valine has been researched along with HbS Disease in 31 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 23 (74.19) | 18.7374 |
1990's | 2 (6.45) | 18.2507 |
2000's | 3 (9.68) | 29.6817 |
2010's | 3 (9.68) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bergendahl, LT; Esin, A; Marsh, JA; Savolainen, V; Warnecke, T | 1 |
Becchi, M; Francina, A; Joly, P; Préhu, C; Riou, J; Wajcman, H; Zanella-Cleon, I | 1 |
Billote, GB; Brittenham, GM; DeBellis, RH; Ender, KL; Erlanger, BF | 1 |
Gali, E; Kaya, H; Oktar, S; Ozcelik, N; Sogut, S; Tutanc, M; Yigit, A; Yilmaz, HR; Yonden, Z | 1 |
HEYWOOD, JD; KARON, M; WEISSMAN, S | 1 |
Ferrone, FA; Roufberg, A | 1 |
Acharya, AS; Ho, C; Ho, NT; Kumar, R; Malavalli, A; Manjula, BN; Nagel, RL; Prabhakaran, M; Rao, MJ; Sun, DP | 1 |
Bechtel, KC; Haycraft, GL; Horne, MK; Jue, DL; Moo-Penn, WF; Nagel, RL; Roth, EF; Schmidt, RM; Wright, JM | 1 |
Cottam, GL; Waterman, MR | 1 |
Manning, JM; Nigen, AM | 1 |
Kirson, LE; Tomaro, AJ | 1 |
Pigoń, H | 1 |
Yang, JT | 1 |
Benjamin, LJ; Manning, JM; Ueno, H; Yatco, E | 1 |
Lalaiants, IE; Milovanova, LS | 1 |
Ben-Bassat, I; Beutler, E; Paniker, NV | 1 |
Itano, HA; Suzuki, H | 1 |
Anderson, WF | 1 |
Cerami, A; Gillette, PN; Herbert, JT; Lu, YS; Peterson, CM | 1 |
Rieder, RF | 1 |
Cerami, A | 1 |
Cerami, A; Gillette, PN; Lee, CK; Manning, JM | 1 |
Lee, CK; Manning, JM | 1 |
Moon, RB; Nelson, MJ; Powars, DF; Richards, JH | 1 |
Cerami, A; Gillette, PN; Manning, JM | 1 |
Camp, FR; Henry, RL; Nalbandian, RM; Nichols, BM; Wolf, PL | 1 |
Ranney, HM | 1 |
Itano, HA; Kazazian, HH | 1 |
Beale, D; Lehmann, H; Marengo-Rowe, AJ | 1 |
Heywood, D; Karon, M; Weissman, S | 1 |
Murayama, M | 1 |
4 review(s) available for valine and HbS Disease
Article | Year |
---|---|
Molecular aspects of sickle cell disease.
Topics: Anemia, Sickle Cell; Electron Spin Resonance Spectroscopy; Erythrocytes; Gels; Glutamates; Hemoglobin A; Hemoglobin, Sickle; Kinetics; Macromolecular Substances; Microscopy, Electron; Oxygen; Protein Conformation; Thermodynamics; Valine; X-Ray Diffraction | 1976 |
[Sickle cell anemia--a world problem].
Topics: Anemia, Sickle Cell; Blood Coagulation; Blood Viscosity; Erythrocyte Aging; Female; Hemoglobins; Heterozygote; Homozygote; Humans; Male; Maternal-Fetal Exchange; Mutation; Phenotype; Pregnancy; Pregnancy Complications; Valine | 1975 |
Variation in beta-alpha synthesis ratios in thalassemia and hemoglobinopathies.
Topics: Anemia, Hemolytic, Autoimmune; Anemia, Sickle Cell; Bone Marrow; Bone Marrow Cells; Carbon Radioisotopes; Erythrocyte Aging; Erythrocytes; Globins; Hemoglobin C Disease; Hemoglobinopathies; Heterozygote; Homozygote; Humans; Leucine; Peptide Chain Termination, Translational; Peptide Fragments; RNA, Messenger; Thalassemia; Tritium; Trypsin; Valine | 1974 |
Review of the development of cyanate as a drug in the treatment of sickle cell anemia.
