Detalhe da pesquisa
1.
Mutations in KIF7 implicated in idiopathic scoliosis in humans and axial curvatures in zebrafish.
Hum Mutat
; 42(4): 392-407, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33382518
2.
Tracking DNA-based antigen-specific T cell receptors during progression to type 1 diabetes.
Sci Adv
; 9(49): eadj6975, 2023 Dec 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38064552
3.
Congruence as a measurement of extended haplotype structure across the genome.
J Transl Med
; 10: 32, 2012 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-22369243
4.
Temporal development of T cell receptor repertoires during childhood in health and disease.
JCI Insight
; 7(18)2022 09 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35998036
5.
Analysis of Human Leukocyte Antigen DR Alleles, Immune-Related Adverse Events, and Survival Associated With Immune Checkpoint Inhibitor Use Among Patients With Advanced Malignant Melanoma.
JAMA Netw Open
; 5(12): e2246400, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36512357
6.
Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease.
Genes (Basel)
; 12(6)2021 06 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34208743
7.
The role of CDHR3 in susceptibility to otitis media.
J Mol Med (Berl)
; 99(11): 1571-1583, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34322716
8.
Failed Genetic Protection: Type 1 Diabetes in the Presence of HLA-DQB1*06:02.
Diabetes
; 69(8): 1763-1769, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32439825
9.
Multi-omic studies on missense PLG variants in families with otitis media.
Sci Rep
; 10(1): 15035, 2020 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-32929111
10.
Defining multiple common "completely" conserved major histocompatibility complex SNP haplotypes.
Clin Immunol
; 132(2): 203-14, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19427271
11.
Identification of Novel Genes and Biological Pathways That Overlap in Infectious and Nonallergic Diseases of the Upper and Lower Airways Using Network Analyses.
Front Genet
; 10: 1352, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-32010199
12.
Methyldopa blocks MHC class II binding to disease-specific antigens in autoimmune diabetes.
J Clin Invest
; 128(5): 1888-1902, 2018 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29438107
13.
Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology.
G3 (Bethesda)
; 8(8): 2663-2672, 2018 07 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-29930198
14.
The fission yeast DNA structure checkpoint protein Rad26ATRIP/LCD1/UVSD accumulates in the cytoplasm following microtubule destabilization.
BMC Cell Biol
; 7: 32, 2006 Aug 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-16930478
15.
Sequencing of the TBX6 Gene in Families with Familial Idiopathic Scoliosis.
Spine Deform
; 3(4): 288-296, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26120555
16.
Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis.
G3 (Bethesda)
; 5(2): 167-74, 2014 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25504735
17.
Replication and further characterization of a Type 1 diabetes-associated locus at the telomeric end of the major histocompatibility complex.
J Diabetes
; 3(3): 238-47, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21631897
18.
Dominant suppression of Addison's disease associated with HLA-B15.
J Clin Endocrinol Metab
; 96(7): 2154-62, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21565792
19.
Haplotype analysis discriminates genetic risk for DR3-associated endocrine autoimmunity and helps define extreme risk for Addison's disease.
J Clin Endocrinol Metab
; 95(10): E263-70, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20631027
20.
Homozygosity of the polymorphism MICA5.1 identifies extreme risk of progression to overt adrenal insufficiency among 21-hydroxylase antibody-positive patients with type 1 diabetes.
J Clin Endocrinol Metab
; 94(11): 4517-23, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19820007