Detalhe da pesquisa
1.
Obliteration of portal venules contributes to portal hypertension in biliary cirrhosis.
J Pathol
; 263(2): 178-189, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38551075
2.
Multiple infusions of ex vivo-expanded regulatory T cells promote CD163+ myeloid cells and kidney allograft survival in non-lymphodepleted non-human primates.
Kidney Int
; 105(1): 84-98, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37839695
3.
Next-generation pathology detection of T cell-antigen-presenting cell immune synapses in human liver allografts.
Hepatology
; 77(2): 355-366, 2023 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35819312
4.
Precision transplant pathology.
Curr Opin Organ Transplant
; 25(4): 412-419, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32520786
5.
MCM9 mutations are associated with ovarian failure, short stature, and chromosomal instability.
Am J Hum Genet
; 95(6): 754-62, 2014 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25480036
6.
Tissue-resident memory T cell maintenance during antigen persistence requires both cognate antigen and interleukin-15.
Sci Immunol
; 8(82): eadd8454, 2023 04 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37083450
7.
Transcriptome and Exome Analyses of Hepatocellular Carcinoma Reveal Patterns to Predict Cancer Recurrence in Liver Transplant Patients.
Hepatol Commun
; 6(4): 710-727, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34725972
8.
Enhancing the Value of Histopathological Assessment of Allograft Biopsy Monitoring.
Transplantation
; 103(7): 1306-1322, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30768568
9.
Functional study of a novel missense single-nucleotide variant of NUP107 in two daughters of Mexican origin with premature ovarian insufficiency.
Mol Genet Genomic Med
; 6(2): 276-281, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29363275
10.
Late graft dysfunction after pediatric heart transplantation is associated with fibrosis and microvasculopathy by automated, digital whole-slide analysis.
J Heart Lung Transplant
; 36(12): 1336-1343, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29055602
11.
Highly heterogeneous genomic landscape of uterine leiomyomas by whole exome sequencing and genome-wide arrays.
Fertil Steril
; 107(2): 457-466.e9, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27889101
12.
Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability.
J Clin Invest
; 125(1): 258-62, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25437880