S. Boikos

发表

A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex

E. Remmers, J. Bertherat, C. Stratakis, 2008, European Journal of Human Genetics.

Carney Complex: Pathology and Molecular Genetics

C. Stratakis, S. Boikos, 2006, Neuroendocrinology.

Catastrophic ATP loss underlies a metabolic combination therapy tailored for MYCN-amplified neuroblastoma

Patricia Greninger, C. Benes, B. Hu, 2021, Proceedings of the National Academy of Sciences.

Bone-targeting agents in prostate cancer

M. Carducci, S. Boikos, D. Suzman, 2014, Cancer and Metastasis Reviews.

Immunotherapy for Prostate Cancer Enters Its Golden Age

E. Antonarakis, S. Boikos, 2012, Clinical Medicine Insights. Oncology.

Systemic Therapy, Clinical Outcomes, and Overall Survival in Locally Advanced or Metastatic Pulmonary Carcinoid: A Brief Report

G. Giaccone, D. Ettinger, C. Rudin, 2014, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Correction: Prognostic Factors of Malignant Pheochromocytoma and Paraganglioma: A Combined SEER and TCGA Databases Review

A. Faber, Steven C. Smith, F. Celi, 2019, Hormone and Metabolic Research.

Molecular and immunohistochemical investigation of protein kinase a regulatory subunit type 1A (PRKAR1A) in odontogenic myxomas

C. Stratakis, S. Boikos, R. Gomez, 2005, Genes, chromosomes & cancer.

Respecting your elders: osimertinib demonstrates preferential activity in elderly patients with T790M positive non-small cell lung cancers.

A. Faber, S. Boikos, H. Ebi, 2019, Journal of thoracic disease.

Increased Synthesis of MCL-1 Protein Underlies Initial Survival of EGFR-Mutant Lung Cancer to EGFR Inhibitors and Provides a Novel Drug Target

Krista M. Powell, Y. Yatabe, H. Harada, 2018, Clinical Cancer Research.

MYCN-Amplified Neuroblastoma Is Addicted to Iron and Vulnerable to Inhibition of the System Xc-/Glutathione Axis

Krista M. Powell, S. Ramamoorthy, M. Dozmorov, 2021, Cancer Research.

A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia

I. Bossis, J. Bertherat, X. Bertagna, 2006, Nature Genetics.

Effects of Cushing disease on bone mineral density in a pediatric population.

C. Stratakis, M. Lodish, J. Reynolds, 2010, The Journal of pediatrics.

Paragangliomas in Carney–Stratakis Syndrome

A. Faber, Steven C. Smith, S. Boikos, 2019, Hormone and Metabolic Research.

Multiple gastrointestinal stromal and other tumors caused by platelet-derived growth factor receptor alpha gene mutations: a case associated with a germline V561D defect.

C. Stratakis, B. Pasini, J. Carney, 2007, The Journal of clinical endocrinology and metabolism.

Unusual Case of Autoimmune Diabetes Mellitus in the Setting of Extra-Adrenal Paraganglioma with Loss of Succinate Dehydrogenase Expression

Steven C. Smith, F. Celi, S. Boikos, 2018, AACE Clinical Case Reports.

A novel, non-functional, COL1A1 polymorphism is not associated with lumbar disk disease in young male Greek subjects unlike that of the Sp1 site

C. Stratakis, C. Simopoulos, S. Garantziotis, 2008, Hormones.

Polymorphisms of the Vitamin D Receptor Gene and Stress Fractures

C. Stratakis, G. Tripsianis, S. Boikos, 2009, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Throat clearing - a novel asthma symptom in children.

S. Boikos, E. Mantzouranis, G. Chlouverakis, 2003, The New England journal of medicine.

Mutations in regulatory subunit type 1A of cyclic adenosine 5'-monophosphate-dependent protein kinase (PRKAR1A): phenotype analysis in 353 patients and 80 different genotypes.

J. Bertherat, X. Bertagna, C. Stratakis, 2009, The Journal of clinical endocrinology and metabolism.

Spontaneous splenic rupture during induction chemotherapy for acute myeloid leukemia

P. Lipsett, D. Efron, S. Boikos, 2014, Leukemia and Lymphoma.

Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropin-independent macronodular adrenal hyperplasia compared with other adrenocortical tumors.

C. Stratakis, A. Lacroix, M. Nesterova, 2009, The Journal of clinical endocrinology and metabolism.

Genetics of adrenal tumors associated with Cushing's syndrome: a new classification for bilateral adrenocortical hyperplasias

C. Stratakis, S. Boikos, 2007, Nature Clinical Practice Endocrinology &Metabolism.

The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes

V. Bours, C. Stratakis, A. Horvath, 2010, Clinical genetics.

Denosumab for the treatment of bisphosphonate-refractory hypercalcemia.

