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The Journal of Clinical Investigation
|
November 1, 1992
Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome
N Shimozawa, T Tsukamoto, Y Suzuki, et al.
The Tohoku Journal of Experimental Medicine
|
October 1, 1975
Three GM1-gangliosidoses and a variant of beta-galactosidase deficiency
T Orii, K Sukegawa, T Kudoh, et al.
Pediatric Research
|
December 1, 1988
Biochemical and morphologic aspects of peroxisomes in the human rectal mucosa: diagnosis of Zellweger syndrome simplified by rectal biopsy
N 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.
Brain Research
|
March 21, 1994
Developmental immunohistochemistry of bifunctional protein in human brain
A Imamura, A Kamei, Y Suzuki, et al.
Journal of Investigational Allergology & Clinical Immunology
|
May 1, 1994
Interleukin-2 and interferon-gamma production by peripheral blood lymphocytes of patients with common variable immunodeficiency
Y Inoue, N Kondo, F Motoyoshi, et al.
Clinical Genetics
|
December 1, 1994
Chediak-Higashi syndrome with cerebellar cortical atrophy detected by MRI
N Kondo, N Shimozawa, J Asano, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1994
IgG subclass levels and southern analysis of DNA in primary immunodeficiency diseases including IgG subclass deficiency
Y Miwa, R Inoue, T Ozawa, et al.
The Tohoku Journal of Experimental Medicine
|
August 1, 1972
A new type of mucolipidosis with -galactosidase deficiency and glycopeptiduria
T Orii, R Minami, K Sukegawa, et al.
The Tohoku Journal of Experimental Medicine
|
July 1, 1973
Pattern of beta-galactosidase deficiency in GM1-gangliosidosis type 1 and type 2
T Orii, K Sukegawa, R Minami, et al.
Page
of 40
Search research articles
Search
Showing results (101-110 of 397) with videos related to
Sort By:
Page
of 40
The Journal of Clinical Investigation
|
November 1, 1992
Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome
N Shimozawa, T Tsukamoto, Y Suzuki, et al.
The Tohoku Journal of Experimental Medicine
|
October 1, 1975
Three GM1-gangliosidoses and a variant of beta-galactosidase deficiency
T Orii, K Sukegawa, T Kudoh, et al.
Pediatric Research
|
December 1, 1988
Biochemical and morphologic aspects of peroxisomes in the human rectal mucosa: diagnosis of Zellweger syndrome simplified by rectal biopsy
N 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.
Brain Research
|
March 21, 1994
Developmental immunohistochemistry of bifunctional protein in human brain
A Imamura, A Kamei, Y Suzuki, et al.
Journal of Investigational Allergology & Clinical Immunology
|
May 1, 1994
Interleukin-2 and interferon-gamma production by peripheral blood lymphocytes of patients with common variable immunodeficiency
Y Inoue, N Kondo, F Motoyoshi, et al.
Clinical Genetics
|
December 1, 1994
Chediak-Higashi syndrome with cerebellar cortical atrophy detected by MRI
N Kondo, N Shimozawa, J Asano, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1994
IgG subclass levels and southern analysis of DNA in primary immunodeficiency diseases including IgG subclass deficiency
Y Miwa, R Inoue, T Ozawa, et al.
The Tohoku Journal of Experimental Medicine
|
August 1, 1972
A new type of mucolipidosis with -galactosidase deficiency and glycopeptiduria
T Orii, R Minami, K Sukegawa, et al.
The Tohoku Journal of Experimental Medicine
|
July 1, 1973
Pattern of beta-galactosidase deficiency in GM1-gangliosidosis type 1 and type 2
T Orii, K Sukegawa, R Minami, et al.
Page
of 40