ライフサイエンスコーパス: taurus

1 olated an ortholog of BRCA1 from cattle (Bos taurus).

2 d 100% of the variation at 172 loci in B. t. taurus.

3 and from chromaffin granule membranes of Bos taurus.

4 yomicroscopy structure of complex I from Bos taurus.

5 Moreover, parallel analysis of Bos taurus alpha-tubulin indicated that oryzalin did not int

6 he two major domestic extant cattle taxa, B. taurus and B. indicus.

7 ies, Q was introgressed into non-European B. taurus and Bos indicus breeds.

8 alysis for 10 bovine breeds derived from Bos taurus and Bos indicus revealed 98 polymorphisms (92 SNP

9 tle resulting from interbreeding between Bos taurus and Bos indicus subspecies.

10 ive, a panel of nine breeds representing Bos taurus and Bos indicus was assembled for sequencing and

11 region in Western China, and detected 21 B. taurus and four Bos indicus (zebu) mtDNA haplotypes.

12 ra americana (pronghorn), and the bovids Bos taurus and Ovis aries.

13 epared from mammalian mitochondria (from Bos taurus) and from the bacterium Paracoccus denitrificans,

14 pancreatic-type ribonucleases from cow (Bos taurus) and human (Homo sapiens) were produced in Escher

15 The method merges the use of bovine (Bos taurus) and poultry (Gallus gallus) specific primers tha

16 howing evidence for positive selection in B. taurus are enriched for neurobiology, growth, metabolism

17 ive recessive lethal in Jersey cattle on Bos taurus autosome 15.

18 WA analysis identified a putative SNP on Bos taurus autosomes (BTA) 2 associated with phenotype 1, an

19 differentiate between the specialized B. t. taurus beef and dairy breeds, despite an average polymor

20 dly in frequency in Northwestern European B. taurus between the 16(th) and 18(th) centuries.

21 oduced by embryo transfer from 77 Angus (Bos taurus), Brahman (Bos indicus), and F1 parents and grand

22 e development of American creole cattle (Bos taurus) breeds.

23 and a high resolution comparative map of Bos taurus (BTA) chromosome 18 were constructed, composed of

24 rectly anchored to cattle chromosome 19 [Bos taurus, (BTA) 19].

25 us, beta-B2 and gamma-B crystallins from Bos taurus, canavalin from Jack bean).

26 purifying selection acting on TLR10 in B. t. taurus cattle.

27 Penaeus californiensis, was compared to Bos taurus chymotrypsin, and its structure-function relation

28 a large portion of the membrane domain of B. taurus complex I that contains two core subunits and a c

29 The structure of Bos taurus complex I, determined to 5-A resolution by electr

30 ility of redox-coupled Na(+) transport by B. taurus complex I.

31 In this article we show that Hp of cow (Bos taurus) contains an alpha-chain, the structure of which

32 designated ovine (O), and the other from Bos taurus, designated bovine (B).

33 In male Onthophagus taurus, dsx transcripts were preferentially expressed in

34 sers using JBrowse and WebApollo for two Bos taurus genome assemblies, the reference genome assembly

35 rch for intact envelope genes within the Bos taurus genome identified 18 candidates belonging to five

36 y and characterize novel LILR within the Bos taurus genome, compare these phylogenetically with LILR

37 EPR studies on complex I from Bos taurus have established that five clusters (positions 1,

38 the relationship between complex I from Bos taurus heart mitochondria, a close model for the human e

39 A resolution structure of complex I from Bos taurus heart mitochondria, a close relative of the human

40 pe sharing between Bos taurus taurus and Bos taurus indicus breeds at every locus, and we were unable

41 taurus taurus oocytes with sperm from a Bos taurus indicus bull to facilitate parent-specific transc

42 an and/or mouse in day approximately 105 Bos taurus indicus x Bos taurus taurus F1 hybrid control and

43 Dung beetles Onthophagus taurus lay their eggs in brood balls within dung pats.

44 (Onchorynchus keta, Ilyanassa obsoleta, Bos taurus, Limulus polyphemus, Saccharyomyces cerevisiae).

45 Height in the Bos taurus lineage was reduced by a factor of 1.5 from the

46 hs as a distinct outgroup to the domestic B. taurus lineage, supporting the predominant Near Eastern

47 bedded in a protostellar core (L1527) in the Taurus molecular cloud, which is only 140 parsecs away f

48 ors in cold molecular clouds, such as in the Taurus Molecular Cloud.

49 the most widespread breeds with strictly Bos taurus morphological features in northern China.

50 grated southwest across a wide area from the Taurus Mountains down into the southern Levant, southeas

51 Samples from Bos taurus, Ovis aries, Sus scrofa domestica, Equus caballus

52 c organisms (Homo sapiens, Mus musculus, Bos taurus, Rattus norvegicus, Danio rerio, Gallus gallus an

53 meleagris), pork (Sus scrofa), and cow (Bos taurus) specific primers that amplify fragments (horse;

54 works revealed haplotype sharing between Bos taurus taurus and Bos taurus indicus breeds at every loc

55 y approximately 105 Bos taurus indicus x Bos taurus taurus F1 hybrid control and LOS fetuses using RN

56 re produced by in vitro fertilization of Bos taurus taurus oocytes with sperm from a Bos taurus indic

57 assay with 54,693 SNP loci developed for Bos taurus taurus to rapidly genotype 678 individuals repres

58 ay CGH panel included 90 animals from 11 Bos taurus, three Bos indicus, and three composite breeds fo

59 ence level to nuclear CPSF isolated from Bos taurus thymus.

60 son (Bison bison) and introduced cattle (Bos taurus) to temperature in tallgrass prairie within the G

61 l and archeological records indicate that B. taurus was introduced to Xinjiang during the second mill

62 group (P) of Piedmontese breed animals (Bos taurus) was included to serve as a comparative model for

63 interactions of sand tiger sharks Carcharias taurus, we observed group behavior that has historically

64 25 male Mongolian cattle samples revealed B. taurus Y chromosome haplotype and no B. indicus haplotyp