Search Results - "Midgen, Craig"
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1
Oral Losartan After Limited Mandibulectomy for Treatment of Desmoid-Type Fibromatosis
Published in Ear, nose, & throat journal (01-02-2023)“…Desmoid-type fibromatosis (DF) is a rare soft tissue lesion with an annual incidence of 2 to 4 per million population and peak incidence occurring at…”
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2
Properdin Regulation of Complement Activation Affects Colitis in Interleukin 10 Gene-Deficient Mice
Published in Inflammatory bowel diseases (01-07-2015)“…Interleukin 10-deficient mice (IL-10(-/-)) are a popular model used to dissect the mechanisms underlying inflammatory bowel diseases. The role of complement, a…”
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3
Molar and nonmolar triploidy: Recurrence or bad luck
Published in Clinical case reports (01-05-2020)“…In triploid pregnancies, the parental origin of the extra genome determines the phenotype and placental and fetal outcomes. Molecular genetics and placental…”
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4
Angiotensin II Type I Receptor Blockade Is Associated with Decreased Cutaneous Scar Formation in a Rat Model
Published in Plastic and reconstructive surgery (1963) (01-11-2019)“…BACKGROUND:Angiotensin II engagement of angiotensin II type 1 receptor (AT1R) is implicated in fibrogenesis, with AT1R blockers used clinically to attenuate…”
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5
miR-34a is a tumor suppressor in zebrafish and its expression levels impact metabolism, hematopoiesis and DNA damage
Published in PLoS genetics (28-05-2024)“…Li-Fraumeni syndrome is caused by inherited TP53 tumor suppressor gene mutations. MicroRNA miR-34a is a p53 target and modifier gene. Interestingly, miR-34…”
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6
Congenital Myenteric Hypoganglionosis
Published in The American journal of surgical pathology (22-01-2021)“…Congenital myenteric hypoganglionosis is a rare developmental disorder characterized clinically by severe and persistent neonatal intestinal pseudoobstruction…”
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Congenital Myenteric Hypoganglionosis
Published in The American journal of surgical pathology (01-08-2021)“…Congenital myenteric hypoganglionosis is a rare developmental disorder characterized clinically by severe and persistent neonatal intestinal pseudoobstruction…”
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Etiology and functional validation of gastrointestinal motility dysfunction in a zebrafish model of CHARGE syndrome
Published in The FEBS journal (01-06-2018)“…CHARGE syndrome is linked to autosomal‐dominant mutations in the CHD7 gene and results in a number of physiological and structural abnormalities, including…”
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9
Bilateral Renal Vein and Inferior Vena Cava Thrombosis Associated With Fetal Vascular Malperfusion and Maternal Diabetes
Published in Canadian journal of diabetes (01-12-2019)Get full text
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Abstract 53: Zebrafish tp53 mutants recapitulate Li-Fraumeni syndrome phenotypes and provide a preclinical platform for evaluating tumor preventive compounds
Published in Cancer research (Chicago, Ill.) (04-04-2023)“…Background: Li-Fraumeni syndrome (LFS) is a hereditary cancer predisposition disorder associated with a highly penetrant and diverse tumor spectrum…”
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A dataset of transcriptomic effects of camptothecin treatment on early zebrafish embryos
Published in Data in brief (01-12-2024)“…Zebrafish (Danio rerio) are a good model for cancer research including studies on chemotherapy treatments. We treated wild-type and miR-34a deletion mutant…”
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A dataset of transcriptomic effects of camptothecin treatment on early zebrafish embryosGene Expression Omnibus
Published in Data in brief (01-12-2024)“…Zebrafish (Danio rerio) are a good model for cancer research including studies on chemotherapy treatments. We treated wild-type and miR-34a deletion mutant…”
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13
Massive Saddle Pulmonary Embolism in a Preterm Neonate With Successful Emergent Open Embolectomy
Published in CJC pediatric and congenital heart disease (01-02-2022)“…Pulmonary embolism in the neonate is a rare, life-threatening emergency. Risk factors for neonatal pulmonary embolism (PE) include sepsis, asphyxia,…”
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14
Painless Nodule on the External Ear
Published in Pediatric dermatology (01-05-2015)Get full text
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15
Massive Saddle Pulmonary Embolism in a Preterm Neonate With Successful Emergent Open EmbolectomyNovel Teaching Points
Published in CJC pediatric and congenital heart disease (01-02-2022)“…Pulmonary embolism in the neonate is a rare, life-threatening emergency. Risk factors for neonatal pulmonary embolism (PE) include sepsis, asphyxia,…”
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16
Whole‐Exome Sequencing Reveals GPIHBP1 Mutations in Infantile Colitis With Severe Hypertriglyceridemia
Published in Journal of pediatric gastroenterology and nutrition (01-07-2014)“…ABSTRACT Severe congenital hypertriglyceridemia (HTG) is a rare disorder caused by mutations in genes affecting lipoprotein lipase (LPL) activity. Here we…”
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17
Molar and nonmolar triploidy: Recurrence or bad luck
Published in Clinical case reports (01-05-2020)“…In triploid pregnancies, the parental origin of the extra genome determines the phenotype and placental and fetal outcomes. Molecular genetics and placental…”
Get full text
Report -
18
Massive Saddle Pulmonary Embolism in a Preterm Neonate With Successful Emergent Open Embolectomy
Published in CJC pediatric and congenital heart disease (01-02-2022)“…Pulmonary embolism in the neonate is a rare, life-threatening emergency. Risk factors for neonatal pulmonary embolism (PE) include sepsis, asphyxia,…”
Get full text
Report