A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes

1992 ◽  
Vol 35 (3) ◽  
Author(s):  
Abdel El Kahloun ◽  
Corine Vernet ◽  
Anne-Marie Jouanolle ◽  
Jo�lle Boretto ◽  
Val�rie Mauvieux ◽  
...  
Author(s):  
S. Grammatikos ◽  
T. Kaimakamis ◽  
S. Panos ◽  
C. Gravalidis ◽  
A. Laskarakis ◽  
...  

1968 ◽  
Vol 243 (6) ◽  
pp. 1204-1211
Author(s):  
H Kitchen ◽  
C W Easley ◽  
F W Putnam ◽  
W J Taylor

1982 ◽  
Vol 257 (5) ◽  
pp. 2708-2712
Author(s):  
G C DuBois ◽  
E Appella ◽  
D E Ryan ◽  
D M Jerina ◽  
W Levin

Author(s):  
W. T. Gowers ◽  
L. Milićević

Abstract Let $G_1, \ldots , G_k$ be finite-dimensional vector spaces over a prime field $\mathbb {F}_p$ . A multilinear variety of codimension at most $d$ is a subset of $G_1 \times \cdots \times G_k$ defined as the zero set of $d$ forms, each of which is multilinear on some subset of the coordinates. A map $\phi$ defined on a multilinear variety $B$ is multilinear if for each coordinate $c$ and all choices of $x_i \in G_i$ , $i\not =c$ , the restriction map $y \mapsto \phi (x_1, \ldots , x_{c-1}, y, x_{c+1}, \ldots , x_k)$ is linear where defined. In this note, we show that a multilinear map defined on a multilinear variety of codimension at most $d$ coincides on a multilinear variety of codimension $O_{k}(d^{O_{k}(1)})$ with a multilinear map defined on the whole of $G_1\times \cdots \times G_k$ . Additionally, in the case of general finite fields, we deduce similar (but slightly weaker) results.


Genetics ◽  
1989 ◽  
Vol 121 (3) ◽  
pp. 539-550
Author(s):  
W C Black ◽  
D K McLain ◽  
K S Rai

Abstract A restriction map was constructed of the ribosomal cistron in a mosquito, Aedes albopictus (Skuse). The 18s, 28s and nontranscribed spacer (NTS) regions were subcloned and used to probe for intraspecific variation. Seventeen populations were examined throughout the world range of the species. No variation was detected in the coding regions but extensive and continuous variation existed in the NTS. The NTS consisted of two nonhomologous regions. The first region contained multiple 190-bp AluI repeats nested within larger XhoI repeats of various sizes. There was a large number of length variants in the AluI repeat region of the NTS. No repeats were found in the second region and it gave rise to relatively fewer variants. An analysis of NTS diversity in individual mosquitoes indicated that most of the diversity arose at the population level. Discriminant analysis was performed on spacer types in individual mosquitoes and demonstrated that individuals within a population carried a unique set of spacers. In contrast with studies of the NTS in Drosophila populations, there seems to be little conservation of spacers in a population. The importance of molecular drive relative to drift and selection in the generation of local population differentiation is discussed.


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