Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2011-6-7
pubmed:abstractText
Steroidogenic acute regulatory protein (StAR) is crucial for transport of cholesterol to mitochondria where biosynthesis of steroids is initiated. Loss of StAR function causes lipoid congenital adrenal hyperplasia (LCAH).
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-10802740, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-11200945, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-11484226, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-12384787, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-12459035, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-13285832, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-13990617, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-14973125, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-1538787, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-15390263, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-15489236, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-15654338, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-15985476, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-16234239, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-16868047, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-16968793, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-16990645, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-17626865, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-18059087, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-18493136, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-1853201, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-19171973, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-19773404, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-20444910, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-20962024, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-2268628, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-7892608, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-8401235, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-8517924, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-8692262, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-8948562, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-9020063, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-9097960, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-9141542, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-9283757, http://linkedlifedata.com/resource/pubmed/commentcorrection/21647419-9283763
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1932-6203
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
e20178
pubmed:meshHeading
pubmed-meshheading:21647419-46, XY Disorders of Sex Development, pubmed-meshheading:21647419-Adolescent, pubmed-meshheading:21647419-Adrenal Hyperplasia, Congenital, pubmed-meshheading:21647419-Adult, pubmed-meshheading:21647419-Amino Acid Sequence, pubmed-meshheading:21647419-Animals, pubmed-meshheading:21647419-Base Sequence, pubmed-meshheading:21647419-Child, pubmed-meshheading:21647419-Cholesterol, pubmed-meshheading:21647419-Female, pubmed-meshheading:21647419-Glucocorticoids, pubmed-meshheading:21647419-Heterozygote, pubmed-meshheading:21647419-Homozygote, pubmed-meshheading:21647419-Humans, pubmed-meshheading:21647419-Infant, pubmed-meshheading:21647419-Infant, Newborn, pubmed-meshheading:21647419-Male, pubmed-meshheading:21647419-Models, Molecular, pubmed-meshheading:21647419-Molecular Sequence Data, pubmed-meshheading:21647419-Mutant Proteins, pubmed-meshheading:21647419-Mutation, pubmed-meshheading:21647419-Phosphoproteins, pubmed-meshheading:21647419-Pregnancy, pubmed-meshheading:21647419-Protein Conformation, pubmed-meshheading:21647419-Receptor, Melanocortin, Type 2, pubmed-meshheading:21647419-Siblings
pubmed:year
2011
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