Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 10, 2007, Pages 4101-4105

  Georgitsi, Marianthi ^a   Raitila, Anniina ^a   Karhu, Auli ^a   Tuppurainen, Karoliina ^b   Mäkinen, Markus J ^b   Vierimaa, Outi ^c   Paschke, Ralf ^d   Saeger, Wolfgang ^e   Van Der Luijt, Rob B ^f   Sane, Timo ^g   Robledo, Mercedes ^h   De Menis, Ernesto ⁱ   Weil, Robert J ^j   Wasik, Anna ^k   Zielinski, Grzegorz ^l   Lucewicz, Olga ^m   Lubinski, Jan ^k,m   Launonen, Virpi ^a   Vahteristo, Pia ^a   Aaltonen, Lauri A ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

^b UNIVERSITY OF OULU   (Finland)

^c OULU UNIVERSITY HOSPITAL   (Finland)

^d UNIVERSITY OF LEIPZIG   (Germany)

^e Marienkrankenhaus Hamburg   (Germany)

^f UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^g HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^h Centro Nacional de Investigaciones Oncológicas   (Spain)

ⁱ GENERAL HOSPITAL   (Italy)

^j LERNER RESEARCH INSTITUTE   (United States)

^k NENCKI INSTITUTE OF EXPERIMENTAL BIOLOGY   (Poland)

^l MILITARY INSTITUTE OF MEDICINE   (Poland)

^m POMERANIAN MEDICAL UNIVERSITY   (Poland)

more..

Author keywords

Acromegaly; Growth hormone; Immunohistochemistry; Prolacting secreting adenomas

Indexed keywords

AROMATIC HYDROCARBON RECEPTOR; ARYL HYDROCARBON RECEPTOR INTERACTING PROTEIN; UNCLASSIFIED DRUG; ARYL HYDROCARBON RECEPTOR-INTERACTING PROTEIN; PROTEIN;

ACROMEGALY; ADOLESCENT; ADULT; AGED; AIP GENE; ARTICLE; CHILD; CONTROLLED STUDY; EUROPE; FAMILIAL CANCER; FAMILY HISTORY; FEASIBILITY STUDY; FEMALE; FINLAND; FOUNDER EFFECT; GENE; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC COUNSELING; GENETIC PREDISPOSITION; GENETIC SUSCEPTIBILITY; GERM LINE; HUMAN; HUMAN TISSUE; HYPOPHYSIS ADENOMA; IMMUNOHISTOCHEMISTRY; MAJOR CLINICAL STUDY; MALE; MEN1 GENE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; UNITED STATES; ETHNOLOGY; GENETICS; HYPOPHYSIS TUMOR; MIDDLE AGED; MOLECULAR GENETICS; MULTIPLE ENDOCRINE NEOPLASIA; MUTATION;

ACROMEGALY; ADOLESCENT; ADULT; CHILD; FEMALE; FOUNDER EFFECT; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MULTIPLE ENDOCRINE NEOPLASIA; MUTATION; PITUITARY NEOPLASMS; PROTEINS;

EID: 34247180053     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0700004104     Document Type: Article

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