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`Mitotic drive' of expanded CTG repeats in myotonic dystrophy type 1 (DM1)
British Library Online Contents | 2001| -
`Other' breast cancer susceptibility genes: searching for more holy grail
British Library Online Contents | 2001| -
3-Hydroxy-3-methylglutaryl-CoA lyase (HL): gene targeting causes prenatal lethality in HL-deficient mice
British Library Online Contents | 1998| -
5' and 3' region variability in the dopamine transporter gene (SLC6A3), pesticide exposure and Parkinson's disease risk: a hypothesis-generating study
British Library Online Contents | 2006| -
5-HT~2~A and 5-HT~2~C receptor polymorphisms and psychopathology in late onset Alzheimer's disease
British Library Online Contents | 1998| -
5-Hydroxymethylcytosine-mediated alteration of transposon activity associated with the exposure to adverse in utero environments in human
British Library Online Contents | 2016| -
5-Hydroxymethylcytosine-mediated alteration of transposon activity associated with the exposure to adverse in utero environments in human
British Library Online Contents | 2016| -
7,8-dihydroxyflavone ameliorates cognitive and motor deficits in a Huntington’s disease mouse model through specific activation of the PLCγ1 pathway
British Library Online Contents | 2017| -
7,8-dihydroxyflavone ameliorates cognitive and motor deficits in a Huntingtons disease mouse model through specific activation of the PLC?1 pathway
British Library Online Contents | 2017| -
14q32 and let-7 microRNAs regulate transcriptional networks in fetal and adult human erythroblasts
British Library Online Contents | 2018| -
15q11.2–13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain
British Library Online Contents | 2011| -
15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders
British Library Online Contents | 2007| -
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy
British Library Online Contents | 2014| -
17-DMAG ameliorates polyglutamine-mediated motor neuron degeneration through well-preserved proteasome function in an SBMA model mouse
British Library Online Contents | 2009| -
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development
British Library Online Contents | 2013| -
82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization
British Library Online Contents | 2003| -
A 3′-UTR mutation creates a microRNA target site in the GFPT1 gene of patients with congenital myasthenic syndrome
British Library Online Contents | 2015| -
a7 nicotinic acetylcholine receptor mRNA expression and binding in postmortem human brain are associated with genetic variation in neuregulin 1
British Library Online Contents | 2007| -
A 27 base-pair deletion of the anti-Muellerian type II receptor gene is the most common cause of the persistent Muellerian duct syndrome
British Library Online Contents | 1996| -
A-44G transition in SMN2 intron 6 protects patients with spinal muscular atrophy
British Library Online Contents | 2017| -
A 94 kb genomic sequence 3' to the murine Xist gene reveals an AT rich region containing a new testis specific gene Tsx
British Library Online Contents | 1996| -
a-Actinin-3 deficiency results in reduced glycogen phosphorylase activity and altered calcium handling in skeletal muscle
British Library Online Contents | 2010| -
AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse model
British Library Online Contents | 2017| -
ABCA4 disease progression and a proposed strategy for gene therapy
British Library Online Contents | 2009| -
ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies
British Library Online Contents | 2005| -
ABCB1/MDR1 gene determines susceptibility and phenotype in ulcerative colitis: discrimination of critical variants using a gene-wide haplotype tagging approach
British Library Online Contents | 2006| -
ABCB1 (MDR1) genetic variants are associated with methadone doses required for effective treatment of heroin dependence
British Library Online Contents | 2008| -
Aberrant actin cytoskeleton leads to accelerated proliferation of corneal epithelial cells in mice deficient for destrin (actin depolymerizing factor)
British Library Online Contents | 2003| -
Aberrant cell cycle reentry in human and experimental inclusion body myositis and polymyositis
British Library Online Contents | 2014| -
Aberrant cortical synaptic plasticity and dopaminergic dysfunction in a mouse model of huntington's disease
British Library Online Contents | 2006| -
Aberrant de novo methylation of the p16INK4A CpG island is initiated post gene silencing in association with chromatin remodelling and mimics nucleosome positioning
British Library Online Contents | 2009| -
Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients
British Library Online Contents | 2007| -
Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3
British Library Online Contents | 2006| -
Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtin
British Library Online Contents | 1999| -
Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion
British Library Online Contents | 2004| -
Aberrant molecular properties shared by familial Parkinson's disease-associated mutant UCH-L1 and carbonyl-modified UCH-L1
British Library Online Contents | 2008| -
Aberrant molecular properties shared by familial Parkinsons disease-associated mutant UCH-L1 and carbonyl-modified UCH-L1
British Library Online Contents | 2008| -
Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in a-dystroglycanopathies
British Library Online Contents | 2006| -
Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer
British Library Online Contents | 2001| -
Aberrant processing of the Fugu (FrHD) mRNA in mouse cells and in transgenic mice
British Library Online Contents | 1997| -
Aberrant recombination involving the granzyme locus occurs in Atm−/− T-cell lymphomas
British Library Online Contents | 2005| -
Aberrant splicing induced by missense mutations in BRCA1: clues from a humanized mouse model
British Library Online Contents | 2003| -
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased A42 secretion
British Library Online Contents | 1999| -
A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity
British Library Online Contents | 2000| -
Ablation of P2X7 receptor exacerbates gliosis and motoneuron death in the SOD1-G93A mouse model of amyotrophic lateral sclerosis
British Library Online Contents | 2013| -
Ablation of the Sam68 gene impairs female fertility and gonadotropin-dependent follicle development
British Library Online Contents | 2010| -
Abnormal association of mutant huntingtin with synaptic vesicles inhibits glutamate release
British Library Online Contents | 2003| -
Abnormal Ca2+ release and catecholamine-induced arrhythmias in mitochondrial cardiomyopathy
British Library Online Contents | 2005|
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