Results 261 to 270 of about 161,067 (287)

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

The Lipoprotein Lipase HindIII Polymorphism And The Susceptibility To Hypertension

The FASEB Journal, 2008
Backgroung: Lipoprotein lipase (LPL) enzyme plays a central role in lipid metabolism. The primary function of LPL enzyme is the hydrolysis of the core triglycerides of circulating chylomicron and very low density lipoprotein. It releases monoglycerides and free fatty acids, which are taken up by skeletal muscle or adipose tissue. Aim:
Neveen Salah El Din Hemimi, Mona Mohamed Abd El Salam, Mahmoud M Abd Elwahab   +2 more
openaire   +1 more source

Chromosomal and nuclear distribution of the HindIII 1.9-kb human DNA repeat segment

Chromosoma, 1984
A human interspersed repetitive DNA cloned in pBR322, the HindIII 1.9-kb (kilobase pair) sequence, was labeled with biotinylated dUTP and hybridized to acid-fixed chromosomes and paraformaldehyde-fixed whole cells in situ. Using our most sensitive detection techniques this probe highlighted on the order of 200 discrete loci, in punctate or banded ...
L, Manuelidis, D C, Ward
openaire   +2 more sources

Nucleotide sequence analysis of variola virus HindIII M, L, I genome fragments

Virus Research, 1993
DNA of the variola major virus strain India-1967 in the region of HindIII M, L, I fragments has been sequenced. Analysis of this sequence of 18029 bp revealed 19 potential open reading frames (ORFs). Four proposed proteins (L2R, H9R, L5L, L6R) contain metal-binding domains. Comparison of the variola virus (VAR) and vaccinia virus strain Copenhagen (COP)
S.N. Shchelkunov, V.M. Blinov, A.V. Totmenin, S.S. Marennikova, A.A. Kolykhalov, I.V. Frolov, V.E. Chizhikov, V.V. Gytorov, P.V. Gashikov, E.F. Belanov, P.A. Belavin, S.M. Resenchuk, O.G. Andzhaparidze, L.S. Sandakhchiev   +13 more
openaire   +2 more sources

The nucleotide sequence of the transforming HindIII-G fragment of adenovirus type 5 DNA the region between map positions 4.5 (HpaI site) and 8.0 (HindIII site)

Gene, 1979
The nucleotide sequence of the region between map positions 4.5 (HpaI-site) and 8.0 (HindIII-site) of adenovirus type 5 (Ad5) DNA has been determined. This stretch of DNA is part of the transforming HindIII-G fragment, which is 2809 nucleotides long. The sequenced segment was found to have a long open reading frame for protein biosynthesis, starting 23
J, Maat, H, Van Ormondt
openaire   +2 more sources

An interleukin-8 (IL-8) cDNA clone identifies a frequent HindIII polymorphism

Human Genetics, 1993
An interleukin-8 cDNA probe detects a biallelic HindIII polymorphism. This frequent restriction fragment length polymorphism (RFLP) provides a new genetic marker for the long arm of chromosome 4.
M F, Fey, A, Tobler
openaire   +2 more sources