automatic sequencer abi prism 377 (Thermo Fisher)
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automatic sequencer abi prism 377
Automatic Sequencer Abi Prism 377, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/377+automatic+sequencer/pm39778672-46-23-24
Average 90 stars, based on 1 article reviews
Automatic Sequencer Abi Prism 377, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/377+automatic+sequencer/pm39778672-46-23-24
Average 90 stars, based on 1 article reviews
automatic sequencer abi prism 377 - by Bioz Stars,
2026-10
90/100 stars
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DNA Sequencing:Article Title: Genetic polymorphisms of TLR3 are associated with Nasopharyngeal carcinoma risk in Cantonese population Article Snippet: .. Automatic DNA sequencing was performed on an Article Title: Complete Genome Sequences of New Xenotropic Murine Leukemia Viruses from the Senescence-Accelerated Mouse (SAM): Molecular and Phylogenetic Analyses Article Snippet: .. The DNA sequencing was conducted on an Polymerase Chain Reaction:Article Title: Genetic polymorphisms of TLR3 are associated with Nasopharyngeal carcinoma risk in Cantonese population Article Snippet: .. Automatic DNA sequencing was performed on an Article Title: An intronic variant in LAMB3 contributes to junctional epidermolysis bullosa and enamel hypoplasia via translational attenuation. Article Snippet: Objectives: This study aimed to investigate the genetic etiology of a family affected by junctional epidermolysis bullosa (JEB) and generalized enamel hypoplasia, and to explore how an intronic variant influenced the 5’ untranslated region (5’UTR), thereby affecting LAMB3 expression and contributing to the pathogenesis of the Article Title: Genetic polymorphisms of TLR3 are associated with Nasopharyngeal carcinoma risk in Cantonese population Article Snippet: .. We then sequenced the PCR products using ABI PRISM Dye Terminator Sequencing Kits and loading the samples onto an ABI Article Title: Enamel defects of Axenfeld-Rieger syndrome and the role of PITX2 in its pathogenesis. Article Snippet: AxenfeldRieger syndrome (ARS) is a group of rare autosomal dominant human diseases with an incidence of 1 in 200,000.. Patients with ARS exhibit specific abnormalities in the anterior segment of the eye, with or without systemic manifestations (Hjalt & Semina, 2005).. The major systemic malformations of ARS involve dental, umbilical, heart, and craniofacial abnormalities (Tümer & BachHolm, 2009). Article Title: Digenic inheritance accounts for phenotypic variability in amelogenesis imperfecta. Article Snippet: Funding information Beijing Natural Science Foundation, Grant/Award Number: 7164311; National Clinical Key Discipline Construction Project, Grant/Award Number: PKUSSNMP-201904 Abstract Amelogenesis imperfecta (AI) represents a group of clinically and genetically heterogeneous disorders that affect enamel formation and mineralization.. Although AI is commonly considered a monogenic disorder, digenic inheritance is rarely reported.. In this study, we recruited two nonconsanguineous Chinese families exhibiting diverse phenotypes of enamel defects among affected family members. Sequencing:Article Title: KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences Article Snippet: .. Automated sequencing was performed at both ends on an Article Title: An intronic variant in LAMB3 contributes to junctional epidermolysis bullosa and enamel hypoplasia via translational attenuation. Article Snippet: Objectives: This study aimed to investigate the genetic etiology of a family affected by junctional epidermolysis bullosa (JEB) and generalized enamel hypoplasia, and to explore how an intronic variant influenced the 5’ untranslated region (5’UTR), thereby affecting LAMB3 expression and contributing to the pathogenesis of the Article Title: Genetic polymorphisms of TLR3 are associated with Nasopharyngeal carcinoma risk in Cantonese population Article Snippet: .. We then sequenced the PCR products using ABI PRISM Dye Terminator Sequencing Kits and loading the samples onto an ABI Article Title: KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences. Article Snippet: .. Automated sequencing was performed at both ends on an Article Title: Complete Genome Sequences of New Xenotropic Murine Leukemia Viruses from the Senescence-Accelerated Mouse (SAM): Molecular and Phylogenetic Analyses Article Snippet: .. The DNA sequencing was conducted on an Article Title: Digenic inheritance accounts for phenotypic variability in amelogenesis imperfecta. Article Snippet: Funding information Beijing Natural Science Foundation, Grant/Award Number: 7164311; National Clinical Key Discipline Construction Project, Grant/Award Number: PKUSSNMP-201904 Abstract Amelogenesis imperfecta (AI) represents a group of clinically and genetically heterogeneous disorders that affect enamel formation and mineralization.. Although AI is commonly considered a monogenic disorder, digenic inheritance is rarely reported.. In this study, we recruited two nonconsanguineous Chinese families exhibiting diverse phenotypes of enamel defects among affected family members. Purification:Article Title: An intronic variant in LAMB3 contributes to junctional epidermolysis bullosa and enamel hypoplasia via translational attenuation. Article Snippet: Objectives: This study aimed to investigate the genetic etiology of a family affected by junctional epidermolysis bullosa (JEB) and generalized enamel hypoplasia, and to explore how an intronic variant influenced the 5’ untranslated region (5’UTR), thereby affecting LAMB3 expression and contributing to the pathogenesis of the Article Title: Enamel defects of Axenfeld-Rieger syndrome and the role of PITX2 in its pathogenesis. Article Snippet: AxenfeldRieger syndrome (ARS) is a group of rare autosomal dominant human diseases with an incidence of 1 in 200,000.. Patients with ARS exhibit specific abnormalities in the anterior segment of the eye, with or without systemic manifestations (Hjalt & Semina, 2005).. The major systemic malformations of ARS involve dental, umbilical, heart, and craniofacial abnormalities (Tümer & BachHolm, 2009). Article Title: Digenic inheritance accounts for phenotypic variability in amelogenesis imperfecta. Article Snippet: Funding information Beijing Natural Science Foundation, Grant/Award Number: 7164311; National Clinical Key Discipline Construction Project, Grant/Award Number: PKUSSNMP-201904 Abstract Amelogenesis imperfecta (AI) represents a group of clinically and genetically heterogeneous disorders that affect enamel formation and mineralization.. Although AI is commonly considered a monogenic disorder, digenic inheritance is rarely reported.. In this study, we recruited two nonconsanguineous Chinese families exhibiting diverse phenotypes of enamel defects among affected family members. Amplification:Article Title: Enamel defects of Axenfeld-Rieger syndrome and the role of PITX2 in its pathogenesis. Article Snippet: AxenfeldRieger syndrome (ARS) is a group of rare autosomal dominant human diseases with an incidence of 1 in 200,000.. Patients with ARS exhibit specific abnormalities in the anterior segment of the eye, with or without systemic manifestations (Hjalt & Semina, 2005).. The major systemic malformations of ARS involve dental, umbilical, heart, and craniofacial abnormalities (Tümer & BachHolm, 2009). |