Global ETD Search
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Showing 1 to 3 of 3 for “"Sall4"”.
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Funktionelle Analyse des murinen Sall4-Gens
Mutationen im humanen SALL4 Gen verursachen das Okihiro Syndrom, eine autosomal-dominante vererbte Erkrankung, die durch eine Kombination von Duane-Anomalie und Fehlbildungen des Radius charakterisiert ist. Daneben sind auch Herzfehler, Hörstörungen und anale Fehlbildungen beschrieben worden. Alle …
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DIRECT REPROGRAMMING OF HUMAN FIBROBLASTS INTO CARDIOMYOCYTES
… regulators and found two new factors, SALL4 and YY1 significantly enhanced reprogramming efficiency in human dermal fibroblasts (HDFs) when working together with GATA4, MEF2C, TBX5, HAND2 and MYOCD (5F). HDFs-generated iCMs exhibited cardiac-like action potential and spontaneously …
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Hox Targeting in Vertebrate Forelimb Induction: Expression and Comparative Genomics
… in genes inducing the forelimb (<em>Tbx5, Salli, Sall4, and Fgf10</em>) have been predicted through comparative genomics, including the use of sequence alignment, phylogenetic footprinting, and related analyses. We have also used comparative genomics to predict potential Lmx1b core binding sites …