-
1
-
-
0030873316
-
Three-dimensional structure of NADPH-cytochrome P450 reductase: prototype for FMN- and FAD-containing enzymes
-
Wang M., Roberts D.L., Paschke R., Shea T.M., Masters B.S., and Kim J.J. Three-dimensional structure of NADPH-cytochrome P450 reductase: prototype for FMN- and FAD-containing enzymes. Proc. Natl. Acad. Sci. USA 94 (1997) 8411-8416
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 8411-8416
-
-
Wang, M.1
Roberts, D.L.2
Paschke, R.3
Shea, T.M.4
Masters, B.S.5
Kim, J.J.6
-
2
-
-
10744224515
-
Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome
-
Flück C.E., Tajima T., Pandey A.V., Arlt W., Okuhara K., Verge C.F., Jabs E.W., Mendonça B.B., Fujieda K., and Miller W.L. Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome. Nat. Genet. 36 (2004) 228-230
-
(2004)
Nat. Genet.
, vol.36
, pp. 228-230
-
-
Flück, C.E.1
Tajima, T.2
Pandey, A.V.3
Arlt, W.4
Okuhara, K.5
Verge, C.F.6
Jabs, E.W.7
Mendonça, B.B.8
Fujieda, K.9
Miller, W.L.10
-
3
-
-
43749123253
-
Genetic and clinical features of P450 oxidoreductase deficiency
-
Scott R.R., and Miller W.L. Genetic and clinical features of P450 oxidoreductase deficiency. Horm. Res. 69 (2008) 266-275
-
(2008)
Horm. Res.
, vol.69
, pp. 266-275
-
-
Scott, R.R.1
Miller, W.L.2
-
4
-
-
66149119440
-
Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients
-
Fukami M., Nishimura G., Homma K., Nagai T., Hanaki K., Uematsu A., Ishii T., Numakura C., Sawada H., Nakacho M., Kowase T., Motomura K., Haruna H., Nakamura M., Ohishi A., Adachi M., Tajima T., Hasegawa Y., Hasegawa T., Horikawa R., Fujieda K., and Ogata T. Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients. J. Clin. Endocrinol. Metab. 94 (2009) 1723-1731
-
(2009)
J. Clin. Endocrinol. Metab.
, vol.94
, pp. 1723-1731
-
-
Fukami, M.1
Nishimura, G.2
Homma, K.3
Nagai, T.4
Hanaki, K.5
Uematsu, A.6
Ishii, T.7
Numakura, C.8
Sawada, H.9
Nakacho, M.10
Kowase, T.11
Motomura, K.12
Haruna, H.13
Nakamura, M.14
Ohishi, A.15
Adachi, M.16
Tajima, T.17
Hasegawa, Y.18
Hasegawa, T.19
Horikawa, R.20
Fujieda, K.21
Ogata, T.22
more..
-
5
-
-
51549116267
-
Retinoic acid synthesis and signaling during early organogenesis
-
Duester G. Retinoic acid synthesis and signaling during early organogenesis. Cell 134 (2008) 921-931
-
(2008)
Cell
, vol.134
, pp. 921-931
-
-
Duester, G.1
-
6
-
-
0035862977
-
The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures
-
Abu-Abed S., Dollé P., Metzger D., Beckett B., Chambon P., and Petkovich M. The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures. Genes Dev. 15 (2001) 226-240
-
(2001)
Genes Dev.
, vol.15
, pp. 226-240
-
-
Abu-Abed, S.1
Dollé, P.2
Metzger, D.3
Beckett, B.4
Chambon, P.5
Petkovich, M.6
-
7
-
-
0347683479
-
A novel human cytochrome P450, CYP26C1, involved in metabolism of 9-cis and all-trans isomers of retinoic acid
-
Taimi M., Helvig C., Wisniewski J., Ramshaw H., White J., Amad M., Korczak B., and Petkovich M. A novel human cytochrome P450, CYP26C1, involved in metabolism of 9-cis and all-trans isomers of retinoic acid. J. Biol. Chem. 279 (2004) 77-85
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 77-85
-
-
Taimi, M.1
Helvig, C.2
Wisniewski, J.3
Ramshaw, H.4
White, J.5
Amad, M.6
Korczak, B.7
Petkovich, M.8
-
8
-
-
0742323064
-
Sonic hedgehog and bone morphogenetic protein 4 expressions in the hindgut region of murine embryos with anorectal malformations
-
Sasaki Y., Iwai N., Tsuda T., and Kimura O. Sonic hedgehog and bone morphogenetic protein 4 expressions in the hindgut region of murine embryos with anorectal malformations. Pediatr. Surg. 39 (2004) 170-173
-
(2004)
Pediatr. Surg.
, vol.39
, pp. 170-173
-
-
Sasaki, Y.1
Iwai, N.2
Tsuda, T.3
Kimura, O.4
-
9
-
-
0036578757
-
Genetic evidence that oxidative derivatives of retinoic acid are not involved in retinoid signaling during mouse development
-
Niederreither K., Abu-Abed S., Schuhbaur B., Petkovich M., Chambon P., and Dollé P. Genetic evidence that oxidative derivatives of retinoic acid are not involved in retinoid signaling during mouse development. Nat. Genet. 31 (2002) 84-88
-
(2002)
Nat. Genet.
, vol.31
, pp. 84-88
-
-
Niederreither, K.1
Abu-Abed, S.2
Schuhbaur, B.3
Petkovich, M.4
Chambon, P.5
Dollé, P.6
-
10
-
-
0035862976
-
The retinoic acid-inactivating enzyme CYP26 is essential for establishing an uneven distribution of retinoic acid along the anterio-posterior axis within the mouse embryo
-
Sakai Y., Meno C., Fujii H., Nishino J., Shiratori H., Saijoh Y., Rossant J., and Hamada H. The retinoic acid-inactivating enzyme CYP26 is essential for establishing an uneven distribution of retinoic acid along the anterio-posterior axis within the mouse embryo. Genes Dev. 15 (2001) 213-225
-
(2001)
Genes Dev.
, vol.15
, pp. 213-225
-
-
Sakai, Y.1
Meno, C.2
Fujii, H.3
Nishino, J.4
Shiratori, H.5
Saijoh, Y.6
Rossant, J.7
Hamada, H.8
-
11
-
-
33847018823
-
Rescue of cytochrome P450 oxidoreductase (Por) mouse mutants reveals functions in vasculogenesis, brain and limb patterning linked to retinoic acid homeostasis
-
Ribes V., Otto D.M., Dickmann L., Schmidt K., Schuhbaur B., Henderson C., Blomhoff R., Wolf C.R., Tickle C., and Dollé P. Rescue of cytochrome P450 oxidoreductase (Por) mouse mutants reveals functions in vasculogenesis, brain and limb patterning linked to retinoic acid homeostasis. Dev. Biol. 303 (2007) 66-81
-
(2007)
Dev. Biol.
, vol.303
, pp. 66-81
-
-
Ribes, V.1
Otto, D.M.2
Dickmann, L.3
Schmidt, K.4
Schuhbaur, B.5
Henderson, C.6
Blomhoff, R.7
Wolf, C.R.8
Tickle, C.9
Dollé, P.10
-
12
-
-
20244367932
-
Diversity and function of mutations in P450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis
-
Huang N., Pandey A.V., Agrawal V., Reardon W., Lapunzina P.D., Mowat D., Jabs E.W., Van Vliet G., Sack J., Fluck C.E., and Miller W.L. Diversity and function of mutations in P450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis. Am. J. Hum. Genet. 76 (2005) 729-749
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 729-749
-
-
Huang, N.1
Pandey, A.V.2
Agrawal, V.3
Reardon, W.4
Lapunzina, P.D.5
Mowat, D.6
Jabs, E.W.7
Van Vliet, G.8
Sack, J.9
Fluck, C.E.10
Miller, W.L.11
-
13
-
-
33745790703
-
Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosterone
-
Homma K., Hasegawa T., Nagai T., Adachi M., Horikawa R., Fujiwara I., Tajima T., Takeda R., Fukami M., and Ogata T. Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosterone. J. Clin. Endocrinol. Metab. 91 (2006) 2643-2649
-
(2006)
J. Clin. Endocrinol. Metab.
, vol.91
, pp. 2643-2649
-
-
Homma, K.1
Hasegawa, T.2
Nagai, T.3
Adachi, M.4
Horikawa, R.5
Fujiwara, I.6
Tajima, T.7
Takeda, R.8
Fukami, M.9
Ogata, T.10
-
14
-
-
0028922231
-
Pharmacokinetics of all-trans retinoic acid in pediatric patients with leukemia
-
Takitani K., Tamai H., Morinobu T., Kawamura N., Miyake M., Fujimoto T., and Mino M. Pharmacokinetics of all-trans retinoic acid in pediatric patients with leukemia. Jpn. J. Cancer Res. 56 (1995) 400-405
-
(1995)
Jpn. J. Cancer Res.
