B. McGee

发表

Genetic variants in ADAMTS13 as well as smoking are major determinants of plasma ADAMTS13 levels.

Jun Z. Li, C. Kimchi-Sarfaty, Brian T. Emmer, 2017, Blood advances.

A von Willebrand factor fragment containing the D'D3 domains is sufficient to stabilize coagulation factor VIII in mice.

D. Ginsburg, A. Yee, Robert D. Gildersleeve, 2014, Blood.

THROMBOSIS AND HEMOSTASIS A von Willebrand factor fragment containing the D 9 D 3 domains is suf fi cient to stabilize coagulation factor VIII in mice

D. Ginsburg, A. Yee, Robert D. Gildersleeve, 2014 .

The ER cargo receptor SURF4 facilitates efficient erythropoietin secretion

Brian T. Emmer, A. B. Ozel, K. Desch, 2019, bioRxiv.

pak2a mutations cause cerebral hemorrhage in redhead zebrafish

Julio D Amigo, P. Jagadeeswaran, J. Shavit, 2007, Proceedings of the National Academy of Sciences.

Combined deficiency of factor V and factor VIII is due to mutations in either LMAN1 or MCFD2.

R. Kaufman, D. Ginsburg, Bin Zhang, 2006, Blood.

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

T. Foroud, S. Shurin, J. McClintick, 2001, Nature.

The Endoplasmic Reticulum Cargo Receptor SURF4 Facilitates Efficient Erythropoietin Secretion

Brian T. Emmer, A. B. Ozel, K. Desch, 2020, Molecular and Cellular Biology.

Expression of the blood-group-related glycosyltransferase B4galnt2 influences the intestinal microbiota in mice

F. Bäckhed, S. Künzel, J. Baines, 2012, The ISME Journal.

Selection on cis-Regulatory Variation at B4galnt2 and Its Influence on von Willebrand Factor in House Mice

D. Tautz, P. Pavlidis, J. Baines, 2008, Molecular biology and evolution.

SEC23A rescues SEC23B-deficient congenital dyserythropoietic anemia type II

J. D. Engel, R. Kurita, T. Saunders, 2021, Science advances.

Functions of the COPII gene paralogs SEC23A and SEC23B are interchangeable in vivo

A. Gingras, A. Nesvizhskii, D. Klionsky, 2018, Proceedings of the National Academy of Sciences.

The Function of the COPII Gene Paralogs SEC23A and SEC23B Are Interchangeable In Vivo

A. Gingras, A. Nesvizhskii, D. Klionsky, 2017, bioRxiv.

Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels.

Jun Z. Li, Y. Guan, Hong-Dong Li, 2014, Blood.

either LMAN1 or MCFD2 Combined deficiency of factor V and factor VIII is due to mutations in

R. Kaufman, D. Ginsburg, F. Peyvandi, 2013 .

Genome‐wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance

L. Brody, J. Mills, D. Ginsburg, 2016, Journal of thrombosis and haemostasis : JTH.

Genom e-wide stud ies of von Willebrand Factor Propeptide I dentify Loci Contributing to Variation in Propeptide Levels and von Willebrand Factor

L. Brody, J. Mills, D. Ginsburg, 2016 .

A von Willebrand factor fragment containing the D'D3 domains is sufficient to stabilize coagulation factor VIII in mice.

D. Ginsburg, A. Yee, Robert D. Gildersleeve, 2014, Blood.

Combined deficiency of factor V and factor VIII is due to mutations in either LMAN1 or MCFD2.

R. Kaufman, D. Ginsburg, Bin Zhang, 2006, Blood.