Detalhe da pesquisa
1.
The SKI proto-oncogene enhances the in vivo repopulation of hematopoietic stem cells and causes myeloproliferative disease.
Haematologica
; 99(4): 647-55, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24415629
2.
Comparison of time to treatment initiation of specialty medications between an integrated health system specialty pharmacy and external specialty pharmacies.
J Manag Care Spec Pharm
; 30(4): 352-362, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38555622
3.
Erythropoietin couples erythropoiesis, B-lymphopoiesis, and bone homeostasis within the bone marrow microenvironment.
Blood
; 117(21): 5631-42, 2011 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-21421837
4.
Darbepoietin-alfa has comparable erythropoietic stimulatory effects to recombinant erythropoietin whilst preserving the bone marrow microenvironment.
Haematologica
; 98(5): 686-90, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23242598
5.
Giant clams as open-source, scalable reef environmental biomonitors.
PLoS One
; 18(1): e0278752, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36602996
6.
Prerequisite endocardial-mesenchymal transition for murine cardiac trabecular angiogenesis.
Dev Cell
; 58(9): 791-805.e4, 2023 05 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37023750
7.
System dynamics in medical education: a tool for life.
Adv Health Sci Educ Theory Pract
; 17(2): 203-10, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20652401
8.
Surf smelt accelerate usage of endogenous energy reserves under climate change.
PLoS One
; 17(6): e0270491, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35759491
9.
Interaction of selective serotonin reuptake inhibitors with neuronal nicotinic acetylcholine receptors.
Biochemistry
; 49(27): 5734-42, 2010 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-20527991
10.
Congenital myasthenic syndrome caused by a frameshift insertion mutation in GFPT1.
Neurol Genet
; 6(4): e468, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32754643
11.
The presence of F cells with a fetal phenotype in adults with hemoglobinopathies limits the utility of flow cytometry for quantitation of fetomaternal hemorrhage.
Cytometry B Clin Cytom
; 94(4): 695-698, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29072803
12.
Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results.
Semin Pediatr Neurol
; 26: 28-32, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29961512
13.
A method to reduce ancestry related germline false positives in tumor only somatic variant calling.
BMC Med Genomics
; 10(1): 61, 2017 10 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29052513
14.
Case Report: Novel mutations in TBC1D24 are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disability.
F1000Res
; 6: 553, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28663785
15.
A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia.
Cold Spring Harb Mol Case Stud
; 2(5): a000851, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27626064
16.
Integration of Downstream Signals of Insulin-like Growth Factor-1 Receptor by Endoplasmic Reticulum Stress for Estrogen-Induced Growth or Apoptosis in Breast Cancer Cells.
Mol Cancer Res
; 13(10): 1367-76, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26116171
17.
Novel pathogenic variants and genes for myopathies identified by whole exome sequencing.
Mol Genet Genomic Med
; 3(4): 283-301, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26247046
18.
An integrated framework for reporting clinically relevant biomarkers from paired tumor/normal genomic and transcriptomic sequencing data in support of clinical trials in personalized medicine.
Pac Symp Biocomput
; : 56-67, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25592568
19.
Loss of the tumor suppressor SMARCA4 in small cell carcinoma of the ovary, hypercalcemic type (SCCOHT).
Rare Dis
; 2(1): e967148, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-26942101
20.
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4.
Nat Genet
; 46(5): 427-9, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24658001