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Showing results 801 - 810 for weill cornell connect patient portal

Intraperitoneal in vivo gene therapy to deliver alpha 1-antitrypsin to

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https://geneticmedicine.weill.cornell.edu/publications/intraperitoneal-vivo-gene-therapy-deliver-alpha-1-antitrypsin-systemic-circulation

Intrapleural Gene Therapy for Alpha-1 Antitrypsin Deficiency-Related

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https://geneticmedicine.weill.cornell.edu/publications/intrapleural-gene-therapy-alpha-1-antitrypsin-deficiency-related-lung-disease

Emphysema mediated by lung overexpression of ADAM10. | Genetic

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https://geneticmedicine.weill.cornell.edu/publications/emphysema-mediated-lung-overexpression-adam10

The promoter of the human cystic fibrosis transmembrane conductance

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https://geneticmedicine.weill.cornell.edu/publications/promoter-human-cystic-fibrosis-transmembrane-conductance-regulator-gene-directing-sv40-t-antigen

Nerve growth factor-induced neuronal differentiation requires

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https://geneticmedicine.weill.cornell.edu/publications/nerve-growth-factor-induced-neuronal-differentiation-requires-generation-rac1-regulated-reactive

Modulation of tropoelastin production and elastin messenger

...Skip to main content About Us About Us The Department of Genetic Medicine at Weill Cornell leads...

https://geneticmedicine.weill.cornell.edu/publications/modulation-tropoelastin-production-and-elastin-messenger-ribonucleic-acid-activity-developing-sheep

A mutation in CFTR produces different phenotypes depending on

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https://geneticmedicine.weill.cornell.edu/publications/mutation-cftr-produces-different-phenotypes-depending-chromosomal-background

Normal alveolar epithelial lining fluid contains high levels of

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https://geneticmedicine.weill.cornell.edu/publications/normal-alveolar-epithelial-lining-fluid-contains-high-levels-glutathione

Noggin regulation of bone morphogenetic protein (BMP) 2/7 heterodimer

...Skip to main content About Us About Us The Department of Genetic Medicine at Weill Cornell leads...

https://geneticmedicine.weill.cornell.edu/publications/noggin-regulation-bone-morphogenetic-protein-bmp-27-heterodimer-activity-vitro

Gene therapy for metachromatic leukodystrophy. | Genetic Medicine

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https://geneticmedicine.weill.cornell.edu/publications/gene-therapy-metachromatic-leukodystrophy

Showing results 801 - 810 for weill cornell connect patient portal