Search Results - "Das Gupta, Ruchira"
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1
Structures of Adnectin/Protein Complexes Reveal an Expanded Binding Footprint
Published in Structure (London) (08-02-2012)“…Adnectins are targeted biologics derived from the tenth type III domain of human fibronectin (10Fn3), a member of the immunoglobulin superfamily…”
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2
Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome
Published in American journal of human genetics (01-06-1995)“…Velo-cardio-facial syndrome (VCFS) is a common genetic disorder among individuals with cleft palate and is associated with hemizygous deletions in human…”
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3
Developing Adnectins That Target SRC Co-Activator Binding to PXR: A Structural Approach toward Understanding Promiscuity of PXR
Published in Journal of molecular biology (27-02-2015)“…The human pregnane X receptor (PXR) is a promiscuous nuclear receptor that functions as a sensor to a wide variety of xenobiotics and regulates expression of…”
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4
Identification, Characterization, and Precise Mapping of a Human Gene Encoding a Novel Membrane-Spanning Protein from the 22q11 Region Deleted in Velo–Cardio–Facial Syndrome
Published in Genomics (San Diego, Calif.) (01-06-1997)“…Velo–cardio–facial syndrome (VCFS) and DiGeorge syndrome (DGS) are characterized by a wide spectrum of phenotypes including cleft palate, conotruncal heart…”
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5
Dual Inhibition of Interleukin-23 and Interleukin-17 Offers Superior Efficacy in Mouse Models of Autoimmunity
Published in The Journal of pharmacology and experimental therapeutics (01-08-2015)“…Therapies targeting either interleukin (IL)-23 or IL-17 have shown promise in treating T helper 17 (Th17)-driven autoimmune diseases. Although IL-23 is a…”
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6
A fibronectin scaffold approach to bispecific inhibitors of epidermal growth factor receptor and insulin-like growth factor-I receptor
Published in mAbs (01-01-2011)“…Engineered domains of human fibronectin (Adnectins™) were used to generate a bispecific Adnectin targeting epidermal growth factor receptor (EGFR) and…”
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7
Germ-line msh6 mutations in colorectal cancer families
Published in Cancer research (Chicago, Ill.) (15-10-1999)“…Hereditary nonpolyposis colorectal carcinoma (HNPCC) is due primarily to inherited mutations in two mismatch repair genes, MSH2 and MLH1, whereas germ-line…”
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Dominant Saccharomyces cerevisiae msh6 Mutations Cause Increased Mispair Binding and Decreased Dissociation from Mispairs by Msh2-Msh6 in the Presence of ATP
Published in The Journal of biological chemistry (12-07-2002)“…A previous study described four dominantmsh6 mutations that interfere with both the Msh2-Msh6 and Msh2-Msh3 mismatch recognition complexes (Das Gupta, R., and…”
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9
Novel dominant mutations in Saccharomyces cerevisiae MSH6
Published in Nature genetics (01-01-2000)“…Inherited mutations in the mismatch repair (MMR) genes MSH2 and MLH1 are found in most hereditary nonpolyposis colon cancer (HNPCC) patients studied…”
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A global benchmark study using affinity-based biosensors
Published in Analytical biochemistry (15-03-2009)“…To explore the variability in biosensor studies, 150 participants from 20 countries were given the same protein samples and asked to determine kinetic rate…”
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11
Developing Adnectins That Target SRC Co-Activator Binding to PXR: A Structural Approach toward Understanding Promiscuity of PXR
Published in Journal of molecular biology (01-02-2015)Get full text
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12
An Integrated Approach for Identifying and Mapping Human Genes
Published in Proceedings of the National Academy of Sciences - PNAS (15-05-1993)“…We have developed a method for generating expressed-sequence maps of human chromosomes. The method involves several steps that begin with libraries of highly…”
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13
Saccharomyces cerevisiae pms2 mutations are alleles of MLH1, and pms2-2 corresponds to a hereditary nonpolyposis colorectal carcinoma-causing missense mutation
Published in Molecular and Cellular Biology (01-06-1996)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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14
Towards a genetic definition of velo-cardio-facial syndrome
Published 01-01-1995“…Velo-cardio-facial syndrome (VCFS) is a relatively common genetic disorder, characterized by clefting of the palate, cardiac anomalies, pharyngeal…”
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Dissertation