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Nature Genetics
|
May 1, 1992
A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism
D B Parkinson, R V Thakker
Journal of Cataract and Refractive Surgery
|
March 1, 1988
Synthetic cataract teaching system for phacoemulsification
W F Maloney, D Hall, D B Parkinson
Glia
|
February 2, 2008
Impaired intercellular adhesion and immature adherens junctions in merlin-deficient human primary schwannoma cells
C Flaiz, T Utermark, D B Parkinson, et al.
Human Genetics
|
April 1, 1993
Parathyroid hormone gene analysis in autosomal hypoparathyroidism using an intragenic tetranucleotide (AAAT)n polymorphism
D B Parkinson, N J Shaw, R L Himsworth, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 19, 2001
Transforming growth factor beta (TGFbeta) mediates Schwann cell death in vitro and in vivo: examination of c-Jun activation, interactions with survival signals, and the relationship of TGFbeta-mediated death to Schwann cell differentiation
D B Parkinson, Z Dong, H Bunting, et al.
The New England Journal of Medicine
|
October 8, 1992
Brief report: autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia
R W Bilous, G Murty, D B Parkinson, et al.
Progress in Brain Research
|
September 8, 2001
Regulation of genes involved in Schwann cell development and differentiation
R Mirsky, D B Parkinson, Z Dong, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Nature Genetics
|
May 1, 1992
A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism
D B Parkinson, R V Thakker
Journal of Cataract and Refractive Surgery
|
March 1, 1988
Synthetic cataract teaching system for phacoemulsification
W F Maloney, D Hall, D B Parkinson
Glia
|
February 2, 2008
Impaired intercellular adhesion and immature adherens junctions in merlin-deficient human primary schwannoma cells
C Flaiz, T Utermark, D B Parkinson, et al.
Human Genetics
|
April 1, 1993
Parathyroid hormone gene analysis in autosomal hypoparathyroidism using an intragenic tetranucleotide (AAAT)n polymorphism
D B Parkinson, N J Shaw, R L Himsworth, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 19, 2001
Transforming growth factor beta (TGFbeta) mediates Schwann cell death in vitro and in vivo: examination of c-Jun activation, interactions with survival signals, and the relationship of TGFbeta-mediated death to Schwann cell differentiation
D B Parkinson, Z Dong, H Bunting, et al.
The New England Journal of Medicine
|
October 8, 1992
Brief report: autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia
R W Bilous, G Murty, D B Parkinson, et al.
Progress in Brain Research
|
September 8, 2001
Regulation of genes involved in Schwann cell development and differentiation
R Mirsky, D B Parkinson, Z Dong, et al.
Page
of 1