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A118G Single Nucleotide Polymorphism of Human μ-Opioid Receptor Gene Influences Pain Perception and Patient-controlled Intravenous Morphine Consumption after Intrathecal Morphine for Postcesarean Analgesia

Anesthesiology (Philadelphia), 2008-09, Vol.109 (3), p.520-526

2008

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Ethnicity and OPRM Variant Independently Predict Pain Perception and Patient-Controlled Analgesia Usage for Post-Operative Pain

Molecular pain, 2009-06, Vol.5 (1), p.32-32

2009

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Influence of Mu-Opioid Receptor Variant on Morphine Use and Self-Rated Pain Following Abdominal Hysterectomy

The journal of pain, 2013-10, Vol.14 (10), p.1045-1052

2013

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Intragenic multi-exon deletion in the FBN1 gene in a child with mildly dilated aortic sinus: a retrotransposal event

Journal of human genetics, 2017-07, Vol.62 (7), p.711-715

2017

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Psychometric Properties of the Chinese Version of the Sarcopenia and Quality of Life, a Quality of Life Questionnaire Specific for Sarcopenia

Calcified tissue international, 2021-10, Vol.109 (4), p.415-422

2021

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Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients

Human genomics, 2015-12, Vol.9 (1), p.33-33, Article 33

2015

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A Novel Interferon Regulatory Factor 6 Mutation in an Asian Family with Van der Woude Syndrome

The Cleft palate-craniofacial journal, 2017-07, Vol.54 (4), p.442-445

2017

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De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability

Gene, 2013-03, Vol.517 (1), p.82-88

2013

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A submicroscopic deletion involving part of the CREBBP gene detected by array-CGH in a patient with Rubinstein–Taybi syndrome

Gene, 2012-05, Vol.499 (1), p.182-185

2012

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Piebaldism with multiple café-au-lait–like hyperpigmented macules and inguinal freckling caused by a novel KIT mutation

JAAD Case Reports, 2018-05, Vol.4 (4), p.318-321

2018

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De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus

Molecular cytogenetics, 2013-08, Vol.6 (1), p.31-31

2013

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De novo trisomy 12p in twin girls with different levels of mosaicism

American journal of medical genetics. Part A, 2013-07, Vol.161A (7), p.1702-1705

2013

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An Additional Case of the Recurrent 15q24.1 Microdeletion Syndrome and Review of the Literature

Twin research and human genetics, 2011-08, Vol.14 (4), p.333-339

2011

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Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern

Molecular cytogenetics, 2014-05, Vol.7 (1), p.32-32

2014

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Identification of IRF6 gene variants in three families with Van der Woude syndrome

International journal of molecular medicine, 2008-06, Vol.21 (6), p.747-751

2008

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Host engulfment pathway controls inflammation in inflammatory bowel disease

The FEBS journal, 2020-09, Vol.287 (18), p.3967-3988

2020

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Diarrhoeal pathogenesis in Salmonella infection may result from an imbalance in intestinal epithelial differentiation through reduced Notch signalling

The Journal of physiology, 2022-04, Vol.600 (8), p.1851-1865

2022

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Gender-specific association of insertion/deletion polymorphisms in the nogo gene and chronic schizophrenia

Brain research. Molecular brain research., 2005-10, Vol.139 (2), p.212-216

2005

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Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders

Genetics in medicine, 2019-01, Vol.21 (1), p.207-212

2019

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976 - The Host Engulfment Pathway: A New Cytosolic Sensor of Bacterial Infection and Inflammation

Gastroenterology (New York, N.Y. 1943), 2017-04, Vol.152 (5), p.S183-S183

2017

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The Host Engulfment Pathway: A New Cytosolic Sensor of Bacterial Infection and Inflammation

Gastroenterology (New York, N.Y. 1943), 2017-04, Vol.152 (5), p.S183-S183

2017

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The host engulfment pathway in enteroids is linked to intestinal inflammation following bacterial infection

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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Reduced Expression of Down‐Regulated in Adenoma (DRA) in Murine Enteroid‐Derived Monolayers Following Infection with Salmonella

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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819 - Dysregulation of the Engulfment Pathway in the Gut Epithelium Fuels Inflammatory Bowel Disease

Gastroenterology (New York, N.Y. 1943), 2018-05, Vol.154 (6), p.S-169-S-169

2018

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AB093. Report of a SMARCA4 variant identified in a patient with Coffin-Siris syndrome

Annals of translational medicine, 2017-09, Vol.5 (S2), p.AB093-AB093

2017

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A118G Single Nucleotide Polymorphism of Human μ-Opioid Receptor Gene Influences Pain Perception and Patient-controlled Intravenous Morphine Consumption after Intrathecal Morphine for Postcesarean Analgesia

Ethnicity and OPRM Variant Independently Predict Pain Perception and Patient-Controlled Analgesia Usage for Post-Operative Pain

Influence of Mu-Opioid Receptor Variant on Morphine Use and Self-Rated Pain Following Abdominal Hysterectomy

Intragenic multi-exon deletion in the FBN1 gene in a child with mildly dilated aortic sinus: a retrotransposal event

Psychometric Properties of the Chinese Version of the Sarcopenia and Quality of Life, a Quality of Life Questionnaire Specific for Sarcopenia

Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients

A Novel Interferon Regulatory Factor 6 Mutation in an Asian Family with Van der Woude Syndrome

De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability

A submicroscopic deletion involving part of the CREBBP gene detected by array-CGH in a patient with Rubinstein–Taybi syndrome

Piebaldism with multiple café-au-lait–like hyperpigmented macules and inguinal freckling caused by a novel KIT mutation

De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus

De novo trisomy 12p in twin girls with different levels of mosaicism

An Additional Case of the Recurrent 15q24.1 Microdeletion Syndrome and Review of the Literature

Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern

Identification of IRF6 gene variants in three families with Van der Woude syndrome

Host engulfment pathway controls inflammation in inflammatory bowel disease

Diarrhoeal pathogenesis in Salmonella infection may result from an imbalance in intestinal epithelial differentiation through reduced Notch signalling

Gender-specific association of insertion/deletion polymorphisms in the nogo gene and chronic schizophrenia

Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders

976 - The Host Engulfment Pathway: A New Cytosolic Sensor of Bacterial Infection and Inflammation

The Host Engulfment Pathway: A New Cytosolic Sensor of Bacterial Infection and Inflammation

The host engulfment pathway in enteroids is linked to intestinal inflammation following bacterial infection

Reduced Expression of Down‐Regulated in Adenoma (DRA) in Murine Enteroid‐Derived Monolayers Following Infection with Salmonella

819 - Dysregulation of the Engulfment Pathway in the Gut Epithelium Fuels Inflammatory Bowel Disease

AB093. Report of a SMARCA4 variant identified in a patient with Coffin-Siris syndrome

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