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Items: 24

1.

The PB2 Polymerase Host Adaptation Substitutions Prime Avian Indonesia Sub Clade 2.1 H5N1 Viruses for Infecting Humans.

Wang P, Song W, Mok BW, Zheng M, Lau SY, Liu S, Chen P, Huang X, Liu H, Cremin CJ, Chen H.

Viruses. 2019 Mar 22;11(3). pii: E292. doi: 10.3390/v11030292.

2.

Base excision repair deficiency signatures implicate germline and somatic MUTYH aberrations in pancreatic ductal adenocarcinoma and breast cancer oncogenesis.

Thibodeau ML, Zhao EY, Reisle C, Ch'ng C, Wong HL, Shen Y, Jones MR, Lim HJ, Young S, Cremin C, Pleasance E, Zhang W, Holt R, Eirew P, Karasinska J, Kalloger SE, Taylor G, Majounie E, Bonakdar M, Zong Z, Bleile D, Chiu R, Birol I, Gelmon K, Lohrisch C, Mungall KL, Mungall AJ, Moore R, Ma YP, Fok A, Yip S, Karsan A, Huntsman D, Schaeffer DF, Laskin J, Marra MA, Renouf DJ, Jones SJM, Schrader KA.

Cold Spring Harb Mol Case Stud. 2019 Apr 1;5(2). pii: a003681. doi: 10.1101/mcs.a003681. Print 2019 Apr.

3.

CDKN2A founder mutation in pancreatic ductal adenocarcinoma patients without cutaneous features of Familial Atypical Multiple Mole Melanoma (FAMMM) syndrome.

Cremin C, Howard S, Le L, Karsan A, Schaeffer DF, Renouf D, Schrader KA.

Hered Cancer Clin Pract. 2018 Mar 7;16:7. doi: 10.1186/s13053-018-0088-y. eCollection 2018.

4.

Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11.

Baert A, Machackova E, Coene I, Cremin C, Turner K, Portigal-Todd C, Asrat MJ, Nuk J, Mindlin A, Young S, MacMillan A, Van Maerken T, Trbusek M, McKinnon W, Wood ME, Foulkes WD, Santamariña M, de la Hoya M, Foretova L, Poppe B, Vral A, Rosseel T, De Leeneer K, Vega A, Claes KBM.

Hum Mutat. 2018 Apr;39(4):515-526. doi: 10.1002/humu.23390. Epub 2018 Jan 22.

PMID:
29280214
5.

Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans.

Jiang L, Yin J, Ye L, Yang J, Hemani G, Liu AJ, Zou H, He D, Sun L, Zeng X, Li Z, Zheng Y, Lin Y, Liu Y, Fang Y, Xu J, Li Y, Dai S, Guan J, Jiang L, Wei Q, Wang Y, Li Y, Huang C, Zuo X, Liu Y, Wu X, Zhang L, Zhou L, Zhang Q, Li T, Chen L, Xu Z, Yang X, Qian F, Xie W, Liu W, Guo Q, Huang S, Zhao J, Li M, Jin Y, Gao J, Lv Y, Wang Y, Lin L, Guo A, Danoy P, Willner D, Cremin C, Hadler J, Zhang F, Zhao Y, Li M, Yue T, Fan X, Guo J, Mu R, Li J, Wu C, Zeng M, Wang J, Li S, Jin L, Wang B, Wang J, Ma X, Sun L, Zhang X, Brown MA, Visscher PM, Su DF, Xu H.

Arthritis Rheumatol. 2014 May;66(5):1121-32. doi: 10.1002/art.38353. Erratum in: Arthritis Rheumatol. 2014 Jul;66(7):1881.

6.

Defective epithelial barrier function in asthma.

Xiao C, Puddicombe SM, Field S, Haywood J, Broughton-Head V, Puxeddu I, Haitchi HM, Vernon-Wilson E, Sammut D, Bedke N, Cremin C, Sones J, Djukanović R, Howarth PH, Collins JE, Holgate ST, Monk P, Davies DE.

J Allergy Clin Immunol. 2011 Sep;128(3):549-56.e1-12. doi: 10.1016/j.jaci.2011.05.038. Epub 2011 Jul 12.

PMID:
21752437
7.

Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.

Duncan EL, Danoy P, Kemp JP, Leo PJ, McCloskey E, Nicholson GC, Eastell R, Prince RL, Eisman JA, Jones G, Sambrook PN, Reid IR, Dennison EM, Wark J, Richards JB, Uitterlinden AG, Spector TD, Esapa C, Cox RD, Brown SD, Thakker RV, Addison KA, Bradbury LA, Center JR, Cooper C, Cremin C, Estrada K, Felsenberg D, Glüer CC, Hadler J, Henry MJ, Hofman A, Kotowicz MA, Makovey J, Nguyen SC, Nguyen TV, Pasco JA, Pryce K, Reid DM, Rivadeneira F, Roux C, Stefansson K, Styrkarsdottir U, Thorleifsson G, Tichawangana R, Evans DM, Brown MA.

PLoS Genet. 2011 Apr;7(4):e1001372. doi: 10.1371/journal.pgen.1001372. Epub 2011 Apr 21.

8.

Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.

