W. Ip

发表

K. Du, H. Yeger, C. Bear, 2014, Chemistry & biology.

Evidence for a Causal Relationship Between Early Exocrine Pancreatic Disease and Cystic Fibrosis–Related Diabetes: A Mendelian Randomization Study

Melissa R. Miller, J. Rommens, L. Strug, 2014, Diabetes.

Impact of Protein Deprivation on Protein and DNA Synthesis in the Developing Rat Pancreas

P. Durie, W. Ip, S. Beharry, 1998, Neonatology.

Is fibrosing colonopathy an immune mediated disease?

W. Ip, Julia Lee, P. Durie, 1997, Archives of disease in childhood.

Endoplasmic reticulum stress is involved in the colonic epithelium damage induced by maternal separation.

Bo Li, B. Li, T. Gonska, 2016, Journal of pediatric surgery.

Orkambi® and amplifier co‐therapy improves function from a rare CFTR mutation in gene‐edited cells and patient tissue

K. Du, R. Pomès, P. Ray, 2017, EMBO molecular medicine.

Shwachman syndrome: phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar.

M. Corey, J. Rommens, L. Heitlinger, 1999, The Journal of pediatrics.

Phenotypic profiling of CFTR modulators in patient-derived respiratory epithelia

J. Rommens, J. Rossant, J. Forman-Kay, 2017, npj Genomic Medicine.

ORKAMBI-Mediated Rescue of Mucociliary Clearance in Cystic Fibrosis Primary Respiratory Cultures Is Enhanced by Arginine Uptake, Arginase Inhibition, and Promotion of Nitric Oxide Signaling to the Cystic Fibrosis Transmembrane Conductance Regulator Channel

C. Bear, T. Moraes, T. Gonska, 2019, Molecular Pharmacology.

Intestinal epithelial tight junctions and permeability can be rescued through the regulation of endoplasmic reticulum stress by amniotic fluid stem cells during necrotizing enterocolitis

Bo Li, T. Gonska, Carol Lee, 2021, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Evidence of a Generalized Defect of Acinar Cell Function in Shwachman-Diamond Syndrome

J. Rommens, P. Durie, M. Stormon, 2010, Journal of pediatric gastroenterology and nutrition.

Magnetic resonance imaging findings of the pancreas in patients with Shwachman-Diamond syndrome and mutations in the SBDS gene.

O. Mäkitie, E. Savilahti, P. Durie, 2008, The Journal of pediatrics.

Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics

J. Rommens, P. Böelle, L. Strug, 2016, Human molecular genetics.

Testing gene therapy vectors in human primary nasal epithelial cultures

Jing Wu, K. Du, H. Yeger, 2015, Molecular therapy. Methods & clinical development.

Breast cancer in a case of Shwachman Diamond syndrome

J. Rommens, A. Shimamura, J. Lipton, 2012, Pediatric blood & cancer.

Structural variation and missense mutation in SBDS associated with Shwachman-Diamond syndrome

David R. Murdock, J. Lupski, R. Gibbs, 2014, BMC Medical Genetics.

Early maternal separation induces alterations of colonic epithelial permeability and morphology

Bo Li, T. Gonska, Carol Lee, 2014, Pediatric Surgery International.

CFTR interactome mapping using the mammalian membrane two‐hybrid high‐throughput screening system

Hugo M. Botelho, I. Jurisica, M. Babu, 2022, Molecular systems biology.

Serum pancreatic enzymes define the pancreatic phenotype in patients with Shwachman-Diamond syndrome.

M. Corey, J. Rommens, P. Durie, 2002, The Journal of pediatrics.

Preclinical Studies of a Rare CF-Causing Mutation in the Second Nucleotide Binding Domain (c.3700A>G) Show Robust Functional Rescue in Primary Nasal Cultures by Novel CFTR Modulators

C. Bear, T. Moraes, T. Gonska, 2020, Journal of personalized medicine.

β-adrenergic sweat secretion as a diagnostic test for cystic fibrosis.

P. Quinton, D. Conrad, E. Tullis, 2012, American journal of respiratory and critical care medicine.

Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurements.

M. Corey, L. Tsui, J. Zieleński, 1998, The Journal of pediatrics.

Inhibition of corticotropin-releasing hormone receptor 1 and activation of receptor 2 protect against colonic injury and promote epithelium repair

Bo Li, T. Gonska, Carol Lee, 2017, Scientific Reports.

Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis

J. Rommens, L. Strug, C. Bear, 2023, Life Science Alliance.

Phenotypic profiling of CFTR modulators in patient-derived respiratory epithelia

J. Rommens, J. Rossant, J. Forman-Kay, 2017, npj Genomic Medicine.

Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics.

J. Rommens, P. Böelle, L. Strug, 2016, Human molecular genetics.

Augmentation of CFTR function in human bronchial epithelial cells via SLC6A14-dependent amino acid uptake: Implications for treatment of Cystic Fibrosis.

K. Du, J. Forman-Kay, C. Bear, 2019, American journal of respiratory cell and molecular biology.

Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis

P. Quinton, T. Gonska, P. Durie, 2009, Thorax.

Exocrine Pancreatic Alterations in Long-Lived Surviving Cystic Fibrosis Mice

M. Corey, P. Durie, W. Ip, 1996, Pediatric Research.

Evidence For a Causal Relationship Between Early Exocrine Pancreatic Disease and Cystic Fibrosis-Related Diabetes: A Mendelian Randomization Study Short Title: Interplay of Morbidities in the CF Pancreas

Melissa R. Miller, J. Rommens, L. Strug, 2014 .

SERUM PANCREATIC ENZYMES IN PATIENTS WITH SHWACHMAN‐DIAMOND SYNDROME

J. Rommens, P. Durie, W. Ip, 1999, Journal of Pediatric Gastroenterology and Nutrition.

WS14.6 Beta-adrenergic sweat secretion rate as accurate biomarker for CFTR function

P. Quinton, D. Conrad, E. Tullis, 2012 .