S. Boikos, H. Hammers, 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Adrenal hyperplasia and adenomas are associated with inhibition of phosphodiesterase 11A in carriers of PDE11A sequence variants that are frequent in the population.

P. Gregersen, E. Remmers, I. Bossis, 2006, Cancer research.

PRKAR1A Mutations and protein kinase A interactions with other signaling pathways in the adrenal cortex.

I. Bossis, C. Stratakis, A. Horvath, 2006, The Journal of clinical endocrinology and metabolism.

Genetics of carney triad: recurrent losses at chromosome 1 but lack of germline mutations in genes associated with paragangliomas and gastrointestinal stromal tumors.

E. Campo, A. Dutra, G. Assié, 2007, The Journal of clinical endocrinology and metabolism.

Genomic screening reveals UBA1 as a potent and druggable target in c-MYC-high TNBC models

C. Benes, B. Hu, J. Harrell, 2022, bioRxiv.

17q22-24 chromosomal losses and alterations of protein kinase a subunit expression and activity in adrenocorticotropin-independent macronodular adrenal hyperplasia.

C. Stratakis, S. Boikos, I. Bourdeau, 2006, The Journal of clinical endocrinology and metabolism.

Pituitary pathology in patients with Carney Complex: growth-hormone producing hyperplasia or tumors and their association with other abnormalities

C. Stratakis, S. Boikos, 2006, Pituitary.

Thyroid hormone inactivation in gastrointestinal stromal tumors.

C. Stratakis, L. Helman, S. Boikos, 2014, New England Journal of Medicine.

Phosphodiesterase 11A Expression in the Adrenal Cortex, Primary Pigmented Nodular Adrenocortical Disease, and other Corticotropin-independent Lesions

I. Bossis, J. Bertherat, C. Stratakis, 2008, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

MYCN upregulates the transsulfuration pathway to suppress the ferroptotic vulnerability in MYCN-amplified neuroblastoma

M. Dozmorov, A. Faber, L. Cowart, 2022, Cell stress.

A Reappraisal of Superficial Pleomorphic Liposarcoma.

C. Jackson-Cook, Steven C. Smith, S. Boikos, 2020, American journal of clinical pathology.

The genetic landscape of gastrointestinal stromal tumor lacking KIT and PDGFRA mutations

C. Stratakis, S. Boikos, 2014, Endocrine.

Clinical and molecular genetics of patients with the Carney–Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD

J. Ellison, E. Baudin, P. Rustin, 2008, European Journal of Human Genetics.

Advances and Challenges on Management of Gastrointestinal Stromal Tumors

M. von Mehren, S. Boikos, M. Idowu, 2018, Front. Oncol..

Classification of gastrointestinal stromal tumor syndromes.

S. Grossman, A. Faber, Steven C. Smith, 2018, Endocrine-related cancer.

Carney complex: the first 20 years

C. Stratakis, S. Boikos, 2007, Current opinion in oncology.

Mouse Prkar1a haploinsufficiency leads to an increase in tumors in the Trp53+/- or Rb1+/- backgrounds and chemically induced skin papillomas by dysregulation of the cell cycle and Wnt signaling.

C. Cheadle, I. Bossis, C. Stratakis, 2010, Human molecular genetics.

Association of the M1V PRKAR1A mutation with primary pigmented nodular adrenocortical disease in two large families.

J. Romijn, C. Stratakis, A. Horvath, 2010, The Journal of clinical endocrinology and metabolism.

Molecular genetics of the cAMP-dependent protein kinase pathway and of sporadic pituitary tumorigenesis.

C. Stratakis, S. Boikos, 2007, Human molecular genetics.

A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds.

P. Chanson, J. Bertherat, X. Bertagna, 2006, The Journal of clinical endocrinology and metabolism.

Tumor lysis syndrome in limited-stage small-cell lung cancer.

P. Forde, S. Boikos, C. Hann, 2013, Journal of Thoracic Oncology.

Recurrent epimutation of SDHC in gastrointestinal stromal tumors

P. Meltzer, J. Walling, Yonghong Wang, 2014, Science Translational Medicine.

Intimal sarcoma of the pulmonary artery treated with neoadjuvant radiation prior to pulmonary artery resection and reconstruction

Timothy J. Harris, J. Grizzard, B. Medalion, 2021, Respiratory medicine case reports.

