Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 49

1.

Spontaneous Irs1 passenger mutation linked to a gene-targeted SerpinB2 allele.

Westrick RJ, Mohlke KL, Korepta LM, Yang AY, Zhu G, Manning SL, Winn ME, Dougherty KM, Ginsburg D.

Proc Natl Acad Sci U S A. 2010 Sep 28;107(39):16904-9. doi: 10.1073/pnas.1012050107. Epub 2010 Sep 13.

2.

Molecular basis of LMAN1 in coordinating LMAN1-MCFD2 cargo receptor formation and ER-to-Golgi transport of FV/FVIII.

Zheng C, Liu HH, Yuan S, Zhou J, Zhang B.

Blood. 2010 Dec 16;116(25):5698-706. doi: 10.1182/blood-2010-04-278325. Epub 2010 Sep 3.

3.

Protein sorting receptors in the early secretory pathway.

Dancourt J, Barlowe C.

Annu Rev Biochem. 2010;79:777-802. doi: 10.1146/annurev-biochem-061608-091319. Review.

PMID:
20533886
4.

Molecular analysis in two Tunisian families with combined factor V and factor VIII deficiency.

Abdallah HE, Gouider E, Amor MB, Jlizi A, Meddeb B, Elgaaied A.

Haemophilia. 2010 Sep 1;16(5):801-4. doi: 10.1111/j.1365-2516.2010.02268.x. Epub 2010 May 19.

PMID:
20491958
5.

Structural basis for the cooperative interplay between the two causative gene products of combined factor V and factor VIII deficiency.

Nishio M, Kamiya Y, Mizushima T, Wakatsuki S, Sasakawa H, Yamamoto K, Uchiyama S, Noda M, McKay AR, Fukui K, Hauri HP, Kato K.

Proc Natl Acad Sci U S A. 2010 Mar 2;107(9):4034-9. doi: 10.1073/pnas.0908526107. Epub 2010 Feb 8.

6.

Crystal structure of the LMAN1-CRD/MCFD2 transport receptor complex provides insight into combined deficiency of factor V and factor VIII.

Wigren E, Bourhis JM, Kursula I, Guy JE, Lindqvist Y.

FEBS Lett. 2010 Mar 5;584(5):878-82. doi: 10.1016/j.febslet.2010.02.009. Epub 2010 Feb 9.

7.

ERp44 and ERGIC-53 synergize in coupling efficiency and fidelity of IgM polymerization and secretion.

Cortini M, Sitia R.

Traffic. 2010 May;11(5):651-9. doi: 10.1111/j.1600-0854.2010.01043.x.

8.

EF-hand domains of MCFD2 mediate interactions with both LMAN1 and coagulation factor V or VIII.

Zheng C, Liu HH, Zhou J, Zhang B.

Blood. 2010 Feb 4;115(5):1081-7. doi: 10.1182/blood-2009-09-241877. Epub 2009 Dec 9.

9.

Sec24b selectively sorts Vangl2 to regulate planar cell polarity during neural tube closure.

Merte J, Jensen D, Wright K, Sarsfield S, Wang Y, Schekman R, Ginty DD.

Nat Cell Biol. 2010 Jan;12(1):41-6; sup pp 1-8. doi: 10.1038/ncb2002. Epub 2009 Dec 6.

10.

A novel missense mutation causing abnormal LMAN1 in a Japanese patient with combined deficiency of factor V and factor VIII.

Yamada T, Fujimori Y, Suzuki A, Miyawaki Y, Takagi A, Murate T, Sano M, Matsushita T, Saito H, Kojima T.

Am J Hematol. 2009 Nov;84(11):738-42. doi: 10.1002/ajh.21532.

11.

Genotype-phenotype correlation in combined deficiency of factor V and factor VIII.

Zhang B, Spreafico M, Zheng C, Yang A, Platzer P, Callaghan MU, Avci Z, Ozbek N, Mahlangu J, Haw T, Kaufman RJ, Marchant K, Tuddenham EG, Seligsohn U, Peyvandi F, Ginsburg D.

Blood. 2008 Jun 15;111(12):5592-600. doi: 10.1182/blood-2007-10-113951. Epub 2008 Apr 7.

12.

Identification of ERGIC-53 as an intracellular transport receptor of alpha1-antitrypsin.

Nyfeler B, Reiterer V, Wendeler MW, Stefan E, Zhang B, Michnick SW, Hauri HP.

J Cell Biol. 2008 Feb 25;180(4):705-12. doi: 10.1083/jcb.200709100. Epub 2008 Feb 18.

13.

That which does not kill me makes me stronger: adapting to chronic ER stress.

Rutkowski DT, Kaufman RJ.

Trends Biochem Sci. 2007 Oct;32(10):469-76.

PMID:
17920280
14.

Sequential steps and checkpoints in the early exocytic compartment during secretory IgM biogenesis.

Anelli T, Ceppi S, Bergamelli L, Cortini M, Masciarelli S, Valetti C, Sitia R.

EMBO J. 2007 Oct 3;26(19):4177-88. Epub 2007 Sep 6.

15.

Receptor-mediated protein transport in the early secretory pathway.

Baines AC, Zhang B.

Trends Biochem Sci. 2007 Aug;32(8):381-8. Epub 2007 Jul 6. Review.

PMID:
17618120
16.

Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India.

Jayandharan G, Spreafico M, Viswabandya A, Chandy M, Srivastava A, Peyvandi F.

Haemophilia. 2007 Jul;13(4):413-9.

PMID:
17610559
17.

Cargo selectivity of the ERGIC-53/MCFD2 transport receptor complex.

Nyfeler B, Zhang B, Ginsburg D, Kaufman RJ, Hauri HP.

Traffic. 2006 Nov;7(11):1473-81. Epub 2006 Oct 1.

18.

Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking.

Boyadjiev SA, Fromme JC, Ben J, Chong SS, Nauta C, Hur DJ, Zhang G, Hamamoto S, Schekman R, Ravazzola M, Orci L, Eyaid W.

Nat Genet. 2006 Oct;38(10):1192-7. Epub 2006 Sep 17.

PMID:
16980979
19.

ER storage diseases: a role for ERGIC-53 in controlling the formation and shape of Russell bodies.

Mattioli L, Anelli T, Fagioli C, Tacchetti C, Sitia R, Valetti C.

J Cell Sci. 2006 Jun 15;119(Pt 12):2532-41. Epub 2006 May 30.

20.

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

Zhang B, McGee B, Yamaoka JS, Guglielmone H, Downes KA, Minoldo S, Jarchum G, Peyvandi F, de Bosch NB, Ruiz-Saez A, Chatelain B, Olpinski M, Bockenstedt P, Sperl W, Kaufman RJ, Nichols WC, Tuddenham EG, Ginsburg D.

Blood. 2006 Mar 1;107(5):1903-7. Epub 2005 Nov 22.

Supplemental Content

Support Center