SCOPUS 정보 검색 플랫폼

Volumn 59, Issue 78, 2001, Pages

Recent insights into the molecular genetics of the homocysteine metabolism

(4) Fodinger M a Wagner, O F a Horl W H a Sunder Plassmann, G a

a MEDICAL UNIVERSITY OF VIENNA (Austria)

Author keywords

Cubilin; CUBN; Folate binding protein; FOLR1; Homocysteine; Methylenetetrahydrofolate reductase; MTHFR

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); CUBILIN; CYANOCOBALAMIN; FOLATE BINDING PROTEIN; FOLIC ACID; HOMOCYSTEINE; CARRIER PROTEIN; CELL SURFACE RECEPTOR; FOLATE-BINDING PROTEIN; INTRINSIC FACTOR COBALAMIN RECEPTOR; INTRINSIC FACTOR-COBALAMIN RECEPTOR; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); OXIDOREDUCTASE;

AMINO ACID METABOLISM; ANIMAL MODEL; CONFERENCE PAPER; GENE MUTATION; GENETIC POLYMORPHISM; HEMODIALYSIS; HUMAN; HYPERHOMOCYSTEINEMIA; KIDNEY DISEASE; KIDNEY FAILURE; KIDNEY TRANSPLANTATION; KNOCKOUT MOUSE; MEGALOBLASTIC ANEMIA; MOUSE; NONHUMAN; PERITONEAL DIALYSIS; PRIORITY JOURNAL; ANIMAL; GENETICS; METABOLISM; MOLECULAR BIOLOGY; MOUSE MUTANT; POINT MUTATION; RENAL REPLACEMENT THERAPY; REVIEW; SYNDROME;

5,10-METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ANEMIA, MEGALOBLASTIC; ANIMALS; CARRIER PROTEINS; HOMOCYSTEINE; HUMANS; HYPERHOMOCYSTEINEMIA; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MICE; MICE, KNOCKOUT; MOLECULAR BIOLOGY; OXIDOREDUCTASES; POINT MUTATION; POLYMORPHISM, GENETIC; RECEPTORS, CELL SURFACE; RENAL REPLACEMENT THERAPY; SYNDROME;

EID: 0035130270 PISSN: 00986577 EISSN: None Source Type: Journal
DOI: None Document Type: Conference Paper

Times cited : (29)

References (24)

1
- 0242567342
- Molecular genetics of homocysteine metabolism
- (1999) Miner Electrolyte Metab , vol.25 , pp. 269-278
- Födinger, M.¹ Buchmayer, H.² Sunder-Plassmann, G.³

2
- 1642586763
- Molecular biology of 5,10-methylenetetrahydrofolate reductase
- (2000) J Nephrol , vol.13 , pp. 20-33
- Födinger, M.¹ Hörl, W.H.² Sunder-Plassmann, G.³

3
- 0031904465
- Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)
- erratum appears in Mamm Genome 10:204, 1999
- (1998) Mamm Genome , vol.9 , pp. 652-656
- Goyette, P.¹ Pai, A.² Milos, R.³ Frosst, P.⁴ Tran, P.⁵ Chen, Z.⁶ Chan, M.⁷ Rozen, R.⁸

4
- 0029049553
- A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
- (1995) Nat Genet , vol.10 , pp. 111-113
- Frosst, P.¹ Blom, H.J.² Milos, R.³ Goyette, P.⁴ Sheppard, C.A.⁵ Matthews, R.G.⁶ Boers, G.J.⁷ Den Heijer, M.⁸ Kluijtmans, L.A.⁹ Van Den Heuvel, L.P.¹⁰ Rozen, R.A.¹¹

5
- 0032573077
- A common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells
- (1998) Proc Natl Acad Sci USA , vol.95 , pp. 13217-13220
- Bagley, P.J.¹ Selhub, J.²

6
- 0031611631
- Whole-blood folate values in subjects with different methylenetetrahydrofolate reductase genotypes: Differences between the radioassay and microbiological assays
- (1998) Clin Chem , vol.44 , pp. 186-188
- Molloy, A.M.¹ Mills, J.L.² Kirke, P.N.³ Whitehead, A.S.⁴ Weir, D.G.⁵ Scott, J.M.⁶

7
- 0030851289
- Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients
- (1997) Kidney Int , vol.52 , pp. 517-523
- Födinger, M.¹ Mannhalter, C.² Wölfl, G.³ Pabinger, I.⁴ Müller, E.⁵ Schmid, R.⁶ Hörl, W.H.⁷ Sunder-Plassmann, G.⁸

8
- 7144226583
- Major determinants of hyperhomocysteinemia in peritoneal dialysis patients
- (1998) Kidney Int , vol.53 , pp. 1775-1782
- Vychytil, A.¹ Födinger, M.² Wölfl, G.³ Enzenberger, B.⁴ Auinger, M.⁵ Prischl, F.⁶ Buxbaum, M.⁷ Wiesholzer, M.⁸ Mannhalter, C.⁹ Hörl, W.H.¹⁰ Sunder-Plassmann, G.¹¹

9
- 0005601318
- Effect of MTHFR 677C→T on plasma total homocysteine levels in renal graft recipients
- (1999) Kidney Int , vol.55 , pp. 1072-1080
- Födinger, M.¹ Wölfl, G.² Fischer, G.³ Rasoul-Rockenschaub, S.⁴ Schmid, R.⁵ Hörl, W.H.⁶ Sunder-Plassmann, G.⁷

