Search Results - "Hodges, Craig"
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Oocyte-Specific Differences in Cell-Cycle Control Create an Innate Susceptibility to Meiotic Errors
Published in Current biology (26-04-2011)“…Segregation of homologs at the first meiotic division (MI) is facilitated by crossovers and by a physical constraint imposed on sister kinetochores that…”
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2
Lung SORT LNPs enable precise homology-directed repair mediated CRISPR/Cas genome correction in cystic fibrosis models
Published in Nature communications (11-11-2023)“…Approximately 10% of Cystic Fibrosis (CF) patients, particularly those with CF transmembrane conductance regulator ( CFTR ) gene nonsense mutations, lack…”
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3
Neutrophil-mediated phagocytic host defense defect in myeloid Cftr-inactivated mice
Published in PloS one (03-09-2014)“…Cystic fibrosis (CF) is a common and deadly inherited disease, caused by mutations in the CFTR gene that encodes a cAMP-activated chloride channel. One…”
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4
Synergy between Readthrough and Nonsense Mediated Decay Inhibition in a Murine Model of Cystic Fibrosis Nonsense Mutations
Published in International journal of molecular sciences (31-12-2020)“…Many heritable genetic disorders arise from nonsense mutations, which generate premature termination codons (PTCs) in transcribed mRNA. PTCs ablate protein…”
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5
Dynamic expression of long noncoding RNAs reveals their potential roles in spermatogenesis and fertility
Published in Biology of reproduction (01-08-2017)“…Mammalian reproduction requires that males and females produce functional haploid germ cells through complex cellular differentiation processes known as…”
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6
Delivering on the promise of gene editing for cystic fibrosis
Published in Genes & diseases (01-06-2019)“…In this review, we describe a path for translation of gene editing into therapy for cystic fibrosis (CF). Cystic fibrosis results from mutations in the CFTR…”
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7
Impaired intestinal free fatty acid transport followed by chylomicron malformation, not pancreatic insufficiency, cause metabolic defects in cystic fibrosis
Published in Journal of lipid research (01-07-2024)“…Intestinal disease is one of the earliest manifestations of cystic fibrosis (CF) in children and is closely tied to deficits in growth and nutrition, both of…”
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Lysophosphatidic Acid Increases Maturation of Brush Borders and SGLT1 Activity in MYO5B-deficient Mice, a Model of Microvillus Inclusion Disease
Published in Gastroenterology (New York, N.Y. 1943) (01-10-2020)“…Myosin VB (MYO5B) is an essential trafficking protein for membrane recycling in gastrointestinal epithelial cells. The inactivating mutations of MYO5B cause…”
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Moving beyond genetics: is FAM13A a major biological contributor in lung physiology and chronic lung diseases?
Published in Journal of medical genetics (01-10-2014)“…Variants in FAM13A have been found in genome-wide association studies (GWAS) to associate with lung function in the general population as well as in several…”
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10
HDAC6 depletion improves cystic fibrosis mouse airway responses to bacterial challenge
Published in Scientific reports (16-07-2019)“…The hypothesis of this study was that Hdac6 depletion would restore cystic fibrosis (CF) responses to bacterial challenge to more wild type profiles using a CF…”
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A G542X cystic fibrosis mouse model for examining nonsense mutation directed therapies
Published in PloS one (20-06-2018)“…Nonsense mutations are present in 10% of patients with CF, produce a premature termination codon in CFTR mRNA causing early termination of translation, and…”
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12
Growth deficits in cystic fibrosis mice begin in utero prior to IGF-1 reduction
Published in PloS one (06-04-2017)“…Growth deficits are common in cystic fibrosis (CF), but their cause is complex, with contributions from exocrine pancreatic insufficiency, pulmonary…”
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13
In vivo editing of lung stem cells for durable gene correction in mice
Published in Science (American Association for the Advancement of Science) (14-06-2024)“…In vivo genome correction holds promise for generating durable disease cures; yet, effective stem cell editing remains challenging. In this work, we…”
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14
Parasympathetic Innervation Regulates Tubulogenesis in the Developing Salivary Gland
Published in Developmental cell (25-08-2014)“…A fundamental question in development is how cells assemble to form a tubular network during organ formation. In glandular organs, tubulogenesis is a multistep…”
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15
Bone Marrow Transplantation Rescues Monocyte Recruitment Defect and Improves Cystic Fibrosis in Mice
Published in The Journal of immunology (1950) (01-02-2022)“…Cystic fibrosis (CF) is an inherited life-threatening disease accompanied by repeated lung infections and multiorgan inflammation that affects tens of…”
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16
Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency
Published in Human molecular genetics (01-06-2018)“…Abstract Primary ovarian insufficiency (POI) is characterized by amenorrhea and loss or dysfunction of ovarian follicles prior to the age of 40. POI has been…”
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17
Linaclotide improves gastrointestinal transit in cystic fibrosis mice by inhibiting sodium/hydrogen exchanger 3
Published in American journal of physiology: Gastrointestinal and liver physiology (01-11-2018)“…Gastrointestinal dysfunction in cystic fibrosis (CF) is a prominent source of pain among patients with CF. Linaclotide, a guanylate cyclase C (GCC) receptor…”
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The Burkholderia cenocepacia Type VI Secretion System Effector TecA Is a Virulence Factor in Mouse Models of Lung Infection
Published in mBio (26-10-2021)“…Burkholderia cenocepacia is a member of the Burkholderia cepacia complex (Bcc), a group of bacteria with members responsible for causing lung infections in…”
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Consuming Genistein Improves Survival Rates in the Absence of Laxative in ΔF508-CF Female Mice
Published in Nutrients (03-10-2018)“…Genistein is a naturally occurring isoflavone found in soy. Genistein has been shown to increase the open probability of the most common cystic fibrosis (CF)…”
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Enhancing Cystic Fibrosis Immune Regulation
Published in Frontiers in pharmacology (13-05-2021)“…In cystic fibrosis (CF), sustained infection and exuberant inflammation results in debilitating and often fatal lung disease. Advancement in CF therapeutics…”
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