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

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

Spontaneous intestinal carcinomas and skin neoplasms in Msh2-deficient miceREITMAIR, A. H; REDSTON, M; JIAN CHUN CAI et al.Cancer research (Baltimore). 1996, Vol 56, Num 16, pp 3842-3849, issn 0008-5472Article

Two polymorphisms for the human G_M2 activator protein geneBAPAT, B; XIE BEI; MAHURAN, D et al.Nucleic acids research. 1991, Vol 19, Num 3, issn 0305-1048, p. 683Article

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10PERCIN, E. F; PLODER, L. A; KOCAK-ALTINTAS, A et al.Nature genetics. 2000, Vol 25, Num 4, pp 397-401, issn 1061-4036Article

Cost comparison of predictive genetic testing versus conventional clinical screening for familial adenomatous polyposisBAPAT, B; NOORANI, H; COHEN, Z et al.Gut. 1999, Vol 44, Num 5, pp 698-703, issn 0017-5749Article

Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometriumMILLAR, A. L; PAL, T; BAPAT, B et al.Human molecular genetics (Print). 1999, Vol 8, Num 5, pp 823-829, issn 0964-6906Article

β-catenin mutations are specific for colorectal carcinomas with microsatellite instability but occur in endometrial carcinomas irrespective of mutator pathwayMIRABELLI-PRIMDAHL, L; GRYFE, R; KIM, H et al.Cancer research (Baltimore). 1999, Vol 59, Num 14, pp 3346-3351, issn 0008-5472Article

Negative genetic test result in familial adenomatous polyposis : Clinical screening implications. Invited editorialBERK, T; COHEN, Z; BAPAT, B et al.Diseases of the colon & rectum. 1999, Vol 42, Num 3, pp 307-312, issn 0012-3706Conference Paper

Genotype-phenotype correlations in attenuated adenomatous polyposis coliSORAVIA, C; BERK, T; MADLENSKY, L et al.American journal of human genetics. 1998, Vol 62, Num 6, pp 1290-1301, issn 0002-9297Article

MSH2 deficient mice are viable and susceptible to lymphoid tumoursREITMAIR, A. H; SCHMITS, R; THOMASON, A et al.Nature genetics. 1995, Vol 11, Num 1, pp 64-70, issn 1061-4036Article

Improved predictive carrier testing for familial adenomatous polyposis using DNA from a single archival specimen and polymorphic markers with multiple allelesBAPAT, B; MITRI, A; GREENBERG, C. R et al.Human pathology. 1993, Vol 24, Num 12, pp 1376-1379, issn 0046-8177Article