Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice. - Wikidata - wikimedia - TriplyDB

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

http://www.wikidata.org/entity/Q33838074

about

Point mutations at the purine nucleoside phosphorylase locus impair thymocyte differentiation in the mouse Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy Telomere shortening and metabolic compromise underlie dystrophic cardiomyopathy Transcriptome-scale similarities between mouse and human skeletal muscles with normal and myopathic phenotypes A duchenne muscular dystrophy gene hot spot mutation in dystrophin-deficient cavalier king charles spaniels is amenable to exon 51 skipping.Proteomic profiling of mdx-4cv serum reveals highly elevated levels of the inflammation-induced plasma marker haptoglobin in muscular dystrophy.MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms Sarcoglycans in muscular dystrophy.Delayed cardiomyopathy in dystrophin deficient mdx mice relies on intrinsic glutathione resource.Gene replacement therapies for duchenne muscular dystrophy using adeno-associated viral vectors.Distinctive serum miRNA profile in mouse models of striated muscular pathologies.Genotyping mdx, mdx3cv, and mdx4cv mice by primer competition polymerase chain reaction.Engraftment potential of dermal fibroblasts following in vivo myogenic conversion in immunocompetent dystrophic skeletal muscle Extraocular muscle satellite cells are high performance myo-engines retaining efficient regenerative capacity in dystrophin deficiency.Phospholipase D1 facilitates second-phase myoblast fusion and skeletal muscle regeneration Nitrosative stress elicited by nNOSµ delocalization inhibits muscle force in dystrophin-null mice Duchenne muscular dystrophy gene therapy: Lost in translation?Syndecan-4-expressing muscle progenitor cells in the SP engraft as satellite cells during muscle regeneration.Sequencing protocols to genotype mdx, mdx(4cv), and mdx(5cv) mice mdx(⁵cv) mice manifest more severe muscle dysfunction and diaphragm force deficits than do mdx Mice β4 integrin marks interstitial myogenic progenitor cells in adult murine skeletal muscle.Simultaneous Pathoproteomic Evaluation of the Dystrophin-Glycoprotein Complex and Secondary Changes in the mdx-4cv Mouse Model of Duchenne Muscular Dystrophy Serum proteomic profiling reveals fragments of MYOM3 as potential biomarkers for monitoring the outcome of therapeutic interventions in muscular dystrophies.Lipogenesis mitigates dysregulated sarcoplasmic reticulum calcium uptake in muscular dystrophy.Label-free mass spectrometric analysis reveals complex changes in the brain proteome from the mdx-4cv mouse model of Duchenne muscular dystrophy.Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype.A contemporary atlas of the mouse diaphragm: myogenicity, vascularity, and the Pax3 connection.A marginal level of dystrophin partially ameliorates hindlimb muscle passive mechanical properties in dystrophin-null mice.Preservation of muscle force in Mdx3cv mice correlates with low-level expression of a near full-length dystrophin protein CpG island promoter region methylation patterns of the inactive-X-chromosome hypoxanthine phosphoribosyltransferase (Hprt) gene Recent developments in the treatment of Duchenne muscular dystrophy and spinal muscular atrophy.Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy sar: a genetic mouse model for human sarcosinemia generated by ethylnitrosourea mutagenesis Animal models of muscular dystrophy Dystrophins carrying spectrin-like repeats 16 and 17 anchor nNOS to the sarcolemma and enhance exercise performance in a mouse model of muscular dystrophy.Dual AAV therapy ameliorates exercise-induced muscle injury and functional ischemia in murine models of Duchenne muscular dystrophy Increased sphingosine-1-phosphate improves muscle regeneration in acutely injured mdx mice.A new immuno-, dystrophin-deficient model, the NSG-mdx(4Cv) mouse, provides evidence for functional improvement following allogeneic satellite cell transplantation Parental imprinting studied by allele-specific primer extension after PCR: paternal X chromosome-linked genes are transcribed prior to preferential paternal X chromosome inactivation.Reversal of neurobehavioral social deficits in dystrophic mice using inhibitors of phosphodiesterases PDE5A and PDE9A.

