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Results: 15

Select item 234828051.

Inactivation of 9q22.3 tumor suppressor genes predict outcome for patients with head and neck squamous cell carcinoma.

Ghosh A, Maiti GP, Bandopadhyay MN, Chakraborty J, Biswas J, Roychoudhury S, Panda CK.

Anticancer Res. 2013 Mar;33(3):1215-20.

PMID:: 23482805; [PubMed - indexed for MEDLINE]

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Select item 221902772.

Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay.

Muller EA, Aradhya S, Atkin JF, Carmany EP, Elliott AM, Chudley AE, Clark RD, Everman DB, Garner S, Hall BD, Herman GE, Kivuva E, Ramanathan S, Stevenson DA, Stockton DW, Hudgins L.

Am J Med Genet A. 2012 Feb;158A(2):391-9. doi: 10.1002/ajmg.a.34216. Epub 2011 Dec 21.

PMID:: 22190277; [PubMed - indexed for MEDLINE]

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Select item 218612283.

Association of FANCC and PTCH1 with the development of early dysplastic lesions of the head and neck.

Ghosh A, Ghosh S, Maiti GP, Mukherjee S, Mukherjee N, Chakraborty J, Roy A, Roychoudhury S, Panda CK.

Ann Surg Oncol. 2012 Jul;19 Suppl 3:S528-38. doi: 10.1245/s10434-011-1991-x. Epub 2011 Aug 23.

PMID:: 21861228; [PubMed - indexed for MEDLINE]

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Select item 214129714.

Overgrowth of prenatal onset associated with submicroscopic 9q22.3 deletion.

Kosaki R, Fujita H, Ueoka K, Torii C, Kosaki K.

Am J Med Genet A. 2011 Apr;155A(4):903-5. doi: 10.1002/ajmg.a.33835. Epub 2011 Mar 15. No abstract available.

PMID:: 21412971; [PubMed - indexed for MEDLINE]

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Select item 213898355.

Multiple (familial) trichoepitheliomas: a clinicopathological and molecular biological study, including CYLD and PTCH gene analysis, of a series of 16 patients.

Kazakov DV, Vanecek T, Zelger B, Carlson JA, Spagnolo DV, Schaller J, Nemcova J, Kacerovska D, Vazmitel M, Sangüeza M, Emberger M, Belousova I, Fernandez-Figueras MT, Kempf W, Meyer DR, Rütten A, Baltaci M, Michal M.

Am J Dermatopathol. 2011 May;33(3):251-65. doi: 10.1097/DAD.0b013e3181f7d373. Erratum in: Am J Dermatopathol. 2011 Dec;33(8):874. Fernandez-Figueraz, Maria Tereza [corrected to Fernandez-Figueras, Maria Tereza].

PMID:: 21389835; [PubMed - indexed for MEDLINE]

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Select item 208758766.

Microdeletion of 22q11.1 is associated with two cases of familial nonsyndromic basal cell carcinoma.

Naderi A.

Cancer Genet Cytogenet. 2010 Oct 15;202(2):133-5. doi: 10.1016/j.cancergencyto.2010.07.123.

PMID:: 20875876; [PubMed - indexed for MEDLINE]

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Select item 193206587.

Clinical features of microdeletion 9q22.3 (pat).

Shimojima K, Adachi M, Tanaka M, Tanaka Y, Kurosawa K, Yamamoto T.

Clin Genet. 2009 Apr;75(4):384-93. doi: 10.1111/j.1399-0004.2008.01141.x.

PMID:: 19320658; [PubMed - indexed for MEDLINE]

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Select item 192434118.

Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: report of two cases and review of the literature.

Yamamoto K, Yoshihashi H, Furuya N, Adachi M, Ito S, Tanaka Y, Masuno M, Chiyo H, Kurosawa K.

Congenit Anom (Kyoto). 2009 Mar;49(1):8-14. doi: 10.1111/j.1741-4520.2008.00212.x.

PMID:: 19243411; [PubMed - indexed for MEDLINE]

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Select item 189902339.

