Found: 22
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Lens induction requires attenuation of ERK signaling by Nf1.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1315, doi. 10.1093/hmg/ddr014
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- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. NP, doi. 10.1093/hmg/ddr052
- Publication type:
- Article
Spatial and temporal correlation between neuron loss and neuroinflammation in a mouse model of neuronopathic Gaucher disease.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1375, doi. 10.1093/hmg/ddr019
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- Publication type:
- Article
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1363, doi. 10.1093/hmg/ddr018
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- Publication type:
- Article
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1285
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- Publication type:
- Article
Wolfram syndrome 1 gene (WFS1) product localizes to secretory granules and determines granule acidification in pancreatic β-cells.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1274, doi. 10.1093/hmg/ddq568
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- Publication type:
- Article
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1411, doi. 10.1093/hmg/ddr022
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- Publication type:
- Article
Preventing the ubiquitin–proteasome-dependent degradation of frataxin, the protein defective in Friedreich's ataxia.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1253, doi. 10.1093/hmg/ddq566
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- Publication type:
- Article
Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1456, doi. 10.1093/hmg/ddq571
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- Publication type:
- Article
Preferential accumulation of N-terminal mutant huntingtin in the nuclei of striatal neurons is regulated by phosphorylation.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1424, doi. 10.1093/hmg/ddr023
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- Publication type:
- Article
Rex1/Zfp42 as an epigenetic regulator for genomic imprinting.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1353, doi. 10.1093/hmg/ddr017
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- Publication type:
- Article
TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1400, doi. 10.1093/hmg/ddr021
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- Publication type:
- Article
An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1306, doi. 10.1093/hmg/ddr013
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- Publication type:
- Article
Myogenic Akt signaling attenuates muscular degeneration, promotes myofiber regeneration and improves muscle function in dystrophin-deficient mdx mice.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1324, doi. 10.1093/hmg/ddr015
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- Publication type:
- Article
Smooth muscle protein-22-mediated deletion of Tsc1 results in cardiac hypertrophy that is mTORC1-mediated and reversed by rapamycin.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1290, doi. 10.1093/hmg/ddq570
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- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. NP, doi. 10.1093/hmg/ddr058
- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. NP, doi. 10.1093/hmg/ddr056
- Publication type:
- Article
Identification of direct downstream targets of Dlx5 during early inner ear development.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1262, doi. 10.1093/hmg/ddq567
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- Publication type:
- Article
Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1438, doi. 10.1093/hmg/ddr024
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- Publication type:
- Article
Germline competency of parthenogenetic embryonic stem cells from immature oocytes of adult mouse ovary.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1339, doi. 10.1093/hmg/ddr016
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- Publication type:
- Article
Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. 1387, doi. 10.1093/hmg/ddr020
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- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 7, p. NP, doi. 10.1093/hmg/ddr054
- Publication type:
- Article