Page last updated: 2024-08-26

nsc-172755 and HbS Disease

nsc-172755 has been researched along with HbS Disease in 32 studies

Research

Studies (32)

Timeframe	Studies, this research(%)	All Research%
pre-1990	7 (21.88)	18.7374
1990's	12 (37.50)	18.2507
2000's	7 (21.88)	29.6817
2010's	5 (15.63)	24.3611
2020's	1 (3.13)	2.80

Authors

Authors	Studies
Jajosky, AN; Jajosky, PG; Jajosky, RP	1
Alsultan, A; Farrell, JJ; Sebastiani, P; Shaikho, EM; Steinberg, MH	1
Anani, L; Baglo, T; Dodo, R; Mehou, J; Zohoun, A	1
Anderson, N; Ballas, SK; Eckman, JR	1
Ahouignan, G; Alihonou, E; Gangbo, A; Rahimy, MC	1
Alagnidé, E; Bagre, F; Fiossi-Kpadonou, E; Kpadonou, GT; Rahimy, MC	1
Anani, L; Latoundji, S; Mullet, E; Sorum, PC; Zounon, O	1
Adorno, EV; Albuquerque, AL; Bomfim, G; Bomfim, GC; Cerqueira, I; dos Reis, MG; Dupuit, MF; Fernandes, GB; Gonçalves, MS; Lyra, I; Maciel, E; Pontes, A; Zanette, A	1
Lalloz, MR; Layton, DM; Ofori-Acquah, SF; Serjeant, G	1
Gala, JL; Glynn, JR; Johnson, RC; Nackers, F; Portaels, F; Robert, A; Slachmuylder, V; Tonglet, R; Zinsou, C	1
Dossou-Yovo, OP; Ducrocq, R; Elion, J; Hauchecorne, M; Krishnamoorthy, R; Lapoumeroulie, C; Rahimy, MC; Zaccaria, I	1
Baya, H; Dunda-Belkhodja, O; Jaeger, G; Labie, D; Nagel, RL; Pagnier, J; Teyssier, J; Zohoun, I	1
Bloch, P; Genin, P; Vouge, M	2
Fabry, ME; Green, NS; Kaptue-Noche, L; Nagel, RL	1
Figueiredo, MS; Guerreiro, JF; Pires, AC; Silva, MC; Souza, GP; Zago, MA	1
Elion, J; Ikuta, T; Krishnamoorthy, R; Labie, D; Lapouméroulie, C; Moi, P; Périchon, B; Ragusa, A; Romand, A	1
Ayadi, H; Fakhfakh, F; Frikha, M; Gargouri, J; Ghali, L; Harrabi, M; Labiadh, Z; Mseddi, S; Souissi, T	1
Rahimy, MC	1
Ahouignan, G; Alihonou, E; Anagonou, S; Boco, V; Gangbo, A; Rahimy, MC	1
Agossou-Voyèmè, AK	1
Ballas, SK; Sarnaik, SA	1
García de la Osa, M; Rodríguez-Ojea Menéndez, A	1
Mérault, G; Reinette, P; Rosa, J; Zohoun, IS	1
Figueiredo, MS; Ogo, SH; Zago, MA	1
Chan, L; Powars, DR; Schroeder, WA	1
Adachi, K; Ballas, SK; Rappaport, E; Schwartz, E; Surrey, S; Talacki, CA	1
Aguessy-Ahyi, B; Akogbeto, M; Chippaux, JP; Ekoue, S; Lanmasso, T; Massougbodji, A	1
Baudin, V; Fabry, ME; Labie, D; Nagel, RL; Pagnier, J; Wajcman, H; Zohoun, I	1
Labie, D; Lombardo, M; Lombardo, T; Nagel, RL; Ragusa, A; Sortino, G	1
Poncz, M; Schwartz, E; Sharon, B; Surrey, S	1
Cresta, M	1

Reviews

1 review(s) available for nsc-172755 and HbS Disease

Article	Year
Beta S-gene-cluster haplotypes in sickle cell anemia: clinical implications. The American journal of pediatric hematology/oncology, 1990,Fall, Volume: 12, Issue:3 Topics: Anemia, Sickle Cell; Benin; Central African Republic; Chromosome Deletion; Chromosomes, Human, Pair 11; Fetal Hemoglobin; Globins; Haplotypes; Hemoglobin, Sickle; Humans; Life Tables; Polymorphism, Restriction Fragment Length; Prognosis; Risk Factors; Senegal; Severity of Illness Index; Survival Rate; Thalassemia; United States	1990

Article

Year

Beta S-gene-cluster haplotypes in sickle cell anemia: clinical implications.

