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TBX6
Autism Multiplex Family with 16P11.2P12.2 Microduplication Syndrome in Monozygotic Twins and Distal 16P11.2 Deletion in Their Brother
Product Description SALSA® MLPA® Probemix P463-A2 MRKH to Be Used with the MLPA General Protocol
Novel ENU-Induced Mutation in Tbx6 Causes Dominant Spondylocostal Dysostosis-Like Vertebral Malformations in the Rat
Analysis of Mouse Embryonic Patterning and Morphogenesis By
Diagnostic Interpretation of Genetic Studies in Patients with Primary
S41419-021-03972-6.Pdf
Greg Whittemore, MS4 MD/MS Candidate Columbia University Vagelos College of Physicians and Surgeons Mentors: Cathy Mendelsohn and Simone Sanna-Cherchi
EXAMINING the POST-TRANSCRIPTIONAL REGULATION of LUNATIC FRINGE (Lfng) in the MOUSE SEGMENTATION CLOCK
FGF8, Wnt8 and Myf5 Are Target Genes of Tbx6 During Anteroposterior Specification in Xenopus Embryo
Identification of Direct T-Box Target Genes in the Developing Zebrafish Mesoderm Aaron T
An Interacting Network of T-Box Genes Directs Gene Expression and Fate in the Zebrafish Mesoderm
The Role of T and Tbx6 During Gastrulation and Determination of Left/Right Asymmetry Daniel Concepcion Submitted in Partial Fulf
Tbx6-Mediated Notch Signaling Controls Somite-Specific Mesp2 Expression
Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes As Potentially Cancer Predisposing in Familial Colorectal Cancer
Cellular Targets Involved in Reovirus-Induced Oncolysis Of
Genetic Variant of TTLL11 Gene and Subsequent Ciliary Defects Are Associated with Idiopathic Scoliosis in a 5-Generation UK Fami
Computational Prediction of CRISPR-Impaired Non-Coding
Uncoupling Heart Cell Specification and Migration in the Simple
Top View
Transcriptional Landscape of Myogenesis from Human Pluripotent
Uncoupling Heart Cell Specification and Migration in The
Downloaded July 2019), 46 In
COMPETITION BETWEEN T-BOX TRANSCRIPTION FACTORS CONTRIBUTES to DEVELOPMENTAL DYNAMICS of the MOUSE EMBRYO by Amy Kristen Wehn Ba
Functional Importance of Evolutionally Conserved Tbx6 Binding Sites in The
TBX6, LHX1 and Copy Number Variations in the Complex Genetics of Müllerian Aplasia
Progress and Perspective of TBX6 Gene in Congenital Vertebral Malformations
Fss/Tbx6 Is Required for Central Dermomyotome Cell Fate in Zebrafish
Ripply2 Recruits Proteasome Complex for Tbx6 Degradation to Define
WNT Signaling, in Synergy with T/TBX6, Controls Notch Signaling by Regulating Dll1 Expression in the Presomitic Mesoderm of Mouse Embryos
TBX6-Associated Congenital Scoliosis (TACS)
Distal Chromosome 16P11.2 Duplications Containing SH2B1 In
Eomes and Brachyury Control Pluripotency Exit and Germ Layer Segregation by Changes of Chromatin State
16P11.2 Microdeletions
Generation and Gene Expression Profiling of 48 Transcription-Factor
An Interacting Network of T-Box Genes Directs Gene Expression and Fate in the Zebrafish Mesoderm
A Divergent Tbx6-Related Gene and Tbx6 Are Both Required for Neural Crest and Intermediate Mesoderm Development in Xenopus