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Results: 1 to 20 of 31

Select item 234315681.

Lytic bone disease as the presenting feature of Philadelphia-positive, derivative chromosome 7 myelodysplasia progressing to acute myeloid leukaemia.

Tucker D, Hamilton MS, Kerr JP, Wickham C, Hunter H.

Gene. 2013 Feb 15;515(1):239. No abstract available.

PMID:: 23431568; [PubMed - indexed for MEDLINE]

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Select item 232125192.

CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemia.

McNerney ME, Brown CD, Wang X, Bartom ET, Karmakar S, Bandlamudi C, Yu S, Ko J, Sandall BP, Stricker T, Anastasi J, Grossman RL, Cunningham JM, Le Beau MM, White KP.

Blood. 2013 Feb 7;121(6):975-83. doi: 10.1182/blood-2012-04-426965. Epub 2012 Dec 3.

PMID:: 23212519; [PubMed - indexed for MEDLINE]

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Select item 229348323.

Acquired copy number neutral loss of heterozygosity of chromosome 7 associated with clonal haematopoiesis in a patient with Shwachman-Diamond syndrome.

Parikh S, Perdigones N, Paessler M, Greenbaum B, Tooke LS, Biegel JA, Mason PJ, Bessler M.

Br J Haematol. 2012 Nov;159(4):480-2. doi: 10.1111/bjh.12032. Epub 2012 Aug 31. No abstract available.

PMID:: 22934832; [PubMed - indexed for MEDLINE]

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Select item 227130844.

Phosphorylation of epidermal growth factor receptor and chromosome 7 polysomy in gastric adenocarcinoma.

Zhang F, Tang JM, Wang L, Shen JY, Zheng L, Wu PP, Zhang M, Yan ZW.

J Dig Dis. 2012 Jul;13(7):350-9. doi: 10.1111/j.1751-2980.2012.00597.x.

PMID:: 22713084; [PubMed - indexed for MEDLINE]

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Select item 226755385.

Genome haploidisation with chromosome 7 retention in oncocytic follicular thyroid carcinoma.

Corver WE, Ruano D, Weijers K, den Hartog WC, van Nieuwenhuizen MP, de Miranda N, van Eijk R, Middeldorp A, Jordanova ES, Oosting J, Kapiteijn E, Hovens G, Smit J, van Wezel T, Morreau H.

PLoS One. 2012;7(6):e38287. doi: 10.1371/journal.pone.0038287. Epub 2012 Jun 1.

PMID:: 22675538; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 225656576.

Sole abnormalities of chromosome 7 in myeloid malignancies: spectrum, histopathologic correlates, and prognostic implications.

Hussain FT, Nguyen EP, Raza S, Knudson R, Pardanani A, Hanson CA, Van Dyke D, Tefferi A.

Am J Hematol. 2012 Jul;87(7):684-6. doi: 10.1002/ajh.23230. Epub 2012 May 6.

PMID:: 22565657; [PubMed - indexed for MEDLINE]

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Select item 225651947.

A novel de novo deletion of chromosome 7 [46,XX,del(7)(p14.2 p15.1)] in a child with feeding problems.

Antunes H, Gonçalves JP, Silva E, Teles N.

Gene. 2012 Jul 15;503(1):152-4. doi: 10.1016/j.gene.2012.04.046. Epub 2012 Apr 29.

PMID:: 22565194; [PubMed - indexed for MEDLINE]

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Select item 224756888.

EGFR protein overexpression correlates with chromosome 7 polysomy and poor prognostic parameters in clear cell renal cell carcinoma.

Dorđević G, Matušan Ilijaš K, Hadžisejdić I, Maričić A, Grahovac B, Jonjić N.

J Biomed Sci. 2012 Apr 5;19:40. doi: 10.1186/1423-0127-19-40.

PMID:: 22475688; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 224280469.

Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.

Caburet S, Zavadakova P, Ben-Neriah Z, Bouhali K, Dipietromaria A, Charon C, Besse C, Laissue P, Chalifa-Caspi V, Christin-Maitre S, Vaiman D, Levi G, Veitia RA, Fellous M.

PLoS One. 2012;7(3):e33412. doi: 10.1371/journal.pone.0033412. Epub 2012 Mar 13.

PMID:: 22428046; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 2228502110.

Single nucleotide polymorphism array-based karyotyping shows sequential genomic changes from monosomy to copy-neutral loss of heterozygosity of chromosome 7 and 20q deletion within a balanced translocation t(14;20) in AML.

Huh J, Mun YC, Seong CM, Chung WS.

Cancer Genet. 2011 Dec;204(12):682-6. doi: 10.1016/j.cancergen.2011.11.003.

PMID:: 22285021; [PubMed - indexed for MEDLINE]

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Select item 2173456111.

Small duplication of chromosome (7)(p22.1p22.2) and consideration of a dup 7p syndrome critical region.

AlFardan J, Brown K, Gessner J, Lunt B, Scharer G.

Clin Dysmorphol. 2011 Oct;20(4):217-21. doi: 10.1097/MCD.0b013e328348b2c6. No abstract available.

PMID:: 21734561; [PubMed - indexed for MEDLINE]

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Select item 2150943512.

Bizarre parosteal osteochondromatous proliferation with an inversion of chromosome 7.

Sakamoto A, Imamura S, Matsumoto Y, Harimaya K, Matsuda S, Takahashi Y, Oda Y, Iwamoto Y.