The American journal of pediatric hematology/oncology, 1990,Fall, Volume: 12, Issue:3

Topics: Anemia, Sickle Cell; Benin; Central African Republic; Chromosome Deletion; Chromosomes, Human, Pair 11; Fetal Hemoglobin; Globins; Haplotypes; Hemoglobin, Sickle; Humans; Life Tables; Polymorphism, Restriction Fragment Length; Prognosis; Risk Factors; Senegal; Severity of Illness Index; Survival Rate; Thalassemia; United States

1990

Other Studies

31 other study(ies) available for nsc-172755 and HbS Disease

Article	Year
"Dual-gene" malaria-resistance: Therapeutically-rational exchange (T-REX) of group-O sickle trait and group-O C-traittrait red blood cells can be evaluated in Benin and Nigeria. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis, 2020, Volume: 59, Issue:3 Topics: ABO Blood-Group System; Anemia, Sickle Cell; Benin; Erythrocytes; Exchange Transfusion, Whole Blood; Female; Humans; Malaria; Malaria, Falciparum; Nigeria	2020
Genetic determinants of HbF in Saudi Arabian and African Benin haplotype sickle cell anemia. American journal of hematology, 2017, Volume: 92, Issue:9 Topics: Adaptor Proteins, Signal Transducing; Anemia, Sickle Cell; Benin; beta-Globins; Black or African American; Carrier Proteins; Fetal Hemoglobin; Genome-Wide Association Study; Haplotypes; Humans; Models, Genetic; N-Acetylglucosaminyltransferases; Nuclear Proteins; p21-Activated Kinases; Phosphoproteins; Polymorphism, Single Nucleotide; Principal Component Analysis; Repressor Proteins; Saudi Arabia; United States	2017
[Emergency treatment of sickle cell diseases in the Blood Diseases Department at the Koutoukou Maga National Teaching Hospital, Cotonou, Benin]. The Pan African medical journal, 2018, Volume: 30 Topics: Acute Pain; Adolescent; Adult; Anemia, Sickle Cell; Benin; Child; Child, Preschool; Emergencies; Female; Hospitalization; Hospitals, Teaching; Humans; Length of Stay; Male; Middle Aged; Retrospective Studies; Treatment Outcome; Young Adult	2018
Beyond the transition of adolescents and young adults with sickle cell disease to adult care: Role of geography. American journal of hematology, 2017, Volume: 92, Issue:6 Topics: Adolescent; Adult; Anemia, Sickle Cell; Benin; Blood Transfusion; Cause of Death; Disease Management; Female; Follow-Up Studies; Geography, Medical; Georgia; Health Services Accessibility; Humans; Iron Overload; Male; Meteorological Concepts; Mortality; Philadelphia; Prospective Studies; Senegal; Transition to Adult Care; Urban Population; Young Adult	2017
Newborn screening for sickle cell disease in the Republic of Benin. Journal of clinical pathology, 2009, Volume: 62, Issue:1 Topics: Anemia, Sickle Cell; Benin; Developing Countries; Health Education; Humans; Infant, Newborn; Midwifery; Neonatal Screening; Pilot Projects; Prenatal Care; Program Evaluation	2009
[Problems of rehabilitation in patients with sickle cell disease in Cotonou, Benin]. Medecine tropicale : revue du Corps de sante colonial, 2011, Volume: 71, Issue:6 Topics: Adolescent; Adult; Aged; Anemia, Sickle Cell; Benin; Child; Child, Preschool; Disease Progression; Female; Hemoglobinopathies; Humans; Male; Middle Aged; Young Adult	2011
Misconceptions about sickle cell disease (SCD) among lay people in Benin. Preventive medicine, 2012, Volume: 55, Issue:3 Topics: Adolescent; Adult; Anemia, Sickle Cell; Benin; Female; Health Knowledge, Attitudes, Practice; Humans; Male; Middle Aged; Surveys and Questionnaires; Young Adult	2012
BetaS-haplotypes in sickle cell anemia patients from Salvador, Bahia, Northeastern Brazil. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 2003, Volume: 36, Issue:10 Topics: Anemia, Sickle Cell; Benin; Brazil; Central African Republic; Female; Fetal Hemoglobin; Genotype; Globins; Haplotypes; Humans; Immunoblotting; Male; Polymerase Chain Reaction; Senegal	2003
Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease. Cellular and molecular biology (Noisy-le-Grand, France), 2004, Volume: 50, Issue:1 Topics: Alleles; Anemia, Sickle Cell; Asia; Benin; Central African Republic; Fetal Hemoglobin; Gene Expression Regulation; Genes, Reporter; Globins; Haplotypes; Humans; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Promoter Regions, Genetic; Senegal; Transcription, Genetic	2004
