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Academic Journal

Naturally occurring anti-PP1P K in a Chinese individual with p phenotype: A case based on compound heterozygosity including one novel allele.

  • Authors : Liang S; Shenzhen Institute of Transfusion Medicine, Shenzhen Blood Center, Shenzhen, China.; Wu F

Subjects: Galactosyltransferases*/Galactosyltransferases*/Galactosyltransferases*/genetics ; Blood Group Antigens*/Blood Group Antigens*/Blood Group Antigens*/genetics; Humans

  • Source: Transfusion [Transfusion] 2022 Nov; Vol. 62 (11), pp. 2184-2187. Date of Electronic Publication: 2022 Oct 20.Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

The differential expression of the blood group P 1 -A4GALT and P 2 -A4GALT alleles is stimulated by the transcription factor early growth response 1.

  • Authors : Yeh CC; Institute of Biochemical Sciences, College of Life Science, National Taiwan University, Taipei, Taiwan.; Chang CJ

Subjects: Gene Expression Regulation* ; Polymorphism, Single Nucleotide*; Early Growth Response Protein 1/Early Growth Response Protein 1/Early Growth Response Protein 1/*physiology

  • Source: Transfusion [Transfusion] 2018 Apr; Vol. 58 (4), pp. 1054-1064. Date of Electronic Publication: 2018 Feb 04.Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

A novel P1PK allele in two Bangladeshi sisters with a history of spontaneous abortion: A4GALT*02N(951C).

  • Authors : Floch A; Immunohematology and Genomics Laboratory, New York Blood Center, Long Island City, New York, USA.; Etablissement francais du sang Ile-de-France, Creteil, France.

Subjects: Abortion, Spontaneous/Abortion, Spontaneous/Abortion, Spontaneous/*genetics ; Galactosyltransferases/Galactosyltransferases/Galactosyltransferases/*genetics; Alleles

  • Source: Transfusion [Transfusion] 2021 Oct; Vol. 61 (10), pp. E71-E72. Date of Electronic Publication: 2021 Sep 03.Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Novel A4GALT gene variation with rare p phenotype in a Chinese family.

  • Authors : Qiu F; Institute of Blood Transfusion of Hubei Province, Wuhan Blood Center, Wuhan, China.; He M

Subjects: Galactosyltransferases/Galactosyltransferases/Galactosyltransferases/*genetics; Asian People/Asian People/Asian People/genetics ; Female

  • Source: Transfusion [Transfusion] 2021 Sep; Vol. 61 (9), pp. E57-E58. Date of Electronic Publication: 2021 Jul 27.Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Novel A4GALT gene variation with rare p phenotype in a compound heterozygous Chinese individual.

  • Authors : Chen Q; Jiangsu Province Blood Center, Nanjing, China.; Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, China.

Subjects: Asian People/Asian People/Asian People/*genetics ; Galactosyltransferases/Galactosyltransferases/Galactosyltransferases/*genetics ; Genetic Variation/Genetic Variation/Genetic Variation/*genetics

  • Source: Transfusion [Transfusion] 2021 Jan; Vol. 61 (1), pp. E5-E6. Date of Electronic Publication: 2020 Oct 28.Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

A systematic study of single-nucleotide polymorphisms in the A4GALT gene suggests a molecular genetic basis for the P1/P2 blood groups.

  • Authors : Lai YJ; Institute of Biochemical Sciences, College of Life Science, National Taiwan University, Taipei, Taiwan; Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan

Subjects: Alleles* ; Genotype* ; Polymorphism, Single Nucleotide*

  • Source: Transfusion [Transfusion] 2014 Dec; Vol. 54 (12), pp. 3222-31. Date of Electronic Publication: 2014 Jul 20.Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems.

  • Authors : Westman JS; Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden.; Hellberg A

Subjects: Alleles*; Galactosyltransferases/Galactosyltransferases/Galactosyltransferases/*genetics ; Globosides/Globosides/Globosides/*immunology

  • Source: Transfusion [Transfusion] 2013 Nov; Vol. 53 (11 Suppl 2), pp. 2928-39. Date of Electronic Publication: 2013 Aug 08.Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Amino-acid substitution in the disordered loop of blood group B-glycosyltransferase enzyme causes weak B phenotype.

  • Authors : Yazer MH; Institute for Transfusion Medicine and Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.; Denomme GA

Subjects: Amino Acid Substitution* ; Phenotype*; ABO Blood-Group System/ABO Blood-Group System/ABO Blood-Group System/*chemistry

  • Source: Transfusion [Transfusion] 2005 Jul; Vol. 45 (7), pp. 1178-82.Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print Cited Medium: Print

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Academic Journal

Generation of histo-blood group B transferase by replacing the N-acetyl-D-galactosamine recognition domain of human A transferase with the galactose-recognition domain of evolutionarily related murine alpha1,3-galactosyltransferase.

  • Authors : Yamamoto F; Department of Tumor Development, Burnham Institute for Medical Research, La Jolla, California, USA. ; Yamamoto M

Subjects: Evolution, Molecular*; Galactosyltransferases/Galactosyltransferases/Galactosyltransferases/*metabolism ; N-Acetylgalactosaminyltransferases/N-Acetylgalactosaminyltransferases/N-Acetylgalactosaminyltransferases/*metabolism

  • Source: Transfusion [Transfusion] 2010 Mar; Vol. 50 (3), pp. 622-30. Date of Electronic Publication: 2009 Nov 20.Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Missense mutations outside the catalytic domain of the ABO glycosyltransferase can cause weak blood group A and B phenotypes.

  • Authors : Seltsam A; Department of Transfusion Medicine, Hannover Medical School, Hannover, Germany.; Blasczyk R

Subjects: Amino Acid Substitution* ; Mutation, Missense*; ABO Blood-Group System/ABO Blood-Group System/ABO Blood-Group System/*metabolism

  • Source: Transfusion [Transfusion] 2005 Oct; Vol. 45 (10), pp. 1663-9.Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print Cited Medium: Print

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  • 1-10 of  52 results for ""Galactosyltransferases""