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• Books and Book Chapters
• Original Articles
• Review Articles

• Editorials and Letters
• Guidelines and Workshop Reports
• Published Abstracts

Daniels G. 
Human blood group systems. 
In: Murphy MF, Pamphilon DH, eds. Practical Transfusion Medicine, 3rd edn. Oxford: Wiley-Blackwell 2009:19-29.

Daniels G, Finning K, Martin P, Massey E. 
Non-invasive prenatal diagnosis for fetal blood group status. 
In: Kehoe S, Chitty L, Homfray T, eds. Reproductive Genetics. London: RCOG Press, 2009:173-182.

Finning K, Martin P, Daniels G. 
The use of maternal plasma for prenatal RhD blood group genotyping. 
In: Bugert P, ed. DNA and RNA profiling in human blood: methods and protocols, vol. 496:143-157. Humana Press: 2009.

Original Articles

Beckman N, Nightingale MJ, Pamphilon D.
Practical guidelines for applying statistical process control to blood component production.
Transfus Med. 2009 Dec;19(6):329-39.

Brown AC, Hallouane D, Mawby WJ, Karet FE, Saleem MA, Howie AJ, Toye AM.
RhCG is the major putative ammonia transporter expressed in human kidney and RhBG is not expressed at detectable levels.
Am J Physiol Renal Physiol. 2009 Jun;296(6):F1279-90.

Bruce LJ, Guizouarn H, Burton NM, Gabillat N, Poole J, Flatt JF, Brady RL, Borgese F, Delaunay J, Stewart GW 
The monovalent cation leak in over-hydrated stomatocytic red blood cells results from amino acid substitutions in the Rh associated glycoprotein (RhAG) 
Blood 113 (6):1350-7(2009)

Clewley JP, Kelly CM, Andrews N, Vogliqi K, Mallinson G, Kaisar M, Hilton DA, Ironside JW, Edwards P, McCardle LM, Ritchie DL, Dabaghian R, Ambrose HE, Gill ON.
Prevalence of disease related prion protein in anonymous tonsil specimens in Britain: cross sectional opportunistic survey
BMJ 2009;338:b1442

Cox CV, Diamanti P, Evely RS, Kearns PR, Blair A.
Expression of CD133 on leukemia initiating cells in childhood ALL. 
Blood 113 (14), 3287-96 (2009)

Flegel WA, von Zabern I, Doescher A, Wagner FF, Strathmann KP, Geisen C, Palfi M, Písacka M, Poole J, Polin H, Gabriel C, Avent ND. 
D variants at the RhD vestibule in the weak D type 4 and Eurasian D clusters. 
Transfusion. 2009 Jun;49(6):1059-69.

Hustinx H, Poole J, Bugert P, Gowland P, Still F, Fontana S, Scharberg EA, Tilley L, Daniels G, Niederhauser C. 
Molecular basis of the Rh antigen RH48 (JAL). 
Vox Sang. 96(3): 234-239 (2009)

Pamphilon D, Apperley JF, Samson D, Slaper-Cortenbach I, McGrath E.
JACIE Accreditation in 2008: Demonstrating Excellence in Stem Cell Transplantation.
Hematol Oncol Stem Cell Ther. 2009;2(2):311-9.

Reesink HW, Panzer S, Dettke M, Gabriel C, Lambermont M, Deneys V, Sondag D, Dickmeiss E, Fischer-Nielsen A, Korhonen M, Krusius T, Ali A, Tiberghien P, Schrezenmeier H, Tonn T, Seifried E, Klüter H, Politis C, Stavropoulou-Gioka A, Parara M, Flesland O, Nascimento F, Balint B, Marin P, Bart T, Chen FE, Pamphilon DH.
New cellular therapies: Is there a role for transfusion services? 
Vox Sang. 97(1):77-90.2009

Richardson BM, Heesom KJ, Parsons SF,  Anstee DJ, Frayne J
Analysis of the differential proteome of human erythroblasts during in vitro erythropoiesis by 2-D DIGE
Proteomics - Clinical Applications (2009) 3: 1123

Review Articles 

Anstee DJ
Red cell genotyping and the future of pre-transfusion testing.
Blood 2009; 114 (2): 248-256.

Bruce LJ. 
Hereditary stomatocytosis and cation-leaky red cells--recent developments. 
Blood Cells Mol Dis. 2009; 42: 216-222

Daniels G. 
The molecular genetics of blood group polymorphism. 
Hum Genet 2009;126: 729-42.

Daniels G. 
Naming blood groups and the genes that control them. 
ISBT Science Series 2009; 4: 118-120.

Daniels G.
Lutheran. 
Immunohematology. 2009;25(4):152-9.

Daniels G, Finning K, Martin P, Massey E. 
Noninvasive prenatal diagnosis of fetal blood group phenotypes: current practice and future prospects. 
Prenat Diagn. 2009 ;29(2):101-7. 

Ellory JC, Guizouarn H, Borgese F, Bruce LJ, Wilkins RJ, Stewart GW. 
Leaky Cl--HCO3- exchangers: cation fluxes via modified AE1. 
Philos Trans R Soc Lond B Biol Sci. 2009; 27;364(1514):189-94.

