Literature DB >> 33037655

Frameshift variations in the RHD coding sequence: Molecular mechanisms permitting protein expression.

Willy A Flegel1, Kshitij Srivastava1.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2020        PMID： 33037655      PMCID： PMC9066700          DOI： 10.1111/trf.16123

Source DB:  PubMed          Journal:  Transfusion        ISSN： 0041-1132            Impact factor:   3.337


× No keyword cloud information.
  85 in total

1.  Weak D caused by a founder deletion in the RHD gene.

Authors:  Yann Fichou; Jian-Min Chen; Cédric Le Maréchal; Déborah Jamet; Isabelle Dupont; Claude Chuteau; Cécile Durousseau; Marie-Jeanne Loirat; Pascal Bailly; Claude Férec
Journal:  Transfusion       Date:  2012-03-15       Impact factor: 3.157

2.  Blood group antibodies and their significance in transfusion medicine.

Authors:  Joyce Poole; Geoff Daniels
Journal:  Transfus Med Rev       Date:  2007-01

3.  Primary myelofibrosis: when the clone manifests with Rh phenotype splitting.

Authors:  Nicoletta Orlando; Rossana Putzulu; Eugenia Rosa Nuzzolo; Maddalena Maresca; Giuseppina Massini; Sara Capodimonti; Gina Zini; Luciana Teofili
Journal:  Ann Hematol       Date:  2013-10-23       Impact factor: 3.673

4.  Mechanism of escape from nonsense-mediated mRNA decay of human beta-globin transcripts with nonsense mutations in the first exon.

Authors:  Gabriele Neu-Yilik; Beate Amthor; Niels H Gehring; Sharif Bahri; Helena Paidassi; Matthias W Hentze; Andreas E Kulozik
Journal:  RNA       Date:  2011-03-09       Impact factor: 4.942

5.  Extensive functional analyses of RHD splice site variants: Insights into the potential role of splicing in the physiology of Rh.

Authors:  Yann Fichou; Pierre Gehannin; Manon Corre; Alice Le Guern; Cédric Le Maréchal; Gérald Le Gac; Claude Férec
Journal:  Transfusion       Date:  2015-03-21       Impact factor: 3.157

Review 6.  Ribosomal frameshifting and transcriptional slippage: From genetic steganography and cryptography to adventitious use.

Authors:  John F Atkins; Gary Loughran; Pramod R Bhatt; Andrew E Firth; Pavel V Baranov
Journal:  Nucleic Acids Res       Date:  2016-07-19       Impact factor: 16.971

7.  Rh mosaicism and aberrant MNSs antigen expression in a patient with chronic myelogenous leukemia.

Authors:  A W Bracey; M H McGinniss; R M Levine; J Whang-Peng
Journal:  Am J Clin Pathol       Date:  1983-03       Impact factor: 2.493

8.  Two populations of Rh groups together with chromosomally abnormal cell lines in the bone marrow.

Authors:  S T Callender; H E Kay; S D Lawler; R E Millard; R Sanger; P A Tippett
Journal:  Br Med J       Date:  1971-01-16

9.  Translational regulation mechanisms of aquaporin-4 supramolecular organization in astrocytes.

Authors:  Francesco Pisani; Andrea Rossi; Grazia Paola Nicchia; Maria Svelto; Antonio Frigeri
Journal:  Glia       Date:  2011-08-17       Impact factor: 7.452

10.  An alternate translation initiation site circumvents an amino-terminal DAX1 nonsense mutation leading to a mild form of X-linked adrenal hypoplasia congenita.

Authors:  Gokhan Ozisik; Giovanna Mantovani; John C Achermann; Luca Persani; Anna Spada; Jeffrey Weiss; Paolo Beck-Peccoz; J Larry Jameson
Journal:  J Clin Endocrinol Metab       Date:  2003-01       Impact factor: 5.958
View more
  2 in total

1.  Proceed with care: the "uncommon" serologic weak D phenotypes.

Authors:  Willy Albert Flegel
Journal:  Blood Transfus       Date:  2021-07       Impact factor: 3.443

2.  NG_007494.1(RHD):c.[4A>T;5G>C;6_7insG] with an RhD-negative phenotype.

Authors:  Kshitij Srivastava; Andrea Doescher; Franz F Wagner; Willy A Flegel
Journal:  Transfusion       Date:  2020-10-11       Impact factor: 3.337
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.