About: Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin

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About: Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin Goto Sponge NotDistinct Permalink

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scientific article published on 01 September 1984

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 1984 (uk) article scientifique publié en 1984 (fr) im September 1984 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 September 1984 (en) artículu científicu espublizáu en setiembre de 1984 (ast)
publication date	wds:Q70639207-FF3A5707-2AD4-4657-88B2-41864C379D52
publication date	1984-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q70639207-BAE7511F-2AEA-4676-B8E2-F4F7F3E1370F
language of work or name	English
cites work	wds:Q70639207-31941AD9-A7B9-4774-9BFF-0A4683F576E3 wds:Q70639207-DA92DD9B-9C32-447A-AF91-2C147A1FAC43
cites work	Structure of prealbumin: secondary, tertiary and quaternary interactions determined by Fourier refinement at 1.8 A Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)
author name string	wds:Q70639207-160566C4-7146-4425-BAE3-FD3FFF570ABF wds:Q70639207-1A201B6A-4BAC-4396-B122-6927C3E49996 wds:Q70639207-52678AB7-64B2-49A2-AE5D-01E317AD1CF8 wds:Q70639207-56616FBA-57BF-4CC8-9CD5-2FE8FD1F7A3A wds:Q70639207-7F982490-9724-4EF6-85E6-AA87FC1D84C4 wds:Q70639207-E10AD151-C1DF-419B-984F-84DF3DFAD0F6
author name string	H Matsuo M Nakazato K Kangawa S Araki S Tawara N Minamino
rdfs:label	Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin (en) Revised analysis of amino acid replacement in a prealbumin variant (nl)
skos:prefLabel	Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin (en) Revised analysis of amino acid replacement in a prealbumin variant (nl)
name	Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin (en) Revised analysis of amino acid replacement in a prealbumin variant (nl)
title	wds:Q70639207-F751386F-AF98-4024-B3BC-809BB0F21F7F
title	Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin (en)
page(s)	wds:Q70639207-29EDD29B-7CC7-407C-A5FA-C1EDF49D2B23
page(s)	921-928
instance of	wds:Q70639207-48592AB0-B392-4083-879F-6B74B5D8629B
instance of	scholarly article
PubMed ID	wds:Q70639207-5939C369-E66B-46D9-926E-F96B9D58B910
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6487335
PubMed ID	6487335
published in	wds:Q70639207-93643842-80E6-4168-A9CB-22777153BA26
published in	Biochemical and Biophysical Research Communications
issue	wds:Q70639207-BCA72A33-20FA-4ABE-B442-ED727A5099E0
volume	wds:Q70639207-6EF62146-532B-442F-9DB5-37D6499D558A
issue	3
volume	123
DOI	wds:Q70639207-3120E000-5BAD-4E18-884A-B5EA69A05867
DOI	http://dx.doi.org/10.1016/S0006-291X(84)80222-3
DOI	10.1016/S0006-291X(84)80222-3
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70639207
is cites work of	Gelsolin-related amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin Tissue-specific and developmental expression of human transthyretin gene in transgenic mice Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis Transthyretin gene mutations in British and French patients with amyloid neuropathy Recent advances in the molecular pathology of familial amyloid polyneuropathy Molecular genetics of amyloid neuropathy in Europe Transthyretin mutations in health and disease. Transthyretin mutations in hyperthyroxinemia and amyloid diseases Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline Genetic Aspects of Amyloidosis Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss). Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis Fibril in senile systemic amyloidosis is derived from normal transthyretin Unifying features of systemic and cerebral amyloidosis Ocular amyloidosis, with special reference to the hereditary forms with vitreous involvement Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. Family studies on the transthyretin (prealbumin)-methionine-30 variant Prealbumin variants in the amyloid fibrils of Swedish familial amyloidotic polyneuropathy Systemic senile amyloidosis. Identification of a new prealbumin (transthyretin) variant in cardiac tissue: immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathy Diagnostic radioimmunoassay for familial amyloidotic polyneuropathy before clinical onset Haplotype analysis of familial amyloidotic polyneuropathy A new transthyretin mutation associated with amyloidotic vitreous opacities. Asparagine for isoleucine at position 84 Evidence for increased amyloid enhancing factor activity in Alzheimer brain extract. Transthyretin is synthesized in the mammalian eye The transthyretin cDNA sequence is normal in transthyretin-derived senile systemic amyloidosis Prealbumin: its association with amyloid Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin A DNA test for Indiana/Swiss hereditary amyloidosis (FAP II) Restriction fragment analysis confirms the position 33 mutation in transthyretin from an Israeli patient (SKO) with familial amyloidotic polyneuropathy The single proline-glutamine substitution at position 5 enhances the potency of amyloid fibril formation of murine apo A-II Prealbumin. A major constituent of vitreous amyloid Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs Metabolism of senile amyloid precursor and amyloidogenesis. Age-related acceleration of apolipoprotein A-II clearance in the senescence accelerated mouse A double-variant transthyretin allele (Ser 6, Ile 33) in the Israeli patient "SKO" with familial amyloidotic polyneuropathy Transthyretin Pro 36 associated with familial amyloidotic polyneuropathy in an Ashkenazic Jewish kindred "Sporadic" prealbumin-related amyloid polyneuropathy: report of two cases Immunohistochemical characterization of amyloid proteins in sural nerves and clinical associations in amyloid neuropathy
is cites work of	wds:Q34540755-08DEFE53-5176-4830-9904-DC188BE0F66B wds:Q37070132-AA003B91-69ED-4443-8006-B55BED1C7366 wds:Q40625745-193837BB-8DFC-483E-B5BB-4A79754EB570 wds:Q35246636-8A275A29-CF53-4C56-A40D-AF10EB612417 wds:Q40340220-69F014EC-A337-457F-8122-9DAFEC5F7F6C wds:Q45086740-DCB96B3E-C797-4864-AE9C-75F80BF38ED7 wds:Q44729232-AC6CF450-8F4E-489A-9776-105D802CFC85 wds:Q34269382-9F3E1F9A-104D-44AA-A8D7-9B6B68B25C2B wds:Q42050857-17A56671-D35D-4DCD-A18E-DB0F50BEF73D wds:Q48142427-FBD29BC4-6132-4AA6-A804-D57695F553C5 wds:Q67516546-C3B68A51-4060-4A58-9E97-F53CD724E2A8 wds:Q67522973-FD32D8B2-B4FB-4F91-BFAA-7D24C60AC75A

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