Alterations in candidate genes PHF2, FANCC, PTCH1 and XPA at chromosomal 9q22.3 region: pathological significance in early- and late-onset breast carcinoma.

Sinha S, Singh RK, Alam N, Roy A, Roychoudhury S, Panda CK.

Mol Cancer. 2008 Nov 6;7:84. doi: 10.1186/1476-4598-7-84.

PMID:: 18990233; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 1851207810.

Novel microdeletion syndromes detected by chromosome microarrays.

Slavotinek AM.

Hum Genet. 2008 Aug;124(1):1-17. doi: 10.1007/s00439-008-0513-9. Epub 2008 May 30. Review.

PMID:: 18512078; [PubMed - indexed for MEDLINE]

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Select item 1832955311.

Loss of the PTCH1 gene locus in cardiac fibroma.

Scanlan D, Radio SJ, Nelson M, Zhou M, Streblow R, Prasad V, Reyes C, Perry D, Fletcher S, Bridge JA.

Cardiovasc Pathol. 2008 Mar-Apr;17(2):93-7. doi: 10.1016/j.carpath.2007.08.001. Epub 2007 Oct 24.

PMID:: 18329553; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 1710282012.

Role of loss of heterozygosity on chromosomes 8 and 9 in the development and progression of cancer bladder.

Abdel Wahab AH, Abo-Zeid HI, El-Husseini MI, Ismail M, El-Khor AM.

J Egypt Natl Canc Inst. 2005 Dec;17(4):260-9.

PMID:: 17102820; [PubMed - indexed for MEDLINE]

Free Article

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Select item 1692739113.

Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.

Chen CP, Lin SP, Wang TH, Chen YJ, Chen M, Wang W.

Prenat Diagn. 2006 Aug;26(8):725-9.

PMID:: 16927391; [PubMed - indexed for MEDLINE]

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Select item 1657007214.

Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome.

Redon R, Baujat G, Sanlaville D, Le Merrer M, Vekemans M, Munnich A, Carter NP, Cormier-Daire V, Colleaux L.

Eur J Hum Genet. 2006 Jun;14(6):759-67.

PMID:: 16570072; [PubMed - indexed for MEDLINE]

Free Article

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Select item 1500568915.

Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes.

Sironi E, Cerri A, Tomasini D, Sirchia SM, Porta G, Rossella F, Grati FR, Simoni G.

J Cutan Pathol. 2004 Apr;31(4):318-22.

PMID:: 15005689; [PubMed - indexed for MEDLINE]

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2 free full-text articles in PubMed Central

Alterations in candidate genes PHF2, FANCC, PTCH1 and XPA at chromosomal 9q22.3 region: pathological significance in early- and late-onset breast carcinoma. [Mol Cancer. 2008]
Alterations in candidate genes PHF2, FANCC, PTCH1 and XPA at chromosomal 9q22.3 region: pathological significance in early- and late-onset breast carcinoma.
Sinha S, Singh RK, Alam N, Roy A, Roychoudhury S, Panda CK. Mol Cancer. 2008 Nov 6; 7:84. Epub 2008 Nov 6.
Loss of the PTCH1 gene locus in cardiac fibroma. [Cardiovasc Pathol. 2008]
Loss of the PTCH1 gene locus in cardiac fibroma.
Scanlan D, Radio SJ, Nelson M, Zhou M, Streblow R, Prasad V, Reyes C, Perry D, Fletcher S, Bridge JA. Cardiovasc Pathol. 2008 Mar-Apr; 17(2):93-7. Epub 2007 Oct 24.

