- Home
- Publications
- Publication Search
- Publication Details
Title
The COPII pathway and hematologic disease
Authors
Keywords
-
Journal
BLOOD
Volume 120, Issue 1, Pages 31-38
Publisher
American Society of Hematology
Online
2012-05-15
DOI
10.1182/blood-2012-01-292086
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1 localization in erythroblasts
- (2011) R. Renella et al. BLOOD
- Mice deficient in LMAN1 exhibit FV and FVIII deficiencies and liver accumulation of 1-antitrypsin
- (2011) B. Zhang et al. BLOOD
- Congenital dyserythropoietic anemias
- (2011) Achille Iolascon et al. CURRENT OPINION IN HEMATOLOGY
- The feelgood mutation in zebrafish dysregulates COPII-dependent secretion of select extracellular matrix proteins in skeletal morphogenesis
- (2011) D. B. Melville et al. Disease Models & Mechanisms
- Mendelian Disorders of Membrane Trafficking
- (2011) Maria Antonietta De Matteis et al. NEW ENGLAND JOURNAL OF MEDICINE
- Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene
- (2010) Roberta Russo et al. AMERICAN JOURNAL OF HEMATOLOGY
- Molecular basis of LMAN1 in coordinating LMAN1-MCFD2 cargo receptor formation and ER-to-Golgi transport of FV/FVIII
- (2010) C. Zheng et al. BLOOD
- Cranio-lenticulo-sutural dysplasia associated with defects in collagen secretion
- (2010) SA Boyadjiev et al. CLINICAL GENETICS
- Planar cell polarity defects and defective Vangl2 trafficking in mutants for the COPII gene Sec24b
- (2010) C. Wansleeben et al. DEVELOPMENT
- Crystal structure of the LMAN1-CRD/MCFD2 transport receptor complex provides insight into combined deficiency of factor V and factor VIII
- (2010) Edvard Wigren et al. FEBS LETTERS
- Sec24D-Dependent Transport of Extracellular Matrix Proteins Is Required for Zebrafish Skeletal Morphogenesis
- (2010) Swapnalee Sarmah et al. PLoS One
- Structural basis for the cooperative interplay between the two causative gene products of combined factor V and factor VIII deficiency
- (2010) M. Nishio et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- EF-hand domains of MCFD2 mediate interactions with both LMAN1 and coagulation factor V or VIII
- (2009) C. Zheng et al. BLOOD
- Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship
- (2009) A. Iolascon et al. HAEMATOLOGICA
- A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis
- (2009) A. Iolascon et al. HAEMATOLOGICA
- The Congenital Dyserythropoietic Anemias
- (2009) Raffaele Renella et al. HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA
- Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in theSEC23Bgene
- (2009) Paola Bianchi et al. HUMAN MUTATION
- Sec24b selectively sorts Vangl2 to regulate planar cell polarity during neural tube closure
- (2009) Janna Merte et al. NATURE CELL BIOLOGY
- Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II
- (2009) Klaus Schwarz et al. NATURE GENETICS
- Combined Factor V and Factor VIII Deficiency
- (2009) Marta Spreafico et al. SEMINARS IN THROMBOSIS AND HEMOSTASIS
- Genotype-phenotype correlation in combined deficiency of factor V and factor VIII
- (2008) B. Zhang et al. BLOOD
- Identification of ERGIC-53 as an intracellular transport receptor of α1-antitrypsin
- (2008) Beat Nyfeler et al. JOURNAL OF CELL BIOLOGY
- New Insights into Multiple Coagulation Factor Deficiency from the Solution Structure of Human MCFD2
- (2008) Jodie E. Guy et al. JOURNAL OF MOLECULAR BIOLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started