Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease.
about
An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattleCalcium homeostasis in myogenic differentiation factor 1 (MyoD)-transformed, virally-transduced, skin-derived equine myotubesPseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutationsCalpain3 is expressed in a proteolitically active form in papillomavirus-associated urothelial tumors of the urinary bladder in cattle.A segmental genomic duplication generates a functional intron.Microarray gene expression profiling of neural tissues in bovine spastic paresisAbsence of canonical Smad signaling in ureteral and bladder mesenchyme causes ureteropelvic junction obstruction.A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle.Calcium pumps in health and disease.Status of the cattle genome map.Endoplasmic-reticulum calcium depletion and disease.The Ca2+ pumps of the endoplasmic reticulum and Golgi apparatus.Inhibition of ubiquitin proteasome system rescues the defective sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA1) protein causing Chianina cattle pseudomyotonia.
P2860
Q27346734-A50EFBBF-1174-451E-9ACE-DFEEF8B76408Q28542525-E826BF91-291D-4CF1-8912-8866D5FBBDB5Q30532432-D36C35E4-16D3-40DD-B8E7-F1201B5D31F2Q33565470-BCC87060-E616-48DE-BA01-6DEE9AAF7622Q34212000-7704274C-E8B9-4021-91DD-EE843F336EDBQ34778026-57D2BDEC-D977-4DFE-AB55-13A362CA6D81Q35853268-CAFFA165-B7AE-4090-9E5D-62AE1D25AA76Q37071895-24EFE1BD-6771-49E3-A58C-395D604DB9B6Q37605483-64B6B8DF-6794-4F4A-ADF1-F55EBE2B2DF4Q37851295-8508D7F4-C269-4D90-B25A-95F47CE2872DQ37858336-05F29A57-E9D9-409F-B250-AA7AFA3B9456Q37858339-A2F6A6A5-FCFF-459E-918A-BD3315B0D176Q43041172-8D24DEF7-5B08-4EF4-A9C0-A93C0877254D
P2860
Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Identification of a missense m ...... model of human Brody disease.
@en
Identification of a missense m ...... model of human Brody disease.
@nl
type
label
Identification of a missense m ...... model of human Brody disease.
@en
Identification of a missense m ...... model of human Brody disease.
@nl
prefLabel
Identification of a missense m ...... model of human Brody disease.
@en
Identification of a missense m ...... model of human Brody disease.
@nl
P2093
P1433
P1476
Identification of a missense m ...... model of human Brody disease.
@en
P2093
Arcangelo Gentile
Cord Drögemüller
Ernesto Damiani
Francesco Mascarello
Marco Rossi
Michaela Drögemüller
Roberta Sacchetto
Stefania Testoni
P304
P356
10.1016/J.YGENO.2008.07.014
P50
P577
2008-09-25T00:00:00Z