P2860

Q24564939-E94A54C4-EB78-4AFD-94B8-3C2DC11FBAB6 Q28084979-9E8F1FD6-CA37-4C78-820C-CE0C81D2C087 Q28315028-A0C89F58-E01F-444C-88B9-B673A1664C1D Q33235717-1F62FAD4-8FEE-44EB-81CF-F8A07EEAC494 Q33523810-B52DB9F2-4D15-459E-B310-5F72EE853C09 Q33675040-55C6A7E0-154D-484D-814A-D8915EDC06FC Q33685967-D957EEFA-8B0B-42A7-A017-A4552A32E733 Q33840940-72957BF6-DCA5-40A3-AF7C-9D9B6DC7E797 Q34086953-031F63C5-7CF8-46EE-A873-4EA4F56A937F Q34566454-47A5C9F9-AEC8-410D-A63D-CD307329F49A Q34589538-6BCC5621-6214-4D1F-BF7D-C678555438EF Q34635190-353A2509-D1E5-4279-9EBE-D87F1431D54A Q34794545-C24E3D65-EB84-4548-B8B9-7ED4596CCC7E Q35023888-F414B2E3-E4CF-449A-9A8C-A30914446906 Q35027582-F286362F-9BC0-42B0-B252-6FD1294A7FB8 Q35027817-B0F6E020-D874-4922-8E2B-13BBB27BBAEA Q35052506-D3155D62-17DA-4863-800D-0CF168AC806A Q35124906-B7C8CCAF-B306-40EB-89DB-4689D22D58C5 Q35163553-6FEBF7A1-D07D-4B70-BA84-406E55B4ACAB Q35474357-452A6924-185A-4F31-B848-0B01941FC334 Q35768128-0730952A-80BF-4C02-8373-255E2124686A Q35837856-77D9C11A-2177-4145-B16E-63EB628F5886 Q35924068-F59A3005-1625-473F-B39D-C1AF549AB045 Q36202652-2FEB1CB3-3A05-4BE6-8641-DECCDB098C7C Q36310649-8F1B6027-6E43-4F5F-9E7C-6C7C01244084 Q36344905-2462A0D1-A8C0-4A57-90BE-4C34BCC74C36 Q36473287-F89F7AEC-A452-460B-B1C5-76888B52F89C Q36493233-A286430D-3A2B-4328-BCFD-DD47509CF1E2 Q36579847-63F3C046-E3B2-46A0-8B91-62A43F1789A0 Q36671501-C18BEC6D-F5BF-49D4-8485-9495941090A0 Q36761839-89173C01-9048-4107-AD72-42B699EDFF7E Q36841572-61E15505-6F4D-4B06-B256-8686ECA599A1 Q36913777-0783CE8C-7649-4571-942A-0CF9A5518158 Q36915922-AA687327-C5A7-408C-A788-68E49F1F6A98 Q37111368-8C1137A3-15F0-425E-AB25-8A0A2984749A Q37111962-16D2FEE9-799E-4E53-8DA4-422F89024E0A Q37114072-3E33CF2D-E7DF-47EA-BFF7-ACFC70BC503E Q37157766-D7C996E2-C8ED-4738-B112-73A1047EA4BF Q37281831-C4AD3807-4A47-4940-9B99-67ABB5F1F518 Q37307216-E6489FFB-2C0A-408A-9A56-D49AF2BEE887

