Search Results - "Devine, Patrick W"
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1
Early patterning and specification of cardiac progenitors in gastrulating mesoderm
Published in eLife (08-10-2014)“…Mammalian heart development requires precise allocation of cardiac progenitors. The existence of a multipotent progenitor for all anatomic and cellular…”
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2
A Mesp1-dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors
Published in Development (Cambridge) (01-05-2023)“…Transcriptional networks governing cardiac precursor cell (CPC) specification are incompletely understood owing, in part, to limitations in distinguishing CPCs…”
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3
ETS Factors Regulate Vegf-Dependent Arterial Specification
Published in Developmental cell (15-07-2013)“…Vegf signaling specifies arterial fate during early vascular development by inducing the transcription of Delta-like 4 (Dll4), the earliest Notch ligand gene…”
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4
Hydra: A mixture modeling framework for subtyping pediatric cancer cohorts using multimodal gene expression signatures
Published in PLoS computational biology (10-04-2020)“…Precision oncology has primarily relied on coding mutations as biomarkers of response to therapies. While transcriptome analysis can provide valuable…”
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5
Requirement for chitin biosynthesis in epithelial tube morphogenesis
Published in Proceedings of the National Academy of Sciences - PNAS (22-11-2005)“…Many organs are composed of branched networks of epithelial tubes that transport vital fluids or gases. The proper size and shape of tubes are crucial for…”
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Genetic ancestry and diagnostic yield of exome sequencing in a diverse population
Published in Npj genomic medicine (03-01-2024)“…It has been suggested that diagnostic yield (DY) from Exome Sequencing (ES) may be lower among patients with non-European ancestries than those with European…”
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A novel reporter allele for monitoring Dll4 expression within the embryonic and adult mouse
Published in Biology open (2018)“…Canonical Notch signaling requires the presence of a membrane bound ligand and a corresponding transmembrane Notch receptor. Receptor engagement induces…”
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8
NTRK fusion cervical sarcoma: a report of three cases, emphasising morphological and immunohistochemical distinction from other uterine sarcomas, including adenosarcoma
Published in Histopathology (01-07-2020)“…Aims A unique fibrosarcoma‐like tumour of the uterine cervix harbouring a rearrangement of a neurotrophic tyrosine kinase receptor (NTRK) gene (NTRK1 or NTRK3)…”
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Cytoplasmic Pattern p53 Immunoexpression in Pelvic and Endometrial Carcinomas With TP53 Mutation Involving Nuclear Localization Domains: An Uncommon But Potential Diagnostic Pitfall With Clinical Implications
Published in The American journal of surgical pathology (01-11-2021)“…A cytoplasmic pattern of p53 immunohistochemical expression has recently been reported in a rare subset of pelvic and endometrial cancers with a TP53 mutation…”
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10
Expanding the phenotype of males with OFD1 pathogenic variants-a case report and literature review
Published in European journal of medical genetics (01-06-2022)“…Pathogenic variants in the OFD1 gene have been classically associated with the Orofaciodigital syndrome type 1 in females, a condition previously considered to…”
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Practical roles for molecular diagnostic testing in ovarian adult granulosa cell tumour, Sertoli–Leydig cell tumour, microcystic stromal tumour and their mimics
Published in Histopathology (01-01-2020)“…Within the last decade, molecular advances have provided insights into the genetics of several ovarian sex cord–stromal tumours that have otherwise been…”
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12
Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis
Published in American journal of obstetrics and gynecology (01-01-2022)“…Next-generation sequencing is increasingly used in prenatal diagnosis. Targeted gene panels and exome sequencing are both available, but the comparative…”
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Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features
Published in Ophthalmology (Rochester, Minn.) (01-06-2020)“…To determine the usefulness of a comprehensive, targeted-capture next-generation sequencing (NGS) assay for the clinical management of children undergoing…”
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14
Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease
Published in Developmental cell (08-02-2021)“…Haploinsufficiency of transcriptional regulators causes human congenital heart disease (CHD); however, the underlying CHD gene regulatory network (GRN)…”
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15
Effective Use of ALK Inhibitors in EML4::ALK‐Positive Lymphatic Malformations
Published in Pediatric blood & cancer (11-11-2024)“…ABSTRACT Genetically targeted medications are emerging as important therapies for lymphatic malformations (LMs) unresponsive to sirolimus. We describe two…”
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16
Genetic and Immunohistochemical Profiling of Mammary Hidradenoma and Comparison to Mucoepidermoid Carcinoma
Published in Modern pathology (01-10-2023)“…Mucoepidermoid carcinoma (MEC) is exceedingly rare in the breast, with <45 cases reported in the literature. Although estrogen receptor/progesterone…”
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Neoadjuvant Osimertinib for the Treatment of Stage I-IIIA Epidermal Growth Factor Receptor-Mutated Non-Small Cell Lung Cancer: A Phase II Multicenter Study
Published in Journal of clinical oncology (10-09-2024)“…To assess the safety and efficacy of the third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor osimertinib as neoadjuvant therapy…”
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Identification of high-risk human papillomavirus and Rb/E2F pathway genomic alterations in mutually exclusive subsets of colorectal neuroendocrine carcinoma
Published in Modern pathology (01-02-2019)“…Colorectal neuroendocrine carcinomas, both small cell and large cell types, are highly aggressive tumors with poor prognosis compared with colorectal…”
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Tumor and Constitutional Sequencing for Neurofibromatosis Type 1
Published in JCO precision oncology (01-05-2022)“…variants in tumors are important to recognize, as multiple mechanisms may give rise to biallelic variants. Both deletions and copy-neutral loss of…”
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HER2 overexpression in urothelial carcinoma with GATA3 and PPARG copy number gains
Published in The oncologist (Dayton, Ohio) (05-08-2024)“…HER2, encoded by the ERBB2 gene, is an important druggable driver of human cancer gaining increasing importance as a therapeutic target in urothelial carcinoma…”
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