Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 130

1.

Confirmation of inherited protein S deficiency by PROS1 mutational screening: Identification of three novel PROS1 mutations and haplotype analysis of p.Q279X recurrence.

Hurtado B, Abasolo N, Domènech-Santasusana P, Fuentes-Prior P, García de Frutos P, Sala N.

Thromb Haemost. 2008 Oct;100(4):721-4. No abstract available.

PMID:
18841302
2.

Characterization and structural impact of five novel PROS1 mutations in eleven protein S-deficient families.

Andersen BD, Bisgaard ML, Lind B, Philips M, Villoutreix B, Thorsen S.

Thromb Haemost. 2001 Dec;86(6):1392-9.

PMID:
11776305
3.

Co-segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1.

Lanke E, Johansson AM, Hillarp A, Lethagen S, Zöller B, Dahlbäck B, Halldén C.

J Thromb Haemost. 2004 Nov;2(11):1918-23.

4.
5.

Identification of eight point mutations in protein S deficiency type I--analysis of 15 pedigrees.

Gómez E, Poort SR, Bertina RM, Reitsma PH.

Thromb Haemost. 1995 May;73(5):750-5.

PMID:
7482398
6.

Large deletions of the PROS1 gene in a large fraction of mutation-negative patients with protein S deficiency.

Johansson AM, Hillarp A, Säll T, Zöller B, Dahlbäck B, Halldén C.

Thromb Haemost. 2005 Nov;94(5):951-7.

PMID:
16363235
7.

Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement.

Alhenc Gelas M, Juin F, de Raucourt E, Gandrille S, Borgel D, Aiach M.

Thromb Haemost. 2007 Apr;97(4):678-80. No abstract available.

PMID:
17393035
8.

Identification of a novel PROS1 c.1113T-->GG frameshift mutation in a family with mixed type I/type III protein S deficiency.

ten Kate MK, Mulder R, Platteel M, Brouwer JL, van der Steege G, van der Meer J.

Haematologica. 2006 Aug;91(8):1151-2.

9.
10.
12.

One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.

Mizukami K, Nakabayashi T, Naitoh S, Takeda M, Tarumi T, Mizoguchi I, Ieko M, Koike T.

Am J Hematol. 2006 Oct;81(10):787-97.

13.

Functional characterization of twelve natural PROS1 mutations associated with anticoagulant protein S deficiency.

Hurtado B, Muñoz X, Mulero MC, Navarro G, Domènech P, García de Frutos P, Pérez-Riba M, Sala N.

Haematologica. 2008 Apr;93(4):574-80. doi: 10.3324/haematol.12090. Epub 2008 Mar 5.

14.

Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency.

Espinosa-Parrilla Y, Morell M, Souto JC, Tirado I, Fontcuberta J, Estivill X, Sala N.

Hum Mutat. 1999;14(1):30-9.

PMID:
10447256
15.

Compound heterozygous mutations in the PROS1 gene responsible for quantitative and qualitative protein S deficiency.

Yamanouchi J, Hato T, Tamura T, Fujiwara H, Yakushijin Y, Yasukawa M.

Int J Hematol. 2009 Nov;90(4):537-9. doi: 10.1007/s12185-009-0430-2. Epub 2009 Oct 14. No abstract available.

PMID:
19826897
16.

Analysis for heterozygosity of protein S mRNA: application to genetic screening and family studies in hereditary protein S deficiency.

Yamazaki T, Hamaguchi M, Takamatsu J, Okamoto Y, Katsumi A, Kagami K, Sugiura I, Kojima T, Saito H.

Int J Hematol. 1996 Aug;64(2):119-25.

PMID:
8854569
17.

DNA sequence analysis of protein S deficiency--identification of four point mutations in twelve Japanese subjects.

Iwaki T, Mastushita T, Kobayashi T, Yamamoto Y, Nomura Y, Kagami K, Nakayama T, Sugiura I, Kojima T, Takamatsu J, Kanayama N, Saito H.

Semin Thromb Hemost. 2001;27(2):155-60.

PMID:
11372770
18.

Molecular basis of protein S deficiency.

García de Frutos P, Fuentes-Prior P, Hurtado B, Sala N.

Thromb Haemost. 2007 Sep;98(3):543-56. Review.

PMID:
17849042
19.

A quantitative protein S deficiency associated with a novel nonsense mutation and markedly reduced levels of mutated mRNA.

Yamazaki T, Hamaguchi M, Katsumi A, Kagami K, Kojima T, Takamatsu J, Saito H.

Thromb Haemost. 1995 Aug;74(2):590-5.

PMID:
8584989
20.

Genotype and laboratory and clinical phenotypes of protein s deficiency.

Duebgen S, Kauke T, Marschall C, Giebl A, Lison S, Hart C, Dick A, Spannagl M.

Am J Clin Pathol. 2012 Feb;137(2):178-84. doi: 10.1309/AJCP40UXNBTXGKUX.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk