Pages that link to "Q30039698"
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The following pages link to Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy (Q30039698):
Displaying 50 items.
- DUX4c is up-regulated in FSHD. It induces the MYF5 protein and human myoblast proliferation (Q21091176) (← links)
- Facioscapulohumeral dystrophy: the path to consensus on pathophysiology (Q21195884) (← links)
- Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD (Q21563357) (← links)
- DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1 (Q24299685) (← links)
- Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy (Q24655776) (← links)
- Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD) (Q24670624) (← links)
- Actinin-associated LIM Protein: Identification of a Domain Interaction between PDZ and Spectrin-like Repeat Motifs (Q24678805) (← links)
- The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure (Q24680328) (← links)
- Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients (Q24800026) (← links)
- An eccentric calpain, CAPN3/p94/calpain-3 (Q26781368) (← links)
- Noncoding RNAs, Emerging Regulators of Skeletal Muscle Development and Diseases (Q26799919) (← links)
- Facioscapulohumeral muscular dystrophy: consequences of chromatin relaxation (Q26998289) (← links)
- Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cells. (Q27687330) (← links)
- Recurrent DUX4 fusions in B cell acute lymphoblastic leukemia of adolescents and young adults (Q27853366) (← links)
- Targeting mRNA for the treatment of facioscapulohumeral muscular dystrophy (Q28069201) (← links)
- Further exclusion of FSHD1B from the telomeric region of 10q (Q28139586) (← links)
- Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element (Q28141267) (← links)
- The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements (Q28145563) (← links)
- beta-1,3-Glucuronyltransferase-1 gene implicated as a candidate for a schizophrenia-like psychosis through molecular analysis of a balanced translocation (Q28188757) (← links)
- Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD) (Q28236842) (← links)
- Population-based incidence and prevalence of facioscapulohumeral dystrophy (Q28245908) (← links)
- Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis (Q28271204) (← links)
- Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4 (Q28283803) (← links)
- Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35 (Q28285889) (← links)
- A unifying genetic model for facioscapulohumeral muscular dystrophy (Q28291033) (← links)
- Characterization of genomic structures and expression profiles of three tandem repeats of a mouse double homeobox gene: Duxbl (Q28504911) (← links)
- Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD) (Q28513387) (← links)
- Influence of Repressive Histone and DNA Methylation upon D4Z4 Transcription in Non-Myogenic Cells (Q28553207) (← links)
- Actinin-associated LIM protein-deficient mice maintain normal development and structure of skeletal muscle (Q28585840) (← links)
- Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy (Q28757194) (← links)
- Endogenous DUX4 expression in FSHD myotubes is sufficient to cause cell death and disrupts RNA splicing and cell migration pathways (Q29010925) (← links)
- The FSHD2 Gene SMCHD1 Is a Modifier of Disease Severity in Families Affected by FSHD1 (Q29026180) (← links)
- Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy (Q29039571) (← links)
- Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B (Q29041262) (← links)
- Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2 (Q29303884) (← links)
- THE COMPLEX STRUCTURE AND DYNAMIC EVOLUTION OF HUMAN SUBTELOMERES (Q29393384) (← links)
- FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit (Q29398634) (← links)
- Inappropriate Gene Activation in FSHD (Q30050619) (← links)
- Facioscapulohumeral Dystrophy (Q30250223) (← links)
- Facioscapulohumeral muscular dystrophy. Clinical picture, atypical forms, diagnostics, genetics (Q30318405) (← links)
- Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3 (Q30438210) (← links)
- The DNA laboratory and neurological practice (Q30495790) (← links)
- Relationships between clinical data and quantitative EMG findings in facioscapulohumeral muscular dystrophy (Q30597862) (← links)
- The D4Z4 macrosatellite repeat acts as a CTCF and A-type lamins-dependent insulator in facio-scapulo-humeral dystrophy. (Q33413043) (← links)
- Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation (Q33483016) (← links)
- Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats. (Q33503626) (← links)
- Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy. (Q33614782) (← links)
- Mouse Dux is myotoxic and shares partial functional homology with its human paralog DUX4. (Q33615189) (← links)
- De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1). (Q33625003) (← links)
- Human skeletal muscle xenograft as a new preclinical model for muscle disorders (Q33649287) (← links)