-
1
-
-
0027370090
-
Pathologic characterization of short-chain acy1-CoA dehydrogenase deficiency in BALB/cByJ mice
-
Armstrong DL, Masiowski ML, Wood PA. 1993. Pathologic characterization of short-chain acy1-CoA dehydrogenase deficiency in BALB/cByJ mice. Am J Med Genet 47:884-892.
-
(1993)
Am J Med Genet
, vol.47
, pp. 884-892
-
-
Armstrong, D.L.1
Masiowski, M.L.2
Wood, P.A.3
-
2
-
-
0002787025
-
Genetics, biochemistry, and molecular basis of variant human phenotypes
-
Scriver CR, Beaudet AL, Sly WS, Valle D, eds. New York: McGraw-Hill
-
Beaudet AL, Scriver CR, Sly WS, Valle D. 1995. Genetics, biochemistry, and molecular basis of variant human phenotypes. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease. 7th ed. New York: McGraw-Hill. p 54.
-
(1995)
The Metabolic and Molecular Bases of Inherited Disease. 7th Ed.
, pp. 54
-
-
Beaudet, A.L.1
Scriver, C.R.2
Sly, W.S.3
Valle, D.4
-
3
-
-
0028131232
-
Metabolic disease and sudden unexpected death in infancy
-
Bennett MJ, Powell S. 1994. Metabolic disease and sudden unexpected death in infancy. Hum Pathol 25:742-746.
-
(1994)
Hum Pathol
, vol.25
, pp. 742-746
-
-
Bennett, M.J.1
Powell, S.2
-
4
-
-
0035914381
-
Lipoprotein secretion and triglyceride stores in the heart
-
Björkegren J, Véniant M, Kim SK, Withycombe SK, Wood PA, Hellerstein MK, Neese RA, Young SG. 2001. Lipoprotein secretion and triglyceride stores in the heart. J Biol Chem 276:38511-38517.
-
(2001)
J Biol Chem
, vol.276
, pp. 38511-38517
-
-
Björkegren, J.1
Véniant, M.2
Kim, S.K.3
Withycombe, S.K.4
Wood, P.A.5
Hellerstein, M.K.6
Neese, R.A.7
Young, S.G.8
-
5
-
-
0032337559
-
Inborn errors of metabolism in infancy: A guide to diagnosis
-
Burton BK. 1998. Inborn errors of metabolism in infancy: A guide to diagnosis. Pediatrics 102:E69.
-
(1998)
Pediatrics
, vol.102
-
-
Burton, B.K.1
-
6
-
-
0024328536
-
Altering the genome by homologous recombination
-
Capecchi MR. 1989. Altering the genome by homologous recombination. Science 244:1288-1292.
-
(1989)
Science
, vol.244
, pp. 1288-1292
-
-
Capecchi, M.R.1
-
7
-
-
0034782503
-
Gestational, pathologic, and biochemical differences between very long-chain acy1-CoA dehydrogenase deficiency and long-chain acy1-CoA dehydrogenase deficiency in the mouse
-
Cox KB, Hamm DA, Millington DS, Matern D, Vockley J, Rinaldo P, Pinkert CA, Rhead WJ, Lindsey JR, Wood PA. 2001. Gestational, pathologic, and biochemical differences between very long-chain acy1-CoA dehydrogenase deficiency and long-chain acy1-CoA dehydrogenase deficiency in the mouse. Hum Mol Genet 10:2069-2077.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2069-2077
-
-
Cox, K.B.1
Hamm, D.A.2
Millington, D.S.3
Matern, D.4
Vockley, J.5
Rinaldo, P.6
Pinkert, C.A.7
Rhead, W.J.8
Lindsey, J.R.9
Wood, P.A.10
-
8
-
-
0031904222
-
Chromosomal locations of the mouse fatty acid oxidation genes Cpt1a, Cpt1b, Cpt2, Acadv1, and metabolically related Crat gene
-
Cox KB, Johnson KR, Wood PA. 1998. Chromosomal locations of the mouse fatty acid oxidation genes Cpt1a, Cpt1b, Cpt2, Acadv1, and metabolically related Crat gene. Mamm Genome 9:608-610.
