Convergent structural alterations define SWItch/Sucrose NonFermentable (SWI/SNF) chromatin remodeler as a central tumor suppressive complex in pancreatic cancer von Shain, A. Hunter, Giacomini, Craig P, Matsukuma, Karen, Karikari, Collins A, Bashyam, Murali D, Hidalgo, Manuel, Maitra, Anirban, Pollack, Jonathan R

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Hormonal regulation of gluconeogenic gene transcription in the liver von Yabaluri, Nirmala, Bashyam, Murali D.

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Genomic profiling identifies GATA6 as a candidate oncogene amplified in pancreatobiliary cancer von Kwei, Kevin A, Bashyam, Murali D, Kao, Jessica, Ratheesh, Raman, Reddy, Edumakanti C, Kim, Young H, Montgomery, Kelli, Giacomini, Craig P, Choi, Yoon-La, Chatterjee, Sreejata, Karikari, Collins A, Salari, Keyan, Wang, Pei, Hernandez-Boussard, Tina, Swarnalata, Gowrishankar, van de Rijn, Matt, Maitra, Anirban, Pollack, Jonathan R

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SMURF1 amplification promotes invasiveness in pancreatic cancer von Kwei, Kevin A, Shain, A Hunter, Bair, Ryan, Montgomery, Kelli, Karikari, Collins A, van de Rijn, Matt, Hidalgo, Manuel, Maitra, Anirban, Bashyam, Murali D, Pollack, Jonathan R

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A novel EDARADD 5′-splice site mutation resulting in activation of two alternate cryptic 5′-splice sites causes autosomal recessive Hypohidrotic Ectodermal Dysplasia von Chaudhary, Ajay K., Girisha, Katta M., Bashyam, Murali D.

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A novel large deletion that encompasses EDA and the downstream gene AWAT2 causes X-linked hypohidrotic/anhidrotic ectodermal dysplasia von Chaudhary, Ajay K, Sankar, V.H, Bashyam, D

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Array-Based Comparative Genomic Hybridization Identifies Localized DNA Amplifications and Homozygous Deletions in Pancreatic Cancer von Bashyam, Murali D., Bair, Ryan, Kim, Young H., Wang, Pei, Hernandez-Boussard, Tina, Karikari, Collins A., Tibshirani, Robert, Maitra, Anirban, Pollack, Jonathan R.

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Multiple oncogenic roles of nuclear β-catenin von Kumar, Raju, Bashyam, Murali D

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Novel oncogenic transcriptional targets of mutant p53 in esophageal squamous cell carcinoma von George, Sara A., Kotapalli, Viswakalyan, Ramaswamy, Pandilla, Kumar, Raju, Gowrishankar, Swarnalata, Uppin, Shantveer G., Bashyam, Murali D.

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Exome sequencing reveals novel oncogenic mutations in early-onset sporadic rectal cancer von Bala, Pratyusha, Gupta, Ravi, Bashyam, Murali D.

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The extracytoplasmic function sigma factors: role in bacterial pathogenesis von Bashyam, Murali D., Hasnain, Seyed E.

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SMARCD1 is a transcriptional target of specific non‐hotspot mutant p53 forms von Adduri, Raju S. R., George, Sara A., Kavadipula, Padmavathi, Bashyam, Murali D.

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Ca2+/nuclear factor of activated T cells signaling is enriched in early-onset rectal tumors devoid of canonical Wnt activation von Kumar, Raju, Raman, Ratheesh, Kotapalli, Viswakalyan, Gowrishankar, Swarnalata, Pyne, Saumyadipta, Pollack, Jonathan R., Bashyam, Murali D.

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PNUTS Functions as a Proto-Oncogene by Sequestering PTEN von KAVELA, Sridhar, SHINDE, Swapnil R, SRINIVASULU, Mukta, JUNJIE CHEN, MADDIKA, Subbareddy, RATHEESH, Raman, VISWAKALYAN, Kotapalli, BASHYAM, Murali D, GOWRISHANKAR, Swarnalata, VAMSY, Mohana, PATTNAIK, Sujit, RAO, Subramanyeshwar, SASTRY, Regulagadda A

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Fucoidan from Turbinaria conoides: A multifaceted ‘deliverable’ to combat pancreatic cancer progression von Delma, Caroline R., Somasundaram, Somasundaram T., Srinivasan, Guru Prasad, Khursheed, Md, Bashyam, Murali D., Aravindan, Natarajan

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The Homologous Region Sequence (hr1) of Autographa californica Multinucleocapsid Polyhedrosis Virus Can Enhance Transcription from Non-baculoviral Promoters in Mammalian Cells von Viswanathan, Priya, Venkaiah, Betapudi, Kumar, M. Senthil, Rasheedi, Sheeba, Vrati, Sudhanshu, Bashyam, Murali D., Hasnain, Seyed E.

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Molecular genetic analysis of MSUD from India reveals mutations causing altered protein truncation affecting the C-termini of E1α and E1β von Bashyam, Murali D., Chaudhary, Ajay K., Sinha, Manjari, Nagarajaram, H.A., Devi, A. Radha Rama, Bashyam, Leena, Reddy, E. Chandrakanth, Dalal, Ashwin

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Understanding cancer metastasis: An urgent need for using differential gene expression analysis von BASHYAM, Murali D

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Nonsense-mediated decay: linking a basic cellular process to human disease von Bashyam, Murali D

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Molecular genetics of familial hypertrophic cardiomyopathy (FHC) von Bashyam, M. D., Savithri, G. R., Kumar, M. S., Narasimhan, C., Nallari, P.

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