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498 results on '"Neovison"'

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401. The American mink: The triumph and tragedy of adaptation out of context

402. ‘Safe spaces’ may save the European mink

403. The gastrointestinal tract of farmed mink (Neovison vison) maintains a diverse mucosa-associated microbiota following a 3-day fasting period

404. Inbreeding affects fecundity of American mink (Neovison vison) in Danish farm mink

406. Helminths of mustelids (Mustelidae) in Lithuania

407. The complete mitochondrial genome sequence of Neovison vison (Carnivora: Mustelidae)

408. Nutrient-specific compensatory feeding in a mammalian carnivore, the mink, Neovison vison

409. Conception rates in farm mink (Neovison vison) in relation to first mating date, age and color variety

410. Comparative morphology of the lingual papillae and their connective tissue cores in the tongue of the American mink, Neovison vison

411. Identifying QTL and genetic correlations between fur quality traits in mink (Neovison vison)

412. High feeding intensity increases the severity of fatty liver in the American mink (Neovison vison) with potential ameliorating role for long-chain n-3 polyunsaturated fatty acids

413. Indirect genetic effects contribute substantially to heritable variation in aggression-related traits in group-housed mink (Neovison vison)

414. Trophic segregation of small carnivorans (Carnivora: Mustelidae and Mephitidae) from the southern cone of south America

415. Low protein provision during the first year of life, but not during foetal life, affects metabolic traits, organ mass development and growth in male mink (Neovison vison)

416. Effects of methylmercury on epigenetic markers in three model species: mink, chicken and yellow perch

417. Invasive crayfish reduce food limitation of alien American mink and increase their resilience to control

418. Age-dependent baseline values of faecal cortisol metabolites in the American mink (Neovison vison) under semi-natural housing conditions

419. Environmentally enriched male mink gain more copulations than stereotypic, barren-reared competitors

420. Development of vocalization and hearing in American mink (Neovison vison)

421. Genetic variability and structure of the water vole Arvicola amphibius across four metapopulations in northern Norway

423. Population viability analysis of American mink (Neovison vison) escaped from Danish mink farms

424. Typing of Pseudomonas aeruginosa from hemorrhagic pneumonia in mink (Neovison vison)

425. Postvaccination wounds associated predominantly withArcanobacterium phocaein mink (Neovison vison) at three mink farms

426. Metabolomic study of plasma from female mink (Neovison vison) with low and high residual feed intake during restrictive and ad libitum feeding

427. Hooded Grebe Podiceps gallardoi population decreased by eighty per cent in the last twenty-five years

428. New tick (Acari: Ixodidae) records from a mink, Neovison vison (Schreber), in Mississippi, U.S.A

429. Investigation of the presence of human or bovine respiratory syncytial virus in the lungs of mink (Neovison vison) with hemorrhagic pneumonia due to Pseudomonas aeruginosa

430. Responses of mink to auditory stimuli: prerequisites for applying the 'cognitive bias' approach

431. Genetic parameters and effect of selection for body weight in lines of mink (Neovion vison) on ad libitum and restricted feeding

432. Body condition and reproduction success in farmed mink males (Neovison vison)

433. Identifying QTL for fur quality traits in mink (Neovison vison)

434. Outbreaks of influenza A virus in farmed mink (Neovison vison) in Denmark: molecular characterization of the viruses

435. Prevalence of embedded shotgun pellets in protected and in legally hunted medium-sized carnivores from Denmark

436. Coat color mutations and the monoamine content in the brain of the farm-bred mink (Neovison vison)

437. Yttrium oxide as an inert marker for nutrient digestibility in ferrets (Mustela putoris furo), mink (Neovison vison) and cats (Felis catus)

438. Validation of the 13C-bicarbonate tracer technique for estimation of CO2 production and energy expenditure in mink (Neovison vison)

439. The regulation role of behavior in coat color formation in mink (Neovison vison)

440. Electrophysiological indices in mink (Neovison vison) during CO and CO2 euthanasia

441. Detection of SNP markers and practical applications in mink (Neovison vison)

442. Comparative digestibility of nutrients and energy in ferrets (Mustela putorius furo), mink (Neovison vison) and cats (Felis catus)

443. The effect of handling and training on measures of the affective state of farmed mink (Neovison vison)

444. Similarity of coat color aberrations in northern fur seal (Callorhinus ursinus), mink (Neovison vison), and sable (Martes zibellina)

445. Application of Ultrasonography for in vivo diagnosis of fatty liver disease in mink (Neovison vison)

446. Consequences of outbreaks of influenza A virus in farmed mink (Neovison vison) in Denmark in 2009 and 2010

447. Exclusion of candidate genes for coat colour phenotypes of the American mink (Neovison vison)

448. Characterization of a Tigger1 element from the genome of the American mink (Neovison vison)

449. Effective Control of Non-Native American Mink by Strategic Trapping in a River Catchment in Mainland Britain

450. Mercury and other heavy metals in free-ranging mink of the lower Great Lakes basin, Canada, 1998-2006

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