Literature DB >> 19373522

Definite diagnosis in Japanese patients with protein C deficiency by identification of causative PROC mutations.

Akira Takagi1,2, Ryoko Tanaka1, Daisuke Nakashima1, Yuta Fujimori1, Takayuki Yamada1, Kaoru Okumura1, Takashi Murate1,2, Midori Yamada3, Yasuo Horikoshi4, Koji Yamamoto5, Akira Katsumi6, Tadashi Matsushita6, Tomoki Naoe6, Tetsuhito Kojima7,8.   

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Year:  2009        PMID： 19373522     DOI： 10.1007/s12185-009-0312-7

Source DB:  PubMed          Journal:  Int J Hematol        ISSN： 0925-5710            Impact factor:   2.490


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  14 in total

1.  Compound heterozygosity for two novel mutations in a severe factor XI deficiency.

Authors:  Akiko Tsukahara; Takayuki Yamada; Akira Takagi; Takashi Murate; Tadashi Matsushita; Hidehiko Saito; Tetsuhito Kojima
Journal:  Am J Hematol       Date:  2003-08       Impact factor: 10.047

2.  Recurrent mutations of factor XI gene in Japanese.

Authors:  Kaoru Okumura; Mayu Kyotani; Reiko Kawai; Akira Takagi; Takashi Murate; Koji Yamamoto; Junki Takamatsu; Tadashi Matsushita; Hidehiko Saito; Tetsuhito Kojima
Journal:  Int J Hematol       Date:  2006-06       Impact factor: 2.490

3.  A neonate with homozygous protein C deficiency with a homozygous Arg178Trp mutation.

Authors:  Ferda Ozlu; Mayu Kyotani; Erdal Taskin; Kenan Ozcan; Tetsuhito Kojima; Tadashi Matsushita; Hacer Yapicioğlu; Akira Takagi; Ilgen Saşmaz; Mehmet Satar; Nejat Narli
Journal:  J Pediatr Hematol Oncol       Date:  2008-08       Impact factor: 1.289

Review 4.  Advances in understanding pathogenic mechanisms of thrombophilic disorders.

Authors:  Björn Dahlbäck
Journal:  Blood       Date:  2008-07-01       Impact factor: 22.113

Review 5.  Protein C deficiency: a database of mutations, 1995 update. On behalf of the Subcommittee on Plasma Coagulation Inhibitors of the Scientific and Standardization Committee of the ISTH.

Authors:  P H Reitsma; F Bernardi; R G Doig; S Gandrille; J S Greengard; H Ireland; M Krawczak; B Lind; G L Long; S R Poort
Journal:  Thromb Haemost       Date:  1995-05       Impact factor: 5.249

Review 6.  Protein-C: biochemistry, physiology, and clinical implications.

Authors:  C T Esmon
Journal:  Blood       Date:  1983-12       Impact factor: 22.113

7.  Genetic analysis of protein C deficiency in nineteen Japanese families: five recurrent defects can explain half of the deficiencies.

Authors:  T Miyata; T Sakata; Y Yasumuro; T Okamura; A Katsumi; H Saito; T Abe; A Shirahata; M Sakai; H Kato
Journal:  Thromb Res       Date:  1998-11-15       Impact factor: 3.944

8.  Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency.

Authors:  K Yamamoto; M Tanimoto; N Emi; T Matsushita; J Takamatsu; H Saito
Journal:  J Clin Invest       Date:  1992-12       Impact factor: 14.808

9.  The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects.

Authors:  P H Reitsma; S R Poort; C F Allaart; E Briët; R M Bertina
Journal:  Blood       Date:  1991-08-15       Impact factor: 22.113

10.  Prevalence of protein C deficiency in the healthy population.

Authors:  R C Tait; I D Walker; P H Reitsma; S I Islam; F McCall; S R Poort; J A Conkie; R M Bertina
Journal:  Thromb Haemost       Date:  1995-01       Impact factor: 5.249
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  1 in total

1.  Congenital protein C deficiency and thrombosis in a dog.

Authors:  Darren Kelly; Florence Juvet; Gary Moore
Journal:  J Vet Intern Med       Date:  2020-04-11       Impact factor: 3.333
  1 in total

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