Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: ST14[original query] |
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St 14 (DX S52) VNTR polymorphism in the Indian population and its application in carrier detection and prenatal diagnosis of haemophilia A families. Haematologia 2000 30 (3): 203-7. Shetty S, Ghosh K, Mohanty |
Carrier detection and prenatal diagnosis in families with haemophilia. The National medical journal of India 0 14 (2): 81-3. Shetty S, Ghosh K, Bhide A, Mohanty |
Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism--Indian experience. Annals of hematology 2003 Jul 82 (7): 427-30. Chowdhury M R, Tiwari M, Kabra M, Menon P S |
Identification of new dinucleotide-repeat polymorphisms in factor VIII gene using fluorescent PCR. Haemophilia : the official journal of the World Federation of Hemophilia 2005 Jan 11 (1): 38-42. Kim J-W, Park S-Y, Kim Y-M, Kim J-M, Kim D-J, Ryu H |
Allele frequencies of three factor VIII gene polymorphisms in Iranian populations and their application in hemophilia A carrier detection. American journal of hematology 2006 May 81 (5): 335-9. Azimifar S Babak, Seyedna S Yoosef, Zeinali Siro |
The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families. Haemophilia : the official journal of the World Federation of Hemophilia 2008 Jun . Hussein IR, El-Beshlawy A, Salem A, Mosaad R, Zaghloul N, Ragab L, Fayek H, Gaber K, El-Ekiabi M |
ST14 gene variant and decreased matriptase protein expression predict poor breast cancer survival. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2010 Sep 19 (9): 2133-42. Kauppinen Jaana M, Kosma Veli-Matti, Soini Ylermi, Sironen Reijo, Nissinen Minna, Nykopp Timo K, Kärjä Vesa, Eskelinen Matti, Kataja Vesa, Mannermaa Ar |
A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome. Orphanet journal of rare diseases 2017 12 12 (1): 176. Youssefian Leila, Touati Andrew, Saeidian Amir Hossein, Zargari Omid, Zeinali Sirous, Vahidnezhad Hassan, Uitto Jou |
Mutant cytoskeletal and ECM peptides sensitive to the ST14 protease are associated with a worse outcome for glioblastoma multiforme. Biochemical and biophysical research communications 2018 6 503 (4): 2218-2225. Zaman Saif, Chobrutskiy Boris I, Patel Jay S, Callahan Blake M, Tong Wei Lue, Blanck Geor |
Prevalence and Subtype Distribution of Blastocystis sp. in Senegalese School Children. Microorganisms 2020 9 8 (9): . Khaled Salma, Gantois Nausicaa, Ly Amadou Tidjani, Senghor Simon, Even Gaël, Dautel Ellena, Dejager Romane, Sawant Manasi, Baydoun Martha, Benamrouz-Vanneste Sadia, Chabé Magali, Ndiaye Seynabou, Schacht Anne-Marie, Certad Gabriela, Riveau Gilles, Viscogliosi Er |
Clinical and molecular characteristics of autosomal recessive congenital ichthyosis in Thailand. Pediatric dermatology 2022 Oct . Supsrisunjai Chavalit, Bunnag Thareena, Chaowalit Prapaipit, Boonpuen Niorn, Kootiratrakarn Tanawatt, Wessagowit Vesar |
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- Page last updated:Apr 22, 2024
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