217 related articles for article (PubMed ID: 25071156)
1. Absence of a red blood cell phenotype in mice with hematopoietic deficiency of SEC23B.
Khoriaty R; Vasievich MP; Jones M; Everett L; Chase J; Tao J; Siemieniak D; Zhang B; Maillard I; Ginsburg D
Mol Cell Biol; 2014 Oct; 34(19):3721-34. PubMed ID: 25071156
[TBL] [Abstract][Full Text] [Related]
2. Functions of the COPII gene paralogs SEC23A and SEC23B are interchangeable in vivo.
Khoriaty R; Hesketh GG; Bernard A; Weyand AC; Mellacheruvu D; Zhu G; Hoenerhoff MJ; McGee B; Everett L; Adams EJ; Zhang B; Saunders TL; Nesvizhskii AI; Klionsky DJ; Shavit JA; Gingras AC; Ginsburg D
Proc Natl Acad Sci U S A; 2018 Aug; 115(33):E7748-E7757. PubMed ID: 30065114
[TBL] [Abstract][Full Text] [Related]
3. Pancreatic SEC23B deficiency is sufficient to explain the perinatal lethality of germline SEC23B deficiency in mice.
Khoriaty R; Everett L; Chase J; Zhu G; Hoenerhoff M; McKnight B; Vasievich MP; Zhang B; Tomberg K; Williams J; Maillard I; Ginsburg D
Sci Rep; 2016 Jun; 6():27802. PubMed ID: 27297878
[TBL] [Abstract][Full Text] [Related]
4. Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.
Schwarz K; Iolascon A; Verissimo F; Trede NS; Horsley W; Chen W; Paw BH; Hopfner KP; Holzmann K; Russo R; Esposito MR; Spano D; De Falco L; Heinrich K; Joggerst B; Rojewski MT; Perrotta S; Denecke J; Pannicke U; Delaunay J; Pepperkok R; Heimpel H
Nat Genet; 2009 Aug; 41(8):936-40. PubMed ID: 19561605
[TBL] [Abstract][Full Text] [Related]
5. Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.
Bianchi P; Fermo E; Vercellati C; Boschetti C; Barcellini W; Iurlo A; Marcello AP; Righetti PG; Zanella A
Hum Mutat; 2009 Sep; 30(9):1292-8. PubMed ID: 19621418
[TBL] [Abstract][Full Text] [Related]
6. SEC23A rescues SEC23B-deficient congenital dyserythropoietic anemia type II.
King R; Lin Z; Balbin-Cuesta G; Myers G; Friedman A; Zhu G; McGee B; Saunders TL; Kurita R; Nakamura Y; Engel JD; Reddy P; Khoriaty R
Sci Adv; 2021 Nov; 7(48):eabj5293. PubMed ID: 34818036
[TBL] [Abstract][Full Text] [Related]
7. Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B gene.
Punzo F; Bertoli-Avella AM; Scianguetta S; Della Ragione F; Casale M; Ronzoni L; Cappellini MD; Forni G; Oostra BA; Perrotta S
Orphanet J Rare Dis; 2011 Dec; 6():89. PubMed ID: 22208203
[TBL] [Abstract][Full Text] [Related]
8. Characteristic phenotypes associated with congenital dyserythropoietic anemia (type II) manifest at different stages of erythropoiesis.
Satchwell TJ; Pellegrin S; Bianchi P; Hawley BR; Gampel A; Mordue KE; Budnik A; Fermo E; Barcellini W; Stephens DJ; van den Akker E; Toye AM
Haematologica; 2013 Nov; 98(11):1788-96. PubMed ID: 23935019
[TBL] [Abstract][Full Text] [Related]
9. SEC23B is required for the maintenance of murine professional secretory tissues.
Tao J; Zhu M; Wang H; Afelik S; Vasievich MP; Chen XW; Zhu G; Jensen J; Ginsburg D; Zhang B
Proc Natl Acad Sci U S A; 2012 Jul; 109(29):E2001-9. PubMed ID: 22745161
[TBL] [Abstract][Full Text] [Related]
10. 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
J Biol Chem; 2022 Jan; 298(1):101536. PubMed ID: 34954140
[TBL] [Abstract][Full Text] [Related]
11. SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells.
Rosato BE; Marra R; D'Onofrio V; Del Giudice F; Della Monica S; Iolascon A; Andolfo I; Russo R
Int J Mol Sci; 2022 Jan; 23(3):. PubMed ID: 35163229
[TBL] [Abstract][Full Text] [Related]
12. The COPII pathway and hematologic disease.
Khoriaty R; Vasievich MP; Ginsburg D
Blood; 2012 Jul; 120(1):31-8. PubMed ID: 22586181
[TBL] [Abstract][Full Text] [Related]
13. RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway.
De Rosa G; Andolfo I; Marra R; Manna F; Rosato BE; Iolascon A; Russo R
Int J Mol Sci; 2020 Aug; 21(15):. PubMed ID: 32759740
[TBL] [Abstract][Full Text] [Related]
14. ER-to-Golgi transport and SEC23-dependent COPII vesicles regulate T cell alloimmunity.
Kim S; Khoriaty R; Li L; McClune M; Kalfa TA; Wu J; Peltier D; Fujiwara H; Sun Y; Oravecz-Wilson K; King RA; Ginsburg D; Reddy P
J Clin Invest; 2021 Jan; 131(2):. PubMed ID: 33463537
[TBL] [Abstract][Full Text] [Related]
15. 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
Am J Hum Genet; 2015 Nov; 97(5):661-76. PubMed ID: 26522472
[TBL] [Abstract][Full Text] [Related]
16. New Cases and Mutations in
Musri MM; Venturi V; Ferrer-Cortès X; Romero-Cortadellas L; Hernández G; Leoz P; Ricard Andrés MP; Morado M; Fernández Valle MDC; Beneitez Pastor D; Ortuño Cabrero A; Moreno Gamiz M; Senent Peris L; Perez-Valencia AI; Pérez-Montero S; Tornador C; Sánchez M
Int J Mol Sci; 2023 Jun; 24(12):. PubMed ID: 37373084
[TBL] [Abstract][Full Text] [Related]
17. Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II.
Russo R; Langella C; Esposito MR; Gambale A; Vitiello F; Vallefuoco F; Ek T; Yang E; Iolascon A
Blood Cells Mol Dis; 2013 Jun; 51(1):17-21. PubMed ID: 23453696
[TBL] [Abstract][Full Text] [Related]
18. Non-canonical role of wild-type SEC23B in the cellular stress response pathway.
Yehia L; Liu D; Fu S; Iyer P; Eng C
Cell Death Dis; 2021 Mar; 12(4):304. PubMed ID: 33753724
[TBL] [Abstract][Full Text] [Related]
19. The congenital dyserythropoieitic anemias: genetics and pathophysiology.
King R; Gallagher PJ; Khoriaty R
Curr Opin Hematol; 2022 May; 29(3):126-136. PubMed ID: 35441598
[TBL] [Abstract][Full Text] [Related]
20. Congenital dyserythropoietic anemia, type II with SEC23B exon 12 c.1385 A → G mutation, and pseudo-Gaucher cells in two siblings.
Sharma P; Das R; Bansal D; Trehan A
Hematology; 2015 Mar; 20(2):104-7. PubMed ID: 24801240
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]