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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2006-7-4
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pubmed:abstractText |
A subset of familial isolated primary hyperparathyroidism (FIHP) is a variant of hyperparathyroidism-jaw tumour syndrome (HPT-JT). AIM/PATIENTS AND METHODS: We investigated the involvement of the HRPT2, MEN1 and CASR genes in 11 provisional FIHP families and two HPT-JT families.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0300-0664
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pubmed:author |
pubmed-author:BenikoMutsuoM,
pubmed-author:FujisawaKenjiK,
pubmed-author:FujisawaMasatoM,
pubmed-author:GolamHossain MdHM,
pubmed-author:IwataTakeoT,
pubmed-author:KamataNobuyukiN,
pubmed-author:MizukoshiTsunenoriT,
pubmed-author:MizusawaNorikoN,
pubmed-author:NagaoDaisukeD,
pubmed-author:NoguchiShiroS,
pubmed-author:SakuraiAkihiroA,
pubmed-author:SanoToshiakiT,
pubmed-author:SuzukiShinichiS,
pubmed-author:SuzukiYasuyoY,
pubmed-author:TaharaHidekiH,
pubmed-author:TsuyuguchiMasaruM,
pubmed-author:UchinoShinyaS,
pubmed-author:YamashitaYoshioY,
pubmed-author:YashiroTohruT,
pubmed-author:YoshimotoKatsuhikoK
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pubmed:issnType |
Print
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pubmed:volume |
65
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
9-16
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:16817812-Adenoma,
pubmed-meshheading:16817812-Adult,
pubmed-meshheading:16817812-Aged,
pubmed-meshheading:16817812-DNA Mutational Analysis,
pubmed-meshheading:16817812-Female,
pubmed-meshheading:16817812-Frameshift Mutation,
pubmed-meshheading:16817812-Gene Deletion,
pubmed-meshheading:16817812-Genes, Tumor Suppressor,
pubmed-meshheading:16817812-Genotype,
pubmed-meshheading:16817812-Germ-Line Mutation,
pubmed-meshheading:16817812-Humans,
pubmed-meshheading:16817812-Hyperparathyroidism, Primary,
pubmed-meshheading:16817812-Jaw Neoplasms,
pubmed-meshheading:16817812-Loss of Heterozygosity,
pubmed-meshheading:16817812-Male,
pubmed-meshheading:16817812-Methylation,
pubmed-meshheading:16817812-Microsatellite Repeats,
pubmed-meshheading:16817812-Middle Aged,
pubmed-meshheading:16817812-Multiple Endocrine Neoplasia Type 1,
pubmed-meshheading:16817812-Mutation,
pubmed-meshheading:16817812-Parathyroid Neoplasms,
pubmed-meshheading:16817812-Pedigree,
pubmed-meshheading:16817812-Promoter Regions, Genetic,
pubmed-meshheading:16817812-Receptors, Calcium-Sensing,
pubmed-meshheading:16817812-Sequence Analysis, DNA,
pubmed-meshheading:16817812-Tumor Suppressor Proteins
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pubmed:year |
2006
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pubmed:articleTitle |
Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome.
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pubmed:affiliation |
Department of Medical Pharmacology, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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