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Analysis of TFAP2A mutations in Branchio- Oculo-Facial Syndrome indicates functional complexity within the AP-2a DNA-binding domain
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Nomor Panggil: Human Molecular Genetics: Volume 22, Issue 16: 15 August 2013: p. 3195-3206
Pengarang: tidak diketahui
Tahun/Penerbit: United Kingdom : Oxford University Press, 2013
Mechanism of Polycomb recruitment to CpG islands revealed by inherited disease-associated mutation
cover
Nomor Panggil: Human Molecular Genetics: Volume 22, Issue 16: 15 August 2013: p. 3187-3194
Pengarang: tidak diketahui
Tahun/Penerbit: United Kingdom : Oxford University Press, 2013
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment
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Nomor Panggil: Human Molecular Genetics: Volume 22, Issue 15: 1 August 2013: p. 3174-3185
Pengarang: tidak diketahui
Tahun/Penerbit: United Kingdom : Oxford University Press, 2013
Genome-wide association study in a Chinese population with diabetic retinopathy
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Nomor Panggil: Human Molecular Genetics: Volume 22, Issue 15: 1 August 2013: p. 3165-3173
Pengarang: tidak diketahui
Tahun/Penerbit: United Kingdom : Oxford University Press, 2013
Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity
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Nomor Panggil: Human Molecular Genetics: Volume 22, Issue 15: 1 August 2013: p. 3152-3164
Pengarang: tidak diketahui
Tahun/Penerbit: United Kingdom : Oxford University Press, 2013
CEP89 is required for mitochondrial metabolism and neuronal function in man and fly
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Nomor Panggil: Human Molecular Genetics: Volume 22, Issue 15: 1 August 2013: p. 3138-3151
Pengarang: tidak diketahui
Tahun/Penerbit: United Kingdom : Oxford University Press, 2013
Smooth muscle hyperplasia due to loss of smooth muscle a-actin is driven by activation of focal adhesion kinase, altered p53 localization and increased levels of platelet-derived growth factor receptor-b
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Nomor Panggil: Human Molecular Genetics: Volume 22, Issue 15: 1 August 2013: p. 3123-3137
Pengarang: tidak diketahui
Tahun/Penerbit: United Kingdom : Oxford University Press, 2013
The dual functions of the extreme N-terminus of TDP-43 in regulating its biological activity and inclusion formation
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Nomor Panggil: Human Molecular Genetics: Volume 22, Issue 15: 1 August 2013: p. 3112-3122
Pengarang: tidak diketahui
Tahun/Penerbit: United Kingdom : Oxford University Press, 2013
Activation of p38 signaling increases utrophin A expression in skeletal muscle via the RNA-binding protein KSRP and inhibition of AU-rich element-mediated mRNA decay: implications for novel DMD therapeutics
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Nomor Panggil: Human Molecular Genetics: Volume 22, Issue 15: 1 August 2013: p. 3093-3111
Pengarang: tidak diketahui
Tahun/Penerbit: United Kingdom : Oxford University Press, 2013
De-repression of FOXO3a death axis by microRNA-132 and -212 causes neuronal apoptosis in Alzheimer?s disease
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Nomor Panggil: Human Molecular Genetics: Volume 22, Issue 15: 1 August 2013: p. 3077-3092
Pengarang: tidak diketahui
Tahun/Penerbit: United Kingdom : Oxford University Press, 2013
 
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