Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Serum haptoglobin types and leukemia.

S Nevo, I Tatarsky

    Human Genetics
    |July 1, 1986
    PubMed
    Summary
    This summary is machine-generated.

    Haptoglobin (Hp) type 1-1 is more common in patients with acute lymphatic leukemia (ALL), acute myeloid leukemia (AML), and chronic myeloid leukemia (CML). This finding suggests a link between Hp type and certain leukemia types.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    Acute bleeding complications in patients after bone marrow transplantation.

    Current opinion in hematology·2001
    Same author

    Acute bleeding and thrombocytopenia after bone marrow transplantation.

    Bone marrow transplantation·2001
    Same author

    Paroxysmal nocturnal hemoglobinuria associated with in vitro inhibition of erythropoiesis by bone marrow T lymphocytes.

    The Israel Medical Association journal : IMAJ·2000
    Same author

    Acute bleeding after allogeneic bone marrow transplantation: association with graft versus host disease and effect on survival.

    Transplantation·1999
    Same author

    Acute bleeding after bone marrow transplantation (BMT)- incidence and effect on survival. A quantitative analysis in 1,402 patients.

    Blood·1998
    Same author

    Genetic polymorphism of AHSG, FXIIIB, HP and PLG serum proteins in six Jewish groups in Israel.

    Human heredity·1997
    Same journal

    AI in variant analysis: fast track to genetic diagnoses.

    Human genetics·2026
    Same journal

    Combined family-based association and linkage analyses in families affected by attention-deficit hyperactivity disorder.

    Human genetics·2026
    Same journal

    Investigating the shared genetic architecture between selective immunoglobulin A deficiency and autoimmune diseases.

    Human genetics·2026
    Same journal

    ARHI as a key regulator of EMT and metastasis in pancreatic cancer via the Notch-1 pathway.

    Human genetics·2026
    Same journal

    Large-scale mitogenome analysis reveals complex maternal genetic connections between Sino-Tibetan- and Altaic-speaking populations.

    Human genetics·2026
    Same journal

    Correction: A comprehensive and accessible model for co-segregation analysis in BRCA1, BRCA2, and PALB2 variant classification.

    Human genetics·2026
    See all related articles

    Area of Science:

    • Hematology
    • Genetics
    • Biochemistry

    Background:

    • Haptoglobin (Hp) is a plasma protein involved in hemoglobin binding.
    • Leukemia encompasses a group of blood cancers affecting white blood cells.
    • Previous research has explored potential associations between Hp types and various diseases.

    Purpose of the Study:

    • To investigate the distribution of haptoglobin types in patients with common leukemia subtypes.
    • To determine if specific haptoglobin types are associated with acute lymphatic leukemia (ALL), chronic lymphatic leukemia (CLL), acute myeloid leukemia (AML), and chronic myeloid leukemia (CML).

    Main Methods:

    • Haptoglobin phenotyping was performed on 211 leukemia patients.
    • Frequency distributions of Hp types (Hp 1-1, Hp 1-2, Hp 2-2) were analyzed.

    Related Experiment Videos

  • Patient data was compared to control populations and previously published studies.
  • Main Results:

    • Significant differences in Hp type frequencies were observed between leukemia patients and controls.
    • An elevated incidence of Hp 1-1 was found in patients with ALL, AML, and CML, but not CLL.
    • Analysis of existing literature corroborated the trend of increased Hp 1-1 in ALL, AML, and CML.

    Conclusions:

    • The study suggests a significant association between haptoglobin type and certain types of leukemia.
    • The Hp 1-1 phenotype appears to be more prevalent in patients diagnosed with ALL, AML, and CML.
    • Further research may elucidate the biological mechanisms underlying this observed association.