Results 21 to 30 of about 19,176 (234)

Prader-Willi syndrome: reflections on seminal studies and future therapies [PDF]

open access: yesOpen Biology, 2020
Prader-Willi syndrome (PWS) is caused by the loss of function of the paternally inherited 15q11-q13 locus. This region is governed by genomic imprinting, a phenomenon in which genes are expressed exclusively from one parental allele.
Michael S. Chung   +3 more
doaj   +1 more source

Investigating spatially autocorrelated consumer preference for multiple ecolabels: Evidence from a choice experiment

open access: yesCleaner and Responsible Consumption, 2022
This study investigates spatial autocorrelation in consumer preferences for diverse ecolabels, such as certified ecolabel (type I) and non-certified ecolabel (type II).
Shinsuke Kyoi   +2 more
doaj   +1 more source

idic(X)(q13) [PDF]

open access: yesAtlas of Genetics and Cytogenetics in Oncology and Haematology, 2010
Review on idic(X)(q13), with data on clinics, and the genes involved.
openaire   +2 more sources

A report on seven fetal cases associated with 15q11‐q13 microdeletion and microduplication

open access: yesMolecular Genetics & Genomic Medicine, 2021
Background The 15q11‐q13 region contains three breakpoints (BP1 to BP3), and copy number variations often occur in the region. Aims 15q11‐q13 microdeletion and microduplication are usually associated with Prader‐Willi and Angelman syndromes, respectively.
Xiuzhu Huang   +9 more
doaj   +1 more source

Director-Generals’ Human and Social Capital, and Management Performance of Farmers’ Cooperatives: Evidence from China’s Fujian

open access: yesInternational Journal of Management and Economics, 2018
Purpose – This study aimed to assess the impact of director-generals’ human and social capitals on the organizational performance of farmers’ cooperatives in Fujian Province.
Liu Bin, Li Zhongbin
doaj   +1 more source

Precision Medicine in a Patient With Multiple Myeloma Presenting With t(2;11) and <i>CCND1</i> Overexpression. [PDF]

open access: yesEJHaem
ABSTRACT Translocations involving CCND1 are well described in multiple myeloma (MM), most frequently t(11;14), but rearrangements involving the immunoglobulin kappa (IGK) locus are rare. We present a case of a 71‐year‐old female with MM harboring t(2;11)(p11.2;q13), resulting in IGK::CCND1, with cyclin D1 and BCL‐2 overexpression.
Siegel A   +7 more
europepmc   +2 more sources

Dimensions of CSR in Online Communication of Pharmaceutical Companies: A Comparative Study

open access: yesInternational Journal of Entrepreneurial Knowledge, 2019
The article focuses on analysis of online communication of pharmaceutical companies in the field of CSR. It is based on the fact that there are specific segments in the economy, which are called sensitive sectors.
Džupin Milan, Džupinová Zuzana
doaj   +1 more source

Investigating the effects of altruism on consumer preference for food from disaster-affected regions: A case of Japan

open access: yesJournal of Agriculture and Food Research, 2021
Consumer's willingness to donate to support the disaster-affected region is known to be related to altruism. This study examines how consumer preference for food from disaster-affected regions is affected by the degree of consumer's altruism level and ...
Kentaka Aruga, Timothy Bolt
doaj   +1 more source

t(11;21)(q13;q22) [PDF]

open access: yesAtlas of Genetics and Cytogenetics in Oncology and Haematology, 2011
Review on t(11;21)(q13;q22), with data on clinics, and the genes involved.
Huret, JL, Xue, Y
openaire   +2 more sources

Artificial Intelligence–Based Online Symptom Assessment Tools for Systemic Lupus Erythematosus Diagnosis: Patient Perspectives

open access: yesArthritis Care &Research, EarlyView.
Objective The objective of this article is to identify perceptions of patients with systemic lupus erythematosus (SLE) regarding artificial intelligence (AI)–based online symptom assessment tools, and the potential of these tools to address diagnostic barriers.
Olivia A. Stein   +7 more
wiley   +1 more source

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