, vol.56
, pp. 400-405
-
-
Takitani, K.1
Tamai, H.2
Morinobu, T.3
Kawamura, N.4
Miyake, M.5
Fujimoto, T.6
Mino, M.7
-
15
-
-
0025321256
-
13-cis-Retinoic acid is an endogenous compound in human serum
-
Tang G.W., and Russell R.M. 13-cis-Retinoic acid is an endogenous compound in human serum. J. Lipid Res. 30 (1990) 175-182
-
(1990)
J. Lipid Res.
, vol.30
, pp. 175-182
-
-
Tang, G.W.1
Russell, R.M.2
-
17
-
-
0036151816
-
Complete mutation analysis panel of the 39 human HOX genes
-
Kosaki K., Kosaki R., Suzuki T., Yoshihashi H., Takahashi T., Sasaki K., Tomita M., McGinnis W., and Matsuo N. Complete mutation analysis panel of the 39 human HOX genes. Teratology 65 (2002) 50-62
-
(2002)
Teratology
, vol.65
, pp. 50-62
-
-
Kosaki, K.1
Kosaki, R.2
Suzuki, T.3
Yoshihashi, H.4
Takahashi, T.5
Sasaki, K.6
Tomita, M.7
McGinnis, W.8
Matsuo, N.9
-
18
-
-
0001539774
-
Rectum and anus
-
Stevenson R.E., Hall J.G., and Goodman R.M. (Eds), Oxford University Press, New York
-
Stevenson R.E. Rectum and anus. In: Stevenson R.E., Hall J.G., and Goodman R.M. (Eds). Human Malformations and Related Anomalies (1993), Oxford University Press, New York 493-499
-
(1993)
Human Malformations and Related Anomalies
, pp. 493-499
-
-
Stevenson, R.E.1
-
19
-
-
77953019707
-
Vesicoureteral reflux
-
Kliegman R.M., Behrman R.E., Jenson H.B., and Stanton B.F. (Eds), Saunders, Elsevier, Inc., Philadelphia
-
Elder J.S. Vesicoureteral reflux. In: Kliegman R.M., Behrman R.E., Jenson H.B., and Stanton B.F. (Eds). Nelson Textbook of Pediatrics (2007), Saunders, Elsevier, Inc., Philadelphia 2228-2234
-
(2007)
Nelson Textbook of Pediatrics
, pp. 2228-2234
-
-
Elder, J.S.1
-
20
-
-
0037155271
-
Association of multiple developmental defects and embryonic lethality with loss of microsomal NADPH-cytochrome P450 oxidoreductase
-
Shen A.L., O'Leary K.A., and Kasper C.B. Association of multiple developmental defects and embryonic lethality with loss of microsomal NADPH-cytochrome P450 oxidoreductase. J. Biol. Chem. 277 (2002) 6536-6541
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 6536-6541
-
-
Shen, A.L.1
O'Leary, K.A.2
Kasper, C.B.3
-
21
-
-
27144524316
-
Apoptosis induced by vitamin A signaling is crucial for connecting the ureters to the bladder
-
Batourina E., Tsai S., Lambert S., Sprenkle P., Viana R., Dutta S., Hensle T., Wang F., Niederreither K., McMahon A.P., Carroll T.J., and Mendelsohn C.L. Apoptosis induced by vitamin A signaling is crucial for connecting the ureters to the bladder. Nat. Genet. 37 (2005) 1082-1089
-
(2005)
Nat. Genet.
, vol.37
, pp. 1082-1089
-
-
Batourina, E.1
Tsai, S.2
Lambert, S.3
Sprenkle, P.4
Viana, R.5
Dutta, S.6
Hensle, T.7
Wang, F.8
Niederreither, K.9
McMahon, A.P.10
Carroll, T.J.11
Mendelsohn, C.L.12
-
22
-
-
0032034141
-
Retinoic acid-induced caudal regression syndrome in the mouse fetus
-
Padmanabhan R. Retinoic acid-induced caudal regression syndrome in the mouse fetus. Reprod. Toxicol. 12 (1998) 139-151
-
(1998)
Reprod. Toxicol.
