Linked Life Data

21816872

Source:http://linkedlifedata.com/resource/pubmed/id/21816872

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2011-8-30
pubmed:abstractText
LKB1 mutations are common in patients with Peutz-Jeghers syndrome, which is characterized by mucocutaneous pigmentation, intestinal polyps and a high incidence of cancers at variable sites. This study investigated the status of the LKB1 gene in mucinous bronchioloalveolar carcinoma with or without Peutz-Jeghers syndrome.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1465-3621
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
41
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1132-7
pubmed:meshHeading
pubmed-meshheading:21816872-Adenocarcinoma, Bronchiolo-Alveolar, pubmed-meshheading:21816872-Adenocarcinoma, Mucinous, pubmed-meshheading:21816872-Adult, pubmed-meshheading:21816872-Female, pubmed-meshheading:21816872-Humans, pubmed-meshheading:21816872-Loss of Heterozygosity, pubmed-meshheading:21816872-Lung Neoplasms, pubmed-meshheading:21816872-Male, pubmed-meshheading:21816872-Middle Aged, pubmed-meshheading:21816872-Mutation, pubmed-meshheading:21816872-Peutz-Jeghers Syndrome, pubmed-meshheading:21816872-Polymerase Chain Reaction, pubmed-meshheading:21816872-Protein-Serine-Threonine Kinases, pubmed-meshheading:21816872-Proto-Oncogene Proteins, pubmed-meshheading:21816872-Receptor, Epidermal Growth Factor, pubmed-meshheading:21816872-Sequence Analysis, DNA, pubmed-meshheading:21816872-Tumor Suppressor Protein p53, pubmed-meshheading:21816872-ras Proteins
pubmed:year
2011
pubmed:articleTitle
LKB1 mutations frequently detected in mucinous bronchioloalveolar carcinoma.
pubmed:affiliation
Department of Thoracic Oncology, National Kyushu Cancer Center, Notame 3-1-1, Minami-ku, Fukuoka 811-1395, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't