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Cited by 78

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Divergent matrix-remodeling strategies distinguish developmental from neoplastic mammary epithelial cell invasion programs.

Feinberg, Tamar Y., Zheng, Huarui, Liu, Rui, Wicha, Max S., Yu, S. Michael, Weiss, Stephen J.·2018·Developmental Cell
DOI 10.1016/j.devcel.2018.08.025PMC PMC6317358
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  • The cytoplasmic tail of MT1-MMP plays an important role in endocytosis of MT1-MMP and the localization of MT1-MMP on specific microdomains in the plasma membrane.

    “The cytoplasmic tail of MT1-MMP plays an important role in endocytosis of MT1-MMP and the localization of MT1-MMP on the specific microdomains in the plasma membrane (19, 23–25).”

    From Identification of amino acid residues in the MT-loop of MT1-MMP critical for its ability to cleave low-density lipoprotein receptor (2022) · cites this paper as [25]

    The Results and Discussion passages address MT1-MMP’s role in collagen remodeling and mammary invasion, not the function of its cytoplasmic tail. Searches for “cytoplasmic tail,” “endocytosis,” and “microdomains” found no passage in our copy connecting the tail to endocytosis or localization at plasma-membrane microdomains; page numbers were unavailable. (LLM, conf=0.76)

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Research works printed but not linked: 50

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Metadata

Authors
Feinberg, T. Y., Zheng, H., Liu, R., Wicha, M. S., Yu, S. M., & Weiss, S. J.
Venue
Developmental Cell
Publisher
Elsevier BV
Published
2018-10
Volume
47
Issue
2
Pages
145-160.e6
ISSN
1534-5807
DOI
10.1016/j.devcel.2018.08.025
PMC
PMC6317358
Cited by
78
References
1
Language
en
Licence
Funders
  • NIH (RO1AR060484)
  • NIDDK
  • University of Utah
  • University of Michigan
  • NCI (CA071699)
  • DOD (W81XWH-12-1-0555)
  • Breast Cancer Research Foundation
  • University of Michigan Rogel Cancer Center Support (P30 CA046592)

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