Literature DB >> 12920580

Analysis of MYH Tyr165Cys and Gly382Asp variants in childhood leukemias.

Cemaliye Boylu Akyerli1, Uğur Ozbek, Müge Aydin-Sayitoğlu, Sema Sirma, Tayfun Ozçelik.   

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Year:  2003        PMID： 12920580     DOI： 10.1007/s00432-003-0483-1

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN： 0171-5216            Impact factor:   4.553


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  9 in total

1.  A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots.

Authors:  Darcy Whiteside; Ross McLeod; Gail Graham; Jamie L Steckley; Karen Booth; Martin J Somerville; Susan E Andrew
Journal:  Cancer Res       Date:  2002-01-15       Impact factor: 12.701

2.  MutY catalytic core, mutant and bound adenine structures define specificity for DNA repair enzyme superfamily.

Authors:  Y Guan; R C Manuel; A S Arvai; S S Parikh; C D Mol; J H Miller; S Lloyd; J A Tainer
Journal:  Nat Struct Biol       Date:  1998-12

Review 3.  Deficient DNA mismatch repair: a common etiologic factor for colon cancer.

Authors:  P Peltomäki
Journal:  Hum Mol Genet       Date:  2001-04       Impact factor: 6.150

4.  Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors.

Authors:  Nada Al-Tassan; Nikolas H Chmiel; Julie Maynard; Nick Fleming; Alison L Livingston; Geraint T Williams; Angela K Hodges; D Rhodri Davies; Sheila S David; Julian R Sampson; Jeremy P Cheadle
Journal:  Nat Genet       Date:  2002-01-30       Impact factor: 38.330

Review 5.  Report of the National Cancer Institute-sponsored workshop on definitions of diagnosis and response in acute myeloid leukemia.

Authors:  B D Cheson; P A Cassileth; D R Head; C A Schiffer; J M Bennett; C D Bloomfield; R Brunning; R P Gale; M R Grever; M J Keating
Journal:  J Clin Oncol       Date:  1990-05       Impact factor: 44.544

Review 6.  The genetics of familial leukemia.

Authors:  M Horwitz
Journal:  Leukemia       Date:  1997-08       Impact factor: 11.528

7.  Neurofibromatosis and early onset of cancers in hMLH1-deficient children.

Authors:  Q Wang; C Lasset; F Desseigne; D Frappaz; C Bergeron; C Navarro; E Ruano; A Puisieux
Journal:  Cancer Res       Date:  1999-01-15       Impact factor: 12.701

8.  Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1.

Authors:  M D Ricciardone; T Ozçelik; B Cevher; H Ozdağ; M Tuncer; A Gürgey; O Uzunalimoğlu; H Cetinkaya; A Tanyeli; E Erken; M Oztürk
Journal:  Cancer Res       Date:  1999-01-15       Impact factor: 12.701

9.  Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations.

Authors:  Siân Jones; Paul Emmerson; Julie Maynard; Jacqueline M Best; Sheila Jordan; Geraint T Williams; Julian R Sampson; Jeremy P Cheadle
Journal:  Hum Mol Genet       Date:  2002-11-01       Impact factor: 6.150
  9 in total
  2 in total

1.  MYH Y165C and G382D mutations in hepatocellular carcinoma and cholangiocarcinoma patients.

Authors:  Linnea M Baudhuin; Lewis R Roberts; Felicity T B Enders; Russell L Swanson; Teresa A Mettler; Ileana Aderca; Linda M Stadheim; W Edward Highsmith
Journal:  J Cancer Res Clin Oncol       Date:  2005-11-15       Impact factor: 4.553

2.  Whole exome sequencing of pediatric leukemia reveals a novel InDel within FLT-3 gene in AML patient from Mizo tribal population, Northeast India.

Authors:  Andrew Vanlallawma; Doris Lallawmzuali; Jeremy L Pautu; Vinod Scaria; Sridhar Sivasubbu; Nachimuthu Senthil Kumar
Journal:  BMC Genom Data       Date:  2022-03-28
  2 in total

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