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9q22.3[TIAB] AND ((deletion[TIAB] OR deletion/1[TIAB] OR deletion/12p13[TIAB] OR deletion/13q[TIAB] OR deletion/16[TIAB] OR deletion/16q[TIAB] OR deletion/17p[TIAB] OR deletion/3p[TIAB] OR deletion/7[TIAB] OR deletion/8[TIAB] OR deletion/9[TIAB] OR deletion/ablation[TIAB] OR deletion/accretion[TIAB] OR deletion/ace[TIAB] OR deletion/activation[TIAB] OR deletion/addition[TIAB] OR deletion/amplification[TIAB] OR deletion/anergy[TIAB] OR deletion/antagonism[TIAB] OR deletion/apoptosis[TIAB] OR deletion/att[TIAB] OR deletion/attg2[TIAB] OR deletion/aupd[TIAB] OR deletion/b[TIAB] OR deletion/blocking[TIAB] OR deletion/cat[TIAB] OR deletion/chimeric[TIAB] OR deletion/chloramphenicol[TIAB] OR deletion/cluster[TIAB] OR deletion/codon[TIAB] OR deletion/complementation[TIAB] OR deletion/compound[TIAB] OR deletion/conversion[TIAB] OR deletion/cx26[TIAB] OR deletion/deficiency[TIAB] OR deletion/deletion[TIAB] OR deletion/derivation[TIAB] OR deletion/digeorge[TIAB] OR deletion/digest/page[TIAB] OR deletion/disruption[TIAB] OR deletion/disruptions[TIAB] OR deletion/downregulation[TIAB] OR deletion/downregulation/overexpression[TIAB] OR deletion/duplication[TIAB] OR deletion/duplications[TIAB] OR deletion/expression[TIAB] OR deletion/fra11a[TIAB] OR deletion/fractionation[TIAB] OR deletion/frameshift[TIAB] OR deletion/fusion[TIAB] OR deletion/g[TIAB] OR deletion/gain[TIAB] OR deletion/gene[TIAB] OR deletion/gus[TIAB] OR deletion/hbh[TIAB] OR deletion/homozygous[TIAB] OR deletion/hybrid[TIAB] OR deletion/hypermethylation[TIAB] OR deletion/hypodiploidy[TIAB] OR deletion/imbalance[TIAB] OR deletion/inactivation[TIAB] OR deletion/inhibition[TIAB] OR deletion/insert[TIAB] OR deletion/insertion[TIAB] OR deletion/insertion/duplication[TIAB] OR deletion/insertion/recombination[TIAB] OR deletion/insertion/substitution[TIAB] OR deletion/insertions[TIAB] OR deletion/interruption[TIAB] OR deletion/inversion[TIAB] OR deletion/inversions[TIAB] OR deletion/knockout[TIAB] OR deletion/knockout/inhibition[TIAB] OR deletion/lacz[TIAB] OR deletion/large[TIAB] OR deletion/loh[TIAB] OR deletion/loss[TIAB] OR deletion/luciferase[TIAB] OR deletion/macroconversion[TIAB] OR deletion/marker[TIAB] OR deletion/methylation[TIAB] OR deletion/methylation/expression[TIAB] OR deletion/methylation/mutation/expression[TIAB] OR deletion/modification[TIAB] OR deletion/monosomy[TIAB] OR deletion/more[TIAB] OR deletion/mutagenesis[TIAB] OR deletion/mutant[TIAB] OR deletion/mutation[TIAB] OR deletion/mutational[TIAB] OR deletion/mutations[TIAB] OR deletion/nondeletion[TIAB] OR deletion/nonsense[TIAB] OR deletion/null[TIAB] OR deletion/one[TIAB] OR deletion/overexpression[TIAB] OR deletion/overexpression/insertion[TIAB] OR deletion/phosphorylation[TIAB] OR deletion/physical[TIAB] OR deletion/point[TIAB] OR deletion/polymorphism[TIAB] OR deletion/presence[TIAB] OR deletion/promoter[TIAB] OR deletion/protein[TIAB] OR deletion/rearrangement[TIAB] OR deletion/rearrangements[TIAB] OR deletion/receptor[TIAB] OR deletion/recombination[TIAB] OR deletion/reduction[TIAB] OR deletion/reintroduction[TIAB] OR deletion/repair[TIAB] OR deletion/replacement[TIAB] OR deletion/reporter[TIAB] OR