About: Bing Yu

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher (ORCID 0000-0001-6013-5220)

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) researcher (ORCID 0000-0001-6013-5220) (en)
rdfs:label	Bing Yu (en) Bing Yu (nl) Bing Yu (ast) Bing Yu (es) Bing Yu (sl)
skos:prefLabel	Bing Yu (en) Bing Yu (nl) Bing Yu (ast) Bing Yu (es) Bing Yu (sl)
name	Bing Yu (en) Bing Yu (nl) Bing Yu (ast) Bing Yu (es) Bing Yu (sl)
Scopus author ID	wds:Q39953946-0CAD1EE0-68C3-4F6E-AE77-ED073C51B4A3
Scopus author ID	35232006200
given name	wds:Q39953946-4DDCE5F1-A86B-4056-9E80-C80525D44771
given name	Bing
instance of	wds:Q39953946-BDD81064-B5A3-465C-BE3F-758433D86319
instance of	Homo sapiens
occupation	wds:Q39953946-CE365666-98D6-4FE4-AD5B-2CF14B368383
employer	wds:Q39953946-E20CB5FA-8795-42A9-9E68-5296A3187466
sex or gender	wds:Q39953946-91C8BEA0-5C13-4CD7-8B93-E389E5FCF088
ISNI	wds:Q39953946-2489EDCC-520E-4E19-B8DB-985210A390AB
VIAF ID	wds:Q39953946-75FA4534-21D5-4F7D-87E1-D5105D623A8A
IdRef ID	wds:Q39953946-C0E73438-59D7-4052-B0E6-878EBCC7E8DD
date of birth	wds:Q39953946-6E646CCB-8915-444B-BC82-39C6467F3BD0
educated at	wds:Q39953946-923B48C2-B147-4E3B-A061-2ACD65261121 wds:Q39953946-DB2A5521-82F1-420B-A2B2-14A6074683FF
VIAF ID	http://viaf.org/viaf/93676944
IdRef ID	http://www.idref.fr/154748889/id
occupation	researcher
employer	University of Sydney
sex or gender	male
ISNI	0000000066646809
VIAF ID	93676944
IdRef ID	154748889
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
educated at	University of Sydney Fudan University
ORCID iD	wds:Q39953946-D90B77D0-0A18-4E6A-9FA3-2A2D5CA1FA01
ORCID iD	https://orcid.org/0000-0001-6013-5220
ORCID iD	0000-0001-6013-5220
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q39953946
is author of	Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis Setting up next-generation sequencing in the medical laboratory Patterns of DNA mutations and ALK rearrangement in resected node negative lung adenocarcinoma. DHPLC can be used to detect low-level mutations in amyotrophic lateral sclerosis. Combined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studies An approach to finding brain-situated mutations in sporadic Parkinson's disease. Dietary sialic acid supplementation improves learning and memory in piglets. The EPAS1 gene influences the aerobic-anaerobic contribution in elite endurance athletes. Genetic susceptibility to environmental toxicants in ALS. SRp54 (SFRS11), a regulator for tau exon 10 alternative splicing identified by an expression cloning strategy Mammary analogue secretory carcinoma: an evaluation of its clinicopathological and genetic characteristics. HER2 insertion YVMA mutant lung cancer: Long natural history and response to afatinib. BRAF mutations in non-small cell lung cancer Pharmacogenetic polymorphisms of the AR and metabolism and susceptibility to hormone-induced azoospermia Plasma total bilirubin levels predict amputation events in type 2 diabetes mellitus: the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study Placental deficiency of interleukin-10 (IL-10) in preeclampsia and its relationship to an IL10 promoter polymorphism Salivary duct carcinoma: Clinicopathologic features, morphologic spectrum, and somatic mutations. PD-L1 expression is a favorable prognostic factor in early stage non-small cell carcinoma. Transmission of C9orf72 hexanucleotide repeat expansions in sporadic amyotrophic lateral sclerosis: an Australian trio study Correlation of BRAF and NRAS mutation status with outcome, site of distant metastasis and response to chemotherapy in metastatic melanoma. A genome-wide analysis of brain DNA methylation identifies new candidate genes for sporadic amyotrophic lateral sclerosis. A gene-environment study of the paraoxonase 1 gene and pesticides in amyotrophic lateral sclerosis BRAF(V600E) and NRAS(Q61L/Q61R) mutation analysis in metastatic melanoma using immunohistochemistry: a study of 754 cases highlighting potential pitfalls and guidelines for interpretation and reporting. Screening for ROS1 gene rearrangements in non-small-cell lung cancers using immunohistochemistry with FISH confirmation is an effective method to identify this rare target. The suitability of small biopsy and cytology specimens for EGFR and other mutation testing in non-small cell lung cancer Mutation surveyor: an in silico tool for sequencing analysis A method of oligochip for single nucleotide polymorphism genotyping in the promoter region of the interleukin-1 beta gene and its clinical application Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS. Looking for differences in copy number between blood and brain in sporadic amyotrophic lateral sclerosis. Using case-parent trios to look for rare de novo genetic variants in adult-onset neurodegenerative diseases. Angiotensin-converting enzyme gene DD genotype is associated with increased systolic blood pressure in an Australian Rural Type 2 Diabetic Cohort Differential effects of calyculin A and okadaic acid on the glucose-induced regulation of glycogen synthase and phosphorylase activities in cultured hepatocytes An online locus-specific mutation database for familial hypertrophic cardiomyopathy Analysis of clinically relevant somatic mutations in high-risk head and neck cutaneous squamous cell carcinoma. Effects of metformin on glucose and glucagon regulated gluconeogenesis in cultured normal and diabetic hepatocytes. Environmental insults: critical triggers for amyotrophic lateral sclerosis Alterations of insulin-like growth factor-1 receptor gene copy number and protein expression are common in non-small cell lung cancer. A comparison of the lengths of androgen receptor triplet repeats in brain and blood in motor neuron diseases Low yield in screening patients with sporadic motor neuron disease for Kennedy disease In silico PCR analysis. An analysis of the entire SOD1 gene in sporadic ALS

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