-
(1998)
Mamm Genome
, vol.9
, pp. 608-610
-
-
Cox, K.B.1
Johnson, K.R.2
Wood, P.A.3
-
9
-
-
0010166460
-
Mouse models of human genetic disorders
-
Scriver CR, Beaudet AL, Valle D, Sly WS, Childs B, Kinzler KW, Vogelstein B, eds. New York: McGraw-Hill
-
Craigen WJ. 2001. Mouse models of human genetic disorders. In: Scriver CR, Beaudet AL, Valle D, Sly WS, Childs B, Kinzler KW, Vogelstein B, eds. The Metabolic and Molecular Bases of Inherited Disease. 8th ed. New York: McGraw-Hill. p 379-416.
-
(2001)
The Metabolic and Molecular Bases of Inherited Disease. 8th Ed.
, pp. 379-416
-
-
Craigen, W.J.1
-
10
-
-
0033911995
-
Phenotypes of patients with "simple" mendelian disorders are complex traits: Thresholds, modifiers, and systems dynamics
-
Dipple KM, McCabe ER. 2000. Phenotypes of patients with "simple" mendelian disorders are complex traits: Thresholds, modifiers, and systems dynamics. Am J Hum Genet 66:1729-1735.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1729-1735
-
-
Dipple, K.M.1
McCabe, E.R.2
-
11
-
-
0002919077
-
Physiologic Stressors inducing sudden death in the very-longchain acy1-CoA dehydrogenase deficient mice
-
Exil VJ, Sims H, Kovacs A, Qin W, Boero J, Khuchua Z, Strauss AW. 1998. Physiologic Stressors inducing sudden death in the very-longchain acy1-CoA dehydrogenase deficient mice. Circulation 98:1-5.
-
(1998)
Circulation
, vol.98
, pp. 1-5
-
-
Exil, V.J.1
Sims, H.2
Kovacs, A.3
Qin, W.4
Boero, J.5
Khuchua, Z.6
Strauss, A.W.7
-
12
-
-
11244257720
-
Stress-induced death in the very-long-chain acy1-CoA dehydrogenase deficient mouse
-
Exil VJ, Sims H, Qin W, Boero J, Khuchua Z, Strauss AW. 1999. Stress-induced death in the very-long-chain acy1-CoA dehydrogenase deficient mouse. Circulation 100:1-492.
-
(1999)
Circulation
, vol.100
, pp. 1-492
-
-
Exil, V.J.1
Sims, H.2
Qin, W.3
Boero, J.4
Khuchua, Z.5
Strauss, A.W.6
-
13
-
-
0035371315
-
Acute fatty liver and HELLP syndrome: Two distinct pregnancy disorders
-
Gracia PV. 2001. Acute fatty liver and HELLP syndrome: Two distinct pregnancy disorders. Int J Gynecol Obstet 73:215-220.
-
(2001)
Int J Gynecol Obstet
, vol.73
, pp. 215-220
-
-
Gracia, P.V.1
-
14
-
-
6844258223
-
Identification of four new mutations in the short-chain acy1-CoA dehydrogenase (SCAD) gene in two patients: One of the varient alleles, 511CT, is present at an unexpectedly high frequency in the general population, as was the case for 625GA, together conferring susceptibility to ethylmalonic aciduria
-
Gregersen N, Winter VS, Corydon MJ, Corydon TJ, Rinaldo P, Ribes A, Martinez G, Mennett MJ, Vianey-Saban C, Bhala A, Hale DE, Lehnert W, Kmoch S, Roig M, Riudor E, Eiberg H, Andersen BS, Bross P, Bolund LA, Kolvraa S. 1998. Identification of four new mutations in the short-chain acy1-CoA dehydrogenase (SCAD) gene in two patients: One of the varient alleles, 511CT, is present at an unexpectedly high frequency in the general population, as was the case for 625GA, together conferring susceptibility to ethylmalonic aciduria. Hum Mol Genet 7:619-627.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 619-627
-
-
Gregersen, N.1
Winter, V.S.2
Corydon, M.J.3
Corydon, T.J.4
Rinaldo, P.5
Ribes, A.6
Martinez, G.7
Mennett, M.J.8
Vianey-Saban, C.9
Bhala, A.10
Hale, D.E.11
Lehnert, W.12
Kmoch, S.13
Roig, M.14
Riudor, E.15
Eiberg, H.16
Andersen, B.S.17
Bross, P.18
Bolund, L.A.19
Kolvraa, S.20
more..
