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index medicus (13) 13
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BMC Cancer, ISSN 1471-2407, 06/2019, Volume 19, Issue 1, pp. 605 - 16
BackgroundProgrammed cell death protein 1(PD-1) blocking antibodies have been used to enhance immunity in solid tumors and achieve durable clinical responses... 
TGFβ signaling pathway | Wnt-β-catenin signaling pathway | M1 macrophage cells | IFN-γ | MSI | PD-1 | TGF signaling pathway | PD-1 BLOCKADE | PTEN | TUMOR-CELLS | Wnt--catenin signaling pathway | EVASION | CHECKPOINT BLOCKADE | IFN | EXCLUSION | ONCOLOGY | RESISTANCE | Viral antibodies | Usage | Care and treatment | Colon cancer | Cell death | Antibodies | Genetic aspects | Research | Biological markers | Gene expression
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 3493 - 9
Thalassemia and hemoglobinopathy are two common inherited disorders, which are highly prevalent in southern China. However, there is little knowledge on the... 
POPULATION | ALPHA-THALASSEMIA | MULTIDISCIPLINARY SCIENCES | PROVINCE | SPECTRUM | BETA-THALASSEMIA | DELETION | CD90 antigen | Hemoglobinopathy | Genetic counseling | Prenatal diagnosis | Hemoglobin | Thalassemia | Mutation | Genotypes | Hereditary diseases
Journal Article
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, ISSN 0960-7692, 07/2019
To follow up the noninvasive prenatal testing (NIPT) results of 31515 singleton pregnancies in Fujian province, southeastern China and assess its performance... 
Journal Article
BMC Complementary and Alternative Medicine, ISSN 1472-6882, 06/2013, Volume 13, Issue 1, pp. 144 - 144
Journal Article
Molecular Cytogenetics, ISSN 1755-8166, 03/2019, Volume 12, Issue 1, pp. 13 - 12
Journal Article
by Wu, XQ and Xu, LP and Li, Y and Lin, N and Su, LJ and Cai, MY and Xie, XR and Zheng, L and Huang, HL and Lin, Y
MOLECULAR CYTOGENETICS, ISSN 1755-8166, 08/2019, Volume 12, Issue 1, pp. 36 - 7
Background Nearly 9.89% of chromosome 16 consists of segmental duplications, which makes it prone to non-homologous recombination. The present study aimed to... 
DUPLICATIONS | AUTISM | 16P13.11 PREDISPOSE | MENTAL-RETARDATION | Chromosomal microarray analysis | MICRODELETION SYNDROME | Prenatal diagnosis | GENETICS & HEREDITY | 16P11.2 | SPECTRUM | Submicroscopic aberrations | Chromosome 16 | DELETIONS | 15Q11.2 | DNA microarrays | Pregnant women | Chromosomes | Analysis
Journal Article
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, ISSN 1003-9406, 08/2019, Volume 36, Issue 8, p. 761
To explore the hematological phenotype and genotype of hemoglobin Q-Thailand in Fujian area. Genomic DNA was extracted from peripheral venous blood samples of... 
Journal Article
by Wang, HW and Wang, XR and Xu, LP and Zhang, J and Cao, H
AGING-US, ISSN 1945-4589, 10/2019, Volume 11, Issue 19, pp. 8587 - 8603
Gene expression based consensus molecular subtypes (CMS) and non-negative matrix factorization (NMF) sub-clusters are robust colon cancer classification... 
CDX2 | VDR | SUBTYPES | BRAF inhibitors | PHENOTYPE | PI3K-mTOR inhibitors | chemotherapy | TUMORS | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | RESPONSES | CETUXIMAB | GASTRIC-CANCER | colon cancer subtypes
Journal Article
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, ISSN 1003-9406, 05/2019, Volume 36, Issue 5, p. 498
To determine the origin of supernumerary small marker chromosomes (sSMCs) carried by two fetuses. Single nucleotide polymorphism array (SNP-array) and... 
Journal Article
Journal of clinical laboratory analysis, ISSN 0887-8013, 09/2019, p. e23025
While congenital anomalies of the kidney and urinary tract (CAKUT) constitute one-third of all congenital malformations, the mechanisms underlying their... 
Journal Article
Journal Article
Medicine, ISSN 0025-7974, 12/2018, Volume 97, Issue 50, p. e13617
Background: Congenital heart disease (CHD) is one of the most common birth defects; however, the mechanisms underlying its development are poorly understood.... 
CHROMOSOMAL MICROARRAY | MEDICINE, GENERAL & INTERNAL | DEFECTS | ABNORMALITIES | congenital heart disease | SNP array | FETUSES | COMPARATIVE GENOMIC HYBRIDIZATION | fetal | PRENATAL-DIAGNOSIS | Care and treatment | Congenital heart disease | Diagnosis | Single nucleotide polymorphisms | Identification and classification
Journal Article