Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

107 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Milk as a source of deoxyribonucleic acid and as a substrate for the polymerase chain reaction.
Lipkin E, Shalom A, Khatib H, Soller M, Friedmann A. Lipkin E, et al. Among authors: shalom a. J Dairy Sci. 1993 Jul;76(7):2025-32. doi: 10.3168/jds.S0022-0302(93)77536-0. J Dairy Sci. 1993. PMID: 8345129
Somatic cells in milk were used as a source of DNA and as a substrate for the polymerase chain reaction. Successful DNA extraction required a minimum total of 17 x 10(6) cells in the milk sample. ...Thus, milk can often substitute for blood as a source …
Somatic cells in milk were used as a source of DNA and as a substrate for the polymerase chain reaction. Successful DNA extrac …
Dinucleotide repeat polymorphism at the bovine HUJ246, HUJII77, HUJ223, HUJVI74 and HUJI75 loci.
Shalom A, Mosig MO, Barendse W, Friedmann A, Soller M. Shalom A, et al. Anim Genet. 1994 Feb;25(1):56. Anim Genet. 1994. PMID: 8161029 No abstract available.
Quantitative trait locus mapping in dairy cattle by means of selective milk DNA pooling using dinucleotide microsatellite markers: analysis of milk protein percentage.
Lipkin E, Mosig MO, Darvasi A, Ezra E, Shalom A, Friedmann A, Soller M. Lipkin E, et al. Among authors: shalom a. Genetics. 1998 Jul;149(3):1557-67. Genetics. 1998. PMID: 9649542 Free PMC article.
A correction procedure was developed on the basis of an observed linear regression between shadow band intensity and allele TG repeat number. Using this procedure, a selective DNA pooling study with respect to milk protein percentage was implemented in Israel-Holste
A correction procedure was developed on the basis of an observed linear regression between shadow band intensity and allele TG repeat
Single-parent segregant pools for allocation of markers to a specified chromosomal region in outcrossing species.
Shalom A, Darvasi A, Barendse W, Cheng H, Soller M. Shalom A, et al. Anim Genet. 1996 Feb;27(1):9-17. doi: 10.1111/j.1365-2052.1996.tb01171.x. Anim Genet. 1996. PMID: 8624049
Bulked co-segregant analysis is a method of rapidly allocating unmapped genetic markers to a specific chromosomal region. Although originally developed for utilization in populations derived from crosses between fully inbred lines, it has been proposed that co-segre …
Bulked co-segregant analysis is a method of rapidly allocating unmapped genetic markers to a specific chromosomal region. Alth …
Dinucleotide repeat polymorphism at the bovine HUJ625 locus.
Shalom A, Soller M, Friedmann A. Shalom A, et al. Anim Genet. 1993 Aug;24(4):328. doi: 10.1111/j.1365-2052.1993.tb00326.x. Anim Genet. 1993. PMID: 8239083 No abstract available.
Dinucleotide repeat polymorphism at the bovine HUJ616 locus.
Shalom A, Soller M, Friedmann A. Shalom A, et al. Anim Genet. 1993 Aug;24(4):327. Anim Genet. 1993. PMID: 8239082 No abstract available.
Dinucleotide repeat polymorphism at the bovine HUJ614 locus.
Shalom A, Soller M, Friedmann A. Shalom A, et al. Anim Genet. 1993 Aug;24(4):327. Anim Genet. 1993. PMID: 8239081 No abstract available.
Dinucleotide repeat polymorphisms at the bovine HUJ673, HUJ121, HUJ174, HUJ225, HUJI13 and HUJI29 loci.
Shalom A, Mosig MO, Barendse W, Soller M, Friedmann A. Shalom A, et al. Anim Genet. 1995 Jun;26(3):202-3. doi: 10.1111/j.1365-2052.1995.tb03166.x. Anim Genet. 1995. PMID: 7793693 No abstract available.
Experimental designs for QTL fine mapping in rodents.
Shalom A, Darvasi A. Shalom A, et al. Methods Mol Biol. 2002;195:199-223. doi: 10.1385/1-59259-176-0:199. Methods Mol Biol. 2002. PMID: 12070882 No abstract available.
Cloning and mapping of CDC40, a Saccharomyces cerevisiae gene with a role in DNA repair.
Kassir Y, Kupiec M, Shalom A, Simchen G. Kassir Y, et al. Among authors: shalom a. Curr Genet. 1985;9(4):253-7. doi: 10.1007/BF00419952. Curr Genet. 1985. PMID: 3916722
It is concluded that the CDC40 gene product has a role in DNA repair, possibly holding together or protecting the DNA during the early stages of repair. The CDC40 gene was cloned on a 2.65 kb DNA fragment. A 2 mu plasmid carrying the gene was integrated and m …
It is concluded that the CDC40 gene product has a role in DNA repair, possibly holding together or protecting the DNA during the earl …
107 results
Jump to page
Feedback