-
15
-
-
0032211811
-
Abnormal nonshivering thermogenesis in mice with inherited defects of fatty acid oxidation
-
Guerra C, Koza RA, Walsh K, Kurtz DM, Wood PA, Kozak LP. 1998. Abnormal nonshivering thermogenesis in mice with inherited defects of fatty acid oxidation. J Clin Invest 102:1724-1731.
-
(1998)
J Clin Invest
, vol.102
, pp. 1724-1731
-
-
Guerra, C.1
Koza, R.A.2
Walsh, K.3
Kurtz, D.M.4
Wood, P.A.5
Kozak, L.P.6
-
16
-
-
0027285713
-
Null allele at bcd-I locus in BALB/cByJ mice is due to a deletion in the short-chain acy1-CoA dehydrogenase gene and results in missplicing of mRNA
-
Hinsdale ME, Kelly CL, Wood PA. 1993. Null allele at bcd-I locus in BALB/cByJ mice is due to a deletion in the short-chain acy1-CoA dehydrogenase gene and results in missplicing of mRNA. Genomics 16:605-611.
-
(1993)
Genomics
, vol.16
, pp. 605-611
-
-
Hinsdale, M.E.1
Kelly, C.L.2
Wood, P.A.3
-
17
-
-
0029165220
-
RNA expression and chromosomal location of the mouse long-chain acy1-CoA dehydrogenase gene
-
Hinsdale ME, Farmer SC, Johnson KR, Davisson MT, Hamm DA, Tolwani RJ, Wood PA. 1995. RNA expression and chromosomal location of the mouse long-chain acy1-CoA dehydrogenase gene. Genomics 28:163-170.
-
(1995)
Genomics
, vol.28
, pp. 163-170
-
-
Hinsdale, M.E.1
Farmer, S.C.2
Johnson, K.R.3
Davisson, M.T.4
Hamm, D.A.5
Tolwani, R.J.6
Wood, P.A.7
-
18
-
-
0029940188
-
Effects of short-chain acy1-CoA dehydrogenase deficiency on developmental expression of metabolic enzyme genes in the mouse
-
Hinsdale ME, Hamm DA, Wood PA. 1996. Effects of short-chain acy1-CoA dehydrogenase deficiency on developmental expression of metabolic enzyme genes in the mouse. Biochem Mol Med 57:106-115.
-
(1996)
Biochem Mol Med
, vol.57
, pp. 106-115
-
-
Hinsdale, M.E.1
Hamm, D.A.2
Wood, P.A.3
-
19
-
-
0034987233
-
Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death
-
Ibdah JA, Paul H, Zhao Y, Binford S, Salleng K, Cline M, Matern D, Bennett MJ, Rinaldo P, Strauss AW. 2001. Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death. J Clin Invest 107:1403-1409.
-
(2001)
J Clin Invest
, vol.107
, pp. 1403-1409
-
-
Ibdah, J.A.1
Paul, H.2
Zhao, Y.3
Binford, S.4
Salleng, K.5
Cline, M.6
Matern, D.7
Bennett, M.J.8
Rinaldo, P.9
Strauss, A.W.10
-
20
-
-
0000736325
-
Obese, a new mutation in the house mouse
-
Ingalls AM, Dickie MM, Snell GD. 1950. Obese, a new mutation in the house mouse. J Hered 41:317-318.
-
(1950)
J Hered
, vol.41
, pp. 317-318
-
-
Ingalls, A.M.1
Dickie, M.M.2
Snell, G.D.3
-
21
-
-
11244294435
-
Defective nonshivering thermogenesis and dicarboxylic aciduria in mice deficient in the 70kDa peroxisomal membrane protein (PMP70)
-
Jimenez-Sanchez G, Hebron KJ, Silva-Zolezzi I, Thomas G, Wood PA, Valle D. 2000. Defective nonshivering thermogenesis and dicarboxylic aciduria in mice deficient in the 70kDa peroxisomal membrane protein (PMP70). Pediatr Res 47:240A.
