-
1
-
-
29244446225
-
Whatever happened to neonatal hepatitis?
-
Balistreri WF, Bezerra JA. Whatever happened to «neonatal hepatitis»? Clin Liver Dis 2006 ; 10 : 27-53.
-
(2006)
Clin Liver Dis
, vol.10
, pp. 27-53
-
-
Balistreri, W.F.1
Bezerra, J.A.2
-
2
-
-
7044229442
-
Neonatal cholestasis
-
Suchy FJ. Neonatal cholestasis. Pediatr Rev 2004 ; 25 : 388-96.
-
(2004)
Pediatr Rev
, vol.25
, pp. 388-396
-
-
Suchy, F.J.1
-
3
-
-
0019521476
-
Severe familial cholestasis in North American Indian children : A clinical model of microfilament dysfunction ?
-
Weber AM, Tuchweber B, Yousef I, et al. Severe familial cholestasis in North American Indian children : a clinical model of microfilament dysfunction ? Gastroenterology 1981 ; 81 : 653-62.
-
(1981)
Gastroenterology
, vol.81
, pp. 653-662
-
-
Weber, A.M.1
Tuchweber, B.2
Yousef, I.3
-
4
-
-
0033809652
-
North American Indian cirrhosis in children : A review of 30 cases
-
Drouin E, Russo P, Tuchweber B, et al. North American Indian cirrhosis in children : a review of 30 cases. J Pediatr Gastroenterol Nutr 2000 ; 31 : 395-404.
-
(2000)
J Pediatr Gastroenterol Nutr
, vol.31
, pp. 395-404
-
-
Drouin, E.1
Russo, P.2
Tuchweber, B.3
-
5
-
-
0033911125
-
Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22 and identification of a shared haplotype
-
Betard C, Rasquin-Weber A, Brewer C, et al. Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22 and identification of a shared haplotype. Am J Hum Genet 2000 ; 67 : 222-8.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 222-228
-
-
Betard, C.1
Rasquin-Weber, A.2
Brewer, C.3
-
6
-
-
0036918537
-
A Missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis
-
Chagnon P, Michaud J, Mitchell GA, et al. A Missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis. Am J Hum Genet 2002 ; 71 : 1443-9.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1443-1449
-
-
Chagnon, P.1
Michaud, J.2
Mitchell, G.A.3
-
7
-
-
0026074570
-
Phenotypic variability in glutaric aciduria type I : Report of fourteen cases in five Canadian Indian kindreds
-
Haworth JC, Booth FA, Chudley AE, et al. Phenotypic variability in glutaric aciduria type I : Report of fourteen cases in five Canadian Indian kindreds. J Pediatr 1991 ; 118 : 52-8.
-
(1991)
J Pediatr
, vol.118
, pp. 52-58
-
-
Haworth, J.C.1
Booth, F.A.2
Chudley, A.E.3
-
8
-
-
0028953615
-
A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the Island Lake variant of glutaric acidemia type I
-
Greenberg CR, Reimer D, Singal R, et al. A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the Island Lake variant of glutaric acidemia type I. Hum Mol Genet 1995 ; 4 : 493-5.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 493-495
-
-
Greenberg, C.R.1
Reimer, D.2
Singal, R.3
-
9
-
-
0021346589
-
The molecular basis for the two different clinical presentations of classical pyruvate carboxylase deficiency
-
Robinson BH, Oei J, Sherwood WG, et al. The molecular basis for the two different clinical presentations of classical pyruvate carboxylase deficiency. Am J Hum Genet 1984 ; 36 : 283-94.
-
(1984)
Am J Hum Genet
, vol.36
, pp. 283-294
-
-
Robinson, B.H.1
Oei, J.2
Sherwood, W.G.3
-
10
-
-
0029845713
-
Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype
-
Weiler T, Greenberg CR, Nylen E, et al. Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype. Am J Hum Genet 1996 ; 59 : 872-8.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 872-878
-
-
Weiler, T.1
Greenberg, C.R.2
Nylen, E.3
-
11
-
-
0030239811
-
Characterization of genes expressed early in mouse spermatogenesis, isolated from a subtractive cDNA library
-
Lopez-Fernandez LA, del Mazo J. Characterization of genes expressed early in mouse spermatogenesis, isolated from a subtractive cDNA library. Mamm Genome 1996 ; 7 : 698-700.
-
(1996)
Mamm Genome
, vol.7
, pp. 698-700
-
-
Lopez-Fernandez, L.A.1
del Mazo, J.2
-
12
-
-
0035981222
-
Prediction of the coding sequences of unidentified human genes. XXII. The complete sequences of 50 new cDNA clones which code for large proteins
-
Nagase T, Kikuno R, Ohara O. Prediction of the coding sequences of unidentified human genes. XXII. The complete sequences of 50 new cDNA clones which code for large proteins. DNA Res 2001 ; 8 : 319-27.
