- ADAM23
ADAM metallopeptidase domain 23, also known as ADAM23, is a human
gene .cite web | title = Entrez Gene: ADAM23 ADAM metallopeptidase domain 23| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8745| accessdate = ]PBB_Summary
section_title =
summary_text = This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. This gene is highly expressed in the brain and may function as an integrin ligand in the brain.cite web | title = Entrez Gene: ADAM23 ADAM metallopeptidase domain 23| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8745| accessdate = ]References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Sagane K, Ohya Y, Hasegawa Y, Tanaka I |title=Metalloproteinase-like, disintegrin-like, cysteine-rich proteins MDC2 and MDC3: novel human cellular disintegrins highly expressed in the brain. |journal=Biochem. J. |volume=334 ( Pt 1) |issue= |pages= 93–8 |year= 1998 |pmid= 9693107 |doi=
*cite journal | author=Roberts CM, Tani PH, Bridges LC, "et al." |title=MDC-L, a novel metalloprotease disintegrin cysteine-rich protein family member expressed by human lymphocytes. |journal=J. Biol. Chem. |volume=274 |issue= 41 |pages= 29251–9 |year= 1999 |pmid= 10506182 |doi=
*cite journal | author=Poindexter K, Nelson N, DuBose RF, "et al." |title=The identification of seven metalloproteinase-disintegrin (ADAM) genes from genomic libraries. |journal=Gene |volume=237 |issue= 1 |pages= 61–70 |year= 1999 |pmid= 10524237 |doi=
*cite journal | author=Cal S, Freije JM, López JM, "et al." |title=ADAM 23/MDC3, a human disintegrin that promotes cell adhesion via interaction with the alphavbeta3 integrin through an RGD-independent mechanism. |journal=Mol. Biol. Cell |volume=11 |issue= 4 |pages= 1457–69 |year= 2000 |pmid= 10749942 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Sun YP, Deng KJ, Wang F, "et al." |title=Two novel isoforms of Adam23 expressed in the developmental process of mouse and human brains. |journal=Gene |volume=325 |issue= |pages= 171–8 |year= 2004 |pmid= 14697522 |doi=
*cite journal | author=Schmitt-Ulms G, Hansen K, Liu J, "et al." |title=Time-controlled transcardiac perfusion cross-linking for the study of protein interactions in complex tissues. |journal=Nat. Biotechnol. |volume=22 |issue= 6 |pages= 724–31 |year= 2005 |pmid= 15146195 |doi= 10.1038/nbt969
*cite journal | author=Brandenberger R, Wei H, Zhang S, "et al." |title=Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation. |journal=Nat. Biotechnol. |volume=22 |issue= 6 |pages= 707–16 |year= 2005 |pmid= 15146197 |doi= 10.1038/nbt971
*cite journal | author=Costa FF, Colin C, Shinjo SM, "et al." |title=ADAM23 methylation and expression analysis in brain tumors. |journal=Neurosci. Lett. |volume=380 |issue= 3 |pages= 260–4 |year= 2005 |pmid= 15862898 |doi= 10.1016/j.neulet.2005.01.050
*cite journal | author=Tao WA, Wollscheid B, O'Brien R, "et al." |title=Quantitative phosphoproteome analysis using a dendrimer conjugation chemistry and tandem mass spectrometry. |journal=Nat. Methods |volume=2 |issue= 8 |pages= 591–8 |year= 2005 |pmid= 16094384 |doi= 10.1038/nmeth776
*cite journal | author=Takada H, Imoto I, Tsuda H, "et al." |title=ADAM23, a possible tumor suppressor gene, is frequently silenced in gastric cancers by homozygous deletion or aberrant promoter hypermethylation. |journal=Oncogene |volume=24 |issue= 54 |pages= 8051–60 |year= 2005 |pmid= 16103878 |doi= 10.1038/sj.onc.1208952PBB_Controls
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