-
(2000)
Pediatr Res
, vol.47
-
-
Jimenez-Sanchez, G.1
Hebron, K.J.2
Silva-Zolezzi, I.3
Thomas, G.4
Wood, P.A.5
Valle, D.6
-
22
-
-
0027361992
-
Cloning and characterization of mouse short-chain acy1-CoA dehydrogenase cDNA
-
Kelly CL, Hinsdale ME, Wood, PA. 1993. Cloning and characterization of mouse short-chain acy1-CoA dehydrogenase cDNA. Genomics 18:137-140.
-
(1993)
Genomics
, vol.18
, pp. 137-140
-
-
Kelly, C.L.1
Hinsdale, M.E.2
Wood, P.A.3
-
23
-
-
0030120816
-
Cloning and characterization of the mouse short-chain acy1-CoA dehydrogenase gene
-
Kelly CL, Wood PA. 1996. Cloning and characterization of the mouse short-chain acy1-CoA dehydrogenase gene. Mamm Genome 7:262-264.
-
(1996)
Mamm Genome
, vol.7
, pp. 262-264
-
-
Kelly, C.L.1
Wood, P.A.2
-
24
-
-
0030774807
-
Functional correction of short-chain acy1-CoA dehydrogenase deficiency in transgenic mice: Implications for gene therapy of human mitochondrial enzyme deficiencies
-
Kelly CL, Rhead WJ, Kutschke WK, Brix AE, Hamm DA, Pinkert CA , Lindsey JR, Wood PA. 1997. Functional correction of short-chain acy1-CoA dehydrogenase deficiency in transgenic mice: Implications for gene therapy of human mitochondrial enzyme deficiencies. Hum Mol Genet 6:1451-1455.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1451-1455
-
-
Kelly, C.L.1
Rhead, W.J.2
Kutschke, W.K.3
Brix, A.E.4
Hamm, D.A.5
Pinkert, C.A.6
Lindsey, J.R.7
Wood, P.A.8
-
25
-
-
13044277575
-
Targeted disruption of a mouse long-chain acy1-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation
-
Kurtz DM, Rinaldo P, Rhead WJ, Tain L, Millington DS, Vockley J, Hamm DA, Brix AE, Lindsey JR, Pinkert CA, O'Brien WE, Wood PA. 1998a. Targeted disruption of a mouse long-chain acy1-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation. Proc Natl Acad Sci U S A 95:15592-15597.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 15592-15597
-
-
Kurtz, D.M.1
Rinaldo, P.2
Rhead, W.J.3
Tain, L.4
Millington, D.S.5
Vockley, J.6
Hamm, D.A.7
Brix, A.E.8
Lindsey, J.R.9
Pinkert, C.A.10
O'Brien, W.E.11
Wood, P.A.12
-
26
-
-
0031863627
-
Structural characterization of the mouse long-chain acy1-CoA dehydrogenase gene and 5′ regulatory region
-
Kurtz DM, Tolwani, RJ, Wood PA. 1998b. Structural characterization of the mouse long-chain acy1-CoA dehydrogenase gene and 5′ regulatory region. Mamm Genome 9:361-365.
-
(1998)
Mamm Genome
, vol.9
, pp. 361-365
-
-
Kurtz, D.M.1
Tolwani, R.J.2
Wood, P.A.3
-
27
-
-
0033574265
-
Molecular heterogeneity in very-long-chain acy1-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death
-
Mathur A, Sims HF, Gopalakrishnan D, Gibson B, Rinaldo P, Vockley J, Hug G, Strauss AW. 1999. Molecular heterogeneity in very-long-chain acy1-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death. Circulation 99:1337-1343.
-
(1999)
Circulation
, vol.99
, pp. 1337-1343
-
-
Mathur, A.1
Sims, H.F.2
Gopalakrishnan, D.3
Gibson, B.4
Rinaldo, P.5
Vockley, J.6
Hug, G.7
Strauss, A.W.8
-
28
-
-
0026683892
-
Prevalence of K329E mutation in the mediumchain acy1-CoA dehydrogenase gene determined from Guthrie cards
-
Matsubara Y, Narisawa K, Tada K, Ikeda H, Yeqi Y, Danks DM, Green A, McCabe ER. 1992. Prevalence of K329E mutation in the mediumchain acy1-CoA dehydrogenase gene determined from Guthrie cards. Prog Clin Biol Res 375:453-462.
