Brain lipid composition in grey-lethal mutant mouse characterized by severe malignant osteopetrosis (Q46378786)

21 December 2017

title

Brain lipid composition in grey-lethal mutant mouse characterized by severe malignant osteopetrosis (English)

1 reference

21 December 2017

author

Alessandro Prinetti

1

1 reference

21 December 2017

Sandro Sonnino

10

1 reference

21 December 2017

author name string

Federica Rocchetta

2

1 reference

21 December 2017

Elvira Costantino

3

1 reference

21 December 2017

Annalisa Frattini

4

1 reference

21 December 2017

Elena Caldana

5

1 reference

21 December 2017

Francesca Rucci

6

1 reference

21 December 2017

Arianna Bettiga

7

1 reference

21 December 2017

Pietro L Poliani

8

1 reference

21 December 2017

Vanna Chigorno

9

1 reference

21 December 2017

publication date

10 September 2008

1 reference

21 December 2017

published in

Glycoconjugate Journal

1 reference

21 December 2017

volume

26

1 reference

21 December 2017

issue

6

1 reference

21 December 2017

page(s)

623-633

1 reference

21 December 2017

Filter-paper partition chromatography of sugars: 1. General description and application to the qualitative analysis of sugars in apple juice, egg white and foetal blood of sheep. with a note by R. G. Westall

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10719-008-9179-8

Physiology and pathophysiology of sphingolipid metabolism and signaling

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10719-008-9179-8

Separation of gluco- and galactocerebrosides by means of borate thin-layer chromatography

21 January 2018

1 reference

12 December 2020

Western blotting analysis of the beta-hexosaminidase alpha- and beta-subunits in cultured fibroblasts from cases of various forms of GM2 gangliosidosis

1 reference

12 December 2020

Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man

1 reference

12 December 2020

OSTM1 regulates beta-catenin/Lef1 interaction and is required for Wnt/beta-catenin signaling

1 reference

12 December 2020

Downregulation of amyloid precursor protein inhibits neurite outgrowth in vitro

1 reference

12 December 2020

Sphingolipid-enriched Membrane Domains from Rat Cerebellar Granule Cells Differentiated in Culture

1 reference

12 December 2020

Phosphorus assay in column chromatography

1 reference

12 December 2020

Spleen Cells Transmit Osteopetrosis in Mice

1 reference

12 December 2020

Sphingosylphosphorylcholine in Niemann-Pick disease brain: accumulation in type A but not in type B.

1 reference

12 December 2020

Identification of a novel mutation in the coding region of the grey-lethal gene OSTM1 in human malignant infantile osteopetrosis

1 reference

12 December 2020

Quantitative estimation of sialic acids. II. A colorimetric resorcinol-hydrochloric acid method

1 reference

12 December 2020

The interaction between Alzheimer amyloid beta(1-40) peptide and ganglioside GM1-containing membranes

1 reference

12 December 2020

Long-term outcome of haematopoietic stem cell transplantation in autosomal recessive osteopetrosis: an EBMT report

1 reference

12 December 2020

Lipid rafts mediate the synaptic localization of alpha-synuclein.

1 reference

12 December 2020

Specific tritium labeling of gangliosides at the 3-position of sphingosines

1 reference

12 December 2020

Progressive accumulation of toxic metabolite in a genetic leukodystrophy

1 reference

12 December 2020

Changes in the lipid turnover, composition, and organization, as sphingolipid-enriched membrane domains, in rat cerebellar granule cells developing in vitro

1 reference

12 December 2020

Bone marrow transplantation for autosomal recessive osteopetrosis. A report from the Working Party on Inborn Errors of the European Bone Marrow Transplantation Group

1 reference

12 December 2020

Reagent for Differentiation of 1,4- and 1,6-Linked Glucosaccharides

1 reference

12 December 2020

Functional Coupling of Glycosyl Transfer Steps for Synthesis of Gangliosides in Golgi Membranes from Neural Retina Cells

1 reference

12 December 2020

Novel mutations in the TCIRG1 gene encoding the a3 subunit of the vacuolar proton pump in patients affected by infantile malignant osteopetrosis

1 reference

12 December 2020

Lipid rafts, protein scaffolds, and neurologic disease

1 reference

12 December 2020

Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains

1 reference

12 December 2020

Modified spray for the detection of phospholipids on thin-layer chromatograms.

1 reference

12 December 2020

Regulation of ganglioside biosynthesis in the nervous system

1 reference

12 December 2020

Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene

1 reference

12 December 2020

Glycosylation of glycolipids in the Golgi complex

1 reference

12 December 2020

Metabolic processing of gangliosides by normal and Salla human fibroblasts in culture. A study performed by administering radioactive GM3 ganglioside

1 reference

12 December 2020

Formation of free sphingosine and ceramide from exogenous ganglioside GM1 by cerebellar granule cells in culture.

1 reference

12 December 2020

Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL.

1 reference

12 December 2020

Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human

1 reference

12 December 2020

Patterns of endogenous gangliosides and metabolic processing of exogenous gangliosides in cerebellar granule cells during differentiation in culture.

1 reference

12 December 2020

Chloride and the endosomal-lysosomal pathway: emerging roles of CLC chloride transporters.

1 reference

12 December 2020

Evaluation of the efficiency of an assay procedure for gangliosides in human serum.

1 reference

12 December 2020

The new domestic cresyl echt violet

1 reference

12 December 2020

Gangliosides as components of lipid membrane domains.

1 reference

12 December 2020

Plasma membrane repair is mediated by Ca(2+)-regulated exocytosis of lysosomes

1 reference

12 December 2020

Mutations in the a3 subunit of the vacuolar H(+)-ATPase cause infantile malignant osteopetrosis

1 reference

12 December 2020

Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis

1 reference

12 December 2020

Cholesterol depletion inhibits the generation of beta-amyloid in hippocampal neurons

1 reference

12 December 2020

Lysosomal storage diseases

1 reference

12 December 2020

Biochemical changes in mouse brain composition during myelination

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Broad screening test for sphingolipid-storage diseases.

1 reference

12 December 2020

Severe malignant osteopetrosis caused by a GL gene mutation.

1 reference

12 December 2020

1 reference

12 December 2020

Twenty five years of the "psychosine hypothesis": a personal perspective of its history and present status

1 reference

12 December 2020

Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis

1 reference

12 December 2020

Caveolae, plasma membrane microdomains for alpha-secretase-mediated processing of the amyloid precursor protein

1 reference

12 December 2020

Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement

1 reference

12 December 2020

ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function

1 reference

12 December 2020

Regulation of ganglioside biosynthesis in the nervous system

1 reference

12 December 2020

10.1007/S10719-008-9179-8

Identifiers

DOI

1 reference

21 December 2017

1 reference

21 December 2017