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hemoglobin J-Paris

alanine at position 12 of alpha chains is replaced by aspartic acid

Also Known As:

Hb J-Paris; Hb J-Paris-I; hemoglobin J-Paris-I; Hemoglobin J Paris

Networked: 5 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843
  - Blood Proteins: 12459
    - Hemoglobins: 37188
      - Abnormal Hemoglobins: 120
        Hemoglobin J: 10
        hemoglobin J-Paris: 5
  - Hemeproteins: 194
    - Globins: 2716
      - Hemoglobins: 37188
        Abnormal Hemoglobins: 120
        Hemoglobin J: 10
        hemoglobin J-Paris: 5

Experts

1.	González, Fernando A: 1 article (07/2019)
2.	Martínez, Rafael: 1 article (07/2019)
3.	Nieto, Jorge M: 1 article (07/2019)
4.	Ropero, Paloma: 1 article (07/2019)
5.	Villegas, Ana: 1 article (07/2019)
6.	de la Fuente-Gonzalo, Félix: 1 article (07/2019)

Related Diseases

1.	beta-Thalassemia (Cooley's Anemia) 01/01/1989 - "No interaction between Hb J-Paris-I and beta-thalassemia in an Indian family." 01/01/1977 - "Double heterozygosis for Hb J Paris and beta-thalassemia." 01/01/1986 - "Normal production of the mutant hemoglobin in heterozygotes for hemoglobin J-Paris and beta-thalassemia." 12/11/1980 - "The interactions between beta-thalassemia and the human hemoglobin (Hb) alpha-chain variants, Hb Hasharon, Hb O Idonesia and Hb J Paris, and between alpha-thalassemia and the beta-chain variants, Hb S, Hb C and Hb G San José, which are characterized by preferential decrease of the abnormal Hb level in peripheral bloods, have been studied. "
2.	alpha-Thalassemia 12/11/1980 - "The interactions between beta-thalassemia and the human hemoglobin (Hb) alpha-chain variants, Hb Hasharon, Hb O Idonesia and Hb J Paris, and between alpha-thalassemia and the beta-chain variants, Hb S, Hb C and Hb G San José, which are characterized by preferential decrease of the abnormal Hb level in peripheral bloods, have been studied. "
3.	Hemoglobinopathies 07/01/2019 - "The alterations responsible for non-deletional α-thalassaemia are most represented by the Hph and Hb Groene Hart and, in the case of structural hemoglobinopathies, Hb Le Lamentin and Hb J-Paris."

Related Drugs and Biologics

1.	Hemoglobins (Hemoglobin)
2.	hemoglobin Groene Hart
3.	hemoglobin Le Lamentin
4.	hemoglobin Sealy