Results 181 to 190 of about 112,497 (212)

Human lipoprotein lipase HindIII polymorphism in young patients with myocardial infarction

Metabolism, 1999
We investigated the possibility that the DNA HindIII polymorphism of human lipoprotein lipase (LPL) is associated with the severity of coronary artery disease (CAD) determined by angiography in young patients who survived a myocardial infarction (MI).
GAMBINO, Roberto, SCAGLIONE L., ALEMANNO N., PAGANO, Gian Franco, CASSADER, Maurizio   +4 more
openaire   +3 more sources

Sequence and transcriptional analysis of the vaccinia virus HindIII I fragment [PDF]

Journal of Virology, 1988
The complete sequence of the vaccinia virus HindIII I fragment, which is composed of 6,498 base pairs, encodes six complete and two incomplete open reading frames (ORFs). Computer analysis revealed an amino acid sequence homology between ORF I 4 and the large subunit of the ribonucleotide reductase complex.
J F, Schmitt, H G, Stunnenberg
exaly   +3 more sources

RFLP Standardization Report for DQ Alpha/HindIII

1989
The DQ alpha probe detects five bands. Bands 1-4 are allelic and correlate broadly, but not exclusively, with the DR types of the cells (Table 2). Band 5 is the DQA2 gene (1,2).
P. A. Biro, J. Cutbush, J. M. Tiercy, G. Paulsen, J. Demopulos, R. T. Acton, S. V. Van Tonder, G. Semana, F. Quillivic   +8 more
openaire   +1 more source

RFLP Standardization Report for DO Beta/HindIII

1989
In the DO beta/HID system, one single band was detected in all the core cell lines (Table 1 and Fig. 1).
G. Paulsen, G. Markussen, J. M. Tiercy, R. Fauchet   +3 more
openaire   +1 more source

HindII, HindIII, and HpaI restriction fragment maps of bacteriophage λ DNA

Gene, 1977
The site-specific restriction endonucleases isolated from Hemophilus influenzae strains Rc (HincII) and Rd (HindII + III), and Hemophilus parainfluenzae (HpaI) were used to digest bacteriophage lambda DNA into 34, 40, and 15 specific fragments, respectively.
L H, Robinson, A, Landy
openaire   +2 more sources

RFLP Standardization Report for DP Alpha/HindIII

1989
DP alpha (Fig. 1) gives rise to three nonpolymorphic (std. bands 1, 2, and 4; Table 1) and two polymorphic, allelic fragments (std. bands 3 and 5). The allelic bands can be correlated with the DP types of the cells (1,2). Band 3 correlates with DP type 1 (and probably 5, 6, and 7) and band 5 associates with DP types 2, 2B, 3, 4, and 4B (Tables 2 and 3).
P. A. Biro, S. Cutbush, J. M. Tiercy, G. Paulsen, G. Semana, F. Quillivic   +5 more
openaire   +1 more source

Cloning, analysis and expression of the HindIII R-M-encoding genes

Gene, 1994
The genes encoding the HindIII restriction endonuclease (R.HindIII ENase) and methyltransferase (M.HindIII MTase) from Haemophilus influenzae Rd were cloned and expressed in Escherichia coli and their nucleotide (nt) sequences were determined. The genes are transcribed in the same orientation, with the ENase-encoding gene (hindIIIR) preceding the MTase-
D O, Nwankwo, L S, Moran, B E, Slatko, P A, Waite-Rees, L F, Dorner, J S, Benner, G G, Wilson   +6 more
openaire   +2 more sources

RFLP Standardization Report for DQ Beta/HindIII

1989
Thirty-four bands were identified in the DQB/HID system (Table 1 and Fig. 1). The distribution of nineteen bands showing high DQB specificity is shown in Table 2.
G. Paulsen, G. Markussen, J. Demopulos, J. M. Tiercy, S. van Tonder, F. Quillivic   +5 more
openaire   +1 more source

A HindIII/BglII dystrophin gene polymorphism in the African-American population

Human Genetics, 1992
We describe a common dystrophin gene polymorphism in the black population that alters both HindIII and BglII restriction sites.
T W, Prior, A C, Papp, P J, Snyder, A H, Burghes, B H, Wallace   +4 more
openaire   +2 more sources

RFLP Standardization Report for Class I/HindIII

1989
Twenty-eight fragments have been defined using the class I probe (Table 1 and Fig. 1). The family studies have revealed the existence of a few additional faint bands that are not detected in every blot. The majority of the fragments are polymorphic, although many of their frequencies are either above 85% or below 15%.
P. A. Biro, S. Cutbush, J. M. Tiercy, G. Paulsen, J. Demopulos, R. T. Acton, S. V. van Tonder, G. Semana, F. Quillivic   +8 more
openaire   +1 more source