scholarly article | Q13442814 |
P356 | DOI | 10.3109/08916930903567492 |
P8608 | Fatcat ID | release_dwbofdfgjbghrb5dsc3jyczf7a |
P953 | full work available at URL | http://www.tandfonline.com/doi/pdf/10.3109/08916930903567492 |
P698 | PubMed publication ID | 21067287 |
P2093 | author name string | Carmen Alaez | |
Clara Gorodezky | |||
Esma Ucisik-Akkaya | |||
Hilario Flores | |||
M. Tevfik Dorak | |||
Brittany A. Morrison | |||
P2860 | cites work | Journal of the National Cancer Institute | Q400279 |
Biochimica et Biophysica Acta | Q864239 | ||
The Journal of Rheumatology | Q7743623 | ||
HLA-associated susceptibility to childhood B-cell precursor ALL: definition and role of HLA-DPB1 supertypes | Q27485629 | ||
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population | Q28259896 | ||
Risk alleles for multiple sclerosis identified by a genomewide study | Q29614890 | ||
A whole-genome association study of major determinants for host control of HIV-1 | Q29614891 | ||
Identification of two independent risk factors for lupus within the MHC in United Kingdom families | Q30837981 | ||
Association of narcolepsy-cataplexy with HLA-DRB1 and DQB1 in Mexican patients: a relationship between HLA and gender is suggested | Q33360439 | ||
HLA-DR 15 is associated with female sex and younger age at diagnosis in multiple sclerosis. | Q35465548 | ||
Family studies in acute leukaemia in childhood: a possible association with autoimmune disease | Q36043180 | ||
Evidence that an HLA-DQA1-DQB1 haplotype influences susceptibility to childhood common acute lymphoblastic leukaemia in boys provides further support for an infection-related aetiology | Q36115300 | ||
Hierarchy of resistance to cervical neoplasia mediated by combinations of killer immunoglobulin-like receptor and human leukocyte antigen loci | Q36403391 | ||
A second major histocompatibility complex susceptibility locus for multiple sclerosis | Q37332571 | ||
Female predominance and X chromosome defects in autoimmune diseases | Q37438936 | ||
An international cohort study of cancer in systemic lupus erythematosus | Q38474206 | ||
Conserved extended haplotypes of the major histocompatibility complex: further characterization. | Q40264243 | ||
Mediterranean and Amerindian MHC class II alleles are associated with multiple sclerosis in Mexicans | Q44041614 | ||
A possible epidemiological association between multiple sclerosis and lymphoma/leukaemia | Q44812372 | ||
Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex | Q46806709 | ||
Genetic difference between Europeans and Indians: tissue and blood types | Q46988277 | ||
Examination of gender effect in birth weight and miscarriage associations with childhood cancer (United Kingdom). | Q47306899 | ||
A Taqman assay for high-throughput genotyping of the multiple sclerosis-associated HLA-DRB1*1501 allele | Q60542802 | ||
The potential effect of gender in combination with common genetic polymorphisms of drug-metabolizing enzymes on the risk of developing acute leukemia | Q62078766 | ||
The influence of HLA-DRB1 genes on disease severity in rheumatoid arthritis | Q67567811 | ||
Acute leukemia with features of systemic lupus erythematosus | Q71010733 | ||
A male-specific increase in the HLA-DRB4 (DR53) frequency in high-risk and relapsed childhood ALL | Q74086440 | ||
Genetic susceptibility to childhood common acute lymphoblastic leukaemia is associated with polymorphic peptide-binding pocket profiles in HLA-DPB1*0201 | Q74327558 | ||
Increased heterozygosity for MHC class II lineages in newborn males | Q74519731 | ||
Lack of association between childhood common acute lymphoblastic leukaemia and an HLA-C locus dimorphism influencing the specificity of natural killer cells | Q77348158 | ||
Systemic lupus erythematosus after acute lymphoblastic leukaemia | Q77493672 | ||
HLA class II DNA typing in a large series of European patients with systemic lupus erythematosus: correlations with clinical and autoantibody subsets | Q78069979 | ||
HLA-DRB1 alleles in juvenile-onset systemic lupus erythematosus: renal histologic class correlations | Q80078876 | ||
IFNG polymorphisms are associated with gender differences in susceptibility to multiple sclerosis | Q81326731 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | leukemia | Q29496 |
childhood leukemia | Q5097982 | ||
multiple sclerosis | Q8277 | ||
P304 | page(s) | 690-697 | |
P577 | publication date | 2010-12-01 | |
P1433 | published in | Autoimmunity | Q4826348 |
P1476 | title | Multiple sclerosis risk markers in HLA-DRA, HLA-C, and IFNG genes are associated with sex-specific childhood leukemia risk | |
P478 | volume | 43 |
Q37432974 | A childhood acute lymphoblastic leukemia genome-wide association study identifies novel sex-specific risk variants. |
Q51219524 | Association between SKIV2L polymorphism rs429608 and age-related macular degeneration: A meta-analysis. |
Q28383437 | Clinical implications of interferon-γ genetic and epigenetic variants |
Q38067314 | Current evidence for an inherited genetic basis of childhood acute lymphoblastic leukemia |
Q37385311 | Genetic variation in the extended major histocompatibility complex and susceptibility to childhood acute lymphoblastic leukemia: a review of the evidence |
Q28391986 | Host genetics and viral load in primary HIV-1 infection: clear evidence for gene by sex interactions |
Q35180032 | Human leukocyte antigen-DRB1 polymorphism in childhood acute lymphoblastic leukemia |
Q36114055 | IFNGR2 genetic polymorphism associated with sex-specific paranoid schizophrenia risk |
Q64944820 | Immunogenetics of new onset diabetes after transplantation in Kuwait. |
Q34469229 | Polymorphisms in the inflammatory genes CIITA, CLEC16A and IFNG influence BMD, bone loss and fracture in elderly women |
Q47130873 | Predominance of girls with cancer in families with multiple childhood cancer cases. |
Q41927543 | Sexual Dimorphism in Innate Immunity. |
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