Literature DB >> 17725672

A novel point mutation in the gene encoding capillary morphogenesis protein 2 in a Japanese patient with juvenile hyaline fibromatosis.

A Hatamochi1, T Sasaki, T Kawaguchi, H Suzuki, S Yamazaki.   

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Year:  2007        PMID： 17725672     DOI： 10.1111/j.1365-2133.2007.08147.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  4 in total

1.  Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading system.

Authors:  Rafael Denadai; Cassio E Raposo-Amaral; Débora Bertola; Chong Kim; Nivaldo Alonso; Thomas Hart; Sangwoo Han; Rafael F Stelini; Celso L Buzzo; Cesar A Raposo-Amaral; P Suzanne Hart
Journal:  Am J Med Genet A       Date:  2012-03-01       Impact factor: 2.802

2.  Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome.

Authors:  Zahraa Haidar; Ramzi Temanni; Eliane Chouery; Puthen Jithesh; Wei Liu; Rashid Al-Ali; Ena Wang; Francesco M Marincola; Nadine Jalkh; Soha Haddad; Wassim Haidar; Lotfi Chouchane; André Mégarbané
Journal:  BMC Genet       Date:  2017-01-19       Impact factor: 2.797

3.  Capillary morphogenesis gene 2 regulates adhesion and invasiveness of prostate cancer cells.

Authors:  Lin Ye; Andrew J Sanders; Ping-Hui Sun; Malcolm D Mason; Wen G Jiang
Journal:  Oncol Lett       Date:  2014-04-04       Impact factor: 2.967

4.  Infantile systemic hyalinosis: Variable grades of severity.

Authors:  Ali Al Kaissi; Marwa Hilmi; Zulfiya Betadolova; Sami Bouchoucha; Svetlana Trofimova; Mohammad Shboul; Guseyn Rustamov; Wiam Dwera; Katharina Sigl; Vladimir Kenis; Susanne Gerit Kircher
Journal:  Afr J Paediatr Surg       Date:  2021 Oct-Dec
  4 in total

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