Molecular Subtypes of KIT/PDGFRA Wild-Type Gastrointestinal Stromal Tumors: A Report From the National Institutes of Health Gastrointestinal Stromal Tumor Clinic.

P. Meltzer, J. Schiffman, C. Stratakis, 2016, JAMA oncology.

Alternate protein kinase A activity identifies a unique population of stromal cells in adult bone

C. Cheadle, C. Stratakis, M. Collins, 2010, Proceedings of the National Academy of Sciences.

Coamplification of miR-4728 protects HER2-amplified breast cancers from targeted therapy

J. Arribas, C. Costa, H. Harada, 2018, Proceedings of the National Academy of Sciences.

Familial GI Stromal Tumor With Loss of Heterozygosity and Amplification of Mutant KIT.

E. Montgomery, B. Park, C. Meyer, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

The Ewing Family of Tumors Relies on BCL-2 and BCL-XL to Escape PARP Inhibitor Toxicity

Krista M. Powell, C. Benes, J. Leverson, 2018, Clinical Cancer Research.

Bone-targeting agents in prostate cancer

M. Carducci, S. Boikos, D. Suzman, 2014, Cancer and Metastasis Reviews.

Gastrointestinal Stromal Tumors: The GIST of Precision Medicine.

S. Grossman, C. Stratakis, J. Trent, 2018, Trends in cancer.

Carney triad can be (rarely) associated with germline succinate dehydrogenase defects

F. Faucz, C. Stratakis, L. Helman, 2015, European Journal of Human Genetics.

Surgical Management of Wild-Type Gastrointestinal Stromal Tumors: A Report From the National Institutes of Health Pediatric and Wildtype GIST Clinic.

J. Schiffman, C. Stratakis, C. Weldon, 2017, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

The cytologic features of primary pseudomyogenic hemangioendothelioma of bone

Steven C. Smith, S. Boikos, Sadia Sayeed, 2021, Diagnostic cytopathology.

Molecular mechanisms of medullary thyroid carcinoma: current approaches in diagnosis and treatment.

C. Stratakis, S. Boikos, 2008, Histology and histopathology.

NCI protocol 10250: A phase II study of temozolomide and olaparib for the treatment of advanced uterine leiomyosarcoma.

M. Burgess, G. Schwartz, S. George, 2020, Journal of Clinical Oncology.

Prognostic Factors of Malignant Pheochromocytoma and Paraganglioma: A Combined SEER and TCGA Databases Review

A. Faber, Steven C. Smith, F. Celi, 2019, Hormone and Metabolic Research.

Unmasking BCL-2 Addiction in Synovial Sarcoma by Overcoming Low NOXA

H. Harada, J. Leverson, M. Dozmorov, 2021, Cancers.

Venetoclax Is Effective in Small-Cell Lung Cancers with High BCL-2 Expression

Krista M. Powell, Patricia Greninger, C. Benes, 2017, Clinical Cancer Research.

Germline AIP, MEN1, PRKAR1A, CDKN1B (p27Kip1) and CDKN2C (p18INK4c) gene mutations in a large cohort of pediatric patients with pituitary adenomas occurring in isolation or with associated syndromic features

V. Bours, C. Stratakis, A. Horvath, 2008 .

Targetable immune checkpoint molecules may be significantly differentially expressed in minority ethnicities.

S. Grossman, C. Szeto, A. Faber, 2020 .

Pharmaceutical Interference of the EWS-FLI1–driven Transcriptome By Cotargeting H3K27ac and RNA Polymerase Activity in Ewing Sarcoma

C. Benes, M. Dozmorov, A. Faber, 2021, Molecular Cancer Therapeutics.

Targeting transcription of MCL-1 sensitizes HER2-amplified breast cancers to HER2 inhibitors

M. Scaltriti, M. Dozmorov, A. Faber, 2021, Cell Death & Disease.

Differences in cortisol levels and body mass index between East Asians and Caucasians with Cushing's syndrome: an ‘East Asian’ phenotype for Cushing syndrome

C. Stratakis, S. Boikos, A. Robinson-White, 2007, Clinical endocrinology.

Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes

C. Stratakis, G. Hammer, L. Metherell, 2007, Clinical endocrinology.

The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes

V. Bours, C. Stratakis, A. Horvath, 2010, Clinical genetics.

Effects of Cushing disease on bone mineral density in a pediatric population.

C. Stratakis, M. Lodish, J. Reynolds, 2010, The Journal of pediatrics.

PRKAR1A gene analysis and protein kinase A activity in endometrial tumors.

C. Stratakis, A. Horvath, M. Nesterova, 2012, Endocrine-related cancer.