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Oocyte-Specific Differences in Cell-Cycle Control Create an Innate Susceptibility to Meiotic Errors

Current biology, 2011-04, Vol.21 (8), p.651-657

2011

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Synergy between Readthrough and Nonsense Mediated Decay Inhibition in a Murine Model of Cystic Fibrosis Nonsense Mutations

International journal of molecular sciences, 2020-12, Vol.22 (1), p.344

2020

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Lung SORT LNPs enable precise homology-directed repair mediated CRISPR/Cas genome correction in cystic fibrosis models

Nature communications, 2023-11, Vol.14 (1), p.7322-7322, Article 7322

2023

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Delivering on the promise of gene editing for cystic fibrosis

Genes & diseases, 2019-06, Vol.6 (2), p.97-108

2019

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Impaired intestinal free fatty acid transport followed by chylomicron malformation, not pancreatic insufficiency, cause metabolic defects in cystic fibrosis

Journal of lipid research, 2024-07, Vol.65 (7), p.100551, Article 100551

2024

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Neutrophil-mediated phagocytic host defense defect in myeloid Cftr-inactivated mice

PloS one, 2014-09, Vol.9 (9), p.e106813

2014

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A G542X cystic fibrosis mouse model for examining nonsense mutation directed therapies

PloS one, 2018-06, Vol.13 (6), p.e0199573-e0199573

2018

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The Burkholderia cenocepacia Type VI Secretion System Effector TecA Is a Virulence Factor in Mouse Models of Lung Infection

mBio, 2021-10, Vol.12 (5), p.e0209821-e0209821

2021

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Growth deficits in cystic fibrosis mice begin in utero prior to IGF-1 reduction

PloS one, 2017-04, Vol.12 (4), p.e0175467-e0175467

2017

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Linaclotide improves gastrointestinal transit in cystic fibrosis mice by inhibiting sodium/hydrogen exchanger 3

American journal of physiology: Gastrointestinal and liver physiology, 2018-11, Vol.315 (5), p.G868-G878

2018

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Enhancing Cystic Fibrosis Immune Regulation

Frontiers in pharmacology, 2021-05, Vol.12, p.573065-573065

2021

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Improved Growth Patterns in Cystic Fibrosis Mice after Loss of Histone Deacetylase 6

Scientific reports, 2017-06, Vol.7 (1), p.3676-11, Article 3676

2017

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Consuming Genistein Improves Survival Rates in the Absence of Laxative in ΔF508-CF Female Mice

Nutrients, 2018-10, Vol.10 (10), p.1418

2018

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Early pulmonary disease manifestations in cystic fibrosis mice

Journal of cystic fibrosis, 2016-11, Vol.15 (6), p.736-744

2016

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Voltage-gated potassium channel proteins and stereoselective S-nitroso-l-cysteine signaling

JCI insight, 2020-09, Vol.5 (18)

2020

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Dynamic expression of long noncoding RNAs reveals their potential roles in spermatogenesis and fertility

Biology of reproduction, 2017-08, Vol.97 (2), p.313-323

2017

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Lysophosphatidic Acid Increases Maturation of Brush Borders and SGLT1 Activity in MYO5B-deficient Mice, a Model of Microvillus Inclusion Disease

Gastroenterology (New York, N.Y. 1943), 2020-10, Vol.159 (4), p.1390-1405.e20

2020

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HDAC6 depletion improves cystic fibrosis mouse airway responses to bacterial challenge

Scientific reports, 2019-07, Vol.9 (1), p.10282-11, Article 10282

2019

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Chromosomal Influence on Meiotic Spindle Assembly: Abnormal Meiosis I in Female Mlh1 Mutant Mice

The Journal of cell biology, 1999-06, Vol.145 (7), p.1395-1406

1999

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Bone Marrow Transplantation Rescues Monocyte Recruitment Defect and Improves Cystic Fibrosis in Mice

The Journal of immunology (1950), 2022-02, Vol.208 (3), p.745-752

2022

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Moving beyond genetics: is FAM13A a major biological contributor in lung physiology and chronic lung diseases?

Journal of Medical Genetics, 2014-10, Vol.51 (10), p.646-649

2014

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Simultaneous analysis of chromosomes and chromosome-associated proteins in mammalian oocytes and embryos

Chromosoma, 2002-09, Vol.111 (3), p.165-169

2002

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In vivo editing of lung stem cells for durable gene correction in mice

Science (American Association for the Advancement of Science), 2024-06, Vol.384 (6701), p.1196-1202

2024

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Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency

Human molecular genetics, 2018-06, Vol.27 (11), p.1913-1926

2018

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SMC1β-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction

Nature genetics, 2005-12, Vol.37 (12), p.1351-1355

2005

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Oocyte-Specific Differences in Cell-Cycle Control Create an Innate Susceptibility to Meiotic Errors

Synergy between Readthrough and Nonsense Mediated Decay Inhibition in a Murine Model of Cystic Fibrosis Nonsense Mutations

Lung SORT LNPs enable precise homology-directed repair mediated CRISPR/Cas genome correction in cystic fibrosis models

Delivering on the promise of gene editing for cystic fibrosis

Impaired intestinal free fatty acid transport followed by chylomicron malformation, not pancreatic insufficiency, cause metabolic defects in cystic fibrosis

Neutrophil-mediated phagocytic host defense defect in myeloid Cftr-inactivated mice

A G542X cystic fibrosis mouse model for examining nonsense mutation directed therapies

The Burkholderia cenocepacia Type VI Secretion System Effector TecA Is a Virulence Factor in Mouse Models of Lung Infection

Growth deficits in cystic fibrosis mice begin in utero prior to IGF-1 reduction

Linaclotide improves gastrointestinal transit in cystic fibrosis mice by inhibiting sodium/hydrogen exchanger 3

Enhancing Cystic Fibrosis Immune Regulation

Improved Growth Patterns in Cystic Fibrosis Mice after Loss of Histone Deacetylase 6

Consuming Genistein Improves Survival Rates in the Absence of Laxative in ΔF508-CF Female Mice

Early pulmonary disease manifestations in cystic fibrosis mice

Voltage-gated potassium channel proteins and stereoselective S-nitroso-l-cysteine signaling

Dynamic expression of long noncoding RNAs reveals their potential roles in spermatogenesis and fertility

Lysophosphatidic Acid Increases Maturation of Brush Borders and SGLT1 Activity in MYO5B-deficient Mice, a Model of Microvillus Inclusion Disease

HDAC6 depletion improves cystic fibrosis mouse airway responses to bacterial challenge

Chromosomal Influence on Meiotic Spindle Assembly: Abnormal Meiosis I in Female Mlh1 Mutant Mice

Bone Marrow Transplantation Rescues Monocyte Recruitment Defect and Improves Cystic Fibrosis in Mice

Moving beyond genetics: is FAM13A a major biological contributor in lung physiology and chronic lung diseases?

Simultaneous analysis of chromosomes and chromosome-associated proteins in mammalian oocytes and embryos

In vivo editing of lung stem cells for durable gene correction in mice

Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency

SMC1β-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction

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