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

HLA class II nucleotide sequences, 1991.

S G Marsh1, J G Bodmer

  • 1Imperial Cancer Research Fund, Lincoln's Inn Fields, London, U.K.

Tissue Antigens
|April 1, 1991
PubMed
Summary
This summary is machine-generated.

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

Polymorphisms in the TNFA gene promoter region show evidence of strong linkage disequilibrium with HLA and are associated with delayed neutrophil engraftment in unrelated donor hematopoietic stem cell transplantation.

Tissue antigens·2004
Same author

The IMGT/HLA sequence database.

Reviews in immunogenetics·2002
Same author

Nomenclature for factors of the HLA system, update April 2001.

European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics·2002
Same author

Nomenclature for factors of the HLA system, update May 2001.

European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics·2002
Same author

Nomenclature for factors of the HLA system, update June 2001.

European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics·2002
Same author

The HLA Dictionary 2001: a summary of HLA-A, -B, -C, -DRB1/3/4/5 and -DQB1 alleles and their association with serologically defined HLA-A, -B, -C, -DR and -DQ antigens.

European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics·2002
Same journal

Corrigendum.

Tissue antigens·2015
Same journal

Nomenclature for factors of the HLA system, update September 2015.

Tissue antigens·2015
Same journal

Nomenclature for factors of the HLA system, update August 2015.

Tissue antigens·2015
Same journal

Nomenclature for factors of the HLA system, update July 2015.

Tissue antigens·2015
Same journal

Four amino acid exchanges located in the alpha-2 domain specify the novel HLA-B*50:20 allele.

Tissue antigens·2015
Same journal

A novel HLA-A*02 variant, HLA-A*02:575, detected in a Taiwanese bone marrow hematopoietic stem cell donor.

Tissue antigens·2015
See all related articles

This compilation presents Human Leukocyte Antigen (HLA) Class II sequences from published literature. It aims to provide an accurate and updated resource for researchers studying HLA genetics and immunology.

Area of Science:

  • Immunogenetics
  • Molecular Biology
  • Genomics

Background:

  • The Human Leukocyte Antigen (HLA) system is crucial for immune response.
  • Accurate HLA Class II sequences are essential for understanding immune system function and disease association.
  • Previous compilations may contain discrepancies or outdated information.

Purpose of the Study:

  • To compile and align Human Leukocyte Antigen (HLA) Class II sequences from existing literature.
  • To resolve discrepancies in reported sequences by contacting original authors.
  • To create an accurate and up-to-date reference for HLA Class II alleles.

Main Methods:

  • Literature review of HLA nomenclature publications from 1989 and 1990.
  • Sequence data extraction and alignment.

Related Experiment Videos

  • Contacting original authors to verify and amend discrepancies.
  • Incorporation of amendments into the final sequence compilation.
  • Main Results:

    • A comprehensive alignment of Human Leukocyte Antigen (HLA) Class II sequences has been generated.
    • Discrepancies in published sequences were addressed through author consultation.
    • Standardized notation for sequence identity (-), unavailability (*), and gaps is used.

    Conclusions:

    • This compilation serves as a valuable, accurate resource for HLA Class II sequences.
    • Ongoing efforts are made to maintain the accuracy of the sequence data.
    • Researchers are encouraged to report any new evidence to improve the compilation.