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Seth J Field

Showing results (31-40 of 35) with videos related to

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Cell|October 20, 2009
GOLPH3 bridges phosphatidylinositol-4- phosphate and actomyosin to stretch and shape the Golgi to promote buddingHolly C Dippold, Michelle M Ng, Suzette E Farber-Katz, et al.
Cancer Cell|June 14, 2011
Receptor tyrosine kinases and TLR/IL1Rs unexpectedly activate myeloid cell PI3kγ, a single convergent point promoting tumor inflammation and progressionMichael C Schmid, Christie J Avraamides, Holly C Dippold, et al.
Cell|July 16, 2003
The PHD finger of the chromatin-associated protein ING2 functions as a nuclear phosphoinositide receptorOr Gozani, Philip Karuman, David R Jones, et al.
Nature Genetics|August 12, 2009
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathiesStephanie L Bielas, Jennifer L Silhavy, Francesco Brancati, et al.
Nature Genetics|April 8, 2015
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunctionNaiara Akizu, Vincent Cantagrel, Maha S Zaki, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Cell|October 20, 2009
GOLPH3 bridges phosphatidylinositol-4- phosphate and actomyosin to stretch and shape the Golgi to promote buddingHolly C Dippold, Michelle M Ng, Suzette E Farber-Katz, et al.
Cancer Cell|June 14, 2011
Receptor tyrosine kinases and TLR/IL1Rs unexpectedly activate myeloid cell PI3kγ, a single convergent point promoting tumor inflammation and progressionMichael C Schmid, Christie J Avraamides, Holly C Dippold, et al.
Cell|July 16, 2003
The PHD finger of the chromatin-associated protein ING2 functions as a nuclear phosphoinositide receptorOr Gozani, Philip Karuman, David R Jones, et al.
Nature Genetics|August 12, 2009
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathiesStephanie L Bielas, Jennifer L Silhavy, Francesco Brancati, et al.
Nature Genetics|April 8, 2015
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunctionNaiara Akizu, Vincent Cantagrel, Maha S Zaki, et al.
Pageof 4