Topics: Adolescent; Adult; Anemia, Sickle Cell; Animals; Bilirubin; Binding Sites; Carbon Dioxide; Carbon Radioisotopes; Cell Survival; Chromium; Cyanates; Erythrocytes; Female; Hematocrit; Hemoglobins; Humans; L-Lactate Dehydrogenase; Male; Mice; Organ Specificity; Oxygen; Protein Binding; Time Factors; Valine | 1974 |
2 trial(s) available for valine and HbS Disease
Article | Year |
---|---|
Safety of short-term valacyclovir as an anti-sickling agent in sickle-cell anemia.
Topics: Acyclovir; Adolescent; Adult; Anemia, Sickle Cell; Antisickling Agents; Antiviral Agents; Erythrocytes, Abnormal; Female; Hemoglobins; Humans; Male; Maximum Tolerated Dose; Prodrugs; Prospective Studies; Safety; Survival Rate; Treatment Outcome; Valacyclovir; Valine; Young Adult | 2011 |
Studies with intravenous sodium cyanate in patients with sickle cell anemia.
Topics: Adolescent; Adult; Amino Acids; Anemia, Sickle Cell; Blood Cell Count; Chromatography, Gas; Clinical Trials as Topic; Cyanates; Diuresis; Feeding and Eating Disorders; Female; Hemoglobins; Humans; Hydantoins; Injections, Intravenous; Male; Middle Aged; Reticulocytes; Thyrotropin; Time Factors; Valine; Vasopressins | 1974 |
25 other study(ies) available for valine and HbS Disease
Article | Year |
---|---|
The genetic basis and evolution of red blood cell sickling in deer.
Topics: Amino Acid Sequence; Anemia, Sickle Cell; Animals; beta-Globins; Deer; Erythrocytes; Phylogeny; Polymorphism, Genetic; Sequence Alignment; Valine | 2018 |
Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr].
Topics: Anemia, Sickle Cell; beta-Globins; Chromatography, Liquid; Female; Glutamic Acid; Hemoglobin, Sickle; Hemoglobins, Abnormal; Humans; Lysine; Mass Spectrometry; Middle Aged; Mutation; Spectrometry, Mass, Electrospray Ionization; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Threonine; Valine | 2009 |
Ala-9Val polymorphism of Mn-SOD gene in sickle cell anemia.
Topics: Adolescent; Adult; Alanine; Alleles; Amino Acid Substitution; Anemia, Sickle Cell; Child; Child, Preschool; Female; Gene Frequency; Genetic Association Studies; Humans; Male; Oxidative Stress; Polymorphism, Genetic; Superoxide Dismutase; Valine | 2011 |
AMINO ACIDS: INCORPORATION INTO ALPHA- AND BETA-CHAINS OF HEMOGLOBIN BY NORMAL AND THALASSEMIC RETICULOCYTES.
Topics: Amino Acids; Anemia, Sickle Cell; Carbon Isotopes; Globins; Hemoglobins; Humans; Leucine; Leukemia; Proteins; Research; Reticulocytes; Thalassemia; Valine | 1964 |
A model for the sickle hemoglobin fiber using both mutation sites.
Topics: Algorithms; Anemia, Sickle Cell; Computer Simulation; Hemoglobin, Sickle; Hemoglobins; Hemoglobinuria; Humans; Models, Biological; Models, Chemical; Mutagenesis, Site-Directed; Protein Binding; Valine | 2000 |
Interspecies hybrid HbS: complete neutralization of Val6(beta)-dependent polymerization of human beta-chain by pig alpha-chains.
Topics: Allosteric Regulation; Amino Acid Sequence; Amino Acid Substitution; Anemia, Sickle Cell; Animals; Binding Sites; Dimerization; Genetic Therapy; Globins; Heme; Hemoglobin, Sickle; Humans; Hydrogen-Ion Concentration; Kinetics; Magnetic Resonance Spectroscopy; Models, Molecular; Oxygen; Protein Engineering; Protein Structure, Quaternary; Recombinant Fusion Proteins; Static Electricity; Swine; Valine | 2000 |
Hemoglobin S Travis: a sickling hemoglobin with two amino acid substitutions [beta6(A3)glutamic acid leads to valine and beta142 (h20) alanine leads to valine).