-
(1992)
Prog Clin Biol Res
, vol.375
, pp. 453-462
-
-
Matsubara, Y.1
Narisawa, K.2
Tada, K.3
Ikeda, H.4
Yeqi, Y.5
Danks, D.M.6
Green, A.7
McCabe, E.R.8
-
29
-
-
0033819105
-
Production of mouse models for the study of human inborn errors of metabolism
-
McDonald JD. 2000. Production of mouse models for the study of human inborn errors of metabolism. Mol Genet Metab 71:240-244.
-
(2000)
Mol Genet Metab
, vol.71
, pp. 240-244
-
-
McDonald, J.D.1
-
30
-
-
11244352678
-
Mutations in the short chain L, 3-hydroxyacyl-CoA dehydrogenase gene
-
London, England
-
O'Brien LK, Gibson B, Charrow J, Rinaldo P, Bennett MJ, Strauss AW. 1998. Mutations in the short chain L, 3-hydroxyacyl-CoA dehydrogenase gene. 4th Fatty Acid and Ketogenesis Conference, London, England, p 61.
-
(1998)
4th Fatty Acid and Ketogenesis Conference
, pp. 61
-
-
O'Brien, L.K.1
Gibson, B.2
Charrow, J.3
Rinaldo, P.4
Bennett, M.J.5
Strauss, A.W.6
-
31
-
-
0001321144
-
A mouse model for medium and short chain L-3-hydroxyacyl-CoA dehydrogenase deficiency
-
O'Brien LK, Sims HF, Bennett MJ, Strauss AW. 2000. A mouse model for medium and short chain L-3-hydroxyacyl-CoA dehydrogenase deficiency. J Inherit Metab Dis 23(S1):127.
-
(2000)
J Inherit Metab Dis
, vol.23
, Issue.S1
, pp. 127
-
-
O'Brien, L.K.1
Sims, H.F.2
Bennett, M.J.3
Strauss, A.W.4
-
32
-
-
0030950114
-
Lipid level and type alter stearyl CoA desaturase mRNA abundance differently in mice with distinct susceptibilities to diet-influenced diseases
-
Park EI, Paisley EA, Mangian HJ, Swartz DA, Wu M, O'Morchoe PJ, Behr SR, Visek WJ, Kaput J. 1997. Lipid level and type alter stearyl CoA desaturase mRNA abundance differently in mice with distinct susceptibilities to diet-influenced diseases. J Nutr 127:566-573.
-
(1997)
J Nutr
, vol.127
, pp. 566-573
-
-
Park, E.I.1
Paisley, E.A.2
Mangian, H.J.3
Swartz, D.A.4
Wu, M.5
O'Morchoe, P.J.6
Behr, S.R.7
Visek, W.J.8
Kaput, J.9
-
33
-
-
0005831234
-
A null activity variant found at the butyryl CoA dehydrogenase (Bcd-1) locus in BALB/cByJ mice
-
Prochazka M, Leiter EH. 1986. A null activity variant found at the butyryl CoA dehydrogenase (Bcd-1) locus in BALB/cByJ mice. Mouse News Lett 78:31.
-
(1986)
Mouse News Lett
, vol.78
, pp. 31
-
-
Prochazka, M.1
Leiter, E.H.2
-
34
-
-
0024312617
-
Disorders of mitochondrial β-oxidation: Prenatal and early postnatal diagnosis and their relevance to Reye's syndrome and sudden infant death
-
Pollitt RJ. 1989. Disorders of mitochondrial β-oxidation: Prenatal and early postnatal diagnosis and their relevance to Reye's syndrome and sudden infant death. J Inher Metab Dis 12(S1):215-230.
-
(1989)
J Inher Metab Dis
, vol.12
, Issue.S1
, pp. 215-230
-
-
Pollitt, R.J.1
-
35
-
-
0027304840
-
Breeding experiments to combine the X-linked sparse-fur (spf) mutation with the autosomal recessive BALB/cByJ strain: Testing the biochemical phenotype of double-mutant mice as a model for ammonia: Fatty acyl CoA synergism
-
Qureshi IA, LeBlanc D, Cyr D, Giguere R, Mitchell G. 1993. Breeding experiments to combine the X-linked sparse-fur (spf) mutation with the autosomal recessive BALB/cByJ strain: Testing the biochemical phenotype of double-mutant mice as a model for ammonia: Fatty acyl CoA synergism. Biochem Biophys Res Commun 191:744-749.