P2860

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

http://www.wikidata.org/entity/Q33838074

description

1989 nî lūn-bûn

@nan

1989 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

1989 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

1989年の論文

@ja

1989年論文

@yue

1989年論文

@zh-hant

1989年論文

@zh-hk

1989年論文

@zh-mo

1989年論文

@zh-tw

1989年论文

@wuu

name

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

@ast

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

@en

type

label

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

@ast

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

@en

prefLabel

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

@ast

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

@en

P1433

Q33838074-1D13B8F0-B92A-41CF-A5F1-FE88ACDBFB1B

P1476

Q33838074-94EB6C94-189C-4110-BF7C-2CDC89CA7029

P2093

Q33838074-4F17FD68-8358-49D2-B7B2-0BE357669C18

Q33838074-5A3B4E5E-9729-41A7-9CC5-E35901AB03CC

Q33838074-B055C30B-F7FE-40C5-B6EA-EEBF92FC628E

Q33838074-F44B53BB-BD41-4184-82CC-7301A3E678D0

P2860

Q33838074-2BE5EF74-065B-47CE-A612-321DD1D279A5

Q33838074-339C2ECC-F4D9-49C2-8607-336FEEE3F414

Q33838074-3D305746-216B-482C-B7C8-170B117F107A

Q33838074-4E4D791A-0F56-4583-8123-0B3AE020EE71

Q33838074-535073EE-8623-492C-BAF3-5D2732E2FE79

Q33838074-6F1B70B3-0CC8-4B0E-A110-3E4F36DD009A

Q33838074-71FFBA8E-493F-4A5C-B137-083EDC209D17

Q33838074-748A5F96-8F85-4218-A158-59EFA8F4B426

Q33838074-7BCF7E05-98EA-45D1-A2E7-35716707E8E5

Q33838074-8BF2C180-9B2A-44D8-A5DB-0FD943766B95

P304

Q33838074-E690E416-91C2-4E77-B9AA-40F9DD3657C6

P31

Q33838074-B983AFC9-6A92-46A7-8C9B-057A6876D5F1

P356

Q33838074-6A743017-0380-43B1-B584-ED8DED752A30

P407

Q33838074-48E87A08-23FD-436A-BFE2-582796C9535A

P433

Q33838074-18815BA3-33BB-449C-B5FA-F44AAD82BC85

P478

Q33838074-C9490C1B-6EF9-4352-B345-D6E28B9BFA88

P577

Q33838074-F9BCCBF8-3928-4E3E-969A-1C9F64296C56

P5875

Q33838074-9B8DBF02-666A-45C8-8FB6-A12167306937

P698

Q33838074-0A73D0E2-9697-488D-AA14-38731625F77C

P932

Q33838074-50DE9538-DDC0-4C31-B803-6199C9913C2E

P356

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

@en

P2093

C T Caskey

http://www.w3.org/2001/XMLSchema#string

D Armstrong

http://www.w3.org/2001/XMLSchema#string

D R Miller

http://www.w3.org/2001/XMLSchema#string

V M Chapman

http://www.w3.org/2001/XMLSchema#string

P2860

Unusual type of benign x-linked muscular dystrophy

Specific-locus test shows ethylnitrosourea to be the most potent mutagen in the mouse

Electrophoretic variation for X chromosome-linked hypoxanthine phosphoribosyl transferase (HPRT) in wild-derived mice.

X chromosome-linked muscular dystrophy (mdx) in the mouse

Electrophoretic variation for x-chromosome-linked phosphoglycerate kinase (pgk-1) in the mouse

Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosome

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

Electrophoretically detected germinal mutations induced in the mouse by ethylnitrosourea.

Localization of the mdx mutation within the mouse dystrophin gene.

Dose--response curve for ethylnitrosourea-induced specific-locus mutations in mouse spermatogonia

P304

1292-1296

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1073/PNAS.86.4.1292

http://www.w3.org/2001/XMLSchema#string

P407

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

86

http://www.w3.org/2001/XMLSchema#string

P577

1989-02-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

20237436

http://www.w3.org/2001/XMLSchema#string

P698

2919177

http://www.w3.org/2001/XMLSchema#string

P932

286674

http://www.w3.org/2001/XMLSchema#string