Zobrazeno 1 - 4
of 4
pro vyhledávání: '"R. D. Obermoeller"'
Autor:
R. D. Obermoeller, Brenda B. McEntire, Rodney S. Nairn, L. Della Coletta, Ronald B. Walter, J M Lacson, D D Moore, Donald C. Morizot
Publikováno v:
Cytogenetic and Genome Research. 75:140-144
We have determined the nucleotide sequence and gene map location of the Xiphophorus mαculαtus homologue of RPS 15 (ribosomal protein S15, alias RIG). The Xiphophorus RPS15 cDNA encodes 145 amino acids, which show 94 % identity compared to deduced m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ae16fd596e8262283f93f94ad8359b6
https://doi.org/10.1159/000134465
https://doi.org/10.1159/000134465
Autor:
H. D. Chapman, Zuoming Deng, Thomas P. Dooley, Charles N. Falany, Michael J. Siciliano, R. D. Obermoeller, Edward H. Leiter
Publikováno v:
Genomics. 18:440-443
We have recently cloned a cDNA encoding the human phenol-preferring phenol sulfotranaferase (P-PST) enzyme. An oligonucleotide primer pair based on the human STP (representing sulfotransferase, phenol-preferring) cDNA sequence was synthesized and was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a24c5da632e130ef2863e6e8ed6988b8
https://doi.org/10.1006/geno.1993.1494
https://doi.org/10.1006/geno.1993.1494
Autor:
Thomas P. Dooley, HM Mitchison, Norman A. Doggett, P. Probst, Michael J. Siciliano, David F. Callen, Sara E. Mole, R. D. Obermoeller
Publikováno v:
American journal of medical genetics. 57(2)
Batten disease (juvenile-onset neuronal ceroid lipofuscinosis; JNCL) is an autosomal recessive neurodegenerative disorder, characterized by the cytosomal accumulation of autofluorescent proteolipopigments in neurons and other cell types. The Batten d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2df8f05037584bc2a993b90b6028ce43
https://pubmed.ncbi.nlm.nih.gov/7668357
https://pubmed.ncbi.nlm.nih.gov/7668357
Autor:
K. D. Kallman, Julie Harless, Donald C. Morizot, Juergen R. Vielkind, Rodney S. Nairn, R. D. Obermoeller, R. Svensson, Ronald B. Walter
Publikováno v:
The Journal of heredity. 86(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4f8bf7f0da323f7e933dc2fc00ed8b1
https://pubmed.ncbi.nlm.nih.gov/7608517
https://pubmed.ncbi.nlm.nih.gov/7608517