Pamphilon D, Siddiq S, Brunskill S, Dorée C, Hyde C, Horowitz M, Stanworth S. 
Stem cell donation - What advice can be given to the donor? 
Br J Haematol. 147(1):71-6 (2009).

Satchwell TJ, Shoemark DK, Sessions RB, Toye AM. 
Protein 4.2: a complex linker. 
Blood Cells Mol Dis. 2009 May-Jun;42(3):201-10.

Siddiq S, Pamphilon D, Brunskill S, Doree C, Hyde C, Stanworth S.
Bone marrow harvest versus peripheral stem cell collection for haemopoietic stem cell donation in healthy donors. 
Cochrane Database Syst Rev. 2009 Jan 21;(1):CD006406.

Editorials and Letters

Diamanti P & Blair A. 
Stem cells in childhood acute lymphoblastic leukemia: identifying the most relevant targets for therapy.
Blood 113 (18), 4477 (2009)

Flatt JF, Bruce LJ. 
The hereditary stomatocytoses. 
Haematologica. 94:1039-1041, 2009.

King MJ, Bruce L, Whiteway A. 
The mutant erythrocyte band 3 protein in Southeast Asian ovalocytosis does not bind eosin-5-maleimide. 
Int J Lab Hematol. 31, 116-117 2009

Guidelines and Workshop Reports

Daniels G, Castilho L, Flegel WA, Fletcher A, Garratty G, Levene C, Lomas-Francis C, Moulds JM, Moulds JJ, Olsson ML, Overbeeke M, Poole J, Reid ME, Rouger P, van der Schoot E, Scott M, Sistonen P, Smart E, Storry JR, Tani Y, Yu LC, Wendel S, Westhoff C, Yahalom V, Zelinski T;
International Society of Blood Transfusion Committee on Terminology for Red Blood Cell Surface Antigens. 
International Society of Blood Transfusion Committee on terminology for red blood cell surface antigens: Macao report. 
Vox Sang. 2009 Feb;96(2):153-6.

Daniels G, van der Schoot CE, Gassner C, Olsson ML.
Report of the Third International Workshop on Molecular Blood Group Genotyping. 
Vox Sang. 2009;96:337-343

van der Schoot CE, de Haas M, Engelfriet CP, Reesink HW, Panzer S, Jungbauer C, Schwartz DMW, Mayr WR, Castilho L, St-Louis M, Long A, Denomme G, Semple E, Fernandes B, Flegel WA, Wagner F, Doescher A, Poli F, Villa MA, Paccapelo C, Karpasitou K, VeldhuisenB, Nogués N, Muñiz-Diaz E, Daniels G, Martin P, Finning K, Reid ME. 
Genotyping for red blood cell polymorphisms. International forum. 
Vox Sang 2009;96:167-169.

Published Abstracts

Crew VK, Bullock T, Poole J, van der Mark-Zoet J, Folman C, Daniels G
A novel Lu mutation giving rise to a new example of the recessive type Lutheran-null phenotype
Transfusion Medicine 2009;19 suppl. 1: 24 (abstract)

Crew VK, Thornton N, Burton N, Poole J, Search S, Daniels G
Two heterozygous mutations in an individual result in the loss of a novel high-incidence Lutheran antigen Lurc
Transfusion Medicine 2009;19 suppl. 1: 10 (abstract)

Daniels G
Red cell genotyping
Transfusion Medicine 2009;19 suppl. 1: 5 (abstract)

Green CA, Tilley L, Poole J, Gaskell A, Ridgwell K, Burton N, Uchikawa M, Tsuneyama H, Daniels GL
Three antigens of a new blood group system: RHAG
Transfusion Medicine 2009;19 suppl. 1: 11 (abstract)

Hegde S, James-Ellison M, Bruce L, Wrong O. 
Anion exchanger 1 mutations as a cause of distal renal tubular acidosis and southeast asian ovalocytosis in a Filipino girl. 
Pediatric Nephrology. 24:286. (Abstract) 2009.

Jackson D, Kumpel B, Massey E
Effect of specific anti-HPA-1A peptides on in-vivo anti-HPA-1A responses
Transfusion Medicine 2009;19 suppl. 1: 30 (abstract)

Needs M, Tilley L, Poole J, Mathlouthi R, Marsh J, Ross, K, Win N
A novel RHCE allele resulting in a D- phenotype
Transfusion Medicine 2009;19 suppl. 1: 24 (abstract)

Pamphilon D
Problems with ABO in stem cell transplantation
Transfusion Medicine 2009;19 suppl. 1: 3 (abstract)

Singleton BK, Fairweather VSS, Lau W, Parsons SF, Burton NM, Frayne J, Brady RL, Anstee DJ.
A novel EKLF mutation in a patient with Dyserythropoietic Anemia: the first association of EKLF with disease in Man. 
Blood 2009; 114(22):72 (abstract)

Tilley L, Mathlouthi R, Needs M, Skidmore I, Stamps R, Malde R, Davis A, Poole J, Daniels G.
Five novel RHD alleles resulting in D variant phenotypes
Transfusion Medicine 2009;19 suppl. 1: 23 (abstract)