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Weaver syndrome in Brown Swiss cattle: clinical signs & pathology.

作者信息

Leipold H W, Blaugh B, Huston K, Edgerly C G, Hibbs C M

出版信息

Vet Med Small Anim Clin. 1973 Jun;68(6):645-7.

PMID:4488646
Abstract
摘要

相似文献

1
Weaver syndrome in Brown Swiss cattle: clinical signs & pathology.
Vet Med Small Anim Clin. 1973 Jun;68(6):645-7.
2
Ultrastructural alterations of motor cortex synaptic junctions in Brown Swiss cattle with weaver syndrome.患有韦弗综合征的瑞士褐牛运动皮质突触连接的超微结构改变
Am J Vet Res. 1985 Aug;46(8):1733-6.
3
[The Weaver syndrome in cattle. Clinical, biochemical and pathologico-anatomic studies in a Braunvieh/Brown Swiss cow with bovine progressive degenerative myeloencephalopathy].[牛的韦弗综合征。对一头患有牛进行性退行性脊髓脑病变的布劳恩维赫/瑞士褐牛母牛的临床、生化及病理解剖学研究]
Tierarztl Prax. 1987;15(2):139-44.
4
Congenital white muscle disease in a calf.
N Z Vet J. 1971 Sep;19(9):222-3. doi: 10.1080/00480169.1971.33970.
5
Lipomatous muscular 'dystrophy' of Piedmontese cattle.皮埃蒙特牛的脂肪性肌肉“营养不良”。
Animal. 2012 Nov;6(11):1839-47. doi: 10.1017/S175173111200081X. Epub 2012 Apr 27.
6
[Bovine progressive degenerative myeloencephalopathy ("Weaver syndrome") in brown Swiss x Braunvieh cattle: reproductive occurrences, results of embryo transfer].[瑞士褐牛×布劳恩维牛中的牛进行性退行性脑脊髓病(“韦弗综合征”):繁殖情况及胚胎移植结果]
Berl Munch Tierarztl Wochenschr. 1994 Dec;107(12):400-4.
7
Histochemical and morphometric studies of peripheral muscle in bovine progressive degenerative myeloencephalopathy of brown Swiss cattle.瑞士褐牛进行性退行性脑脊髓病外周肌肉的组织化学和形态计量学研究
Zentralbl Veterinarmed A. 1992 Jun;39(5):321-7. doi: 10.1111/j.1439-0442.1992.tb00189.x.
8
Ultrastructural changes in hereditary muscular hypertrophy in cattle.牛遗传性肌肉肥大的超微结构变化
Acta Vet Scand. 1979;20(2):245-57. doi: 10.1186/BF03546616.
9
[Muscular dystrophy in young ruminants].[幼龄反刍动物的肌肉萎缩症]
Ann Nutr Aliment. 1966;20(3):rev:13-39.
10
[Recognition of congenital unilateral kidney agenesia in domestic animals. I. Agenesia of the right kidney including the urethra with compensatory hypertrophy of the left kidney in a 10 year-old brown Swiss cow].
Schweiz Arch Tierheilkd. 1971 May;113(5):221-6.

引用本文的文献

1
Mining massive genomic data of two Swiss Braunvieh cattle populations reveals six novel candidate variants that impair reproductive success.从两个瑞士褐牛群体的大量基因组数据中挖掘出六个影响繁殖成功率的新候选变异。
Genet Sel Evol. 2021 Dec 16;53(1):95. doi: 10.1186/s12711-021-00686-3.
2
A 0.5-Mbp deletion on bovine chromosome 23 is a strong candidate for stillbirth in Nordic Red cattle.牛23号染色体上一段0.5兆碱基对的缺失是北欧红牛死产的一个强有力候选因素。
Genet Sel Evol. 2016 Apr 18;48:35. doi: 10.1186/s12711-016-0215-z.
3
Confirmation of a non-synonymous SNP in PNPLA8 as a candidate causal mutation for Weaver syndrome in Brown Swiss cattle.
确认PNPLA8中一个非同义单核苷酸多态性作为瑞士褐牛韦弗综合征的候选致病突变。
Genet Sel Evol. 2016 Mar 18;48:21. doi: 10.1186/s12711-016-0201-5.
4
Fine mapping for Weaver syndrome in Brown Swiss cattle and the identification of 41 concordant mutations across NRCAM, PNPLA8 and CTTNBP2.在瑞士褐牛中对 Weaver 综合征进行精细定位,并在 NRCAM、PNPLA8 和 CTTNBP2 中鉴定出 41 个一致突变。
PLoS One. 2013;8(3):e59251. doi: 10.1371/journal.pone.0059251. Epub 2013 Mar 20.
5
Identification of a nonsense mutation in CWC15 associated with decreased reproductive efficiency in Jersey cattle.鉴定与泽西牛繁殖效率降低相关的 CWC15 无义突变。
PLoS One. 2013;8(1):e54872. doi: 10.1371/journal.pone.0054872. Epub 2013 Jan 22.
6
Bovine progressive degenerative myeloencephalopathy (weaver syndrome) in brown swiss cattle in Canada: a literature review and case report.加拿大褐牛中的牛进行性退行性脊髓脑病(韦弗综合征):文献综述与病例报告
Can Vet J. 1988 Apr;29(4):370-7.
7
Microsatellite mapping of the gene causing weaver disease in cattle will allow the study of an associated quantitative trait locus.
Proc Natl Acad Sci U S A. 1993 Feb 1;90(3):1058-62. doi: 10.1073/pnas.90.3.1058.
8
Abiotrophy in domestic animals: a review.家畜营养缺失:综述
Can J Vet Res. 1990 Jan;54(1):65-76.