SCOPUS 정보 검색 플랫폼

American Journal of Human Genetics

Volumn 62, Issue 4, 1998, Pages 765-767

Are we ready to try to cure alkaptonuria?

(1) La Du B N , Jr a

a UNIVERSITY OF MICHIGAN HEALTH SYSTEM (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HOMOGENTISIC ACID; TYROSINE;

ALKAPTONURIA; AMINO ACID METABOLISM; EDITORIAL; ENZYME RECONSTITUTION; FRAMESHIFT MUTATION; GENE ISOLATION; GENE THERAPY; HUMAN; MOLECULAR CLONING; PRIORITY JOURNAL;

EID: 0031901425 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/301810 Document Type: Editorial

Times cited : (23)

References (9)

1
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- Mutation and polymorphism analysis of the human homogentisate 1,2-dioxygenase gene in alkaptonuria patients
- D Beltrán-Valero de Bernabé B Granadino I Chiarelli B Porfirio E Mayatepek R Aquaron MM Moore Mutation and polymorphism analysis of the human homogentisate 1,2-dioxygenase gene in alkaptonuria patients Am J Hum Genet 62 1998 776 784 (in this issue)
- (1998) Am J Hum Genet , vol.62 , pp. 776-784
- Beltrán-Valero de Bernabé, D¹ Granadino, B² Chiarelli, I³ Porfirio, B⁴ Mayatepek, E⁵ Aquaron, R⁶ Moore, MM⁷

2
- 0029740946
- The molecular basis of alkaptonuria
- JM Fernandez-Canon B Granadino D Beltran-Valero de Bernabe M Renedo E Fernandez-Ruiz MA Penalva S Rodriguez de Cordoba The molecular basis of alkaptonuria Nat Genet 14 1996 19 24
- (1996) Nat Genet , vol.14 , pp. 19-24
- Fernandez-Canon, JM¹ Granadino, B² Beltran-Valero de Bernabe, D³ Renedo, M⁴ Fernandez-Ruiz, E⁵ Penalva, MA⁶ Rodriguez de Cordoba, S⁷

3
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- The Croonian lectures on inborn errors of metabolism: lecture II: alkaptonuria
- AE Garrod The Croonian lectures on inborn errors of metabolism: lecture II: alkaptonuria Lancet 2 1908 73 79
- (1908) Lancet , vol.2 , pp. 73-79
- Garrod, AE¹

4
- 0030935941
- Molecular defects in alkaptonuria
- A Gehrig SR Schmidt CR Muller S Srsen K Srsnova W Kress Molecular defects in alkaptonuria Cytogenet Cell Genet 76 1997 14 16
- (1997) Cytogenet Cell Genet , vol.76 , pp. 14-16
- Gehrig, A¹ Schmidt, SR² Muller, CR³ Srsen, S⁴ Srsnova, K⁵ Kress, W⁶

5
- 0031571117
- The human homogentisicate 1,2-dioxygenase (HGO) gene
- B Granadino D Beltran-Valero de Bernabe JM Fernandez-Canon MA Penalva S Rodriguez de Cordoba The human homogentisicate 1,2-dioxygenase (HGO) gene Genomics 43 1997 115 122
- (1997) Genomics , vol.43 , pp. 115-122
- Granadino, B¹ Beltran-Valero de Bernabe, D² Fernandez-Canon, JM³ Penalva, MA⁴ Rodriguez de Cordoba, S⁵

6
- 0000465301
- The nature of the defect in tyrosine metabolism in alcaptonuria
- BN La Du VG Zannoni L Laster JE Seegmiller The nature of the defect in tyrosine metabolism in alcaptonuria J Biol Chem 230 1958 251 260
- (1958) J Biol Chem , vol.230 , pp. 251-260
- La Du, BN¹ Zannoni, VG² Laster, L³ Seegmiller, JE⁴

7
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- Alkaptonuria
- BN La Du Alkaptonuria CR Scriver AL Beaudet W Sly D Valle The metabolic and molecular bases of inherited disease 7th ed 1995 McGraw-Hill New York 1371 1386
- (1995) , pp. 1371-1386
- La Du, BN¹

8
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- Hypertyrosinemia
- GA Mitchell M Lambert RM Tanguay Hypertyrosinemia CR Scriver AL Beaudet W Sly D Valle The metabolic and molecular bases of inherited disease 7th ed 1995 McGraw-Hill New York 1077 1106
- (1995) , pp. 1077-1106
- Mitchell, GA¹ Lambert, M² Tanguay, RM³

9
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- aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16
- X Montagutelli A Lalouette M Coude P Kamoun M Forest J-L Guenet aku , a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16 Genomics 19 1994 9 11
- (1994) Genomics , vol.19 , pp. 9-11
- Montagutelli, X¹ Lalouette, A² Coude, M³ Kamoun, P⁴ Forest, M⁵ Guenet, J-L⁶

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