Gardie B, Remenieras A, Kattygnarath D, Bombled J, Lefèvre S, Perrier-Trudova V, Rustin P, Barrois M, Slama A, Avril MF, Bessis D, Caron O, Caux F, Collignon P, Coupier I, Cremin C, Dollfus H, Dugast C, Escudier B, Faivre L, Field M, Gilbert-Dussardier B, Janin N, Leport Y, Leroux D, Lipsker D, Malthieu F, McGilliwray B, Maugard C, Méjean A, Mortemousque I, Plessis G, Poppe B, Pruvost-Balland C, Rooker S, Roume J, Soufir N, Steinraths M, Tan MH, Théodore C, Thomas L, Vabres P, Van Glabeke E, Meric JB, Verkarre V, Lenoir G, Joulin V, Deveaux S, Cusin V, Feunteun J, Teh BT, Bressac-de Paillerets B, Richard S; French National Cancer Institute "Inherited predisposition to kidney cancer" network.

J Med Genet. 2011 Apr;48(4):226-34. doi: 10.1136/jmg.2010.085068. Epub 2011 Mar 12. Erratum in: J Med Genet. 2011 Aug;48(8):576.

9.

Genetics: factor V Leiden.

Cremin C, Carroll JC, Allanson J, Blaine SM, Dorman H, Gibbons CA, Honeywell C, Meschino WS, Permaul J, Wilson BJ.

Can Fam Physician. 2010 Apr;56(4):353. No abstract available.

10.

Genetics: Preimplantation genetic diagnosis.

Gibbons CA, Allanson J, Blaine SM, Cremin C, Dorman H, Honeywell C, Meschino WS, Permaul J, Carroll JC.

Can Fam Physician. 2010 Mar;56(3):247. No abstract available.

11.

Genetics: familial melanoma.

Cremin C, Blaine SM, Allanson J, Dorman H, Gibbons CA, Honeywell C, Meschino WS, Permaul J, Carroll JC.

Can Fam Physician. 2010 Jan;56(1):31. No abstract available.

12.

Genetics: schizophrenia.

Rideout AL, Carroll JC, Blaine SM, Cremin C, Dorman H, Gibbons CA, Honeywell C, Meschino WS, Permaul J, Allanson J.

Can Fam Physician. 2009 Dec;55(12):1207. No abstract available.

13.

Genetics: Hypertrophic cardiomyopathy.

Honeywell C, Meschino WS, Allanson J, Blaine SM, Cremin C, Dorman H, Gibbons CA, Permaul J, Carroll JC.

Can Fam Physician. 2009 Nov;55(11):1095. No abstract available.

14.

The identification of Lynch syndrome in British Columbia.

Cremin CM, Armstrong L, Gill S, Huntsman D, Bajdik C.

Can J Gastroenterol. 2009 Nov;23(11):761-7.

15.

Genetics: Newborn screening for sickle cell anemia.

Meschino WS, Gibbons CA, Allanson J, Blaine SM, Cremin C, Dorman H, Honeywell C, Permaul J, Wilson BJ, Carroll JC.

Can Fam Physician. 2009 Oct;55(10):1001. No abstract available.

16.

Genetics: type 2 diabetes.

Dorman H, Meschino WS, Allanson J, Blaine SM, Cremin C, Gibbons CA, Honeywell C, Permaul J, Carroll JC.

Can Fam Physician. 2009 Sep;55(9):893. No abstract available.

17.

Validation of predictive models for germline mutations in DNA mismatch repair genes in colorectal cancer.

Monzon JG, Cremin C, Armstrong L, Nuk J, Young S, Horsman DE, Garbutt K, Bajdik CD, Gill S.

Int J Cancer. 2010 Feb 15;126(4):930-9. doi: 10.1002/ijc.24808.

18.

Genetics: prostate cancer.

Blaine SM, Honeywell C, Allanson J, Cremin C, Dorman H, Gibbons CA, Meschino WS, Permaul J, Carroll JC.

Can Fam Physician. 2009 Jul;55(7):710. No abstract available.

19.

Genetics: Alzheimer disease.

Dorman H, Meschino WS, Allanson J, Blaine SM, Cremin C, Gibbons CA, Honeywell C, Permaul J, Carroll JC.

Can Fam Physician. 2009 Jun;55(6):603. No abstract available.

20.

Genetics: newborn screening for MCAD deficiency.

Carroll JC, Gibbons CA, Blaine SM, Cremin C, Dorman H, Honeywell C, Meschino WS, Permaul J, Allanson J.

Can Fam Physician. 2009 May;55(5):487. Review. No abstract available.

21.

Genetics: Codeine metabolism.

Gibbons CA, Blaine SM, Allanson J, Cremin C, Dorman H, Honeywell C, Meschino WS, Permaul J, Carroll JC.

Can Fam Physician. 2009 Feb;55(2):164. No abstract available.

22.

Genetics: hereditary hemochromatosis.

Allanson J, Honeywell C, Blaine SM, Cremin C, Dorman H, Gibbons CA, Grimshaw J, Meschino WS, Permaul J, Wilson BJ, Carroll JC.

Can Fam Physician. 2009 Jan;55(1):53. No abstract available.

23.

Hereditary breast and ovarian cancers.

Carroll JC, Cremin C, Allanson J, Blaine SM, Dorman H, Gibbons CA, Grimshaw J, Honeywell C, Meschino WS, Permaul J, Wilson BJ.

Can Fam Physician. 2008 Dec;54(12):1691-2. Review. No abstract available.

24.

Nonovarian pelvic cancers in BRCA1/2 mutation carriers and the BRCAPRO statistical model.

Cremin C, Wong N, Buzaglo K, Paradis AJ, Foulkes W.

J Clin Oncol. 2002 Sep 15;20(18):3936; author reply 3936-7. No abstract available.

PMID:
12228218

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