Association between haemoglobin variants S and C and Mycobacterium ulcerans disease (Buruli ulcer): a case-control study in Benin. Tropical medicine & international health : TM & IH, 2007, Volume: 12, Issue:4 Topics: Adolescent; Adult; Age Distribution; Aged; Aged, 80 and over; Anemia, Sickle Cell; Benin; Case-Control Studies; Child; Child, Preschool; Female; Gene Frequency; Genotype; Hemoglobin C; Hemoglobin C Disease; Hemoglobin, Sickle; Hemoglobins; Humans; Infant; Male; Middle Aged; Mycobacterium Infections, Nontuberculous; Mycobacterium ulcerans; Osteomyelitis; Risk Factors; Sex Distribution	2007
Variants of the mannose-binding lectin gene in the Benin population: heterozygosity for the p.G57E allele may confer a selective advantage. Human biology, 2007, Volume: 79, Issue:6 Topics: Adolescent; Adult; Alleles; Anemia, Sickle Cell; Benin; Genetics, Population; Heterozygote; Humans; Infant, Newborn; Mannose-Binding Lectin; Middle Aged	2007
alpha-Thalassemia among sickle cell anemia patients in various African populations. Human genetics, 1984, Volume: 68, Issue:4 Topics: Adolescent; Adult; Anemia, Sickle Cell; Benin; Central African Republic; Child; Child, Preschool; Epistasis, Genetic; Gene Frequency; Humans; Infant; Senegal; Thalassemia	1984
[Osteonecrosis of the femoral head of sickle-cell origin. Apropos of 19 cases observed during a year in Benin. Proposal for radiologic classification]. Journal de radiologie, 1984, Volume: 65, Issue:10 Topics: Adolescent; Adult; Anemia, Sickle Cell; Benin; Child; Female; Femur Head Necrosis; Humans; Male; Radiography	1984
Senegal haplotype is associated with higher HbF than Benin and Cameroon haplotypes in African children with sickle cell anemia. American journal of hematology, 1993, Volume: 44, Issue:2 Topics: Anemia, Sickle Cell; Benin; Cameroon; Child, Preschool; Fetal Hemoglobin; Haplotypes; Humans; Infant; Senegal	1993
The heterogeneity of the beta s cluster haplotypes in Brazil. Gene geography : a computerized bulletin on human gene frequencies, 1994, Volume: 8, Issue:1 Topics: Anemia, Sickle Cell; Benin; Black People; Brazil; Central African Republic; Genetic Heterogeneity; Haplotypes; Hemoglobin, Sickle; Homozygote; Humans; Linkage Disequilibrium; Senegal	1994
Inter-ethnic polymorphism of the beta-globin gene locus control region (LCR) in sickle-cell anemia patients. Human genetics, 1993, Volume: 91, Issue:5 Topics: Algeria; Anemia, Sickle Cell; Base Sequence; Benin; Black People; Cameroon; Central African Republic; Globins; Haplotypes; Humans; India; Linkage Disequilibrium; Molecular Sequence Data; Nucleic Acid Conformation; Polymerase Chain Reaction; Polymorphism, Genetic; Regulatory Sequences, Nucleic Acid; Repetitive Sequences, Nucleic Acid; Senegal; Sequence Analysis, DNA; Sicily	1993
[Hemoglobin beta S haplotype in the Kebili region (southern Tunisia)]. Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine, 1998, Volume: 5, Issue:2 Topics: Adolescent; Adult; alpha-Thalassemia; Anemia, Sickle Cell; Benin; Child; Consanguinity; Ethnicity; Female; Fetal Hemoglobin; Gene Frequency; Genetic Heterogeneity; Globins; Haplotypes; Hemoglobin, Sickle; Humans; Male; Polymorphism, Restriction Fragment Length; Severity of Illness Index; Sickle Cell Trait; Tunisia	1998
[Early detection and medical management of sickle cell anemia: five years of experience in Cotonou]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 1999, Volume: 6 Suppl 2 Topics: Anemia, Sickle Cell; Benin; Female; Genetic Carrier Screening; Humans; Infant, Newborn; Parents; Pregnancy	1999
Outpatient management of fever in children with sickle cell disease (SCD) in an African setting. American journal of hematology, 1999, Volume: 62, Issue:1 Topics: Abdominal Pain; Administration, Oral; Ambulatory Care; Amoxicillin; Anemia, Sickle Cell; Bacterial Infections; Benin; Ceftriaxone; Child; Child, Preschool; Cohort Studies; Combined Modality Therapy; Developing Countries; Drug Costs; Drug Therapy, Combination; Female; Fever; Fluid Therapy; Follow-Up Studies; Hospitalization; Humans; Infant; Injections, Intramuscular; Malaria, Falciparum; Male; Pilot Projects; Recurrence	1999