, vol.12
, pp. 139-151
-
-
Padmanabhan, R.1
-
23
-
-
0038507099
-
Liver-specific deletion of the NADPH-cytochrome P450 reductase gene: impact on plasma cholesterol homeostasis and the function and regulation of microsomal cytochrome P450 and heme oxygenase
-
Gu J., Weng Y., Zhang Q.Y., Cui H., Behr M., Wu L., Yang W., Zhang L., and Ding X. Liver-specific deletion of the NADPH-cytochrome P450 reductase gene: impact on plasma cholesterol homeostasis and the function and regulation of microsomal cytochrome P450 and heme oxygenase. J. Biol. Chem. 278 (2003) 5895-5901
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 5895-5901
-
-
Gu, J.1
Weng, Y.2
Zhang, Q.Y.3
Cui, H.4
Behr, M.5
Wu, L.6
Yang, W.7
Zhang, L.8
Ding, X.9
-
24
-
-
67650641859
-
Removal of maternal retinoic acid by embryonic CYP26 is required for correct Nodal expression during early embryonic patterning
-
Uehara M., Yashiro K., Takaoka K., Yamamoto M., and Hamada H. Removal of maternal retinoic acid by embryonic CYP26 is required for correct Nodal expression during early embryonic patterning. Genes Dev. 23 (2009) 1689-1698
-
(2009)
Genes Dev.
, vol.23
, pp. 1689-1698
-
-
Uehara, M.1
Yashiro, K.2
Takaoka, K.3
Yamamoto, M.4
Hamada, H.5
-
25
-
-
0041468898
-
Identification of novel roles of the cytochrome p450 system in early embryogenesis: effects on vasculogenesis and retinoic Acid homeostasis
-
Otto D.M., Henderson C.J., Carrie D., Davey M., Gundersen T.E., Blomhoff R., Adams R.H., Tickle C., and Wolf C.R. Identification of novel roles of the cytochrome p450 system in early embryogenesis: effects on vasculogenesis and retinoic Acid homeostasis. Mol. Cell. Biol. 23 (2003) 6103-6116
-
(2003)
Mol. Cell. Biol.
, vol.23
, pp. 6103-6116
-
-
Otto, D.M.1
Henderson, C.J.2
Carrie, D.3
Davey, M.4
Gundersen, T.E.5
Blomhoff, R.6
Adams, R.H.7
Tickle, C.8
Wolf, C.R.9
-
26
-
-
0024745470
-
Penile agenesis and syndrome of multiple abnormalities associated with the ingestion of retinoic acid by the mother
-
(in Spanish)
-
Martínez Tallo M.E., Galán Gómez E., Cordero Carrasco J.L., Hidalgo Barquero E.H., Campo Sampedro F.M., and Cardesa García J.J. Penile agenesis and syndrome of multiple abnormalities associated with the ingestion of retinoic acid by the mother. An. Esp. Pediatr. 31 (1989) 399-400 (in Spanish)
-
(1989)
An. Esp. Pediatr.
, vol.31
, pp. 399-400
-
-
Martínez Tallo, M.E.1
Galán Gómez, E.2
Cordero Carrasco, J.L.3
Hidalgo Barquero, E.H.4
Campo Sampedro, F.M.5
Cardesa García, J.J.6
-
27
-
-
33745133051
-
Molecular genetic cascades for external genitalia formation: an emerging organogenesis program
-
Yamada G., Suzuki K., Haraguchi R., Miyagawa S., Satoh Y., Kamimura M., Nakagata N., Kataoka H., Kuroiwa A., and Chen Y. Molecular genetic cascades for external genitalia formation: an emerging organogenesis program. Dev. Dyn. 235 (2006) 1738-1752
-
(2006)
Dev. Dyn.
, vol.235
, pp. 1738-1752
-
-
Yamada, G.1
Suzuki, K.2
Haraguchi, R.3
Miyagawa, S.4
Satoh, Y.5
Kamimura, M.6
Nakagata, N.7
Kataoka, H.8
Kuroiwa, A.9
Chen, Y.10
-
28
-
-
0344953585
-
A defective response to Hedgehog signaling in disorders of cholesterol biosynthesis
-
Cooper M.K., Wassif C.A., Krakowiak P.A., Taipale J., Gong R., Kelley R.I., Porter F.D., and Beachy P.A. A defective response to Hedgehog signaling in disorders of cholesterol biosynthesis. Nat. Genet. 33 (2003) 508-513
-
(2003)
Nat. Genet.
, vol.33
, pp. 508-513
-
-
Cooper, M.K.1
Wassif, C.A.2
Krakowiak, P.A.3
Taipale, J.4
Gong, R.5
Kelley, R.I.6
Porter, F.D.7
Beachy, P.A.8
-
29
-
-
0037387601
-
Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromes
-
Herman G.E. Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromes. Hum. Mol. Genet. 12 S1 (2003) R75-R88
-
(2003)
Hum. Mol. Genet.
, vol.12
, Issue.SUPPL.1
-
-
Herman, G.E.1
|