18301Detail in contemporary glass architecture
This book presents 50 of the most recently completed and influential glass designs for residential, public and commercial architecture. Each project is presented with colour photographs, site plans and sections and elevations, as well as numerous construction details. There is also a descriptive text, detailed captions and in-depth information for each project, including the location, client, architectural project team, main consultants and contractors.
18302Detail in contemporary timber architecture
It provides analysis of both the technical and the aesthetic importance of details in modern timber architecture. Featuring the work of internationally renowned architects, this book presents 50 of the most recent and influential designs for residential and commercial timber architecture.
18303Details in architecture 1-2
Providing images, specifications and graphics design about architecture works, such as: Skybridge in Malaysia, Star city in Australia, Glass Facade in Brazil,...
18304Details in architecture 4: Creative detailing
The CD features an abundance of sketches, drawings and relevant photographs of specific details which have been selected and submitted by the architect to place the architectural details into perspective. Each project also includes a 250-word descriptive text. The emerging trends which will be followed by architects and designers for years to come are presented in clear and concise layouts. Many details are functional, but many are also decorative. Details can be used to make a building design environment friendly, or called upon to link a building with place, tradition and history.
18305Detection of 16S rRNA and 23S rRNA gene mutations in multidrug resistant Salmonella serovars isolated from different sources using RNA sequencing method
The aim of this study was to support for finding novel mechanisms that render bacteria resistant to the ribosome targeting antibiotics, we screen for antibiotics resistant 16S and 23S ribosomal RNAs in multidrug resistant Salmonella serovars isolated from raw retail meats isolated from Hanoi, Vietnam.
18306Detection of -28(A>G) beta thalassemia mutation using amplification refractory mutation system (ARMS)-PCR = Phát hiện đột biến -28(A>G) gây bệnh beta thalassemia bằng kỹ thuật AMRS-PCR
Nghiên cứu các cặp mồi của kỹ thuật ARMS_PCR được thiết kế và điều kiện PCR được tối ưu để phát hiện đột biến -28(A>G) trong 263 bệnh nhân được chẩn đoán β thalassem.
18307Detection of an EDA mutation causing hypohidrotic ectodermal dysplasia in a Vietnamese patient
Hypohidrotic ectodermal dysplasia (HED) is a rare disease characterized by abnormal development of the structures derived from the ectoderm layer, including hair, teeth, nails, and sweat glands. The most observed form of HED, which is known as X-linked hypohidrotic ectodermal dysplasia (XLHED), is commonly attributed to genetic abnormalities in the ectodysplasin A (EDA) gene.
18308Detection of c.G2194A mutation in AR gene of a vietnamese patient with androgen insensitivity syndrome: a case report
In this study, whole-exome sequencing was performed to screen mutations in the AR gene as well as genes related to disorders of sex development (DSD). Sanger sequencing was applied to validate the mutations in the patient. One missense mutation in the AR gene which was reported previously was identified in the patient. In this site, nucleotide G is changed to A at position 2194 on cDNA (c.G2194A), leading to a substitution of aspartic at position 732 aspartic to asparagine (p.Asp732Asn). However, this is the first published case in a Vietnamese with this mutation. Our study expands the mutation spectrum of the AR gene in Vietnamese patients and confirms the usefulness of whole-exome sequencing in the diagnosis of AIS. The results of the study are the basis for supporting doctors in prenatal diagnosis and giving reasonable advice to patients and families.
18309Detection of pathogenic variants related to severe dominant monogenic diseases by non-invasive prenatal testing (NIPT-SGD)
Report describes the first cases in Vietnam that identified pathogenic/likely pathogenic variants by NIPT-SGD in fetuses. These findings were compared with the diagnostic testing (whole exome sequencing/WES) on amniotic fluid/placenta tissue/umbilical cord blood samples. Single-gene NIPT detected pathogenic variants in the fetuses on TSC2, FGFR3, FGFR2 (two cases), and PTPN11 genes. All results coincided with the subsequent diagnosis. Preliminary research showed the potential of cell-free fetal DNA analysis for prenatal screening of dominant single-gene mutations.
18310Determinants affecting the satisfaction of forwarders with container delivery services: an examination of the Da Nang port joint stock company - a case study
Chapter 1: Introduction; Chapter 2: Literature review; Chapter 3: Research design and methodology; Chapter 4: Data analysis; Chapter 5: A case study of strategy and action plan for Da Nang port joint stock company; Chapter 6: Recommendations and conclusion.