Functional complementation in mouse — human radiation hybrids assigns the putative murine scid gene to the pericentric region of human chromosome 8

1993 ◽  
Vol 2 (7) ◽  
pp. 1031-1034 ◽  
Author(s):  
Kenshi Komatsu ◽  
Tohru Ohta ◽  
Yoshihiro Jinno ◽  
Norio Nlikawa ◽  
Yutaka Okumura
Genomics ◽  
1991 ◽  
Vol 11 (4) ◽  
pp. 857-869 ◽  
Author(s):  
Susan Halloran Blanton ◽  
John R. Heckenlively ◽  
Anne W. Cottingham ◽  
Jackie Friedman ◽  
Lori A. Sadler ◽  
...  

Genomics ◽  
1994 ◽  
Vol 21 (1) ◽  
pp. 208-216 ◽  
Author(s):  
Manika Sapru ◽  
Jessie Gu ◽  
Xiang Gu ◽  
David Smith ◽  
Chang-En Yu ◽  
...  

Genomics ◽  
1998 ◽  
Vol 49 (1) ◽  
pp. 129-132
Author(s):  
Jörg W. Bartsch ◽  
Hideyuki Mukai ◽  
Nobuaki Takahashi ◽  
Melanie Ronsiek ◽  
Sonja Fuchs ◽  
...  

1992 ◽  
Vol 18 (4) ◽  
pp. 371-379 ◽  
Author(s):  
Gursurinder P. Kaur ◽  
Augustinus Rinaldy ◽  
R. Stephen Lloyd ◽  
Raghbir S. Athwal

1997 ◽  
Vol 230 (2) ◽  
pp. 315-319 ◽  
Author(s):  
Noriyuki Suzuki ◽  
Minoru Sugawara ◽  
Masanobu Sugimoto ◽  
Mitsuo Oshimura ◽  
Yasuhiro Furuichi

Blood ◽  
1988 ◽  
Vol 71 (6) ◽  
pp. 1713-1719 ◽  
Author(s):  
WM Mars ◽  
P van Tuinen ◽  
HA Drabkin ◽  
JW White ◽  
GF Saunders

Abstract A myeloid-related sequence (mrs) has previously been identified that is highly expressed in selected subpopulations of myeloid leukocytes. Nucleotide sequence analysis indicates that mrs encodes what is apparently a unique 93-amino acid protein that includes an 18-amino acid leader sequence. Hybridization of an mrs cDNA probe to a Southern blot made from somatic cell hybrid DNAs shows 100% concordance with human chromosome 8, thus indicating that mrs localizes to this chromosome. In situ hybridization to metaphase chromosomes further sublocalizes mrs to bands 8q21.1–23 as 58% of the grains displayed on chromosome 8 were clustered in this region. This area encompasses the translocation breakpoint 8q22, which is rearranged in an estimated 18% of patients diagnosed with the M2 subclassification of acute nonlymphocytic leukemia (M2-ANLL). When Southern blot hybridization was performed by using somatic cell hybrid DNAs harboring either a single 8q- or a single 21q+ chromosome from two different patients with M2- ANLL, a signal was only detected in the hybrid containing the 8q- chromosome.


1993 ◽  
Vol 64 (3-4) ◽  
pp. 133-146 ◽  
Author(s):  
Dennis Drayna ◽  
Robin J. Leach ◽  
Stephen Wood

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