(Q48202303)

9 February 2018

title

I-cell disease-like phenotype in mice deficient in mannose 6-phosphate receptors (English)

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9 February 2018

author name string

F Dittmer

1

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9 February 2018

A Hafner

2

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9 February 2018

E J Ulbrich

3

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9 February 2018

J D Moritz

4

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9 February 2018

P Schmidt

5

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9 February 2018

W Schmahl

6

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9 February 2018

R Pohlmann

7

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9 February 2018

K V Figura

8

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9 February 2018

publication date

1 November 1998

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9 February 2018

published in

Transgenic Research

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9 February 2018

volume

7

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9 February 2018

issue

6

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9 February 2018

page(s)

473-483

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9 February 2018

https://scigraph.springernature.com/pub.10.1023/a:1008823315416

exact match

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cites work

Ultrastructural studies in fetal I-cell disease

1 reference

12 December 2020

Mannose-6-phosphate/insulin-like growth factor-II receptor is a receptor for retinoic acid

1 reference

12 December 2020

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

1 reference

12 December 2020

Structure and function of the mannose 6-phosphate/insulinlike growth factor II receptors

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12 December 2020

Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality

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12 December 2020

Theearly andlate processing of lysosomal enzymes: Proteolysis and compartmentation

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12 December 2020

Differential biallelic activation of three insulin-like growth factor II promoters in the mouse central nervous system.

1 reference

12 December 2020

A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

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12 December 2020

Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

12 December 2020

Targeted disruption of the arylsulfatase B gene results in mice resembling the phenotype of mucopolysaccharidosis VI

1 reference

12 December 2020

Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds

1 reference

12 December 2020

Rescue of the T-associated maternal effect in mice carrying null mutations in Igf-2 and Igf2r, two reciprocally imprinted genes

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12 December 2020

Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures

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12 December 2020

Trafficking of lysosomal enzymes in normal and disease states

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12 December 2020

[A new specimen radiography device with a maximum 20-fold magnification for breast diagnosis]

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12 December 2020

Mannose 6-phosphate receptors in sorting and transport of lysosomal enzymes

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12 December 2020

Spontaneous mucolipidosis in a cat: an animal model of human I-cell disease

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12 December 2020

I-cell disease. A further report on its pathology

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12 December 2020

Targeted disruption of the M(r) 46,000 mannose 6-phosphate receptor gene in mice results in misrouting of lysosomal proteins

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12 December 2020

I-cell disease. A case report and review of the literature

1 reference

12 December 2020

Mouse mutants lacking the cation-independent mannose 6-phosphate/insulin-like growth factor II receptor are impaired in lysosomal enzyme transport: comparison of cation-independent and cation-dependent mannose 6-phosphate receptor-deficient mice

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12 December 2020

Regulation of embryonic growth and lysosomal targeting by the imprinted Igf2/Mpr gene

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12 December 2020

Protein measurement with the Folin phenol reagent

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12 December 2020

The Two Mannose 6-Phosphate Receptors Transport Distinct Complements of Lysosomal Proteins

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12 December 2020

Targeted disruption of the mouse cation-dependent mannose 6-phosphate receptor results in partial missorting of multiple lysosomal enzymes.

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1008823315416

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9 February 2018

Dimensions Publication ID

1044407476

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9 February 2018