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Scandinavian Journal of Rheumatology. Supplement
|
January 1, 1986
Effects of immunosuppressive drugs on the morphology of the microvilli in Sjögren's syndrome
J M Scharf, E Meyer, J A Scharf, et al.
Genomics
|
March 10, 2000
Evolutionary divergence of the mouse and human Lgn1/SMA repeat structures
J D Growney, J M Scharf, L M Kunkel, et al.
European Child & Adolescent Psychiatry
|
July 16, 2015
Parental mood during pregnancy and post-natally is associated with offspring risk of Tourette syndrome or chronic tics: prospective data from the Avon Longitudinal Study of Parents and Children (ALSPAC)
Y Ben-Shlomo, J M Scharf, L L Miller, et al.
The EMBO Journal
|
January 3, 1995
Concerted evolution of the tandem array encoding primate U2 snRNA occurs in situ, without changing the cytological context of the RNU2 locus
T Pavelitz, L Rusché, A G Matera, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 25, 1995
Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene
S Selig, S Bruno, J M Scharf, et al.
Genomics
|
December 15, 1996
The mouse region syntenic for human spinal muscular atrophy lies within the Lgn1 critical interval and contains multiple copies of Naip exon 5
J M Scharf, D Damron, A Frisella, et al.
Gene Therapy
|
September 1, 1994
Antitumor activity and reporter gene transfer into rat brain neoplasms inoculated with herpes simplex virus vectors defective in thymidine kinase or ribonucleotide reductase
E J Boviatsis, J M Scharf, M Chase, et al.
Genomics
|
September 16, 1999
Comparative sequence analysis of the mouse and human Lgn1/SMA interval
M Endrizzi, S Huang, J M Scharf, et al.
Nature Genetics
|
September 10, 1998
Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics
J M Scharf, M G Endrizzi, A Wetter, et al.
Human Genetics
|
September 10, 1999
Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminoma
F von Deimling, J M Scharf, T Liehr, et al.
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Showing results (1-10 of 14) with videos related to
Sort By:
Page
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Scandinavian Journal of Rheumatology. Supplement
|
January 1, 1986
Effects of immunosuppressive drugs on the morphology of the microvilli in Sjögren's syndrome
J M Scharf, E Meyer, J A Scharf, et al.
Genomics
|
March 10, 2000
Evolutionary divergence of the mouse and human Lgn1/SMA repeat structures
J D Growney, J M Scharf, L M Kunkel, et al.
European Child & Adolescent Psychiatry
|
July 16, 2015
Parental mood during pregnancy and post-natally is associated with offspring risk of Tourette syndrome or chronic tics: prospective data from the Avon Longitudinal Study of Parents and Children (ALSPAC)
Y Ben-Shlomo, J M Scharf, L L Miller, et al.
The EMBO Journal
|
January 3, 1995
Concerted evolution of the tandem array encoding primate U2 snRNA occurs in situ, without changing the cytological context of the RNU2 locus
T Pavelitz, L Rusché, A G Matera, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 25, 1995
Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene
S Selig, S Bruno, J M Scharf, et al.
Genomics
|
December 15, 1996
The mouse region syntenic for human spinal muscular atrophy lies within the Lgn1 critical interval and contains multiple copies of Naip exon 5
J M Scharf, D Damron, A Frisella, et al.
Gene Therapy
|
September 1, 1994
Antitumor activity and reporter gene transfer into rat brain neoplasms inoculated with herpes simplex virus vectors defective in thymidine kinase or ribonucleotide reductase
E J Boviatsis, J M Scharf, M Chase, et al.
Genomics
|
September 16, 1999
Comparative sequence analysis of the mouse and human Lgn1/SMA interval
M Endrizzi, S Huang, J M Scharf, et al.
Nature Genetics
|
September 10, 1998
Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics
J M Scharf, M G Endrizzi, A Wetter, et al.
Human Genetics
|
September 10, 1999
Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminoma
F von Deimling, J M Scharf, T Liehr, et al.
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of 2