Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mark Arnholt"'
Autor:
Alisha Hoefs, Madeleine Herro, Diane H. Munzenmaier, Abigail Hawkins, Lilly Betts, Farren Powers, Brooke Sill, Mark Arnholt
Publikováno v:
The FASEB Journal. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0721536822882d067910dcde6c37732
https://doi.org/10.1096/fasebj.2019.33.1_supplement.lb319
https://doi.org/10.1096/fasebj.2019.33.1_supplement.lb319
Autor:
Mark Arnholt, Margaret Colwell, Theodore Colwell, Evelyn Anderson, Cara Kennedy, Cassidy Benson, Rachel Zuern, Delaney Hennes, Emma Witt, Diane H. Munzenmaier, Tate Stoeckmann, Julia Brown, Gabriel Hoffmann, Lauren Hautala, Michael Flanagan, Leah Lisowski
Publikováno v:
The FASEB Journal. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ff8ad4b6bf97831015c77c39d560bdd
https://doi.org/10.1096/fasebj.2019.33.1_supplement.lb297
https://doi.org/10.1096/fasebj.2019.33.1_supplement.lb297
Autor:
F. Rrahmani, S. Schmitt, J. Spudich, M. Cina, B. Lane, C. Kennedy, A. O'Bryon, A. Downing, E. Witt, K. Tadlock, Mark T. McNally, M. Bohn, L. Hautala, M. Tomashek, J. Pepin, Mark Arnholt, S. Staus, A. Jaeke, Michael Flanagan, E. Rohloff
Publikováno v:
The FASEB Journal. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ee10b035c10308fdf24ca575470bf87
https://doi.org/10.1096/fasebj.2018.32.1_supplement.lb203
https://doi.org/10.1096/fasebj.2018.32.1_supplement.lb203
Autor:
C Wilkins, L Krupski, J Bade, A Kellicut, J Killoren, L Semler, C Czerniak, Mark Arnholt, S Daley, Melissa Wilk
Publikováno v:
The FASEB Journal. 29
The average person's eyes adapt to darkness within minutes. For those with Oguchi's disease, adaptation can be slowed to several hours. Oguchi disease is an autosomal recessive disorder that results in greatly slowed phototransduction. Phototransduct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e155f32d942ae745aef0317ccf3a79bc
https://doi.org/10.1096/fasebj.29.1_supplement.lb63
https://doi.org/10.1096/fasebj.29.1_supplement.lb63
Autor:
Mark Arnholt, Gabrielle Rigden, Jessica Griesmer, Kayla Erickson, Megan Heimermann, Brandy Lewandowski, Mary Daley, Olivia Hoffman, Mark T. McNally, Julia Loosen
Publikováno v:
The FASEB Journal. 28
Spinal muscular atrophy (SMA) is a genetic disorder leading to death before age two. This is caused by degeneration of motor neurons in the spine and affects one in six thousand babies yearly (Fami...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72677b8db5a11a253edc2c46a1cf2d89
https://doi.org/10.1096/fasebj.28.1_supplement.lb94
https://doi.org/10.1096/fasebj.28.1_supplement.lb94