Compounds > phenylalanine

phenylalanine and Anemia, Hemolytic

phenylalanine has been researched along with Anemia, Hemolytic in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19905 (71.43)18.7374
1990's1 (14.29)18.2507
2000's0 (0.00)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Li, DZ; Li, R; Wang, T; Xie, XM1
Artymiuk, PJ; Chang, ML; Hollán, S; Lammi, A; Maquat, LE; Wu, X1
Bruckheimer, S; Burkert, LB; Pisciotta, AV; Ranney, HM; Sharma, VS1
Dan, K; Ito, T; Kajita, A; Nomura, T; Nozawa, Y; Ogata, K; Okazaki, T1
De Weinstein, BI; Lehmann, H; White, JM; Wiltshire, BG1
Carrell, RW; Owen, MC1
Bank, A; Marks, PA1

Other Studies

7 other study(ies) available for phenylalanine and Anemia, Hemolytic

ArticleYear
Case report: prenatal diagnosis of Hb Hammersmith [β42(CD1)Phe→Ser; HBB: c.128T > C] in a family with an adult male patient.
    Hemoglobin, 2014, Volume: 38, Issue:2

    Topics: Adult; Anemia, Hemolytic; Base Sequence; beta-Globins; Child, Preschool; Cyanosis; DNA Mutational Analysis; Family Health; Female; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Male; Mutation, Missense; Phenylalanine; Pregnancy; Prenatal Diagnosis; Serine; Splenomegaly

2014
Human triosephosphate isomerase deficiency resulting from mutation of Phe-240.
    American journal of human genetics, 1993, Volume: 52, Issue:6

    Topics: Adolescent; Adult; Anemia, Hemolytic; Base Sequence; Cells, Cultured; DNA; Enzyme Stability; Homozygote; Hot Temperature; Humans; Male; Molecular Sequence Data; Mutation; Neuromuscular Diseases; Phenylalanine; RNA, Messenger; Triose-Phosphate Isomerase

1993
Hemoglobin M equon beta 41 (C7) phenylalanine leads to tyrosine.
    Blood, 1976, Volume: 48, Issue:5

    Topics: Adult; Amino Acids; Anemia, Hemolytic; Electrophoresis, Cellulose Acetate; Female; Hemoglobins, Abnormal; Humans; Methemoglobin; Oxygen Consumption; Peptides; Phenylalanine; Tyrosine; Wisconsin

1976
Hemoglobin Sendagi (beta 42 Phe----Val): a new unstable hemoglobin variant having an amino acid substitution at CD1 of the beta-chain.
    Hemoglobin, 1986, Volume: 10, Issue:5

    Topics: Anemia, Hemolytic; Chromatography, High Pressure Liquid; Electrophoresis; Hemoglobins, Abnormal; Humans; Japan; Male; Middle Aged; Oxygen; Phenylalanine; Protein Conformation

1986
A new unstable haemoglobin: Hb Buenos Aires, beta 85 (F1) Phe leads to Ser.
    Acta haematologica, 1973, Volume: 50, Issue:6

    Topics: Adolescent; Anemia, Hemolytic; Child; Electrophoresis, Starch Gel; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Male; Phenylalanine; Serine

1973
A new approach to haemoglobin variant identification. Haemoglobin Christchurch beta-71 (E15) phenylalanine leads to serine.
    Biochimica et biophysica acta, 1971, Jun-29, Volume: 236, Issue:3

    Topics: Adolescent; Amino Acid Sequence; Amino Acids; Anemia, Hemolytic; Anemia, Pernicious; Autoradiography; Carbon Isotopes; Chromatography, Thin Layer; Drug Stability; Electrophoresis; Erythrocytes; Female; Heme; Hemoglobinopathies; Hemoglobins; Hemoglobins, Abnormal; Hemolysis; Humans; Methods; New Zealand; Peptides; Phenylalanine; Serine

1971
Protein synthesis in a cell free human reticulocyte system: ribosome function in thalassemia.
    The Journal of clinical investigation, 1966, Volume: 45, Issue:3

    Topics: Amino Acids; Anemia, Hemolytic; Anemia, Sickle Cell; Humans; In Vitro Techniques; Phenylalanine; Proteins; Reticulocytes; Ribosomes; Thalassemia

1966