[Radiologic morphometry of the hip in Beninese black children]. Journal de radiologie, 2000, Volume: 81, Issue:9 Topics: Acetabulum; Adolescent; Age Factors; Anemia, Sickle Cell; Benin; Cartilage, Articular; Child; Child, Preschool; Female; Femur Head; Femur Head Necrosis; Femur Neck; Hip Joint; Humans; Infant; Legg-Calve-Perthes Disease; Linear Models; Male; Osteoarthritis, Hip; Radiography; Sex Factors	2000
Molecular characteristics of pediatric patients with sickle cell anemia and stroke. American journal of hematology, 2001, Volume: 67, Issue:3 Topics: alpha-Thalassemia; Anemia, Sickle Cell; Benin; Cameroon; Central African Republic; Cerebral Infarction; Child; Child, Preschool; Cohort Studies; Comorbidity; DNA Mutational Analysis; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genotype; Globins; Haplotypes; Hemoglobin, Sickle; Humans; Infant; Infant, Newborn; Male; Michigan; Risk Factors; Senegal; Sex Factors	2001
[Malaria and sickle-cell anemia. A correlation of the clinical and epidemiological aspects]. Revista cubana de medicina tropical, 1992, Volume: 44, Issue:1 Topics: Adolescent; Adult; Age Distribution; Anemia, Sickle Cell; Benin; Female; Hemoglobin SC Disease; Hemoglobins; Humans; Malaria, Falciparum; Male; Middle Aged; Prevalence; Sex Distribution	1992
[Health policies and sickle cell disease]. La Revue du praticien, 1992, Oct-01, Volume: 42, Issue:15 Topics: Anemia, Sickle Cell; Benin; France; Health Policy; Humans; West Indies	1992
Bantu beta s cluster haplotype predominates among Brazilian blacks. American journal of physical anthropology, 1992, Volume: 88, Issue:3 Topics: Anemia, Sickle Cell; Benin; Black People; Brazil; Central African Republic; Gene Frequency; Haplotypes; Hemoglobin, Sickle; Humans; Multigene Family; Polymorphism, Genetic; Senegal	1992
The Xmn I site (-158, C----T) 5' to the G gamma gene: correlation with the Senegalese haplotype and G gamma globin expression. Hemoglobin, 1991, Volume: 15, Issue:5 Topics: Adolescent; Adult; Aged; Anemia, Sickle Cell; Benin; Child; Child, Preschool; Deoxyribonucleases, Type II Site-Specific; Female; Fetal Hemoglobin; Gene Expression Regulation; Globins; Haplotypes; Humans; Middle Aged; Pennsylvania; Polymorphism, Restriction Fragment Length; Regulatory Sequences, Nucleic Acid; Senegal	1991
[The transplacental transport of Plasmodium falciparum in non-febrile parturient women in a holoendemic region]. Bulletin de la Societe de pathologie exotique (1990), 1991, Volume: 84, Issue:5 Pt 5 Topics: Anemia, Sickle Cell; Animals; Benin; Female; Humans; Infant, Newborn; Malaria, Falciparum; Placenta; Plasmodium falciparum; Pregnancy; Pregnancy Complications, Infectious; Prevalence	1991
Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type. The New England journal of medicine, 1985, Apr-04, Volume: 312, Issue:14 Topics: Adult; Analysis of Variance; Anemia, Sickle Cell; Benin; Child; Child, Preschool; Erythrocyte Count; Fetal Hemoglobin; Globins; Haploidy; Hematocrit; Humans; Senegal; Thalassemia	1985
Beta S gene in Sicily is in linkage disequilibrium with the Benin haplotype: implications for gene flow. American journal of hematology, 1988, Volume: 27, Issue:2 Topics: Anemia, Sickle Cell; Benin; Child; Gene Frequency; Genetic Linkage; Genetics, Population; Haplotypes; Hemoglobin, Sickle; Humans; Polymorphism, Restriction Fragment Length; Sicily	1988
Non-random association of the Rsa I polymorphic site 5' to the beta-globin gene with major sickle cell haplotypes. Hemoglobin, 1988, Volume: 12, Issue:2 Topics: Anemia, Sickle Cell; Benin; Central African Republic; Chromosomes, Human, Pair 11; Deoxyribonucleases, Type II Site-Specific; DNA Restriction Enzymes; Globins; Humans; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Senegal	1988
[Osteonecrosis of the femur head caused by sickle cell anemia in Benin. Epidemiologic and radiologic aspects]. Bulletin de la Societe de pathologie exotique et de ses filiales, 1985, Volume: 78, Issue:2 Topics: Adolescent; Adult; Anemia, Sickle Cell; Benin; Child; Female; Femur Head Necrosis; Humans; Male; Radiography	1985
Letter: Energy expenditure in sicklemia. JAMA, 1974, Apr-15, Volume: 228, Issue:3 Topics: Adult; Anemia, Sickle Cell; Basal Metabolism; Benin; Energy Metabolism; Humans; Physical Exertion	1974