Search Results 31-40 of 15067 for hla genotype

  1. Stevens-Johnson syndrome - Diagnosis & treatment - Mayo Clinic

    HLA genotype and carbamazepine-induced cutaneous adverse drug reactions: A systematic review. Clinical Pharmacology and Therapeutics. 2012;92:757. Wetter DA ...

  2. Genotyping - Genome Analysis Core - Mayo Clinic Research

    Genotyping services, genome wide single nucleotide polymorphism (SNP) arrays and methylation analyses are offered by Mayo Clinic's Genome Analysis Core.

  3. A Study to Evaluate the Safety and Efficacy of A2B694, a Logic-gated CAR T, in Subjects With Solid Tumors That Express MSLN and Have Lost HLA-A*02 Expression - Mayo Clinic

    A Study to Evaluate the Safety and Efficacy of A2B694, a Logic-gated CAR T, in Subjects With Solid Tumors That Express MSLN and Have Lost HLA-A*02 Expression.

  4. Study of the Safety, Tolerability, Pharmacokinetics and Biomarker of DONQ52 in Celiac Disease Patients - Mayo Clinic

    5 genotype (HLA-DQA1*05 and HLA-DQB1*02) (homozygous or heterozygous) ... genotyping must submit a blood sample to determine whether an eligible HLA-DQ2.

  5. Genetic testing - Mayo Clinic

    Genetic testing: Learn why it's done, how to prepare and what to expect from diagnostic tests, carrier tests, prenatal tests and newborn screening.

  6. Mayo Clinic Q and A: Bone marrow transplants save lives - more donors are needed

    An ideal bone marrow donor should be HLA-matched to the transplant recipient. HLA stands for human leukocyte antigens — markers on the surface of the cells in ...

  7. Gregory A. Poland, M.D. - Mayo Clinic Faculty Profiles

    ... HLA typing for immunogenetic studies; and high-throughput assays, such as ... genotype information. Through research, Dr. Poland and his team aim to ...

  8. A Study of Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of KAN-101 in People With Celiac Disease - Mayo Clinic

    - HLA-DQ8 genotype. - Previous oral gluten challenge within 12 months. - Selective IgA deficiency. - Diagnosis of Type-1 diabetes. - Active gastrointestinal ...

  9. Primary Hyperoxaluria Mutation Genotyping/Phenotyping - Mayo Clinic

    About this study. Specific mutations relating to hyperoxaluria will be determined via DNA analysis by the Mayo RKSC research staff.

  10. Maternal-Infant Haplotypes and Tissue Rejection Pathways in Placental Villitis Examination - Mayo Clinic

    In our first aim, we will evaluate the associations between maternal-infant HLA alleles, eplets and VUE. ... Abnormal genotype. Note: Other protocol ...