Menkes and Wilson diseases.

Menkes and Wilson diseases.

Dades bibliogràfiques
Autors principals:	Monaco, A, Chelly, J
Format:	Journal article
Idioma:	English
Publicat:	1995

Ítems similars

Wilson disease and Menkes disease: new handles on heavy-metal transport.
per: Bull, P, et al.
Publicat: (1994)

Cloning the Wilson disease gene.
per: Chelly, J, et al.
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Characterization of the exon structure of the Menkes disease gene using vectorette PCR.
per: Tümer, Z, et al.
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A Golgi localization signal identified in the Menkes recombinant protein.
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Analysis of Mnk, the murine homologue of the locus for Menkes disease, in normal and mottled (Mo) mice.
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IDENTIFICATION OF A COPPER-BINDING ATPASE HOMOLOGOUS TO THE MENKES GENE - A CANDIDATE FOR THE WILSON DISEASE GENE
per: Cox, D, et al.
Publicat: (1994)

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene.
per: Bull, P, et al.
Publicat: (1993)

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein.
per: Chelly, J, et al.
Publicat: (1993)

Genetics of Menkes Disease
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Publicat: (1994-11-01)

Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease.
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Biochemical Marker for Menkes Disease
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Novel membrane traffic steps regulate the exocytosis of the Menkes disease ATPase.
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Menkes kinky hair disease
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Emergence of kinky hair in Menkes disease
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Reduced Neutrophil Extracellular Trap (NET) Formation During Systemic Inflammation in Mice With Menkes Disease and Wilson Disease: Copper Requirement for NET Release
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Menkes Maple Syrup Urine Disease: Treatment
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Molecular basis of neurodegeneration and neurodevelopmental defects in Menkes disease
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Response of Fibroblasts from Menkes’ and Wilson’s Copper Metabolism-Related Disorders to Ionizing Radiation: Influence of the Nucleo-Shuttling of the ATM Protein Kinase
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Almost misdiagnosed Menkes disease: A case report
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Clinical expression of Menkes disease in females with normal karyotype
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Mottled mice and non-mammalian models of Menkes disease
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Non-Menkes Type Copper Deficiency
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The Menkes disease ATPase (ATP7A) is internalized via a Rac1-regulated, clathrin- and caveolae-independent pathway.
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Menkes disease as a differential diagnosis of child abuse Doença de Menkes como diagnóstico diferencial de abuso de criança
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Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
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Is It a Pathogenic ATP7A Variation and Is It Menkes Disease?
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Menkes Kinky Hair Syndrome: A Rare Neurodegenerative Disease
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Vacuolization in Myeloid and Erythroid Precursors in a Child with Menkes Disease
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Imaging findings of Menkes disease, a radiographic mimic of abusive trauma
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