-
(1993)
Biochem Biophys Res Commun
, vol.191
, pp. 744-749
-
-
Qureshi, I.A.1
LeBlanc, D.2
Cyr, D.3
Giguere, R.4
Mitchell, G.5
-
36
-
-
0030748497
-
Decompensation of hepatic and cerebral acy1-CoA metabolism in BALB/cByJ mice by chronic riboflavin deficiency: Restoration by acetyl-L-carnitine
-
Rao KVR, Qureshi IA. 1997. Decompensation of hepatic and cerebral acy1-CoA metabolism in BALB/cByJ mice by chronic riboflavin deficiency: Restoration by acetyl-L-carnitine. Can J Physiol Pharmacol 75:423-4360.
-
(1997)
Can J Physiol Pharmacol
, vol.75
, pp. 423-4360
-
-
Rao, K.V.R.1
Qureshi, I.A.2
-
37
-
-
0000576457
-
Mitochondrial fatty acid oxidation disorders
-
Scriver CR, Beaudet AL, Sly WS, Valle D, eds. New York: McGraw-Hill. CD-ROM ed.
-
Roe CR, Coates PM. 1997. Mitochondrial fatty acid oxidation disorders. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease. 7th ed. New York: McGraw-Hill. p 1501-1533. CD-ROM ed.
-
(1997)
The Metabolic and Molecular Bases of Inherited Disease. 7th Ed.
, pp. 1501-1533
-
-
Roe, C.R.1
Coates, P.M.2
-
38
-
-
0000044868
-
Mitochondrial fatty acid oxidation disorders
-
Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B, eds. New York: McGraw-Hill
-
Roe CR, Ding J. 2001. Mitochondrial fatty acid oxidation disorders. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B, eds. The Metabolic and Molecular Bases of Inherited Disease. 8th ed. New York: McGraw-Hill. p 2297-2326.
-
(2001)
The Metabolic and Molecular Bases of Inherited Disease. 8th Ed.
, pp. 2297-2326
-
-
Roe, C.R.1
Ding, J.2
-
39
-
-
0028817917
-
Molecular basis of human mitochondrial very-long-chain acy1-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood
-
Strauss AW, Powell CK, Hale DE, Anderson MM, Ahuja A, Brackett JC, Sims HF. 1995. Molecular basis of human mitochondrial very-long-chain acy1-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood. Proc Natl Acad Sci U S A 92:10496-10500.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 10496-10500
-
-
Strauss, A.W.1
Powell, C.K.2
Hale, D.E.3
Anderson, M.M.4
Ahuja, A.5
Brackett, J.C.6
Sims, H.F.7
-
40
-
-
0030005955
-
Structure and chromosomal location of the mouse medium-chain acy1-CoA dehydrogenase gene and its promoter
-
Tolwani RJ, Farmer SC, Kurtz DM, Johnson KR, Davisson MT, Hinsdale ME, Cresci S, Kelly DP, Wood PA. 1996. Structure and chromosomal location of the mouse medium-chain acy1-CoA dehydrogenase gene and its promoter. Gene 170:165-171.
-
(1996)
Gene
, vol.170
, pp. 165-171
-
-
Tolwani, R.J.1
Farmer, S.C.2
Kurtz, D.M.3
Johnson, K.R.4
Davisson, M.T.5
Hinsdale, M.E.6
Cresci, S.7
Kelly, D.P.8
Wood, P.A.9
-
41
-
-
0028086583
-
Molecular cloning and characterization of the mouse-medium-chain acy1-CoA dehydrogenase cDNA
-
Tolwani RJ, Farmer SC, Wood PA. 1994. Molecular cloning and characterization of the mouse-medium-chain acy1-CoA dehydrogenase cDNA. Genomics 23:247-249.
