Wei W - Search Results

1

Analysis of MCFD2- and LMAN1-deficient mice demonstrates distinct functions in vivo.

Zhu M, Zheng C, Wei W, Everett L, Ginsburg D, Zhang B. Zhu M, et al. Among authors: wei w. Blood Adv. 2018 May 8;2(9):1014-1021. doi: 10.1182/bloodadvances.2018018317. Blood Adv. 2018. PMID: 29735583 Free PMC article.

2

LMAN1-MCFD2 complex is a cargo receptor for the ER-Golgi transport of α1-antitrypsin.

Zhang Y, Zhu M, Zheng C, Wei W, Emmer BT, Zhang B. Zhang Y, et al. Among authors: wei w. Biochem J. 2022 Apr 14;479(7):839-855. doi: 10.1042/BCJ20220055. Biochem J. 2022. PMID: 35322856 Free PMC article.

3

Missense mutations near the N-glycosylation site of the A2 domain lead to various intracellular trafficking defects in coagulation factor VIII.

Wei W, Zheng C, Zhu M, Zhu X, Yang R, Misra S, Zhang B. Wei W, et al. Sci Rep. 2017 Mar 22;7:45033. doi: 10.1038/srep45033. Sci Rep. 2017. PMID: 28327546 Free PMC article.

4

Molecular mechanisms of missense mutations that generate ectopic N-glycosylation sites in coagulation factor VIII.

Wei W, Misra S, Cannon MV, Yang R, Zhu X, Gilmore R, Zhu M, Zhang B. Wei W, et al. Biochem J. 2018 Mar 6;475(5):873-886. doi: 10.1042/BCJ20170884. Biochem J. 2018. PMID: 29444815 Free PMC article.

5

A common human missense mutation of vesicle coat protein SEC23B leads to growth restriction and chronic pancreatitis in mice.

Wei W, Liu Z, Zhang C, Khoriaty R, Zhu M, Zhang B. Wei W, et al. J Biol Chem. 2022 Jan;298(1):101536. doi: 10.1016/j.jbc.2021.101536. Epub 2021 Dec 24. J Biol Chem. 2022. PMID: 34954140 Free PMC article.

6

Neural tube opening and abnormal extraembryonic membrane development in SEC23A deficient mice.

Zhu M, Tao J, Vasievich MP, Wei W, Zhu G, Khoriaty RN, Zhang B. Zhu M, et al. Among authors: wei w. Sci Rep. 2015 Oct 23;5:15471. doi: 10.1038/srep15471. Sci Rep. 2015. PMID: 26494538 Free PMC article.

7

Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer.

Yehia L, Niazi F, Ni Y, Ngeow J, Sankunny M, Liu Z, Wei W, Mester JL, Keri RA, Zhang B, Eng C. Yehia L, et al. Among authors: wei w. Am J Hum Genet. 2015 Nov 5;97(5):661-76. doi: 10.1016/j.ajhg.2015.10.001. Epub 2015 Oct 29. Am J Hum Genet. 2015. PMID: 26522472 Free PMC article.

8

Factor VIII and vWF deficiency in STT3A-CDG.

Chang IJ, Byers HM, Ng BG, Merritt JL 2nd, Gilmore R, Shrimal S, Wei W, Zhang Y, Blair AB, Freeze HH, Zhang B, Lam C. Chang IJ, et al. Among authors: wei w. J Inherit Metab Dis. 2019 Mar;42(2):325-332. doi: 10.1002/jimd.12021. Epub 2019 Jan 30. J Inherit Metab Dis. 2019. PMID: 30701557 Free PMC article.

9

Allosteric activation of PP2A inhibits experimental abdominal aortic aneurysm.

Zhou X, Zhang C, Xie F, Wei W, Li R, Xu Q, Wang Y, Klenotic PA, Narla G, Dong N, Lin Z. Zhou X, et al. Among authors: wei w. Clin Sci (Lond). 2021 Sep 17;135(17):2085-2097. doi: 10.1042/CS20210315. Clin Sci (Lond). 2021. PMID: 34402501 Free PMC article.

10

CALR mutation screening in pediatric primary myelofibrosis.

An W, Wan Y, Guo Y, Chen X, Ren Y, Zhang J, Chang L, Wei W, Zhang P, Zhu X. An W, et al. Among authors: wei w. Pediatr Blood Cancer. 2014 Dec;61(12):2256-62. doi: 10.1002/pbc.25211. Epub 2014 Aug 30. Pediatr Blood Cancer. 2014. PMID: 25176567

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

13,600 results

Search Page

Filters