Topics: Alanine; Amino Acids; Anemia, Sickle Cell; Female; Genetic Variation; Glutamates; Hemoglobin, Sickle; Humans; Hydrogen-Ion Concentration; Kinetics; Male; Oxygen; Pedigree; Peptide Fragments; Valine | 1977 |
Inhibition of erythrocyte sickling in vitro by DL-glyceraldehyde.
Topics: Anemia, Sickle Cell; Erythrocytes, Abnormal; Gels; Glyceraldehyde; Hemoglobin, Sickle; Humans; Lysine; Oxygen; Valine | 1977 |
Mental nerve paresthesia secondary to sickle-cell crisis.
Topics: Adolescent; Adult; Anemia, Sickle Cell; Hemoglobins; Humans; Lip; Male; Mandibular Nerve; Paresthesia; Thalassemia; Valine | 1979 |
Intermolecular contacts of deoxyhemoblogin S: a hypothesis and search for possible anti-sickling agents.
Topics: Amino Acid Sequence; Amino Acids; Anemia, Sickle Cell; Binding Sites; Glutamates; Hemoglobin, Sickle; Hemoglobins; Hemoglobins, Abnormal; Humans; Macromolecular Substances; Models, Biological; Protein Binding; Protein Conformation; Valine | 1975 |
Effects of methyl acetyl phosphate, a covalent antisickling agent, on the density profiles of sickle erythrocytes.
Topics: Anemia, Sickle Cell; Antisickling Agents; Cell Fractionation; Cell Separation; Centrifugation, Density Gradient; Erythrocyte Count; Erythrocytes, Abnormal; Hemoglobin, Sickle; Humans; Oxygen; Phosphonoacetic Acid; Valine | 1992 |
[The role of "valine substitution" in oncogene functioning (a hypothesis)].
Topics: Anemia, Sickle Cell; GTP Phosphohydrolases; Humans; In Vitro Techniques; Malaria; Models, Molecular; Neoplasms; Oncogene Protein p21(ras); Oncogenes; Peptide Chain Initiation, Translational; Peptide Chain Termination, Translational; Valine; X-Ray Diffraction | 1991 |
Evaluation of sickle hemoglobin and desickling agents by falling ball viscometry.
Topics: 6-Phytase; Anemia, Sickle Cell; Aspirin; Blood Viscosity; Carbamates; Cyanates; Drug Storage; Fructose; Glyceraldehyde; Glyceric Acids; Hemoglobins, Abnormal; Humans; Inositol; Methemoglobin; NAD; Phosphoric Acids; Potassium; Pyridoxal Phosphate; Time Factors; Urea; Valine; Vinblastine | 1972 |
Delayed removal of N-terminal methionine from nascent globin chains in sickle-cell anemia reticulocytes.
Topics: Anemia, Sickle Cell; Animals; Chromatography; Hemoglobin, Sickle; Hemoglobins; Hemoglobins, Abnormal; Humans; In Vitro Techniques; Lysine; Methionine; Peptide Biosynthesis; Peptide Chain Elongation, Translational; Peptides; Rabbits; Reticulocytes; Sulfur Isotopes; Tritium; Valine | 1973 |
Isolation and translation of messenger RNA from beta-thalassemia red cells.
Topics: Anemia; Anemia, Sickle Cell; Animals; Bone Marrow; Bone Marrow Cells; Carbon Radioisotopes; Cell-Free System; Chromatography, Ion Exchange; Erythroblastosis, Fetal; Erythrocytes; Female; Globins; Glycine; Humans; Leucine; Methionine; Peptide Fragments; Peptide Initiation Factors; Phenylhydrazines; Pregnancy; Rabbits; Reticulocytes; Ribosomes; RNA, Messenger; RNA, Transfer; Thalassemia; Valine | 1974 |
Gas chromatographic determination of the carbamylation of hemoglobin S by cyanate.
