Cross-talk between Rac1 GTPase and dysregulated Wnt signaling pathway leads to cellular redistribution of β-catenin and TCF/LEF-mediated transcriptional activationESUFALI, S; BAPAT, B.Oncogene (Basingstoke). 2004, Vol 23, Num 50, pp 8260-8271, issn 0950-9232, 12 p.Article

Bent dissociative states of CO²⁺2BAPAT, B; SHARMA, Vandana.Journal of physics. B. Atomic, molecular and optical physics (Print). 2007, Vol 40, Num 1, pp 13-19, issn 0953-4075, 7 p.Article

An apparatus for studying momentum-resolved electron-impact dissociative and non-dissociative ionisationSHARMA, V; BAPAT, B.The European physical journal. D, Atomic, molecular and optical physics (Print). 2005, Vol 37, Num 2, pp 223-229, issn 1434-6060, 7 p.Article

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial diseaseWOODS, M. O; YOUNGHUSBAND, H. B; DE LA CHAPELLE, A et al.Gut. 2010, Vol 59, Num 10, pp 1369-1377, issn 0017-5749, 9 p.Article

Intraductal papillary mucinous neoplasm of the pancreas in a patient with attenuated familial adenomatous polyposisCHETTY, R; SALAHSHOR, S; BAPAT, B et al.Journal of clinical pathology. 2005, Vol 58, Num 1, pp 97-101, issn 0021-9746, 5 p.Article

Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor)TEJPAR, S; NOLLET, F; ALMAN, B. A et al.Oncogene (Basingstoke). 1999, Vol 18, Num 47, pp 6615-6620, issn 0950-9232Article

Lifetime measurements for some n = 2 levels in Be-like CI XIV and S XIIIBHATTACHARYA, N; BAPAT, B; RANGWALA, S. A et al.The European physical journal. D, Atomic, molecular and optical physics (Print). 1998, Vol 2, Num 2, pp 125-129, issn 1434-6060Article

Cloning and sequence analysis of a cDNA encoding the 8.8-subunit of mouse β-hexosaminidaseBAPAT, B; ETHIER, M; NEOTE, K et al.FEBS letters. 1988, Vol 237, Num 1-2, pp 191-195, issn 0014-5793Article

Polarization dependence in non-resonant photo-triple-ionization of CO₂KUSHAWAHA, R. K; SUNIL KUMAR, S; PRAJAPATI, I. A et al.Journal of physics. B. Atomic, molecular and optical physics (Print). 2009, Vol 42, Num 10, issn 0953-4075, 105201.1-105201.5Article

An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1MUTTER, P; WIJNEN, J; WU, J et al.Journal of medical genetics. 2002, Vol 39, Num 5, pp 323-327, issn 0022-2593Article

STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patientsJIANG, C.-Y; ESUFALI, S; BERK, T et al.Clinical genetics. 1999, Vol 56, Num 2, pp 136-141, issn 0009-9163Article

Using genetic information to make surgical decisions : Report of a case of a 13-year-old boy with colon cancerMADLENSKY, L; BAPAT, B; REDSTON, M et al.Diseases of the colon & rectum. 1997, Vol 40, Num 2, pp 240-243, issn 0012-3706Conference Paper

Promoter methylation of Wnt5a is associated with microsatellite instability and BRAF V600E mutation in two large populations of colorectal cancer patientsRAWSON, J. B; MRKONJIC, M; GALLINGER, S et al.British journal of cancer. 2011, Vol 104, Num 12, pp 1906-1912, issn 0007-0920, 7 p.Article

Family history and molecular features of children, adolescents, and young adults with colorectal carcinomaDURNO, C; ARONSON, M; BAPAT, B et al.Gut. 2005, Vol 54, Num 8, pp 1146-1150, issn 0017-5749, 5 p.Article

A novel aberrant splice site mutation in the APC geneCHARAMES, G. S; CHENG, H; GILPIN, C. A et al.Journal of medical genetics. 2002, Vol 39, Num 10, pp 754-757, issn 0022-2593Article

Overexpression of the nonpancreatic secretory group II PLA₂ messenger RNA and protein in colorectal adenomas from familial adenomatous polyposis patientsKENNEDY, B. P; SORAVIA, C; MOFFAT, J et al.Cancer research (Baltimore). 1998, Vol 58, Num 3, pp 500-503, issn 0008-5472Article

Identification of somatic APC gene mutations in periampullary adenomas in a patient with familial adenomatous polyposis (FAP)BAPAT, B; ODZE, R; MITRI, A et al.Human molecular genetics (Print). 1993, Vol 2, Num 11, pp 1957-1959, issn 0964-6906Article

Triple F⁺ ejection from SF₆ bombarded by swift ionsKUSHAWAHA, R. K; SUNIL KUMAR, S; JANA, M. R et al.Journal of physics. B. Atomic, molecular and optical physics (Print). 2010, Vol 43, Num 20, issn 0953-4075, 205204.1-205204.5Article

A germline mutation at the extreme 3' end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumorCOUTURE, J; MITRI, A; LAGACE, R et al.Clinical genetics. 2000, Vol 57, Num 3, pp 205-212, issn 0009-9163Article

A rare insertion/deletion polymorphism at eht HEXA locusNEOTE, K; BAPAT, B; MAHURAN, D et al.Nucleic acids research. 1991, Vol 19, Num 3, issn 0305-1048, p. 683Article

The human tyrosine kinase gene (FRE) detects an RFLP with BgllBAPAT, B; GROFFEN, J; RAY, P. N et al.Nucleic acids research. 1991, Vol 19, Num 15, issn 0305-1048, p. 4310Article

Association of apolipoprotein E polymorphisms and dietary factors in colorectal cancerMRKONJIC, M; CHAPPELL, E; PETHE, V. V et al.British journal of cancer. 2009, Vol 100, Num 12, pp 1966-1974, issn 0007-0920, 9 p.Article

Adenomatous polyposis coli gene mutation alters proliferation through its β-catenin-regulatory function in aggressive fibromatosis (desmoid tumor)LI, C; BAPAT, B; ALMAN, B. A et al.The American journal of pathology. 1998, Vol 153, Num 3, pp 709-714, issn 0002-9440Article

Distinct regions of frequent loss of heterozygosity of chromosome 5p and 5q in human esophageal cancerPERALTA, R. C; CASSON, A. G; WANG, R.-N et al.International journal of cancer. 1998, Vol 78, Num 5, pp 600-605, issn 0020-7136Article

A truncated hMSH2 transcript occurs as a common variant in the population : Implications for genetic diagnosisXIA, L; SHEN, W; RITACCA, F et al.Cancer research (Baltimore). 1996, Vol 56, Num 10, pp 2289-2292, issn 0008-5472Article