A Hereditary Enteropathy Caused by Mutations in the SLCO2A1 Gene, Encoding a Prostaglandin Transporter

PLoS Genetics

Volumn 11, Issue 11, 2015, Pages

  Umeno, Junji ^a   Hisamatsu, Tadakazu ^b,c   Esaki, Motohiro ^a   Hirano, Atsushi ^a   Kubokura, Naoya ^a   Asano, Kouichi ^a   Kochi, Shuji ^d   Yanai, Shunichi ^a   Fuyuno, Yuta ^a   Shimamura, Katsuyoshi ^b   Hosoe, Naoki ^b   Ogata, Haruhiko ^b   Watanabe, Takashi ^e   Aoyagi, Kunihiko ^e   Ooi, Hidehisa ^f   Watanabe, Kenji ^g   Yasukawa, Shigeyoshi ^h   Hirai, Fumihito ^h   Matsui, Toshiyuki ^h   Iida, Mitsuo ^a,i   Yao, Tsuneyoshi ^h,j   Hibi, Toshifumi ^k   Kosaki, Kenjiro ^b   Kanai, Takanori ^b   Kitazono, Takanari ^a   Matsumoto, Takayuki ^a,l   more..

^a KYUSHU UNIVERSITY   (Japan)

^b KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c KYORIN UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d MATSUYAMA RED CROSS HOSPITAL   (Japan)

^e FUKUOKA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^f IMAMURA GENERAL HOSPITAL   (Japan)

^g OSAKA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^h Fukuoka University Chikushi Hospital   (Japan)

ⁱ Kyushu Central Hospital   (Japan)

^j Department of Surgery   (Japan)

^k KITASATO INSTITUTE HOSPITAL   (Japan)

^l IWATE MEDICAL UNIVERSITY   (Japan)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; GUANINE; MESSENGER RNA; PROSTAGLANDIN E2; PROSTAGLANDIN TRANSPORTER; ORGANIC ANION TRANSPORTER; SLCO2A1 PROTEIN, HUMAN;

ABDOMINAL PAIN; AGED; ANEMIA; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CELL MEMBRANE; CELLULAR DISTRIBUTION; CHRONIC NONSPECIFIC MULTIPLE ULCERS OF THE SMALL INTESTINE; CONTROLLED STUDY; CROHN DISEASE; CYTOSOL; DIGITAL CLUBBING; EDEMA; ENDOTHELIUM CELL; ENTEROPATHY; EXOME; EXON; FEMALE; GENE; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; HYPOPROTEINEMIA; IMMUNOFLUORESCENCE TEST; IMMUNOHISTOCHEMISTRY; INTRON; LOSS OF FUNCTION MUTATION; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; OSTEOARTHROPATHY; PATHOPHYSIOLOGY; PROSTAGLANDIN URINE LEVEL; PROTEIN ANALYSIS; PROTEIN DEPLETION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; RARE DISEASE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA SPLICING; SEGREGATION ANALYSIS; SEQUENCE ANALYSIS; SLCO2A1 GENE; SMALL INTESTINE MUCOSA; STOP CODON; VASCULAR ENDOTHELIUM; GENETIC SCREENING; GENETICS; MUTATION; PATHOLOGY; PEDIGREE; SMALL INTESTINE;

FEMALE; GENETIC TESTING; HUMANS; INTESTINAL DISEASES; INTESTINE, SMALL; MALE; MUTATION; ORGANIC ANION TRANSPORTERS; PEDIGREE;

EID: 84949294796     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1005581     Document Type: Article

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