-
(1994)
Genomics
, vol.23
, pp. 247-249
-
-
Tolwani, R.J.1
Farmer, S.C.2
Wood, P.A.3
-
42
-
-
0033819241
-
Genomics of the human carnitine acyltransferase genes
-
van der Leij FR, Huijkman NC, Boomsma C, Kuipers JR, Bartelds B. 2000. Genomics of the human carnitine acyltransferase genes. Mol Genet Metab 71:139-153.
-
(2000)
Mol Genet Metab
, vol.71
, pp. 139-153
-
-
Van Der Leij, F.R.1
Huijkman, N.C.2
Boomsma, C.3
Kuipers, J.R.4
Bartelds, B.5
-
43
-
-
0033803952
-
Synergistic heterozygosity: Disease resulting from multiple partial defects in one or more metabolic pathways
-
Vockley J, Rinaldo P, Bennett MJ, Matern D, Vladutiu GD. 2000. Synergistic heterozygosity: Disease resulting from multiple partial defects in one or more metabolic pathways. Mol Genet Metab 71:10-18.
-
(2000)
Mol Genet Metab
, vol.71
, pp. 10-18
-
-
Vockley, J.1
Rinaldo, P.2
Bennett, M.J.3
Matern, D.4
Vladutiu, G.D.5
-
45
-
-
0024496544
-
Short-chain acy1-coenzyme A dehydrogenase deficiency in mice
-
Wood PA, Amendt BA, Rhead WJ, Millington DS, Inoue F, Armstrong D. 1989. Short-chain acy1-coenzyme A dehydrogenase deficiency in mice. Pediatr Res 25:38-43.
-
(1989)
Pediatr Res
, vol.25
, pp. 38-43
-
-
Wood, P.A.1
Amendt, B.A.2
Rhead, W.J.3
Millington, D.S.4
Inoue, F.5
Armstrong, D.6
-
46
-
-
0032916807
-
Defects in mitochondrial β-oxidation of fatty acids
-
Wood, PA. 1999. Defects in mitochondrial β-oxidation of fatty acids. Curr Opin Lipidol 10:107-112.
-
(1999)
Curr Opin Lipidol
, vol.10
, pp. 107-112
-
-
Wood, P.A.1
-
47
-
-
0008055469
-
Lessons learned from the mouse model of short-chain acy1-CoA dehydrogenase deficiency
-
Quant PA, Eaton S, eds. New York: Kluwer Academic/ Plenum Press
-
Wood PA, Kelly-Kurtz L, Hinsdale ME, Hamm DA, Rhead WJ. 1999. Lessons learned from the mouse model of short-chain acy1-CoA dehydrogenase deficiency. In: Quant PA, Eaton S, eds. Current Views of Fatty Acid Oxidation and Ketogenesis. New York: Kluwer Academic/ Plenum Press. p 395-402.
-
(1999)
Current Views of Fatty Acid Oxidation and Ketogenesis
, pp. 395-402
-
-
Wood, P.A.1
Kelly-Kurtz, L.2
Hinsdale, M.E.3
Hamm, D.A.4
Rhead, W.J.5
-
48
-
-
11244287875
-
Gestational loss is a complex trait in the long-chain acy1-CoA dehydrogenase deficient mouse model
-
Wood PA, Berger PS, Hamm DA, Pinkert CA. 2001. Gestational loss is a complex trait in the long-chain acy1-CoA dehydrogenase deficient mouse model. Eur J Hum Genet 9(S1):335.
-
(2001)
Eur J Hum Genet
, vol.9
, Issue.S1
, pp. 335
-
-
Wood, P.A.1
Berger, P.S.2
Hamm, D.A.3
Pinkert, C.A.4
-
49
-
-
0027207327
-
Identification of very-long-chain-acy1-CoA dehydrogenase deficiency in three patients previously diagnosed with long-chain acy1-CoA dehydrogenase deficiency
-
Yamaguchi S, Indo Y, Coates PM, Hashimoto T, Tanaka K. 1993. Identification of very-long-chain-acy1-CoA dehydrogenase deficiency in three patients previously diagnosed with long-chain acy1-CoA dehydrogenase deficiency. Pediatr Res 34:111-113.
-
(1993)
Pediatr Res
, vol.34
, pp. 111-113
-
-
Yamaguchi, S.1
Indo, Y.2
Coates, P.M.3
Hashimoto, T.4
Tanaka, K.5
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