-
(2001)
DNA Res
, vol.8
, pp. 319-327
-
-
Nagase, T.1
Kikuno, R.2
Ohara, O.3
-
13
-
-
0037182878
-
A large nucleolar U3 ribonucleoprotein required for 18S ribosomal RNA biogenesis
-
Dragon F, Gallagher JE, Compagnone-Post PA, et al. A large nucleolar U3 ribonucleoprotein required for 18S ribosomal RNA biogenesis. Nature 2002 ; 417 : 967-70.
-
(2002)
Nature
, vol.417
, pp. 967-970
-
-
Dragon, F.1
Gallagher, J.E.2
Compagnone-Post, P.A.3
-
14
-
-
0035664074
-
WD-repeat proteins : Structure characteristics, biological function, and their involvement in human diseases
-
Li D, Roberts R. WD-repeat proteins : structure characteristics, biological function, and their involvement in human diseases. Cell Mol Life Sci 2001 ; 58 : 2085-97.
-
(2001)
Cell Mol Life Sci
, vol.58
, pp. 2085-2097
-
-
Li, D.1
Roberts, R.2
-
15
-
-
27744436483
-
Nucleolar localization of cirhin, the protein mutated in North American Indian childhood cirrhosis
-
Yu B, Mitchell GA, Richter A. Nucleolar localization of cirhin, the protein mutated in North American Indian childhood cirrhosis. Exp Cell Res 2005 ; 311 : 218-28.
-
(2005)
Exp Cell Res
, vol.311
, pp. 218-228
-
-
Yu, B.1
Mitchell, G.A.2
Richter, A.3
-
16
-
-
0036856312
-
Functional proteomic analysis of human nucleolus
-
Scherl A, Coute Y, Deon C, et al. Functional proteomic analysis of human nucleolus. Mol Biol Cell 2002 ; 13 : 4100-9.
-
(2002)
Mol Biol Cell
, vol.13
, pp. 4100-4109
-
-
Scherl, A.1
Coute, Y.2
Deon, C.3
-
19
-
-
0034193778
-
The nucleolus : An old factory with unexpected capabilities
-
Olson MO, Dundr M, Szebeni A. The nucleolus : an old factory with unexpected capabilities. Trends Cell Biol 2000 ; 10 : 189-96.
-
(2000)
Trends Cell Biol
, vol.10
, pp. 189-196
-
-
Olson, M.O.1
Dundr, M.2
Szebeni, A.3
-
21
-
-
0037154983
-
The contribution of nuclear compartmentalization to gene regulation
-
Carmo-Fonseca M. The contribution of nuclear compartmentalization to gene regulation. Cell 2002 ; 108 : 513-21.
-
(2002)
Cell
, vol.108
, pp. 513-521
-
-
Carmo-Fonseca, M.1
-
22
-
-
0034847625
-
Using the yeast interaction trap and other two-hybrid-based approaches to study protein-protein interactions
-
Toby GG, Golemis EA. Using the yeast interaction trap and other two-hybrid-based approaches to study protein-protein interactions. Methods 2001 ; 24 : 201-17.
-
(2001)
Methods
, vol.24
, pp. 201-217
-
-
Toby, G.G.1
Golemis, E.A.2
-
23
-
-
0035145907
-
Structure of the human zinc finger protein HIVEP3 : Molecular cloning, expression, exon-intron structure, and comparison with paralogous genes HIVEP1 and HIVEP2
-
Hicar MD, Liu Y, Allen CE, Wu LC. Structure of the human zinc finger protein HIVEP3 : molecular cloning, expression, exon-intron structure, and comparison with paralogous genes HIVEP1 and HIVEP2. Genomics 2001 ; 71 : 89-100.
-
(2001)
Genomics
, vol.71
, pp. 89-100
-
-
Hicar, M.D.1
Liu, Y.2
Allen, C.E.3
Wu, L.C.4
-
24
-
-
33645271646
-
Advances in NF-kappaB signaling transduction and transcription
-
Xiao W. Advances in NF-kappaB signaling transduction and transcription. Cell Mol Immunol 2004 ; 1 : 425-35.
-
(2004)
Cell Mol Immunol
, vol.1
, pp. 425-435
-
-
Xiao, W.1
-
26
-
-
0033529707
-
Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis
-
Winzeler EA, Shoemaker DD, Astromoff A, et al Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis. Science 1999 ; 285 : 901-6.
-
(1999)
Science
, vol.285
, pp. 901-906
-
-
Winzeler, E.A.1
Shoemaker, D.D.2
Astromoff, A.3
-
27
-
-
85088334509
-
Embryonic lethality in mice deficient in tex292, ortholog of the North American Indian childhood cirrhosis (NAIC) gene CIRH1A
-
octobre, abstract
-
th Annual Meeting, octobre 2005 (abstract).
-
(2005)
th Annual Meeting
-
-
Yu, B.1
Mitchell, G.A.2
Richter, A.3
|