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Similar articles for PubMed (Select 22684231)

1.

BRCA1 and BRCA2 unclassified variants and missense polymorphisms in Algerian breast/ovarian cancer families.

Cherbal F, Salhi N, Bakour R, Adane S, Boualga K, Maillet P.

Dis Markers. 2012;32(6):343-53. doi: 10.3233/DMA-2012-0893.

2.

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity, and is a familial breast cancer risk factor.

Peterlongo P, Catucci I, Colombo M, Caleca L, Mucaki E, Bogliolo M, Marin M, Damiola F, Bernard L, Pensotti V, Volorio S, Dall'Olio V, Meindl A, Bartram C, Sutter C, Surowy H, Sornin V, Dondon MG, Eon-Marchais S, Stoppa-Lyonnet D, Andrieu N, Sinilnikova OM; GENESIS, Mitchell G, James PA, Thompson E; kConFab; SWE-BRCA, Marchetti M, Verzeroli C, Tartari C, Capone G, Putignano AL, Genuardi M, Medici V, Marchi I, Federico M, Tognazzo S, Matricardi L, Agata S, Dolcetti R, Della Puppa L, Cini G, Gismondi V, Viassolo V, Perfumo C, Mencarelli MA, Baldassarri M, Peissel B, Roversi G, Silvestri V, Rizzolo P, Spina F, Vivanet C, Tibiletti MG, Caligo MA, Gambino G, Tommasi S, Pilato B, Tondini C, Corna C, Bonanni B, Barile M, Osorio A, Benitez J, Balestrino L, Ottini L, Manoukian S, Pierotti MA, Renieri A, Varesco L, Couch FJ, Wang X, Devilee P, Hilbers FS, van Asperen CJ, Viel A, Montagna M, Cortesi L, Diez O, Balmaña J, Hauke J, Schmutzler RK, Papi L, Pujana MA, Lázaro C, Falanga A, Offit K, Vijai J, Campbell I, Burwinkel B, Kvist A, Ehrencrona H, Mazoyer S, Pizzamiglio S, Verderio P, Surralles J, Rogan PK, Radice P.

Hum Mol Genet. 2015 Jun 30. pii: ddv251. [Epub ahead of print]

PMID:
26130695
3.

RECQL: a new breast cancer susceptibility gene.

Banerjee T, Brosh RM Jr.

Cell Cycle. 2015 Jun 30:0. [Epub ahead of print]

PMID:
26125302
4.

Referral of Ovarian Cancer Patients for Genetic Counselling by Oncologists: Need for Improvement.

Ricci MT, Sciallero S, Mammoliti S, Gismondi V, Franiuk M, Bruzzi P, Varesco L.

Public Health Genomics. 2015 Jun 24. [Epub ahead of print]

PMID:
26111740
5.

BRCA1 and BRCA2 mutations in Iranian breast cancer patients: A systematic review.

Neamatzadeh H, Shiryazdi SM, Kalantar SM.

J Res Med Sci. 2015 Mar;20(3):284-93. Review.

6.

AGO Austria recommendations for genetic testing of patients with ovarian cancer.

Marth C, Hubalek M, Petru E, Polterauer S, Reinthaller A, Schauer C, Scholl-Firon T, Singer CF, Zschocke J, Zeimet AG.

Wien Klin Wochenschr. 2015 Jun 25. [Epub ahead of print]

PMID:
26109557
7.

Molecular aspects of breast cancer resistance to drugs (Review).

Calaf GM, Zepeda AB, Castillo RL, Figueroa CA, Arias C, Figueroa E, Farías JG.

Int J Oncol. 2015 Jun 18. doi: 10.3892/ijo.2015.3055. [Epub ahead of print]

PMID:
26094681
8.

Detection of novel germline mutations for breast cancer in non-BRCA1/2 families.

Aloraifi F, McDevitt T, Martiniano R, McGreevy J, McLaughlin R, Egan CM, Cody N, Meany M, Kenny E, Green AJ, Bradley DG, Geraghty JG, Bracken AP.

FEBS J. 2015 Jun 20. doi: 10.1111/febs.13352. [Epub ahead of print]

PMID:
26094658
9.

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.

