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New Zealand Veterinary Journal
|
July 21, 2005
Polyglucosan body disease in a mixed-breed dog
R D Jolly, F I Hill, J A Hill, et al.
The Journal of Biological Chemistry
|
April 5, 1989
Ovine ceroid lipofuscinosis. The major lipopigment protein and the lipid-binding subunit of mitochondrial ATP synthase have the same NH2-terminal sequence
D N Palmer, R D Martinus, S M Cooper, et al.
American Journal of Medical Genetics
|
June 5, 1995
Hematopoietic cell transplantation in fetal lambs with ceroid-lipofuscinosis
V J Westlake, R D Jolly, B R Jones, et al.
The Biochemical Journal
|
December 1, 1978
Characterization of the mutant alpha-mannosidase in bovine mannosidosis
L J Burditt, N C Phillips, D Robinson, et al.
Plos One
|
December 19, 2017
Familial episodic ataxia in lambs is potentially associated with a mutation in the fibroblast growth factor 14 (FGF14) gene
K E Dittmer, R D Jolly, I G Mayhew, et al.
The Biochemical Journal
|
June 15, 1990
The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase
I M Fearnley, J E Walker, R D Martinus, et al.
New Zealand Veterinary Journal
|
March 20, 2023
A lower motor neuron disease in takahē (<i>Porphyrio hochstetteri</i>) is an endoplasmic reticulum storage disease
R D Jolly, M R Perrott, M R Alley, et al.
Veterinary Research Communications
|
January 1, 1991
Bovine ceroid-lipofuscinosis (Batten's disease): the major component stored is the DCCD-reactive proteolipid, subunit C, of mitochondrial ATP synthase
R D Martinus, P A Harper, R D Jolly, et al.
American Journal of Medical Genetics
|
February 15, 1992
Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)
D N Palmer, I M Fearnley, J E Walker, et al.
New Zealand Veterinary Journal
|
February 15, 2012
Mucopolysaccharidosis type VI in a Miniature Poodle-type dog caused by a deletion in the arylsulphatase B gene
R D Jolly, J J Hopwood, N R Marshall, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 142) with videos related to
Sort By:
Page
of 15
New Zealand Veterinary Journal
|
July 21, 2005
Polyglucosan body disease in a mixed-breed dog
R D Jolly, F I Hill, J A Hill, et al.
The Journal of Biological Chemistry
|
April 5, 1989
Ovine ceroid lipofuscinosis. The major lipopigment protein and the lipid-binding subunit of mitochondrial ATP synthase have the same NH2-terminal sequence
D N Palmer, R D Martinus, S M Cooper, et al.
American Journal of Medical Genetics
|
June 5, 1995
Hematopoietic cell transplantation in fetal lambs with ceroid-lipofuscinosis
V J Westlake, R D Jolly, B R Jones, et al.
The Biochemical Journal
|
December 1, 1978
Characterization of the mutant alpha-mannosidase in bovine mannosidosis
L J Burditt, N C Phillips, D Robinson, et al.
Plos One
|
December 19, 2017
Familial episodic ataxia in lambs is potentially associated with a mutation in the fibroblast growth factor 14 (FGF14) gene
K E Dittmer, R D Jolly, I G Mayhew, et al.
The Biochemical Journal
|
June 15, 1990
The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase
I M Fearnley, J E Walker, R D Martinus, et al.
New Zealand Veterinary Journal
|
March 20, 2023
A lower motor neuron disease in takahē (<i>Porphyrio hochstetteri</i>) is an endoplasmic reticulum storage disease
R D Jolly, M R Perrott, M R Alley, et al.
Veterinary Research Communications
|
January 1, 1991
Bovine ceroid-lipofuscinosis (Batten's disease): the major component stored is the DCCD-reactive proteolipid, subunit C, of mitochondrial ATP synthase
R D Martinus, P A Harper, R D Jolly, et al.
American Journal of Medical Genetics
|
February 15, 1992
Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)
D N Palmer, I M Fearnley, J E Walker, et al.
New Zealand Veterinary Journal
|
February 15, 2012
Mucopolysaccharidosis type VI in a Miniature Poodle-type dog caused by a deletion in the arylsulphatase B gene
R D Jolly, J J Hopwood, N R Marshall, et al.
Page
of 15