deletion/rescue[TIAB] OR deletion/retention[TIAB] OR deletion/reversion[TIAB] OR deletion/ring[TIAB] OR deletion/s[TIAB] OR deletion/selection[TIAB] OR deletion/silencing[TIAB] OR deletion/site[TIAB] OR deletion/skipping[TIAB] OR deletion/splicing[TIAB] OR deletion/substitution[TIAB] OR deletion/substitution/addition[TIAB] OR deletion/substitutions[TIAB] OR deletion/t790m[TIAB] OR deletion/tetranucleotide[TIAB] OR deletion/tp53[TIAB] OR deletion/transcriptionally[TIAB] OR deletion/translocation[TIAB] OR deletion/truncation[TIAB] OR deletion/unaltered[TIAB] OR deletion/variant[TIAB] OR deletion/vcf/digeorge[TIAB] OR deletion/vcfs[TIAB] OR deletion/wild[TIAB] OR deletion/zymosan/camp[TIAB] OR deletion'[TIAB] OR deletion's[TIAB] OR deletion322[TIAB] OR deletionaag[TIAB] OR deletional[TIAB] OR deletional/duplicational[TIAB] OR deletional/insertional[TIAB] OR deletional/mutational[TIAB] OR deletionally[TIAB] OR deletione[TIAB] OR deletioninversion[TIAB] OR deletionless[TIAB] OR deletionmutation[TIAB] OR deletionof[TIAB] OR deletionogenic[TIAB] OR deletionrcolon[TIAB] OR deletions[TIAB] OR deletions/100,000[TIAB] OR deletions/8q[TIAB] OR deletions/additions[TIAB] OR deletions/cell/generation[TIAB] OR deletions/centric[TIAB] OR deletions/conversions[TIAB] OR deletions/depletions[TIAB] OR deletions/dicentrics[TIAB] OR deletions/duplication[TIAB] OR deletions/duplications[TIAB] OR deletions/extra[TIAB] OR deletions/frameshift[TIAB] OR deletions/gains[TIAB] OR deletions/imbalances[TIAB] OR deletions/inactivating[TIAB] OR deletions/indels[TIAB] OR deletions/insertion[TIAB] OR deletions/insertions[TIAB] OR deletions/insertions/duplications[TIAB] OR deletions/insertions/rearrangements[TIAB] OR deletions/inversions[TIAB] OR deletions/large[TIAB] OR deletions/loss[TIAB] OR deletions/monosomy[TIAB] OR deletions/monosony13[TIAB] OR deletions/multiplications[TIAB] OR deletions/multiplications/copy[TIAB] OR deletions/mutations[TIAB] OR deletions/person[TIAB] OR deletions/polymorphisms[TIAB] OR deletions/rare[TIAB] OR deletions/rearran[TIAB] OR deletions/rearrangement[TIAB] OR deletions/rearrangements[TIAB] OR deletions/rearrangements/insertions[TIAB] OR deletions/replacements[TIAB] OR deletions/revisions[TIAB] OR deletions/splices[TIAB] OR deletions/stop[TIAB] OR deletions/substitutions[TIAB] OR deletions/translocations[TIAB] OR deletions/transpositions[TIAB] OR deletions/truncations[TIAB] OR deletions'[TIAB] OR deletionsinsertions[TIAB]) OR (microdeletion[TIAB] OR microdeletion/digeorge[TIAB] OR microdeletion/duplication[TIAB] OR microdeletion/duplications[TIAB] OR microdeletion/insertion[TIAB] OR microdeletion/microduplication[TIAB] OR microdeletion/microduplications[TIAB] OR microdeletion/microinsertion[TIAB] OR microdeletion/supernumerary[TIAB] OR microdeletion/syndrome[TIAB] OR microdeletional[TIAB] OR microdeletions[TIAB] OR microdeletions/chromosomal[TIAB] OR microdeletions/duplications[TIAB] OR microdeletions/insertions[TIAB] OR microdeletions/microduplications[TIAB] OR microdeletions/microindels[TIAB] OR microdeletions/microinsertions[TIAB])) AND english[la] AND "humans"[MeSH Terms] AND "2003/07/15"[dp] : "2013/05/22"[dp]

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