1-8 of 8
Peter LOBEL
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Articles

Lysosomal protein thermal stability does not correlate with cellular half-life: global observations and a case study of tripeptidyl-peptidase 1

Available to Purchase
Aaron M. Collier, Yuliya Nemtsova, Narendra Kuber, Whitney Banach-Petrosky, Anurag Modak, David E. Sleat, Vikas Nanda, Peter Lobel
Journal: Biochemical Journal
Biochem J (2020) 477 (3): 727–745.
https://doi.org/10.1042/BCJ20190874
Published: 14 February 2020
View articletitled, Lysosomal protein thermal stability does not correlate with cellular half-life: global observations and a case study of tripeptidyl-peptidase 1
Open the PDF for Lysosomal protein thermal stability does not correlate with cellular half-life: global observations and a case study of tripeptidyl-peptidase 1 in another window
Includes: Supplementary data
Articles

Glial fibrillary acidic protein is elevated in the lysosomal storage disease classical late-infantile neuronal ceroid lipofuscinosis, but is not a component of the storage material

Available to Purchase
Su Xu, David E. Sleat, Michel Jadot, Peter Lobel
Journal: Biochemical Journal
Biochem J (2010) 428 (3): 355–362.
https://doi.org/10.1042/BJ20100128
Published: 27 May 2010
View articletitled, Glial fibrillary acidic protein is elevated in the lysosomal storage disease classical late-infantile neuronal ceroid lipofuscinosis, but is not a component of the storage material
Open the PDF for Glial fibrillary acidic protein is elevated in the lysosomal storage disease classical late-infantile neuronal ceroid lipofuscinosis, but is not a component of the storage material in another window
Includes: Supplementary data
Articles

Dipeptidyl-peptidase I does not functionally compensate for the loss of tripeptidyl-peptidase I in the neurodegenerative disease late-infantile neuronal ceroid lipofuscinosis

Available to Purchase
Kwi-Hye Kim, Christine T. Pham, David E. Sleat, Peter Lobel
Journal: Biochemical Journal
Biochem J (2008) 415 (2): 225–232.
https://doi.org/10.1042/BJ20080411
Published: 25 September 2008
View articletitled, Dipeptidyl-peptidase I does not functionally compensate for the loss of tripeptidyl-peptidase I in the neurodegenerative disease late-infantile neuronal ceroid lipofuscinosis
Open the PDF for Dipeptidyl-peptidase I does not functionally compensate for the loss of tripeptidyl-peptidase I in the neurodegenerative disease late-infantile neuronal ceroid lipofuscinosis in another window
Articles

Do mammalian NPC1 and NPC2 play a role in intestinal cholesterol absorption?

Available to Purchase
Sayali S. Dixit, David E. Sleat, Ann M. Stock, Peter Lobel
Journal: Biochemical Journal
Biochem J (2007) 408 (1): 1–5.
https://doi.org/10.1042/BJ20071167
Published: 29 October 2007
View articletitled, Do mammalian NPC1 and NPC2 play a role in intestinal cholesterol absorption?
Open the PDF for Do mammalian NPC1 and NPC2 play a role in intestinal cholesterol absorption? in another window
Articles

Production and characterization of recombinant human CLN2 protein for enzyme-replacement therapy in late infantile neuronal ceroid lipofuscinosis

Available to Purchase
Li LIN, Peter LOBEL
Journal: Biochemical Journal
Biochem J (2001) 357 (1): 49–55.
https://doi.org/10.1042/bj3570049
Published: 25 June 2001
View articletitled, Production and characterization of recombinant human CLN2 protein for enzyme-replacement therapy in late infantile neuronal ceroid lipofuscinosis
Open the PDF for Production and characterization of recombinant human CLN2 protein for enzyme-replacement therapy in late infantile neuronal ceroid lipofuscinosis in another window
Articles

Specific alterations in levels of mannose 6-phosphorylated glycoproteins in different neuronal ceroid lipofuscinoses

Available to Purchase
David E. SLEAT, Istvan SOHAR, Premila S. PULLARKAT, Peter LOBEL, Raju K. PULLARKAT
Journal: Biochemical Journal
Biochem J (1998) 334 (3): 547–551.
https://doi.org/10.1042/bj3340547
Published: 15 September 1998
View articletitled, Specific alterations in levels of mannose 6-phosphorylated glycoproteins in different neuronal ceroid lipofuscinoses
Open the PDF for Specific alterations in levels of mannose 6-phosphorylated glycoproteins in different neuronal ceroid lipofuscinoses in another window
Articles

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

Available to Purchase
Istvan SOHAR, David SLEAT, Chang-Gong LIU, Thomas LUDWIG, Peter LOBEL
Journal: Biochemical Journal
Biochem J (1998) 330 (2): 903–908.
https://doi.org/10.1042/bj3300903
Published: 01 March 1998
View articletitled, 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
Open the PDF for 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 in another window
Articles

α -Glucosidase and N -acetylglucosamine-6-sulphatase are the major mannose-6-phosphate glycoproteins in human urine

Available to Purchase
David E. SLEAT, Stephen R. KRAUS, Istvan SOHAR, Henry LACKLAND, Peter LOBEL
Journal: Biochemical Journal
Biochem J (1997) 324 (1): 33–39.
https://doi.org/10.1042/bj3240033
Published: 15 May 1997
View articletitled, α -Glucosidase and N -acetylglucosamine-6-sulphatase are the major mannose-6-phosphate glycoproteins in human urine
Open the PDF for α -Glucosidase and N -acetylglucosamine-6-sulphatase are the major mannose-6-phosphate glycoproteins in human urine in another window