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S Shackleton

Showing results (11-20 of 19) with videos related to

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Human Mutation|January 1, 1994
Identification of rare and novel mutations in the CFTR genes of CF patients in southern EnglandS Shackleton, J Hull, S Dear, et al.
The British Journal of Dermatology|April 27, 2007
Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literatureJ Mazereeuw-Hautier, L C Wilson, S Mohammed, et al.
Journal of Medical Genetics|June 7, 2005
Compound heterozygous ZMPSTE24 mutations reduce prelamin A processing and result in a severe progeroid phenotypeS Shackleton, D T Smallwood, P Clayton, et al.
Journal of Science Education and Technology|May 21, 2019
Learning Neuroscience with Technology: A Scaffolded, Active Learning ApproachKatrina B Schleisman, S Selcen Guzey, Richard Lie, et al.
Frontiers in Neuroscience|September 13, 2024
Ergogenic effects of spinal cord stimulation on exercise performance following spinal cord injuryDaniel D Hodgkiss, Alison M M Williams, Claire S Shackleton, et al.
Nature Genetics|February 2, 2000
LMNA, encoding lamin A/C, is mutated in partial lipodystrophyS Shackleton, D J Lloyd, S N Jackson, et al.
Diabetes|November 15, 2000
Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophyC Vigouroux, J Magré, M C Vantyghem, et al.
Nature Communications|May 12, 2025
<sup>81</sup>Kr dating of 1 kg Antarctic iceF Ritterbusch, J S Wang, X Feng, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 2025
Miocene and Pliocene ice and air from the Allan Hills blue ice area, East AntarcticaS Shackleton, V Hishamunda, L Davidge, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Human Mutation|January 1, 1994
Identification of rare and novel mutations in the CFTR genes of CF patients in southern EnglandS Shackleton, J Hull, S Dear, et al.
The British Journal of Dermatology|April 27, 2007
Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literatureJ Mazereeuw-Hautier, L C Wilson, S Mohammed, et al.
Journal of Medical Genetics|June 7, 2005
Compound heterozygous ZMPSTE24 mutations reduce prelamin A processing and result in a severe progeroid phenotypeS Shackleton, D T Smallwood, P Clayton, et al.
Journal of Science Education and Technology|May 21, 2019
Learning Neuroscience with Technology: A Scaffolded, Active Learning ApproachKatrina B Schleisman, S Selcen Guzey, Richard Lie, et al.
Frontiers in Neuroscience|September 13, 2024
Ergogenic effects of spinal cord stimulation on exercise performance following spinal cord injuryDaniel D Hodgkiss, Alison M M Williams, Claire S Shackleton, et al.
Nature Genetics|February 2, 2000
LMNA, encoding lamin A/C, is mutated in partial lipodystrophyS Shackleton, D J Lloyd, S N Jackson, et al.
Diabetes|November 15, 2000
Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophyC Vigouroux, J Magré, M C Vantyghem, et al.
Nature Communications|May 12, 2025
<sup>81</sup>Kr dating of 1 kg Antarctic iceF Ritterbusch, J S Wang, X Feng, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 2025
Miocene and Pliocene ice and air from the Allan Hills blue ice area, East AntarcticaS Shackleton, V Hishamunda, L Davidge, et al.
Pageof 2