(Q24595262)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

The molecular basis of alkaptonuria

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

A review of canine inherited bleeding disorders: biochemical and molecular strategies for disease characterization and carrier detection

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Large animal models and gene therapy

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

The Dalmatian defect: a hepatic endocrinopathy of urate transport

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

The nature of the defect in tyrosine metabolism in alcaptonuria

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Animal models for mucopolysaccharidoses and their clinical relevance.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Therapeutic neonatal hepatic gene therapy in mucopolysaccharidosis VII dogs

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Canine genetics comes of age.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Molecular basis of feline beta-glucuronidase deficiency: an animal model of mucopolysaccharidosis VII.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Naturally occurring xanthine urolithiasis in a domestic shorthair cat.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Beta-glucuronidase deficiency in a dog: a model of human mucopolysaccharidosis VII.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Research on genetic diseases: reciprocal benefits to animals and man.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Alpha-L-iduronidase Deficiency in a Cat: A Model of Mucopolysaccharidosis I

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Beta-galactosidase deficiency in a Korat cat: a new form of feline GM1-gangliosidosis.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

MRI and electrophysiological abnormalities in a case of canine globoid cell leucodystrophy

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Sulfamidase deficiency in a family of Dachshunds: a canine model of mucopolysaccharidosis IIIA (Sanfilippo A).

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

D-(+)-glyceric aciduria in an Afghan hound

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Methylmalonic and malonic aciduria in a dog with progressive encephalomyelopathy.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

The molecular defect underlying canine fucosidosis.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Neuronal GM 1 Gangliosidosis in a Siamese Cat with β-Galactosidase Deficiency

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Mannosidosis in a litter of Persian cats

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Enzymological characterization of a putative canine analogue of primary hyperoxaluria type 1.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

L-2-hydroxyglutaric aciduria in a West Highland white terrier.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Mucopolysaccharidosis type VII in a German Shepherd Dog.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Inheritance, biochemical abnormalities, and clinical features of feline mucolipidosis II: the first animal model of human I-cell disease

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

A model of mucopolysaccharidosis IIIB (Sanfilippo syndrome type IIIB): N‐acetyl‐α‐D‐glucosaminidase deficiency in Schipperke dogs

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Mitochondrial myopathy in a german shepherd dog.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

L-2-Hydroxyglutaric aciduria in Staffordshire Bull Terriers

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Mitochondriopathy with regional encephalic mineralization in a Jack Russell Terrier.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Globoid cell-like leukodystrophy in a domestic longhaired cat.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

GM1-gangliosidosis in Alaskan huskies: clinical and pathologic findings.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Canine cystinuria: polymorphism in the canine SLC3A1 gene and identification of a nonsense mutation in cystinuric Newfoundland dogs

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Mucopolysaccharidosis VII in a cat.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Investigating demyelination in the brain in a canine model of globoid cell leukodystrophy (Krabbe disease) using magnetization transfer contrast: preliminary results.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Globoid cell leukodystrophy in cairn and West Highland white terriers

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Clinical and morphologic features of mucopolysaccharidosis type II in a dog: naturally occurring model of Hunter syndrome

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Myopathy in an irish terrier with a metabolic defect of the isolated mitochondria.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Episodic weakness associated with exertional lactic acidosis and myopathy in Old English sheepdog littermates

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3132193

Hyperammonaemic encephalopathy secondary to selective cobalamin deficiency in a juvenile Border collie

28 November 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Primary hyperoxaluria andl-glyceric aciduria in the cat

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Alaskan Husky encephalopathy--a canine neurodegenerative disorder resembling subacute necrotizing encephalomyelopathy (Leigh syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Persistent cobalamin deficiency causing failure to thrive in a juvenile beagle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Inherited selective intestinal cobalamin malabsorption and cobalamin deficiency in dogs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

The incidence of alkaptonuria: a study in chemical individuality. 1902 [classical article]

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Feline mucopolysaccharidosis VII due to beta-glucuronidase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Canine fucosidosis: a biochemical and genetic investigation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Mitochondrial myopathy in the Sussex spaniel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Mucopolysaccharidosis IIIA (Sanfilippo syndrome) in a New Zealand Huntaway dog with ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Bilateral xanthine nephrolithiasis in a dog

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Clinical vignette. Mucopolysaccharidosis VI in a miniature pinscher

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Suspected mitochondrial myopathy in a Jack Russell terrier

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Genetic predisposition to purine uroliths in Dalmatian dogs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Sandhoff disease in a golden retriever dog

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

Canine mitochondrial myopathy associated with reduced mitochondrial mRNA and altered cytochrome c oxidase activities in fibroblasts and skeletal muscle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2006.08.017

7 January 2021

inferred from DOI database lookup

Screening for inborn errors of metabolism in dogs and cats

1 reference

12 December 2020

Inheritance of cystinuria and renal defect in Newfoundlands

1 reference

12 December 2020

Lactic acidosis in a Clumber spaniel

1 reference

12 December 2020

GM2-gangliosidosis variant 0 (Sandhoff-like disease) in a family of Japanese domestic cats

1 reference

12 December 2020