10
- 0031971515
- A second common mutation in the methylenetetrahydrofolate reductase gene: An additional risk factor for neural-tube defects?
- (1998) Am J Hum Genet , vol.62 , pp. 1044-1051
- Van Der Put, N.M.¹ Gabreels, F.² Stevens, E.M.³ Smeitink, J.A.⁴ Trijbels, F.J.⁵ Eskes, T.K.⁶ Van Den Heuvel, L.P.⁷ Blom, H.J.⁸

11
- 0031687887
- A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
- (1998) Mol Genet Metab , vol.64 , pp. 169-172
- Weisberg, I.¹ Tran, P.² Christenses, B.³ Sibani, S.⁴ Rozen, R.⁵

12
- 0033779530
- 12 plasma concentrations in kidney graft recipients
- (2000) J Am Soc Nephrol , vol.11 , pp. 1918-1925
- Födinger, M.¹ Buchmayer, H.² Heinz, G.³ Papagiannopoulos, M.⁴ Kletzmayr, J.⁵ Rasoul-Rockenschaub, S.⁶ Hörl, W.H.⁷ Sunder-Plassmann, G.⁸

13
- 0024415796
- Molecular cloning and characterization of the human folate-binding protein cDNA from placenta and malignant tissue culture (KB) cells
- (1989) J Biol Chem , vol.264 , pp. 14893-14901
- Elwood, P.C.¹

14
- 0031036589
- The divergent 5′ termini of the alpha human folate receptor (hFR) mRNAs originate from two tissue-specific promoters and alternative splicing: Characterization of the alpha hFR gene structure
- (1997) Biochemistry , vol.36 , pp. 1467-1478
- Elwood, P.C.¹ Nachmanoff, K.² Saikawa, Y.³ Page, S.T.⁴ Pacheco, P.⁵ Roberts, S.⁶ Chung, K.N.⁷

15
- 0025336152
- Folate-binding proteins
- (1990) Annu Rev Nutr , vol.10 , pp. 319-335
- Henderson, G.B.¹

16
- 0032884078
- Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development
- (1999) Nat Genet , vol.23 , pp. 228-232
- Piedrahita, J.A.¹ Oetama, B.² Bennett, G.D.³ Van Waes, J.⁴ Kamen, B.A.⁵ Richardson, J.⁶ Lacey, S.W.⁷ Anderson, R.G.⁸ Finnell, R.H.⁹

17
- 0032525203
- 12 receptor, cubilin: Molecular characterization and chromosomal mapping of the gene to 10p within the autosomal recessive megaloblastic anemia (MGA1) region
- erratum appears in Blood 92:2608, 1998
- (1998) Blood , vol.91 , pp. 3593-3600
- Kozyraki, R.¹ Kristiansen, M.² Silahtaroglu, A.³ Hansen, C.⁴ Jacobsen, C.⁵ Tommerup, N.⁶ Verroust, P.J.⁷ Moestrup, S.K.⁸

18
- 0031576218
- 12 and binds receptor-associated protein
- (1997) J Biol Chem , vol.272 , pp. 26497-26504
- Birn, H.¹ Verroust, P.J.² Nexo, E.³ Hager, H.⁴ Jacobsen, C.⁵ Christensen, E.I.⁶ Moestrup, S.K.⁷

19
- 0033056072
- 12 receptor, cubilin, is a high-affinity apolipoprotein A-I receptor facilitating endocytosis of high-density lipoprotein
- (1999) Nat Med , vol.5 , pp. 656-661
- Kozyraki, R.¹ Fyfe, J.² Kristiansen, M.³ Gerdes, C.⁴ Jacobsen, C.⁵ Cui, S.⁶ Christensen, E.I.⁷ Aminoff, M.⁸ De La Chapelle, A.⁹ Krahe, R.¹⁰ Verroust, P.J.¹¹ Moestrup, S.K.¹²

20
- 0033051889
- 12 receptor, cubilin, cause hereditary megaloblastic anaemia 1
- (1999) Nat Genet , vol.21 , pp. 309-313
- Aminoff, M.¹ Carter, J.E.² Chadwick, R.B.³ Johnson, C.⁴ Gräsbeck, R.⁵ Abdelaal, M.A.⁶ Broch, H.⁷ Jenner, L.B.⁸ Verroust, P.J.⁹ Moestrup, S.K.¹⁰ De La Chapelle, A.¹¹ Krahe, R.¹²

21
- 0032054038
- Lack of association between mutations in the folate receptor-alpha gene and spina bifida
- erratum appears in Am J Med Genet 79:231, 1998
- (1998) Am J Med Genet , vol.76 , pp. 310-317
- Barber, R.C.¹ Shaw, G.M.² Lammer, E.J.³ Greer, K.A.⁴ Biela, T.A.⁵ Lacey, S.W.⁶ Wasserman, C.R.⁷ Finnell, R.H.⁸

22
- 0032815305
- Influence of 5,10-methylenetetrahydrofolate reductase gene polymorphism on plasma homocysteine concentration in patients with end-stage renal disease
- (1999) Am J Kidney Dis , vol.34 , pp. 259-263
- Lee, H.A.¹ Choi, J.S.² Ha, K.S.³ Yang, D.H.⁴ Chang, S.K.⁵ Hong, S.Y.⁶

23
- 0344699328
- Response of hyperhomocysteinemia to folic acid supplementation in patients with end-stage renal disease
- (1999) Clin Nephrol , vol.51 , pp. 108-115
- Dierkes, J.¹ Domröse, U.² Ambrosch, A.³ Bosselmann, H.P.⁴ Neumann, K.H.⁵ Luley, C.⁶

24
- 0034058544
- The C677T methylenetetrahydrofolate reductase gene mutation in hemodialysis patients
- (2000) J Am Soc Nephrol , vol.11 , pp. 885-893
- Kimura, H.¹ Gejyo, F.² Suzuki, S.³ Miyazaki, R.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.