Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Paul Litman"'
Publikováno v:
Journal of Circadian Rhythms, Vol 17, Iss 1 (2019)
Cystic fibrosis (CF) is autosomal recessive disease that affects multiple body systems. CF patients often experience sleep disturbances, altered sleep patterns, and sleep apnea. Sleep in mammals is controlled in part by circadian clock genes, includi
Externí odkaz:
https://doaj.org/article/08796973e9b547d7b5526e1c214bea39
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Scientific Reports
Scientific Reports
Cystic fibrosis (CF) is an autosomal recessive disease caused by dysfunctional cystic fibrosis transmembrane conductance regulator (CFTR) protein, and is marked by an accumulation of mucus in affected airways resulting in persistent infection and chr
Autor:
Paul Litman, Niraj B Desai, Christine Horvat Davey, Rebecca J. Darrah, Allison R. Webel, Joachim G. Voss, Chao-Pin Hsiao, Ashwini R. Sehgal, Federico Perez
Publikováno v:
Western Journal of Nursing Research. 42:1042-1049
Fatigue is a prevalent symptom associated with decreased quality of life and increased mortality in individuals with end stage renal disease (ESRD), yet causes of fatigue in individuals with ESRD remain poorly understood. We examined gene expression
Autor:
Paul Litman, Christine Horvat Davey, Richard Josephson, Rebecca J. Darrah, Vitor H F Oliveira, Allison R. Webel, Chris T. Longenecker, Marianne Vest, Trevor Jenkins, Jackson Currie
Publikováno v:
J Assoc Nurses AIDS Care
People living with HIV (PLHIV) experience high rates of fatigue which can be improved with physical activity. We examined the relationship between HIV infection, fatigue, cardiorespiratory fitness, physical activity, and myokines. Twenty HIV-positive
Publikováno v:
Biol Res Nurs
Introduction: Cystic fibrosis (CF) is an autosomal recessive disease that affects many organ systems, most notably the pulmonary and gastrointestinal systems. Through genome-wide association studies, multiple genetic regions modifying CF-related pulm
Publikováno v:
Journal of Circadian Rhythms
Journal of Circadian Rhythms, Vol 17, Iss 1 (2019)
Journal of Circadian Rhythms; Vol 17 (2019); 2
Journal of Circadian Rhythms, Vol 17, Iss 1 (2019)
Journal of Circadian Rhythms; Vol 17 (2019); 2
Cystic fibrosis (CF) is autosomal recessive disease that affects multiple body systems. CF patients often experience sleep disturbances, altered sleep patterns, and sleep apnea. Sleep in mammals is controlled in part by circadian clock genes, includi
Autor:
Garry R. Cutting, David E. Nethery, Mitchell L. Drumm, Eric Barbato, Neha Joshi, Paul Litman, Cara Campanaro, Abdus Sattar, Rebecca J. Darrah, Michael R. Knowles, Frank J. Jacono, Lisa J. Strug, Craig A. Hodges, Anna L. Mitchell, Harriet Corvol, Jennifer Frey
Publikováno v:
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis, 2019, 18 (1), pp.127-134. ⟨10.1016/j.jcf.2018.05.013⟩
Journal of Cystic Fibrosis, Elsevier, 2019, 18 (1), pp.127-134. ⟨10.1016/j.jcf.2018.05.013⟩
Journal of Cystic Fibrosis, 2019, 18 (1), pp.127-134. ⟨10.1016/j.jcf.2018.05.013⟩
Journal of Cystic Fibrosis, Elsevier, 2019, 18 (1), pp.127-134. ⟨10.1016/j.jcf.2018.05.013⟩
International audience; BACKGROUND: Pulmonary disease remains the primary cause of morbidity and mortality for individuals with cystic fibrosis (CF). Variants at a locus on the X-chromosome containing the type 2 angiotensin II receptor gene (AGTR2) w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4164aed56a6f38eab59d091222ea319
https://hal.sorbonne-universite.fr/hal-02041563
https://hal.sorbonne-universite.fr/hal-02041563
Autor:
Paul Litman, LiPuma Jj, Tracey L. Bonfield, Rebecca J. Darrah, Craig A. Hodges, Mitchell L. Drumm, Frank J. Jacono
Publikováno v:
Journal of Infectious Pulmonary Diseases. 3
Chronic pulmonary disease and infection is the primary cause of morbidity and mortality in people with cystic fibrosis (CF). Though Pseudomonas aeruginosa, is most commonly found in the airways of individuals with CF, there is increasing appreciation
Publikováno v:
American Journal of Physiology-Cell Physiology. 305:C133-C146
Mice deficient in Na-K-2Cl cotransporter (NKCC1) have been generated by targeted disruption of the gene encoding NKCC1 involving the carboxy terminus (CT-NKCC1) but not the amino terminus. We hypothesize that the resulting physiological defects are d
Autor:
Mitchell L. Drumm, Anna L. Mitchell, Paul Litman, Frank J. Jacono, Craig A. Hodges, Eric Barbato, Cara Campanaro, Abdus Sattar, Rebecca J. Darrah
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 15(6)
Background Altered pulmonary function is present early in the course of cystic fibrosis (CF), independent of documented infections or onset of pulmonary symptoms. New initiatives in clinical care are focusing on detection and characterization of prec