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Report of cerebellar hypoplasia in three calves
(2013-03-01)
Hereditary or acquired cerebellar hypoplasia (CH) is commonly diagnosed in Holstein, Guernsey, Shorthorn and Jersey cattle. Bovine viral diarrhea (BVD) has been associated to acquired CH due to viral infection during the ...
Report of cerebellar hypoplasia in three calves
(2013-03-01)
Hereditary or acquired cerebellar hypoplasia (CH) is commonly diagnosed in Holstein, Guernsey, Shorthorn and Jersey cattle. Bovine viral diarrhea (BVD) has been associated to acquired CH due to viral infection during the ...
Deletion of the α subunit of the heterotrimeric Go protein impairs cerebellar cortical development in mice
(BioMed Central, 2019-06)
Go is a member of the pertussis toxin-sensitive Gi/o family. Despite its abundance in the central nervous system, the precise role of Go remains largely unknown compared to other G proteins. In the present study, we explored ...
Congenital tremor in piglets: Is bovine viral diarrhea virus an etiological cause?
(2018-07-01)
Congenital tremor in pigs involves several etiologies, including pestivirus, which may cause neurological injuries in different animal species. To evaluate whether bovine viral diarrhea virus (BVDV), an important pestivirus, ...
Congenital ataxia due to cerebellar malformation presenting with unilateral hypoplasia
(Academia Brasileira de Neurologia - ABNEURO, 2013-03-01)
The chromatin remodeling factor CHD7 controls cerebellar development by regulating reelin expression
(Amer Soc Clinical Investigation Inc, 2017-03-01)
The mechanisms underlying the neurodevelopmental deficits associated with CHARGE syndrome, which include cerebellar hypoplasia, developmental delay, coordination problems, and autistic features, have not been identified. ...
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development
(Springer Nature, 2012)
Charged multivesicular body protein 1A (CHMP1A; also known as chromatin-modifying protein 1A) is a member of the ESCRT-III (endosomal sorting complex required for transport-III) complex but is also suggested to localize ...
Deletion of the α subunit of the heterotrimeric Go protein impairs cerebellar cortical development in mice
(BMC, 2019)
Abtract: Go is a member of the pertussis toxin-sensitive Gi/o family. Despite its abundance in the central nervous system, the precise role of Go remains largely unknown compared to other G proteins. In the present study, ...