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M D Benson

Showing results (181-190 of 227) with videos related to

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The Journal of Clinical Investigation|January 1, 1988
Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysisM R Wallace, F E Dwulet, E C Williams, et al.
Obstetrics and Gynecology|March 29, 2001
Immunologic studies in presumed amniotic fluid embolismM D Benson, H Kobayashi, R K Silver, et al.
Annals of Neurology|May 1, 1990
Diagnosis of Maryland/German familial amyloidotic polyneuropathy using allele-specific, enzymatically amplified, genomic DNAJ R Mendell, X S Jiang, J R Warmolts, et al.
The Journal of Biological Chemistry|February 5, 1993
X-ray crystal structure of the Ala-109-->Thr variant of human transthyretin which produces euthyroid hyperthyroxinemiaL K Steinrauf, J A Hamilton, B C Braden, et al.
Journal of Medical Genetics|June 1, 1993
RFLP analysis for APP 717 mutations associated with Alzheimer's diseaseS R Zeldenrust, J Murrell, M Farlow, et al.
American Journal of Veterinary Research|August 1, 1989
Serum amyloid A protein concentration measured by radial immunodiffusion in Abyssinian and non-Abyssinian catsS P DiBartola, J A Reiter, J B Cornacoff, et al.
Nature|December 12, 1970
Antigenic determinants in amyloid depositsE S Cathcart, M S Skinner, A S Cohen, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1993
Thyroxine interactions with transthyretin: a comparison of 10 different naturally occurring human transthyretin variantsH N Rosen, A C Moses, J R Murrell, et al.
Science (New York, N.Y.)|February 3, 1989
Autocrine induction of collagenase by serum amyloid A-like and beta 2-microglobulin-like proteinsC E Brinckerhoff, T I Mitchell, M J Karmilowicz, et al.
Neuromuscular Disorders : NMD|June 1, 1997
A European family with histidine 58 transthyretin mutation in familial amyloid polyneuropathyH H Goebel, S Seddigh, H C Hopf, et al.
Pageof 23

Showing results (181-190 of 227) with videos related to

Sort By:
Pageof 23
The Journal of Clinical Investigation|January 1, 1988
Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysisM R Wallace, F E Dwulet, E C Williams, et al.
Obstetrics and Gynecology|March 29, 2001
Immunologic studies in presumed amniotic fluid embolismM D Benson, H Kobayashi, R K Silver, et al.
Annals of Neurology|May 1, 1990
Diagnosis of Maryland/German familial amyloidotic polyneuropathy using allele-specific, enzymatically amplified, genomic DNAJ R Mendell, X S Jiang, J R Warmolts, et al.
The Journal of Biological Chemistry|February 5, 1993
X-ray crystal structure of the Ala-109-->Thr variant of human transthyretin which produces euthyroid hyperthyroxinemiaL K Steinrauf, J A Hamilton, B C Braden, et al.
Journal of Medical Genetics|June 1, 1993
RFLP analysis for APP 717 mutations associated with Alzheimer's diseaseS R Zeldenrust, J Murrell, M Farlow, et al.
American Journal of Veterinary Research|August 1, 1989
Serum amyloid A protein concentration measured by radial immunodiffusion in Abyssinian and non-Abyssinian catsS P DiBartola, J A Reiter, J B Cornacoff, et al.
Nature|December 12, 1970
Antigenic determinants in amyloid depositsE S Cathcart, M S Skinner, A S Cohen, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1993
Thyroxine interactions with transthyretin: a comparison of 10 different naturally occurring human transthyretin variantsH N Rosen, A C Moses, J R Murrell, et al.
Science (New York, N.Y.)|February 3, 1989
Autocrine induction of collagenase by serum amyloid A-like and beta 2-microglobulin-like proteinsC E Brinckerhoff, T I Mitchell, M J Karmilowicz, et al.
Neuromuscular Disorders : NMD|June 1, 1997
A European family with histidine 58 transthyretin mutation in familial amyloid polyneuropathyH H Goebel, S Seddigh, H C Hopf, et al.
Pageof 23