S. Ravichandran

发表

Synthesis and Biological Evaluation of Fluorescent Bryostatin Analogues

P. Blumberg, N. Lewin, Kevin M McGowan, 2018, Chembiochem : a European journal of chemical biology.

Mannose receptor (CD206) activation in tumor-associated macrophages enhances adaptive and innate antitumor immune responses

Jason B. White, M. Ferrer, Noel Southall, 2020, Science Translational Medicine.

In search of genetic factors predisposing to familial hairy cell leukemia (HCL): exome-sequencing of four multiplex HCL pedigrees

M. Dyer, M. Greene, A. Brooks-Wilson, 2020, Leukemia.

Pharmacophore model of the quercetin binding site of the SIRT6 protein.

B. Luke, S. Fugmann, Stuart Maudsley, 2014, Journal of molecular graphics & modelling.

A Comparison of Genome-wide and Exome-wide Somatic Mutation Patterns in Tumors

B. Luke, S. Ravichandran, E. Mulhern, 2016 .

The identification of a novel SIRT6 modulator from Trigonella foenum-graecum using ligand fishing with protein coated magnetic beads.

S. Fugmann, R. Moaddel, Kevin Spelman, 2014, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Can structural features of kinase receptors provide clues on selectivity and inhibition? A molecular modeling study.

B. Luke, J. Collins, S. Ravichandran, 2015, Journal of molecular graphics & modelling.

Identification of IL-23p19 as an endothelial proinflammatory peptide that promotes gp130-STAT3 signaling

B. Luke, G. Tosato, M. Cid, 2016, Science Signaling.

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

X. Hua, Jianxin Shi, S. Chanock, 2014, Nature Genetics.

Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility.

G. Marti, S. Chanock, M. Yeager, 2016, Blood.

Abstract 2756: Whole-exome sequencing reveals a novel germline variant in CEBPA-associated familial acute myeloid leukemia: 45-year follow-up of a large family

M. Yeager, B. Luke, J. Mulvihill, 2015 .

Cbl-b interacts with ubiquitinated proteins; differential functions of the UBA domains of c-Cbl and Cbl-b

M. Nau, S. Lipkowitz, S. Ettenberg, 2004, Oncogene.

Plasma metabolomic profiling of a ketamine and placebo crossover trial of major depressive disorder and healthy control subjects

L. Ferrucci, T. Gould, C. Zarate, 2018, Psychopharmacology.

A molecular model of the enantioselective liquid chromatographic separation of (R,S)-ifosfamide and its N-dechloroethylated metabolites on a teicoplanin aglycon chiral stationary phase.

J. Collins, S. Ravichandran, Nagendra S. Singh, 2012, Journal of chromatography. A.

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

Jianxin Shi, Florence Demenais, Maria Teresa Landi, 2014, Nature Genetics.

The evolutionary landscape of chronic lymphocytic leukemia treated with ibrutinib targeted therapy

D. Neuberg, I. Bozic, D. Landau, 2017, Nature Communications.

Somatic Genomics and Clinical Features of Lung Adenocarcinoma: A Retrospective Study

X. Hua, Jianxin Shi, S. Chanock, 2016, PLoS medicine.

Natural polyphenols as sirtuin 6 modulators

L. Ferrucci, M. Lahtela-Kakkonen, T. Kulikowicz, 2018, Scientific Reports.

Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family

M. Yeager, B. Luke, J. Mulvihill, 2016, Haematologica.

Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family

A. Dutra, M. Greene, M. Yeager, 2015, Human Genetics.

Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene

S. Chanock, M. Yeager, M. Tucker, 2016, Haematologica.

Deep sequencing of HPV16 genomes: A new high-throughput tool for exploring the carcinogenicity and natural history of HPV16 infection

M. Laptewicz, M. Yeager, S. Wacholder, 2015, Papillomavirus research.

Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family

A. Dutra, M. Greene, M. Yeager, 2015, Human Genetics.

Associations of CDH1 germline variant location and cancer phenotype in families with hereditary diffuse gastric cancer (HDGC)

S. Wacholder, S. Hewitt, K. Calzone, 2019, Journal of Medical Genetics.

Transcriptomic profiling and quantitative high-throughput (qHTS) drug screening of CDH1 deficient hereditary diffuse gastric cancer (HDGC) cells identify treatment leads for familial gastric cancer

M. Ferrer, B. Gryder, Y. Bian, 2017, Journal of Translational Medicine.

Structural conservation of interferon gamma among vertebrates.

J. Collins, H. Young, R. Savan, 2009, Cytokine & growth factor reviews.

AVIA v2.0: annotation, visualization and impact analysis of genomic variants and genes

Jack R. Collins, Brian T. Luke, Hue Vuong, 2015, Bioinform..

AVIA 3.0: interactive portal for genomic variant and sample level analysis

Sarangan Ravichandran, Anney Che, Brian T Luke, 2020, Bioinform..

Natural polyphenols as sirtuin 6 modulators

L. Ferrucci, M. Lahtela-Kakkonen, R. Moaddel, 2018, Scientific Reports.

A molecular model of the enantioselective liquid chromatographic separation of (R,S)-ifosfamide and its N-dechloroethylated metabolites on a teicoplanin aglycon chiral stationary phase.

J. Collins, S. Ravichandran, Nagendra S. Singh, 2012, Journal of chromatography. A.