Karageorgos I, Mizzi C, Giannopoulou E, Pavlidis C, Peters BA, Zagoriti Z, Stenson PD, Mitropoulos K, Borg J, Kalofonos HP, Drmanac R, Stubbs A, van de Spek P, Cooper DN, Katsila T, Patrinos GP.

Hum Genomics. 2015 Jun 20;9(1):12. [Epub ahead of print]

10.

OGG1 Mutations and Risk of Female Breast Cancer: Meta-Analysis and Experimental Data.

Ali K, Mahjabeen I, Sabir M, Mehmood H, Kayani MA.

Dis Markers. 2015;2015:690878. doi: 10.1155/2015/690878. Epub 2015 May 19.

11.

Computational Analysis of Missense Variants of G Protein-Coupled Receptors Involved in the Neuroendocrine Regulation of Reproduction.

Min L, Nie M, Zhang A, Wen J, Noel SD, Lee V, Carroll RS, Kaiser UB.

Neuroendocrinology. 2015 Jun 18. [Epub ahead of print]

PMID:
26088945
12.

BRCA1 gene variant p.P142H associated with male breast cancer: a two-generation genealogic study and literature review.

Spinelli C, Strambi S, Piccini L, Rossi L, Aretini P, Caligo A.

Fam Cancer. 2015 Jun 18. [Epub ahead of print]

PMID:
26085381
13.

Tumour spectrum in non-BRCA hereditary breast cancer families in Sweden.

Wendt C, Lindblom A, Arver B, von Wachenfeldt A, Margolin S.

Hered Cancer Clin Pract. 2015 Jun 16;13(1):15. doi: 10.1186/s13053-015-0036-z. eCollection 2015.

14.

DNA repair capacity is impaired in healthy BRCA1 heterozygous mutation carriers.

Vaclová T, Gómez-López G, Setién F, Bueno JM, Macías JA, Barroso A, Urioste M, Esteller M, Benítez J, Osorio A.

Breast Cancer Res Treat. 2015 Jun 14. [Epub ahead of print]

PMID:
26071757
15.

Functional and in silico assessment of MAX variants of unknown significance.

Comino-Méndez I, Leandro-García LJ, Montoya G, Inglada-Pérez L, de Cubas AA, Currás-Freixes M, Tysoe C, Izatt L, Letón R, Gómez-Graña Á, Mancikova V, Apellániz-Ruiz M, Mannelli M, Schiavi F, Favier J, Gimenez-Roqueplo AP, Timmers HJ, Roncador G, Garcia JF, Rodríguez-Antona C, Robledo M, Cascón A.

J Mol Med (Berl). 2015 Jun 14. [Epub ahead of print]

PMID:
26070438
16.

Absence of the FANCM c.5101C>T mutation in BRCA1/2-negative triple-negative breast cancer patients from Pakistan.

Rashid MU, Muhammad N, Khan FA, Hamann U.

Breast Cancer Res Treat. 2015 Jul;152(1):229-30. doi: 10.1007/s10549-015-3457-5. Epub 2015 Jun 12. No abstract available.

PMID:
26067930
17.

Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic.

Janatova M, Soukupova J, Stribrna J, Kleiblova P, Vocka M, Boudova P, Kleibl Z, Pohlreich P.

PLoS One. 2015 Jun 9;10(6):e0127711. doi: 10.1371/journal.pone.0127711. eCollection 2015.

18.

Predicting the Pathogenic Potential of BRCA1 and BRCA2 Gene Variants Identified in Clinical Genetic Testing.

Brookes C, Lai S, Doherty E, Love DR.

Sultan Qaboos Univ Med J. 2015 May;15(2):e218-25. Epub 2015 May 28.

19.

Ten modifiers of BRCA1 penetrance validated in a Norwegian series.

Heramb C, Ekstrøm PO, Tharmaratnam K, Hovig E, Møller P, Mæhle L.

Hered Cancer Clin Pract. 2015 May 30;13(1):14. doi: 10.1186/s13053-015-0035-0. eCollection 2015.

20.

BRCA Mutations Increase Fertility in Families at Hereditary Breast/Ovarian Cancer Risk.

Kwiatkowski F, Arbre M, Bidet Y, Laquet C, Uhrhammer N, Bignon YJ.

PLoS One. 2015 Jun 5;10(6):e0127363. doi: 10.1371/journal.pone.0127363. eCollection 2015.

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