000 | 02049 a2200649 4500 | ||
---|---|---|---|
005 | 20250515170200.0 | ||
264 | 0 | _c20090803 | |
008 | 200908s 0 0 eng d | ||
022 | _a1088-9051 | ||
024 | 7 |
_a10.1101/gr.092668.109 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aPittman, Alan M | |
245 | 0 | 0 |
_aThe colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression. _h[electronic resource] |
260 |
_bGenome research _cJun 2009 |
||
300 |
_a987-93 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAged |
650 | 0 | 4 | _aAlleles |
650 | 0 | 4 | _aAnimals |
650 | 0 | 4 | _aCell Line, Tumor |
650 | 0 | 4 | _aChromosome Mapping |
650 | 0 | 4 |
_aChromosomes, Human, Pair 18 _xgenetics |
650 | 0 | 4 |
_aColorectal Neoplasms _xgenetics |
650 | 0 | 4 | _aElectrophoretic Mobility Shift Assay |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGene Expression |
650 | 0 | 4 | _aGene Frequency |
650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
650 | 0 | 4 | _aGenetic Variation |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 |
_aNuclear Proteins _xmetabolism |
650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
650 | 0 | 4 | _aProtein Binding |
650 | 0 | 4 | _aRisk Factors |
650 | 0 | 4 | _aSequence Analysis, DNA |
650 | 0 | 4 |
_aSmad7 Protein _xgenetics |
650 | 0 | 4 |
_aXenopus laevis _xembryology |
700 | 1 | _aNaranjo, Silvia | |
700 | 1 | _aWebb, Emily | |
700 | 1 | _aBroderick, Peter | |
700 | 1 | _aLips, Esther H | |
700 | 1 | _avan Wezel, Tom | |
700 | 1 | _aMorreau, Hans | |
700 | 1 | _aSullivan, Kate | |
700 | 1 | _aFielding, Sarah | |
700 | 1 | _aTwiss, Philip | |
700 | 1 | _aVijayakrishnan, Jayaram | |
700 | 1 | _aCasares, Fernando | |
700 | 1 | _aQureshi, Mobshra | |
700 | 1 | _aGómez-Skarmeta, José Luis | |
700 | 1 | _aHoulston, Richard S | |
773 | 0 |
_tGenome research _gvol. 19 _gno. 6 _gp. 987-93 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1101/gr.092668.109 _zAvailable from publisher's website |
999 |
_c18826127 _d18826127 |