(Q28591663)

31 January 2017

title

Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9 (English)

1 reference

neuronal ceroid lipofuscinosis

31 January 2017

main subject

1 reference

R. T. Bronson

1

1 reference

31 January 2017

L. R. Donahue

2

1 reference

31 January 2017

K. R. Johnson

3

1 reference

31 January 2017

A. Tanner

4

1 reference

31 January 2017

P. W. Lane

5

1 reference

31 January 2017

J. R. Faust

6

1 reference

31 January 2017

publication date

26 May 1998

1 reference

American Journal of Medical Genetics Part A

31 January 2017

published in

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31 January 2017

volume

77

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31 January 2017

issue

4

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31 January 2017

page(s)

289–297

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Ceroid-lipofuscinosis in two Saluki dogs

31 January 2017

cites work

1 reference

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Hydrocephalus with hop gait (hyh): a new mutation on chromosome 7 in the mouse.

21 January 2018

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Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)

21 January 2018

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21 January 2018

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The ultrastructural characteristics of the abnormal cytosomes in Batten-Kufs' disease

21 January 2018

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Neuronal ceroidosis (ceroid-lipofuscinosis) in a Blue Heeler dog.

21 January 2018

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DNA sequences of a bovine gene and of two related pseudogenes for the proteolipid subunit of mitochondrial ATP synthase

21 January 2018

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The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase

21 January 2018

1 reference

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CpG island in the region of an autosomal dominant polycystic kidney disease locus defines the 5' end of a gene encoding a putative proton channel

21 January 2018

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Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis)

21 January 2018

1 reference

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Molecular cloning of cDNA encoding the 16 KDa subunit of vacuolar H+-ATPase from mouse cerebellum

21 January 2018

1 reference

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English setter model and juvenile ceroid-lipofuscinosis in man.

21 January 2018

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Isolation and chromosomal mapping of a mouse homolog of the Batten disease gene CLN3.

21 January 2018

1 reference

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Isolation of a novel gene underlying batten disease, CLN3

21 January 2018

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Evidence that lysosomal storage of proteolipids is a cell autonomous process in the motor neuron degeneration (mnd) mouse, a model of neuronal ceroid lipofuscinosis

21 January 2018

1 reference

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A Macintosh program for storage and analysis of experimental genetic mapping data

21 January 2018

1 reference

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Characterization of the expressed genes for subunit c of mitochondrial ATP synthase in sheep with ceroid lipofuscinosis

21 January 2018

1 reference

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Mapping of the motor neuron degeneration (Mnd) gene, a mouse model of amyotrophic lateral sclerosis (ALS)

21 January 2018

1 reference

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Retinal degeneration in motor neuron degeneration (mnd) mutant mice

21 January 2018

1 reference

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Genetics of primary and timing effects in the mnd mouse

21 January 2018

1 reference

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Tibetan terrier model of canine ceroid lipofuscinosis

21 January 2018

1 reference

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Loci for classical and a variant late infantile neuronal ceroid lipofuscinosis map to chromosomes 11p15 and 15q21-23.

21 January 2018

1 reference

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Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

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Clinical features of ceroid lipofuscinosis in border collie dogs

21 January 2018

1 reference

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Neuronal ceroid-lipofuscinosis in older dachshunds

21 January 2018

1 reference

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Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

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Sequence analysis and mapping of a novel human mitochondrial ATP synthase subunit 9 cDNA (ATP5G3)

21 January 2018

1 reference

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10.1002/(SICI)1096-8628(19980526)77:4<289::AID-AJMG8>3.0.CO;2-I

21 January 2018

Identifiers

DOI

0 references

1 reference