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Pathophysiology of intraabdominal hypertension and abdominal compartment syndrome and relevance to veterinary critical care

Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000), 2022-01, Vol.32 (S1), p.48-56

2022

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Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment

Nature communications, 2024-02, Vol.15 (1), p.1210-1210, Article 1210

2024

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The Link between Inactivation and High-Affinity Block of hERG1 Channels

Molecular pharmacology, 2015-06, Vol.87 (6), p.1042-1050

2015

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How to perform a percutaneous cecal or colonic trocarization in horses with severe abdominal tympany

Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000), 2022-01, Vol.32 (S1), p.57-62

2022

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A Focal Epilepsy and Intellectual Disability Syndrome Is Due to a Mutation in TBC1D24

American journal of human genetics, 2010-09, Vol.87 (3), p.371-375

2010

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A multicenter retrospective case–cohort study on the prevalence of incisional morbidities in late pregnant mares following exploratory celiotomy (2014–2019): 579 cases

Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000), 2023-01, Vol.33 (1), p.59-69

2023

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Intrasinus bolstering of traumatic maxillary sinus fractures by using Foley catheter balloons in two foals

Veterinary surgery, 2020-08, Vol.49 (6), p.1255-1261

2020

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A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability

American journal of human genetics, 2012-10, Vol.91 (4), p.694-702

2012

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Deficiency of phospholipase A2 group 7 decreases intestinal polyposis and colon tumorigenesis in Apc(Min/+) mice

Cancer research (Chicago, Ill.), 2013-05, Vol.73 (9), p.2806

2013

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Identification of a Domain That Mediates Association of Platelet-activating Factor Acetylhydrolase with High Density Lipoprotein

The Journal of biological chemistry, 2008-06, Vol.283 (25), p.17099-17106

2008

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Molecular basis for susceptibility of plasma platelet-activating factor acetylhydrolase to oxidative inactivation

The FASEB journal, 2007-04, Vol.21 (4), p.1164-1176

2007

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Novel mechanism for regulation of plasma platelet-activating factor acetylhydrolase expression in mammalian cells

Biochemical journal, 2010-06, Vol.428 (2), p.269-279

2010

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Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse

Nature genetics, 1998-10, Vol.20 (2), p.149-156

1998

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Presentation of a four-year-old Friesian mare to a referral hospital with signs of abdominal pain and thoracic and pericardial effusion

Journal of the American Veterinary Medical Association, 2024-03, Vol.262 (3), p.418-4

2024

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A Goat Cadaver as a Cost-effective Resource for Teaching Emergency Medicine Procedures in Kijabe, Kenya

Pediatric emergency care, 2022-03, Vol.38 (3), p.e1097-e1103

2022

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Concatenated hERG1 tetramers reveal stoichiometry of altered channel gating by RPR-260243

Molecular pharmacology, 2015-03, Vol.87 (3), p.401-409

2015

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Cooperative subunit interactions mediate fast C‐type inactivation of hERG1 K+ channels

The Journal of physiology, 2014-10, Vol.592 (20), p.4465-4480

2014

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Human nuclear hormone receptor activity contributes to malaria parasite liver stage development

Cell chemical biology, 2023-05, Vol.30 (5), p.486-498.e7

2023

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Molecular mechanisms of Slo2 K+ channel closure

The Journal of physiology, 2017-04, Vol.595 (7), p.2321-2336

2017

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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

American journal of human genetics, 2012-01, Vol.90 (1), p.152-160

2012

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C-Linker Accounts for Differential Sensitivity of ERG1 and ERG2 K+ Channels to RPR260243-Induced Slow Deactivation

Molecular pharmacology, 2015-07, Vol.88 (1), p.19-28

2015

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Ginsenoside Rg3, a Gating Modifier of EAG Family K+ Channels

Molecular pharmacology, 2016-10, Vol.90 (4), p.469-482

2016

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Stoichiometry of altered hERG1 channel gating by small molecule activators

The Journal of general physiology, 2014-04, Vol.143 (4), p.499-512

2014

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Molecular and Functional Analyses of the Human and Mouse Genes Encoding AFG3L1, a Mitochondrial Metalloprotease Homologous to the Human Spastic Paraplegia Protein

Genomics (San Diego, Calif.), 2001-08, Vol.76 (1-3), p.58-65

2001

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Pathophysiology of intraabdominal hypertension and abdominal compartment syndrome and relevance to veterinary critical care

Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment

The Link between Inactivation and High-Affinity Block of hERG1 Channels

How to perform a percutaneous cecal or colonic trocarization in horses with severe abdominal tympany

A Focal Epilepsy and Intellectual Disability Syndrome Is Due to a Mutation in TBC1D24

A multicenter retrospective case–cohort study on the prevalence of incisional morbidities in late pregnant mares following exploratory celiotomy (2014–2019): 579 cases

Intrasinus bolstering of traumatic maxillary sinus fractures by using Foley catheter balloons in two foals

A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability

Deficiency of phospholipase A2 group 7 decreases intestinal polyposis and colon tumorigenesis in Apc(Min/+) mice

Identification of a Domain That Mediates Association of Platelet-activating Factor Acetylhydrolase with High Density Lipoprotein

Molecular basis for susceptibility of plasma platelet-activating factor acetylhydrolase to oxidative inactivation

Novel mechanism for regulation of plasma platelet-activating factor acetylhydrolase expression in mammalian cells

Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse

Presentation of a four-year-old Friesian mare to a referral hospital with signs of abdominal pain and thoracic and pericardial effusion

A Goat Cadaver as a Cost-effective Resource for Teaching Emergency Medicine Procedures in Kijabe, Kenya

Concatenated hERG1 tetramers reveal stoichiometry of altered channel gating by RPR-260243

Cooperative subunit interactions mediate fast C‐type inactivation of hERG1 K+ channels

Human nuclear hormone receptor activity contributes to malaria parasite liver stage development

Molecular mechanisms of Slo2 K+ channel closure

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

C-Linker Accounts for Differential Sensitivity of ERG1 and ERG2 K+ Channels to RPR260243-Induced Slow Deactivation

Ginsenoside Rg3, a Gating Modifier of EAG Family K+ Channels

Stoichiometry of altered hERG1 channel gating by small molecule activators

Molecular and Functional Analyses of the Human and Mouse Genes Encoding AFG3L1, a Mitochondrial Metalloprotease Homologous to the Human Spastic Paraplegia Protein

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