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N Shimozawa

Showing results (31-40 of 167) with videos related to

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Pediatric Research|December 1, 1988
Biochemical and morphologic aspects of peroxisomes in the human rectal mucosa: diagnosis of Zellweger syndrome simplified by rectal biopsyN Shimozawa, Y Suzuki, T Orii, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|January 1, 1993
[Peroxisomal disorders--DNA analysis]T Orii, Y Suzuki, N Shimozawa, et al.
Clinical Genetics|December 1, 1994
Chediak-Higashi syndrome with cerebellar cortical atrophy detected by MRIN Kondo, N Shimozawa, J Asano, et al.
Brain & Development|January 1, 1986
The syndrome of the absence of a septum pellucidum with porencephalyN Shimozawa, K Ohno, S Takashima, et al.
Biochemical and Biophysical Research Communications|May 20, 1998
A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6pS Tamura, N Shimozawa, Y Suzuki, et al.
American Journal of Human Genetics|September 1, 2000
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group GK Ghaedi, M Honsho, N Shimozawa, et al.
Experimental Cell Research|August 1, 1992
Transformation and characterization of mutant human fibroblasts defective in peroxisome assemblyH Okamoto, Y Suzuki, N Shimozawa, et al.
Annals of the New York Academy of Sciences|December 27, 1996
Peroxisomal disorders: clinical aspectsY Suzuki, N Shimozawa, Y Takahashi, et al.
The Japanese Journal of Human Genetics|March 1, 1996
Incidence of peroxisomal disorders in JapanY Suzuki, N Shimozawa, S Yajima, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Disorders of peroxisome biogenesis: complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency)R J Wanders, P A Mooijer, C Dekker, et al.
Pageof 17

Showing results (31-40 of 167) with videos related to

Sort By:
Pageof 17
Pediatric Research|December 1, 1988
Biochemical and morphologic aspects of peroxisomes in the human rectal mucosa: diagnosis of Zellweger syndrome simplified by rectal biopsyN Shimozawa, Y Suzuki, T Orii, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|January 1, 1993
[Peroxisomal disorders--DNA analysis]T Orii, Y Suzuki, N Shimozawa, et al.
Clinical Genetics|December 1, 1994
Chediak-Higashi syndrome with cerebellar cortical atrophy detected by MRIN Kondo, N Shimozawa, J Asano, et al.
Brain & Development|January 1, 1986
The syndrome of the absence of a septum pellucidum with porencephalyN Shimozawa, K Ohno, S Takashima, et al.
Biochemical and Biophysical Research Communications|May 20, 1998
A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6pS Tamura, N Shimozawa, Y Suzuki, et al.
American Journal of Human Genetics|September 1, 2000
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group GK Ghaedi, M Honsho, N Shimozawa, et al.
Experimental Cell Research|August 1, 1992
Transformation and characterization of mutant human fibroblasts defective in peroxisome assemblyH Okamoto, Y Suzuki, N Shimozawa, et al.
Annals of the New York Academy of Sciences|December 27, 1996
Peroxisomal disorders: clinical aspectsY Suzuki, N Shimozawa, Y Takahashi, et al.
The Japanese Journal of Human Genetics|March 1, 1996
Incidence of peroxisomal disorders in JapanY Suzuki, N Shimozawa, S Yajima, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Disorders of peroxisome biogenesis: complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency)R J Wanders, P A Mooijer, C Dekker, et al.
Pageof 17