Contribution of germline BRCA1 and BRCA2 sequence alterations to breast cancer in Northern India

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Contribution of germline BRCA1 and BRCA2 sequence alterations to breast cancer in Northern India is …
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scholarly articleQ13442814

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P6179Dimensions Publication ID1018130265
P356DOI10.1186/1471-2350-7-75
P932PMC publication ID1617095
P698PubMed publication ID17018160
P5875ResearchGate publication ID6777217

P50authorSunita SaxenaQ30351631
David GoldgarQ91793745
Csilla I. SzaboQ96064531
P2093author name stringGilbert Lenoir
Prakash C Sharma
Sanjeev Kotwal
Veena K Sharma
Mishi Kaushal
Anil K Aggarwal
Anurupa Chakraborty
Chintamani Chintamani
Dinesh Bhatanager
Ravindar S Mohil
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In search of the tumour-suppressor functions of BRCA1 and BRCA2Q28748477
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Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage ConsortiumQ29619206
Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2Q33910123
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Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populationsQ78105304
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Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencingQ34144140
BRCA1 and BRCA2 and the genetics of breast and ovarian cancerQ34189009
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsQ34294785
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.Q34334383
BRCA1 physically associates with p53 and stimulates its transcriptional activity.Q34467604
Cancer risks in BRCA2 mutation carriersQ34504452
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Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage ConsortiumQ34724404
Evidence for a transcriptional activation function of BRCA1 C-terminal regionQ34736712
Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?Q35238904
Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1.Q35436601
Haplotype and cancer risk analysis of two common mutations, BRCA1 4184del4 and BRCA2 2157delG, in high risk northwest England breast/ovarian familiesQ35444717
Preventive intervention in breast cancer, but when?Q35593597
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international studyQ35881432
The 185delAG BRCA1 mutation originated before the dispersion of Jews in the diaspora and is not limited to AshkenazimQ38892074
Novel germline mutations in breast cancer susceptibility genes BRCA1, BRCA2 and p53 gene in breast cancer patients from IndiaQ39701378
The complete BRCA2 gene and mutations in chromosome 13q-linked kindredsQ41226231
Do regular ovulatory cycles increase breast cancer risk?Q41500964
Common BRCA1 variants and transcriptional activation.Q43104950
Population genetics of BRCA1 and BRCA2.Q43109039
Conformation-sensitive gel electrophoresis for detecting BRCA1 mutationsQ44460352
BRCA1 and BRCA2 mutations in women from Shanghai ChinaQ47197575
BRCA1 germline mutations in Indian familial breast cancerQ48268212
Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancerQ48610385
Internal repeats in the BRCA2 protein sequenceQ53173241
Epidemiologic evidence for the increased cell proliferation model of carcinogenesis.Q53501721
Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families.Q54694066
Transcriptional activation by BRCA1Q59072814
BRCA1 Inhibition of Estrogen Receptor Signaling in Transfected CellsQ60568779
Mutations and alternative splicing of the BRCA1 gene in UK breast/ovarian cancer familiesQ73259292
Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer familiesQ73282154
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central ItalyQ73692286
Germline BRCA1 mutation analysis in Indian breast/ovarian cancer familiesQ74595265
Mutation analysis of the BRCA1 gene in Malaysian breast cancer patientsQ74630713
Novel germline mutations in the BRCA1 and BRCA2 genes in Indian breast and breast-ovarian cancer familiesQ75259366
BRCA1 and BRCA2 mutations among breast cancer patients from the PhilippinesQ77839463
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancerQ77845970
Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletionsQ77931925
P921main subjectIndiaQ668
P304page(s)75
P577publication date2006-10-04
P1433published inBMC Medical GeneticsQ15759918
P1476titleContribution of germline BRCA1 and BRCA2 sequence alterations to breast cancer in Northern India
P478volume7

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Q42181679A comprehensive focus on global spectrum of BRCA1 and BRCA2 mutations in breast cancer
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