DNA rearrangements in the α5(IV) collagen gene (COL4A5) of individuals with alport syndrome: Further refinement using pulsed-field gel electrophoresis (Q57635565)

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English	DNA rearrangements in the α5(IV) collagen gene (COL4A5) of individuals with alport syndrome: Further refinement using pulsed-field gel electrophoresis	article

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scholarly article

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14 September 2019

DNA rearrangements in the alpha 5(IV) collagen gene (COL4A5) of individuals with Alport syndrome: further refinement using pulsed-field gel electrophoresis (English)

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14 September 2019

Alport syndrome

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inferred from title

1

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14 September 2019

author name string

E Boye

2

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14 September 2019

F Flinter

3

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14 September 2019

M Bobrow

4

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14 September 2019

A Harris

5

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publication date

1 November 1992

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14 September 2019

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14 September 2019

14

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14 September 2019

3

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14 September 2019

624-633

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HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

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High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers

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https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980161-2

7 January 2021

based on heuristic

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Identification of mutations in the COL4A5 collagen gene in Alport syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980161-2

7 January 2021

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CpG-rich islands and the function of DNA methylation

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7 January 2021

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Major rearrangements in the α5(IV) collagen gene in three patients with alport syndrome

1 reference

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7 January 2021

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Localization of the gene for X-linked Alport's syndrome

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7 January 2021

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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Localization of the gene for classic Alport syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980161-2

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Genetics of classic Alport's syndrome

1 reference

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Variants of Alport's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980161-2

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Multipoint linkage analysis in X-linked Alport syndrome

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Duplication of seven exons in LDL receptor gene caused by Alu-Alu recombination in a subject with familial hypercholesterolemia

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Removal of repeated sequences from hybridisation probes

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The arrangement of intra- and intermolecular disulfide bonds in the carboxyterminal, non-collagenous aggregation and cross-linking domain of basement-membrane type IV collagen

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

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7 January 2021

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Linkage studies in X-linked Alport's syndrome

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Long-range mapping of the gene for the human alpha 5(IV) collagen chain at Xq22-q23.

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Construction of a yeast artificial chromosome contig encompassing the human alpha 5(IV) collagen gene (COL4A5).

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The glomerular basal lamina in hereditary nephritis

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Single base mutation in α5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980161-2

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Characterization of the 3' half of the human type IV collagen alpha 5 gene that is affected in the Alport syndrome

1 reference

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Identifiers

10.1016/S0888-7543(05)80161-2

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Europe PubMed Central

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14 September 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1330889%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

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