Detalhe da pesquisa
1.
Preparation of Tetrandrine Nanocrystals by Microfluidic Method and Its In Vitro and In Vivo Evaluation.
AAPS PharmSciTech
; 25(1): 4, 2023 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38114843
2.
EGR2 is a hub-gene in myocardial infarction and aggravates inflammation and apoptosis in hypoxia-induced cardiomyocytes.
BMC Cardiovasc Disord
; 22(1): 373, 2022 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35971091
3.
Optimizing genomic prediction model given causal genes in a dairy cattle population.
J Dairy Sci
; 103(11): 10299-10310, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-32952023
4.
Dynamic DNA methylation of ovaries during pubertal transition in gilts.
BMC Genomics
; 20(1): 510, 2019 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31221102
5.
Genome wide association study on feed conversion ratio using imputed sequence data in chickens.
Asian-Australas J Anim Sci
; 32(4): 494-500, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30381748
6.
Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities.
Am J Med Genet A
; 176(2): 319-329, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29194955
7.
Pallister-Killian syndrome: a study of 22 British patients.
J Med Genet
; 52(7): 454-64, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25888713
8.
A reliable method for the detection of BRCA1 and BRCA2 mutations in fixed tumour tissue utilising multiplex PCR-based targeted next generation sequencing.
BMC Clin Pathol
; 15: 5, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25859162
9.
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
Am J Hum Genet
; 87(5): 618-30, 2010 Nov 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-21055719
10.
Identification of a diagnostic model and molecular subtypes of major depressive disorder based on endoplasmic reticulum stress-related genes.
Front Psychiatry
; 14: 1168516, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37649561
11.
Bibliometric and visual analysis in the field of traditional Chinese medicine in cancer from 2002 to 2022.
Front Pharmacol
; 14: 1164425, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37469862
12.
Using the spring constant method to analyze arterial elasticity in type 2 diabetic patients.
Cardiovasc Diabetol
; 11: 39, 2012 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-22531211
13.
Analysis of using the tongue deviation angle as a warning sign of a stroke.
Biomed Eng Online
; 11: 53, 2012 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-22908956
14.
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
N Engl J Med
; 359(16): 1685-99, 2008 Oct 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-18784092
15.
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Genet Med
; 13(9): 777-84, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21844811
16.
Transmitted deletions of medial 5p and learning difficulties; does the cadherin cluster only become penetrant when flanking genes are deleted?
Am J Med Genet A
; 155A(11): 2807-15, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21965044
17.
Germline FFPE inherited cancer panel testing in deceased family members: implications for clinical management of unaffected relatives.
Eur J Hum Genet
; 29(5): 861-871, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33654310
18.
The Improvement Effect of Different Doses of Gamma Globulin on the Disease Condition of Infants with Hemolytic Disease of Newborn and Their Effects on Immune Factors in Serum.
Iran J Public Health
; 49(5): 914-922, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32953679
19.
Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4).
Hum Genet
; 125(2): 181-8, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19104840
20.
15q overgrowth syndrome: a newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q.
Am J Med Genet A
; 149A(2): 147-54, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19133692