F. Hantash

发表

OncoKB: A Precision Oncology Knowledge Base.

Moriah H Nissan, B. Taylor, N. Schultz, 2017, JCO precision oncology.

Membrane Association of the Escherichia coli Enterobactin Synthase Proteins EntB/G, EntE, and EntF

F. Hantash, C. Earhart, 2000, Journal of bacteriology.

Enterobactin synthase polypeptides of Escherichia coli are present in an osmotic-shock-sensitive cytoplasmic locality.

F. Hantash, C. Earhart, M. Ammerlaan, 1997, Microbiology.

Activation of extracellular signal-regulated kinase and c-Jun-NH(2)-terminal kinase but not p38 mitogen-activated protein kinases is required for RRR-alpha-tocopheryl succinate-induced apoptosis of human breast cancer cells.

F. Hantash, B. G. Sanders, K. Kline, 2001, Cancer research.

CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotype

Aubrey Milunsky, Arlene Buller, Franklin Quan, 2006, Genetics in Medicine.

High contents of homo-α-linolenic acid (20:3 ω3) in gametophores of two mosses

F. Hantash, S. Radwan, R. Al-Hasan, 1991 .

Targeted Next-Generation Sequencing Reveals Exceptionally High Rates of Molecular Driver Mutations in Never-Smokers With Lung Adenocarcinoma

E. Schadt, W. Oh, F. Hirsch, 2021, The oncologist.

Mutational analysis using next generation sequencing in pediatric thyroid cancer reveals BRAF and fusion oncogenes are common.

F. Hantash, R. Newfield, Wen Jiang, 2022, International journal of pediatric otorhinolaryngology.

Mutational Analysis in Pediatric Thyroid Cancer and Correlations with Age, Ethnicity, and Clinical Presentation

F. Waldman, F. Hantash, M. Mcphaul, 2016, Thyroid : official journal of the American Thyroid Association.

Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening

Weimin Sun, C. Strom, F. Hantash, 2006, Human Genetics.

Frequency of the cystic fibrosis 3199del6 mutation in individuals heterozygous for I148T

C. Strom, F. Hantash, J. Redman, 2004, Genetics in Medicine.

Relationship between insulin resistance and amino acids in women and men

G. Reaven, F. Hantash, F. Abbasi, 2015, Physiological reports.

Relationship among 25-hydroxyvitamin D concentrations, insulin action, and cardiovascular disease risk in patients with essential hypertension.

G. Reaven, F. Hantash, F. Abbasi, 2015, American journal of hypertension.

Extensive Sequencing of the CFTR gene: lessons learned from the first 157 patient samples

Weimin Sun, C. Strom, F. Hantash, 2005, Human Genetics.

Activation of Extracellular Signal-regulated Kinase and c-Jun-NH 2 -terminal Kinase but not p38 Mitogen-activated Protein Kinases Is Required for RRR- (cid:1) -Tocopheryl Succinate-induced Apoptosis of Human Breast Cancer Cells

F. Hantash, B. G. Sanders, K. Kline, 2001 .

Succinate-induced Apoptosis of Human Breast Cancer Cells-Tocopheryl α Protein Kinases Is Required for RRR-- terminal Kinase but not p 38 Mitogen-activated 2 c-Jun-NH Activation of Extracellular Signal-regulated Kinase and Updated

F. Hantash, B. G. Sanders, K. Kline, 2001 .

Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: Implications for fragile X syndrome carrier and newborn screening

Weimin Sun, C. Strom, F. Hantash, 2010, Genetics in Medicine.

Development of a novel, accurate, automated, rapid, high-throughput technique suitable for population-based carrier screening for Fragile X syndrome

Weimin Sun, C. Strom, F. Hantash, 2007, Genetics in Medicine.

OncoKB: Annotation of the oncogenic effect and treatment implications of somatic mutations in cancer.

N. Schultz, M. Ladanyi, S. Chandarlapaty, 2016 .

Clinical actionability and utilization of next-generation sequencing for prostate cancer in a changing treatment landscape

W. Oh, M. Galsky, F. Hantash, 2022, Frontiers in Urology.

Apparent homozygosity of a novel frame shift mutation in the CFTR gene because of a large deletion.

Weimin Sun, C. Strom, F. Hantash, 2009, The Journal of molecular diagnostics : JMD.

Mutation Yield of a 34-Gene Solid Tumor Panel in Community-Based Tumor Samples

F. Waldman, J. Catanese, J. Sninsky, 2016, Molecular Diagnosis & Therapy.

Inherited and de novo 22q11.2 distal duplications in two patients with autistic features, speech delay and no dysmorphology

C. Strom, F. Hantash, R. Owen, 2012, Journal of Pediatric Genetics.

FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: Insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States

Weimin Sun, C. Strom, F. Hantash, 2011, Genetics in Medicine.

Enriching marine macroalgae with eicosatetraenoic (arachidonic) and eicosapentaenoic acids by chilling

F. Hantash, S. Radwan, R. Al-Hasan, 1991, Applied Microbiology and Biotechnology.

Response to letter regarding article, "lipoprotein(a) concentrations, rosuvastatin therapy, and residual vascular risk: an analysis from the JUPITER trial (justification for the use of statins in prevention: an intervention trial evaluating rosuvastatin)".

A. Khera, P. Ridker, S. Mora, 2014, Circulation.

Lipoprotein(a) Concentrations, Rosuvastatin Therapy, and Residual Vascular Risk: An Analysis From the JUPITER Trial (Justification for the Use of Statins in Prevention An Intervention Trial Evaluating Rosuvastatin)

A. Khera, P. Ridker, S. Mora, 2013, Circulation.

Abstract 10170: Lipoprotein(a) Concentrations, Rosuvastatin Therapy, and Residual Vascular Risk: An Analysis From the JUPITER Trial

A. Khera, P. Ridker, S. Mora, 2013 .

Low circulating 25-hydroxyvitamin D concentrations are associated with defects in insulin action and insulin secretion in persons with prediabetes.

G. Reaven, F. Hantash, C. Blasey, 2015, The Journal of nutrition.

Genetically characterized positive control cell lines derived from residual clinical blood samples.

S. Thibodeau, D. H. Farkas, C. Strom, 2005, Clinical chemistry.

Direct visualization of cystic fibrosis transmembrane regulator mutations in the clinical laboratory setting.

David D. Clark, Weimin Sun, Charles M Strom, 2004, Clinical chemistry.

A large deletion in the CFTR gene in CBAVD

Weimin Sun, C. Strom, F. Hantash, 2006, Genetics in Medicine.

Characterization of a recurrent novel large duplication in the cystic fibrosis transmembrane conductance regulator gene.

Weimin Sun, C. Strom, F. Hantash, 2007, The Journal of molecular diagnostics : JMD.

Rapid one-step carrier detection assay of mucolipidosis IV mutations in the Ashkenazi Jewish population.

Weimin Sun, C. Strom, F. Hantash, 2006, The Journal of molecular diagnostics : JMD.

Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening

Weimin Sun, C. Strom, F. Hantash, 2006, Human Genetics.

A. Khera, P. Ridker, S. Mora, 2014, Circulation.

Consultations in Molecular Diagnostics Characterization of a Recurrent Novel Large Duplication in the Cystic Fibrosis Transmembrane Conductance Regulator Gene

Weimin Sun, C. Strom, F. Hantash, 2007 .

A. Khera, P. Ridker, S. Mora, 2013, Circulation.

Lipoprotein ( a ) Concentrations , Rosuvastatin Therapy , and Residual Vascular Risk An Analysis From the JUPITER Trial ( Justification for the Use of Statins in Prevention : An Intervention Trial Evaluating Rosuvastatin

P. Ridker, F. Hantash, Brendan M. Everett, 2022 .

Targeted Next-Generation Sequencing Reveals Exceptionally High Rates of Molecular Driver Mutations in Never-Smokers With Lung Adenocarcinoma

E. Schadt, W. Oh, Rong Chen, 2022, The oncologist.