SCOPUS 정보 검색 플랫폼

Current Opinion in Neurology

Volumn 14, Issue 6, 2001, Pages 783-787

Peroxisomal disorders

(1) Raymond, Gerald V a

a KENNEDY KRIEGER INSTITUTE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LONG CHAIN FATTY ACID; MATRIX PROTEIN; MEMBRANE PROTEIN;

ADRENOLEUKODYSTROPHY; DISORDERS OF PEROXISOMAL FUNCTIONS; ENZYME DEFICIENCY; HUMAN; PATHOGENESIS; PEROXISOME; PHENOTYPE; PROTEIN TARGETING; REVIEW; X CHROMOSOME LINKED DISORDER; ZELLWEGER SYNDROME;

ADRENOLEUKODYSTROPHY; ADULT; BRAIN; CENTRAL NERVOUS SYSTEM DISEASES; CHILD; FEMALE; HUMANS; MALE; NEUROLOGIC EXAMINATION; PEROXISOMAL DISORDERS; PEROXISOMES; PHENOTYPE; SPINAL CORD;

EID: 0035684152 PISSN: 13507540 EISSN: None Source Type: Journal
DOI: 10.1097/00019052-200112000-00017 Document Type: Review

Times cited : (9)

References (20)

1
- 0001687866
- The peroxisome biogenesis disorders
- Scriver CR, Beaudet AL, Sly WS, Valle D (editors). New York: McGraw-Hill
- (2001) The metabolic and molecular basis of inherited disease , pp. 3181-3218
- Gould, S.J.¹ Raymond, G.V.² Valle, D.³

2
- 10144261887
- A unified nomenclature for peroxisome biogenesis factors
- (1996) J Cell Biol , vol.135 , pp. 1-3
- Distel, B.¹ Erdmann, R.² Gould, S.J.³

3
- 0029010680
- Import of stably folded proteins into peroxisomes
- (1995) Mol Biol Cell , vol.6 , pp. 675-683
- Walton, P.A.¹ Hill, P.E.² Subramani, S.³

4
- 0035805208
- Peroxisomal protein import: The paradigm shifts
- (2001) Cell , vol.105 , pp. 293-296
- Smith, M.D.¹ Schnell, D.J.²

5
- 0035917528
- The human peroxisomal targeting signal receptor, Pex5p, is translocated into the peroxisomal matrix and recycled to the cytosol
- (2001) Cell , vol.105 , pp. 187-196
- Dammai, V.¹ Subramani, S.²

6
- 0035844874
- Multiple distinct targeting signals in integral peroxisomal membrane proteins
- (2001) J Cell Biol , vol.153 , pp. 1141-1150
- Jones, J.M.¹ Morrell, J.C.² Gould, S.J.³

7
- 0034972812
- Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences
- (2001) Mol Cell Biol , vol.21 , pp. 4413-4424
- Fransen, M.¹ Wylin, T.² Brees, C.³

8
- 0034964726
- Disorders of peroxisome biogenesis due to mutations in pex1: Phenotypes and pex1 protein levels
- (2001) Am J Hum Genet , vol.69 , pp. 35-48
- Walter, C.¹ Gootjes, J.² Mooijer, P.A.³

9
- 0033840419
- Neuronal migration disorder in Zellweger mice is secondary to glutamate receptor dysfunction
- (2000) Ann Neurol , vol.48 , pp. 336-343
- Gressens, P.¹ Baes, M.² Leroux, P.³

10
- 0035953036
- Enhanced expression of a-series gangliosides in fibroblasts of patients with peroxisome biogenesis disorders
- (2001) Biochim Biophys Acta , vol.1535 , pp. 285-293
- Tatsumi, K.¹ Saito, M.² Lin, B.³

11
- 0002277381
- X-linked adrenoleukodystrophy
- Scriver CR, Beaudet AL, Valle D, Sly WS (editors). New York: McGraw-Hill Medical Publishing Division
- (2001) The metabolic and molecular basis of inherited disease , pp. 3257-3302
- Moser, H.W.¹ Smith, K.D.² Watkins, P.A.³

12
- 0035071054
- Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening
- (2001) Ann. Neurol , vol.49 , pp. 512-517
- Bezman, L.¹ Moser, A.B.² Raymond, G.V.³

13
- 0343133942
- Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously described
- (2000) Hum Murat , vol.15 , pp. 348-353
- Lachtermacher, M.B.¹ Seuanez, H.N.² Moser, A.B.³

14
- 0032893407
- X-linked adrenoleukodystrophy: Genes, mutations, and phenotypes
- (1999) Neurochem Res , vol.24 , pp. 521-535
- Smith, K.D.¹ Kemp, S.² Braiterman, L.T.³

15
- 0033030905
- Mutational analysis and the pathogenesis of variant X-linked adrenoleukodystrophy phenotypes
- (1999) Arch Neurol , vol.56 , pp. 273-275
- Moser, H.W.¹ Kemp, S.² Smith, K.D.³

16
- 0034327372
- Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: Implications for gene therapy of X-linked adrenoleukodystrophy
- (2000) Hum Mol Genet , vol.9 , pp. 2609-2616
- Unterrainer, G.¹ Molzer, B.² Forss-Petter, S.³ Berger, J.⁴

17
- 0035138765
- Evolution of phenotypes in adult male patients with X-linked adrenoleukodystrophy
- (2001) Ann Neurol , vol.49 , pp. 186-194
- Van Geel, B.M.¹ Bezman, L.² Loes, D.J.³

18
- 0029788562
- Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotype
- (1996) Ann Neurol , vol.40 , pp. 254-257
- Korenke, G.C.¹ Fuchs, S.² Krasemann, E.³

19
- 0035005817
- The dorsal root ganglia in adrenomyeloneuropathy: Neuronal atrophy and abnormal mitochondria
- (2001) J Neuropathol Exp Neurol , vol.60 , pp. 493-501
- Powers, J.M.¹ DeCiero, D.P.² Cox, C.³

20
- 0033970326
- Adrenomyeloneuropathy: A neuropathologic review featuring its noninflammatory myelopathy
- (2000) J Neuropathol Exp Neurol , vol.59 , pp. 89-102
- Powers, J.M.¹ DeCiero, D.P.² Ito, M.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.