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Brain Research. Molecular Brain Research
|
September 1, 1994
Novel cDNA clones obtained by antibody screening of a mouse cerebellar cDNA expression library
M Kambouris, L C Triarhou, S R Dlouhy, et al.
American Journal of Medical Genetics
|
February 13, 1995
Pelizaeus-Merzbacher disease in a family of Portuguese origin caused by a point mutation in exon 5 of the proteolipid protein gene
V M Pratt, S Boyadjiev, S R Dlouhy, et al.
Neuropsychiatry, Neuropsychology, and Behavioral Neurology
|
September 10, 2002
Longitudinal personality changes among presymptomatic Huntington disease gene carriers
Sandra Close Kirkwood, Eric Siemers, Richard Viken, et al.
American Journal of Medical Genetics
|
February 13, 1995
In-frame deletion in the proteolipid protein gene of a family with Pelizaeus-Merzbacher disease
D O Kleindorfer, S R Dlouhy, V M Pratt, et al.
Brain Research. Molecular Brain Research
|
September 1, 1994
Molecular characterization of a novel cDNA from murine cerebellum, developmental expression, and distribution in brain
M Kambouris, L Sangameswaran, L C Triarhou, et al.
Molecular Biology & Medicine
|
October 1, 1984
A complementary DNA sequence that predicts a human pancreatic amylase primary structure consistent with the electrophoretic mobility of the common isozyme, Amy2 A
R J Wise, R C Karn, S H Larsen, et al.
Cytogenetics and Cell Genetics
|
January 1, 1976
Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA)
A D Merritt, B H Petersen, A A Biegel, et al.
Birth Defects Original Article Series
|
January 1, 1976
Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA)
A D Merritt, B H Petersen, A A Biegel, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
January 1, 1987
Distribution of phosphodiesterase I in normal human tissues
D J Morley, D M Hawley, T M Ulbright, et al.
FEBS Letters
|
July 15, 1996
The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2
Y Tong, J Wei, S Zhang, et al.
Page
of 15
Search research articles
Search
Showing results (111-120 of 144) with videos related to
Sort By:
Page
of 15
Brain Research. Molecular Brain Research
|
September 1, 1994
Novel cDNA clones obtained by antibody screening of a mouse cerebellar cDNA expression library
M Kambouris, L C Triarhou, S R Dlouhy, et al.
American Journal of Medical Genetics
|
February 13, 1995
Pelizaeus-Merzbacher disease in a family of Portuguese origin caused by a point mutation in exon 5 of the proteolipid protein gene
V M Pratt, S Boyadjiev, S R Dlouhy, et al.
Neuropsychiatry, Neuropsychology, and Behavioral Neurology
|
September 10, 2002
Longitudinal personality changes among presymptomatic Huntington disease gene carriers
Sandra Close Kirkwood, Eric Siemers, Richard Viken, et al.
American Journal of Medical Genetics
|
February 13, 1995
In-frame deletion in the proteolipid protein gene of a family with Pelizaeus-Merzbacher disease
D O Kleindorfer, S R Dlouhy, V M Pratt, et al.
Brain Research. Molecular Brain Research
|
September 1, 1994
Molecular characterization of a novel cDNA from murine cerebellum, developmental expression, and distribution in brain
M Kambouris, L Sangameswaran, L C Triarhou, et al.
Molecular Biology & Medicine
|
October 1, 1984
A complementary DNA sequence that predicts a human pancreatic amylase primary structure consistent with the electrophoretic mobility of the common isozyme, Amy2 A
R J Wise, R C Karn, S H Larsen, et al.
Cytogenetics and Cell Genetics
|
January 1, 1976
Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA)
A D Merritt, B H Petersen, A A Biegel, et al.
Birth Defects Original Article Series
|
January 1, 1976
Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA)
A D Merritt, B H Petersen, A A Biegel, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
January 1, 1987
Distribution of phosphodiesterase I in normal human tissues
D J Morley, D M Hawley, T M Ulbright, et al.
FEBS Letters
|
July 15, 1996
The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2
Y Tong, J Wei, S Zhang, et al.
Page
of 15