scholarly article | Q13442814 |
P2093 | author name string | Bulmaro Cisneros | |
Federico Centeno-Cruz | |||
Efraín Garrido | |||
Rocío Suárez-Sánchez | |||
Marcela Villarreal-Silva | |||
P2860 | cites work | Alteration of nuclear lamin organization inhibits RNA polymerase II-dependent transcription | Q22066149 |
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Dystrophin Dp71 is required for neurite outgrowth in PC12 cells | Q24293534 | ||
Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor | Q24561804 | ||
Mitotic checkpoint slippage in humans occurs via cyclin B destruction in the presence of an active checkpoint | Q24648791 | ||
Different dystrophin-like complexes are expressed in neurons and glia | Q24684826 | ||
Dystrophin Dp71 in PC12 cell adhesion | Q28569063 | ||
Inheriting nuclear organization: can nuclear lamins impart spatial memory during post-mitotic nuclear assembly? | Q51048937 | ||
Mitotic regulation of TFIID: inhibition of activator-dependent transcription and changes in subcellular localization. | Q52521588 | ||
Dystrophin and utrophin complexed with different associated proteins in cardiac Purkinje fibres | Q58052198 | ||
Characterization of a novel Dp71 dystrophin-associated protein complex (DAPC) present in the nucleus of HeLa cells: Members of the nuclear DAPC associate with the nuclear matrix | Q60708115 | ||
Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening | Q74051627 | ||
Interaction of cadmium with actin microfilaments in vitro | Q84722532 | ||
Dystrophin Dp71f associates with the beta1-integrin adhesion complex to modulate PC12 cell adhesion | Q28578480 | ||
In vitro disassembly of the nuclear lamina and M phase-specific phosphorylation of lamins by cdc2 kinase | Q28647498 | ||
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals | Q30050310 | ||
Dystrophin is transcribed in brain from a distant upstream promoter. | Q33517277 | ||
Functions and dysfunctions of the nuclear lamin Ig-fold domain in nuclear assembly, growth, and Emery-Dreifuss muscular dystrophy. | Q34081419 | ||
Function and genetics of dystrophin and dystrophin-related proteins in muscle | Q34120764 | ||
The nuclear lamina comes of age. | Q34390408 | ||
A mitotic lamin B matrix induced by RanGTP required for spindle assembly | Q34502865 | ||
Lamins: building blocks or regulators of gene expression? | Q34988332 | ||
Regulation of the differentiation of PC12 pheochromocytoma cells | Q35032923 | ||
The nuclear lamina and its functions in the nucleus | Q35200844 | ||
A lamin A protein isoform overexpressed in Hutchinson-Gilford progeria syndrome interferes with mitosis in progeria and normal cells | Q35677842 | ||
A role for the p34cdc2 kinase and phosphatases in the regulation of phosphorylation and disassembly of lamin B2 during the cell cycle | Q35923400 | ||
Useful cell lines derived from the adrenal medulla | Q35947549 | ||
A role for nuclear lamins in nuclear envelope assembly | Q36377945 | ||
Mitotic arrest and cell fate: why and how mitotic inhibition of transcription drives mutually exclusive events | Q36716332 | ||
A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues | Q37055980 | ||
Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues | Q37152720 | ||
Reorganization of the nuclear envelope during open mitosis | Q37269387 | ||
Chromosome segregation machinery and cancer | Q37477348 | ||
How do anti-mitotic drugs kill cancer cells? | Q37558986 | ||
Dystrophin Dp71 is critical for stability of the DAPs in the nucleus of PC12 cells | Q39794386 | ||
Mcl-1 mediates tumor necrosis factor-related apoptosis-inducing ligand resistance in human cholangiocarcinoma cells. | Q40554408 | ||
Dystrophin-glycoprotein complex: molecular organization and critical roles in skeletal muscle. | Q40935234 | ||
Eleutherobin, a novel cytotoxic agent that induces tubulin polymerization, is similar to paclitaxel (Taxol). | Q41056495 | ||
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy gene | Q41748776 | ||
Targeting of dystroglycan to the cleavage furrow and midbody in cytokinesis. | Q42819879 | ||
Nocodazole induces mitotic cell death with apoptotic-like features in Saccharomyces cerevisiae. | Q43095405 | ||
The cyclin-dependent kinase inhibitor flavopiridol induces apoptosis in multiple myeloma cells through transcriptional repression and down-regulation of Mcl-1. | Q44214979 | ||
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression | Q46160928 | ||
Expression and regulation of the dystrophin Purkinje promoter in human skeletal muscle, heart, and brain | Q48066766 | ||
A housekeeping type promoter, located in the 3' region of the Duchenne muscular dystrophy gene, controls the expression of Dp71, a major product of the gene | Q48093856 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cytokinesis | Q1447198 |
P304 | page(s) | e23504 | |
P577 | publication date | 2011-01-01 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Knockdown of dystrophin Dp71 impairs PC12 cells cycle: localization in the spindle and cytokinesis structures implies a role for Dp71 in cell division | |
P478 | volume | 6 |
Q37619815 | Decreased Dp71 expression is associated with gastric adenocarcinoma prognosis |
Q88778329 | Detection of Dystrophin Dp71 in Human Skeletal Muscle Using an Automated Capillary Western Assay System |
Q64988592 | Dp71 depleted HBE cells displayed increased DNA damage and apoptosis induced by H2O2. |
Q38719209 | Dystrophin Dp71 Isoforms Are Differentially Expressed in the Mouse Brain and Retina: Report of New Alternative Splicing and a Novel Nomenclature for Dp71 Isoforms. |
Q91974710 | Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy |
Q24298098 | Dystrophin Dp71: the smallest but multifunctional product of the Duchenne muscular dystrophy gene |
Q100533732 | Dystrophin Dp71ab is monoclonally expressed in human satellite cells and enhances proliferation of myoblast cells |
Q35162006 | Generation of induced pluripotent stem cells from muscular dystrophy patients: efficient integration-free reprogramming of urine derived cells |
Q48796965 | HEK293 cells express dystrophin Dp71 with nucleus-specific localization of Dp71ab |
Q35078823 | HSF1 functions as a transcription regulator for Dp71 expression |
Q38809940 | Knocking down Dp71 expression in A549 cells reduces its malignancy in vivo and in vitro |
Q41395588 | Myelination is delayed during postnatal brain development in the mdx mouse model of Duchenne muscular dystrophy |
Q36105739 | Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains |
Q98159750 | Single-transcript multiplex in situ hybridisation reveals unique patterns of dystrophin isoform expression in the developing mammalian embryo |
Q42000124 | The shortest isoform of dystrophin (Dp40) interacts with a group of presynaptic proteins to form a presumptive novel complex in the mouse brain |
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