-
Miller YE, Kao B (1989) Monoclonal antibody based immunoassay for human aminoacylase-1. J Immunoass 10:129-152
-
(1989)
J Immunoass
, vol.10
, pp. 129-152
-
-
Miller, Y.E.1
Kao, B.2
-
11
-
-
0025074829
-
Human Aminoacylase-1: Cloning, regional assignment to distal chromosome 3p21.1, and identification of a cross-hybridizing sequence on chromosome 18
-
Miller YE, Drabkin H, Jones C, Fisher JH (1990) Human Aminoacylase-1: cloning, regional assignment to distal chromosome 3p21.1, and identification of a cross-hybridizing sequence on chromosome 18. Genomics 8:149-154
-
(1990)
Genomics
, vol.8
, pp. 149-154
-
-
Miller, Y.E.1
Drabkin, H.2
Jones, C.3
Fisher, J.H.4
-
12
-
-
0018380801
-
Bioautographic visualization of Aminoacylase-1: Assignment of the structural gene ACY1 to chromosome 3 in man
-
Naylor SL, Shows TB, Klebe RJ (1979) Bioautographic visualization of Aminoacylase-1: assignment of the structural gene ACY1 to chromosome 3 in man. Somatic Cell Genet 5:11-21
-
(1979)
Somatic Cell Genet
, vol.5
, pp. 11-21
-
-
Naylor, S.L.1
Shows, T.B.2
Klebe, R.J.3
-
13
-
-
0020048660
-
Mapping of Aminoacylase-1 and beta-galactosidase-A to homologous regions of human chromosome 3 and mouse chromosome 9 suggets location of additional genes
-
Naylor SL, Elliott RW, Brown JA, Shows TB (1982) Mapping of Aminoacylase-1 and beta-galactosidase-A to homologous regions of human chromosome 3 and mouse chromosome 9 suggets location of additional genes. Am J Hum Genet 34:235-244
-
(1982)
Am J Hum Genet
, vol.34
, pp. 235-244
-
-
Naylor, S.L.1
Elliott, R.W.2
Brown, J.A.3
Shows, T.B.4
-
14
-
-
23044509196
-
Catabolism of intracellular N-terminal acetylated proteins: Involvement of acylpeptide hydrolase and acylase
-
Perrier J, Durand A, Giardina T, Puigserver A (2005) Catabolism of intracellular N-terminal acetylated proteins: involvement of acylpeptide hydrolase and acylase. Biochimie 87:673-685
-
(2005)
Biochimie
, vol.87
, pp. 673-685
-
-
Perrier, J.1
Durand, A.2
Giardina, T.3
Puigserver, A.4
-
15
-
-
33344460531
-
Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism
-
Sass JO, Mohr V, Olbrich H, Engelke U, Horvath J et al. (2006) Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism. Am J Hum Genet 78:401-409
-
(2006)
Am J Hum Genet
, vol.78
, pp. 401-409
-
-
Sass, J.O.1
Mohr, V.2
Olbrich, H.3
Engelke, U.4
Horvath, J.5
-
16
-
-
34250361341
-
Neurological findings in aminoacylase 1 deficiency
-
Sass JO, Olbrich H, Mohr V, Hart C, Woldseth B, Krywawych S, Bjurulf B, Lakhani PK, Buchdahl RM, Omran H (2007) Neurological findings in aminoacylase 1 deficiency. Neurology 68:2151-2153
-
(2007)
Neurology
, vol.68
, pp. 2151-2153
-
-
Sass, J.O.1
Olbrich, H.2
Mohr, V.3
Hart, C.4
Woldseth, B.5
Krywawych, S.6
Bjurulf, B.7
Lakhani, P.K.8
Buchdahl, R.M.9
Omran, H.10
-
18
-
-
33747164766
-
Comparative proteomics in neurodegenerative and non-neurodegenerative diseases suggest nodal point proteins in regulatory networking
-
Zabel C, Sagi D, Kaindl AM et al. (2006) Comparative proteomics in neurodegenerative and non-neurodegenerative diseases suggest nodal point proteins in regulatory networking. J Proteome Res 5:1948-1958
-
(2006)
J Proteome Res
, vol.5
, pp. 1948-1958
-
-
Zabel, C.1
Sagi, D.2
Kaindl, A.M.3
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