Topics: Anemia, Sickle Cell; Chemical Phenomena; Chemistry; Chromatography, Gas; Cyanates; Hemoglobin, Sickle; Hemoglobins, Abnormal; Humans; Hydantoins; Methods; Time Factors; Valine | 1973 |
Kinetics of the carbamylation of the amino groups of sickle cell hemoglobin by cyanate.
Topics: Anemia, Sickle Cell; Binding, Competitive; Carbamates; Carbon Dioxide; Carbon Isotopes; Carboxyhemoglobin; Countercurrent Distribution; Cyanates; Erythrocytes; Hemoglobins; Hemoglobins, Abnormal; Hemolysis; Humans; Hydrogen-Ion Concentration; Hydroxymercuribenzoates; Kinetics; Oxyhemoglobins; Peptides; Potassium; Sodium; Trypsin; Valine | 1973 |
13C magnetic resonance studies of hemoglobin carbamylation.
Topics: Adult; Amino Acid Sequence; Anemia, Sickle Cell; Binding Sites; Carbon Isotopes; Carbon Monoxide; Carboxyhemoglobin; Cyanates; Evaluation Studies as Topic; Fourier Analysis; Hemoglobins; Heparin; Humans; Hydrogen-Ion Concentration; Lysine; Magnetic Resonance Spectroscopy; Methods; Protein Binding; Protein Conformation; Valine | 1974 |
Increased survival of sickle-cell erythrocytes after treatment in vitro with sodium cyanate.
Topics: Adolescent; Adult; Anemia, Sickle Cell; Chromium Isotopes; Cyanates; Erythrocytes; Erythrocytes, Abnormal; Female; Half-Life; Hemoglobins; Humans; In Vitro Techniques; Male; Time Factors; Valine | 1971 |
Molecular basis for a simple, specific test for S hemoglobin: the Murayama test.
Topics: Adolescent; Adult; Aged; Anemia, Sickle Cell; Chemical Phenomena; Chemistry; Child; Child, Preschool; Female; Gels; Glutamates; Hemoglobin C; Hemoglobins, Abnormal; Heterozygote; Homozygote; Humans; Male; Methods; Middle Aged; Models, Structural; Temperature; Valine | 1970 |
Interactions of other hemoglobin variants with sickle-cell hemoglobin.
Topics: Anemia, Sickle Cell; Binding Sites; Gels; Glutamates; Hemoglobin C; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Models, Theoretical; Oxygen; Polymers; Valine | 1970 |
Studies on the quantitative control of polypeptide synthesis in human reticulocytes.
Topics: Anemia, Sickle Cell; Carbon Isotopes; Erythrocytes; Hemoglobins; Hemoglobins, Abnormal; Histidine; Humans; In Vitro Techniques; Leucine; Male; Peptide Biosynthesis; Reticulocytes; RNA, Messenger; Time Factors; Trypsin; Valine | 1968 |
New human haemoglobin variant from southern Arabia: G-Audhali (alpha-23(B4) glutamic acid--valine) and the variability of B4 in human haemoglobin.
Topics: Amino Acid Sequence; Amino Acids; Anemia, Sickle Cell; Arabia; Blood Protein Electrophoresis; Chymotrypsin; Glutamates; Hemoglobins, Abnormal; Humans; Peptides; Thalassemia; Trypsin; Valine | 1968 |
Asymmetrical incorporation of amino acids in the alpha and beta chains of hemoglobin synthesized by thalassemic reticulocytes.
Topics: Anemia, Sickle Cell; Dinitrophenols; Hemoglobins; Humans; In Vitro Techniques; Leucine; Leukemia, Lymphoid; Peptide Biosynthesis; Reticulocytes; Thalassemia; Valine | 1965 |
Tertiary structure of sickle cell hemoglobin and its functional significance.
Topics: Amino Acid Sequence; Anemia, Sickle Cell; Erythrocytes; Glutamates; Hemoglobins, Abnormal; Humans; Methane; Microscopy, Electron; Models, Theoretical; Temperature; Valine | 1966 |