Skeletal Radiol. 2011 Nov;40(11):1487-90. doi: 10.1007/s00256-011-1173-8. Epub 2011 Apr 21.

PMID:: 21509435; [PubMed - indexed for MEDLINE]

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Select item 2134387913.

A sensitive and specific diagnostic panel to distinguish diffuse astrocytoma from astrocytosis: chromosome 7 gain with mutant isocitrate dehydrogenase 1 and p53.

Camelo-Piragua S, Jansen M, Ganguly A, Kim JC, Cosper AK, Dias-Santagata D, Nutt CL, Iafrate AJ, Louis DN.

J Neuropathol Exp Neurol. 2011 Feb;70(2):110-5. doi: 10.1097/NEN.0b013e31820565f9.

PMID:: 21343879; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 2105670414.

Interstitial deletion of 7q31.32 → q33 secondary to a paracentric inversion of a maternal chromosome 7.

Paskulin GA, Riegel M, Machado Rosa RF, Graziadio C, Gazzola Zen PR.

Eur J Med Genet. 2011 Mar-Apr;54(2):181-5. doi: 10.1016/j.ejmg.2010.10.012. Epub 2010 Nov 5.

PMID:: 21056704; [PubMed - indexed for MEDLINE]

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Select item 2088462315.

EGFR fluorescence in situ hybridization pattern of chromosome 7 disomy predicts resistance to cetuximab in KRAS wild-type metastatic colorectal cancer patients.

Li YH, Wang F, Shen L, Deng YM, Shao Q, Feng F, An X, Wang FH, Wang ZQ, Xu RH, Shao JY.

Clin Cancer Res. 2011 Jan 15;17(2):382-90. doi: 10.1158/1078-0432.CCR-10-0208. Epub 2010 Sep 30.

PMID:: 20884623; [PubMed - indexed for MEDLINE]

Free Article

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Select item 2080920116.

Ring/marker chromosome derived from chromosome 7 in childhood acute megakaryoblastic leukemia with monosomy 7.

Fujino H, Fujita N, Hamamoto K, Oobu S, Kita M, Tanaka A, Matsubara H, Watanabe K, Heike T, Adachi S.

Int J Hematol. 2010 Sep;92(2):386-90. doi: 10.1007/s12185-010-0663-0. Epub 2010 Sep 1.

PMID:: 20809201; [PubMed - indexed for MEDLINE]

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Select item 2068401117.

Atypical Silver-Russell phenotype resulting from maternal uniparental disomy of chromosome 7.

Stark Z, Ryan MM, Bruno DL, Burgess T, Savarirayan R.

Am J Med Genet A. 2010 Sep;152A(9):2342-5. doi: 10.1002/ajmg.a.33590.

PMID:: 20684011; [PubMed - indexed for MEDLINE]

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Select item 2064265218.

C1q nephropathy associated with deletion of long arm of chromosome 7.

Judkins A, Townshend S, Willis F.

J Paediatr Child Health. 2010 Jun;46(6):364-5. doi: 10.1111/j.1440-1754.2010.01785.x. No abstract available.

PMID:: 20642652; [PubMed - indexed for MEDLINE]

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Select item 2063505919.

Polysomy and amplification of chromosome 7 defined for EGFR gene in squamous cell carcinoma of the lung together with exons 19 and 21 wild type.

Couceiro P, Sousa V, Alarcão A, Silva M, Carvalho L.

Rev Port Pneumol. 2010 May-Jun;16(3):453-62. English, Portuguese.

PMID:: 20635059; [PubMed - indexed for MEDLINE]

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Select item 2063377020.

A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome.

Lizcova L, Zemanova Z, Malinova E, Jarosova M, Mejstrikova E, Smisek P, Pospisilova D, Stary J, Michalova K.

Cancer Genet Cytogenet. 2010 Aug;201(1):52-6. doi: 10.1016/j.cancergencyto.2010.05.004.

PMID:: 20633770; [PubMed - indexed for MEDLINE]

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6 free full-text articles in PubMed Central

Genome haploidisation with chromosome 7 retention in oncocytic follicular thyroid carcinoma. [PLoS One. 2012]
Genome haploidisation with chromosome 7 retention in oncocytic follicular thyroid carcinoma.
Corver WE, Ruano D, Weijers K, den Hartog WC, van Nieuwenhuizen MP, de Miranda N, van Eijk R, Middeldorp A, Jordanova ES, Oosting J, et al. PLoS One. 2012; 7(6):e38287. Epub 2012 Jun 1.
EGFR protein overexpression correlates with chromosome 7 polysomy and poor prognostic parameters in clear cell renal cell carcinoma. [J Biomed Sci. 2012]
EGFR protein overexpression correlates with chromosome 7 polysomy and poor prognostic parameters in clear cell renal cell carcinoma.
Dorđević G, Matušan Ilijaš K, Hadžisejdić I, Maričić A, Grahovac B, Jonjić N. J Biomed Sci. 2012 Apr 5; 19:40. Epub 2012 Apr 5.
Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure. [PLoS One. 2012]
Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.
Caburet S, Zavadakova P, Ben-Neriah Z, Bouhali K, Dipietromaria A, Charon C, Besse C, Laissue P, Chalifa-Caspi V, Christin-Maitre S, et al. PLoS One. 2012; 7(3):e33412. Epub 2012 Mar 13.

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