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Journal articles on the topic 'Lenok'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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1

Si, Shengjuan, Ying Wang, Gefeng Xu, Shiyong Yang, Zhenbo Mou, and Zhaobin Song. "Complete mitochondrial genomes of two lenoks,Brachymystax lenokandBrachymystax lenok tsinlingensis." Mitochondrial DNA 23, no. 5 (2012): 338–40. http://dx.doi.org/10.3109/19401736.2012.690749.

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2

Liu, Yang, Jiashou Liu, Shaowen Ye, et al. "Global metabolic responses of the lenok (Brachymystax lenok) to thermal stress." Comparative Biochemistry and Physiology Part D: Genomics and Proteomics 29 (March 2019): 308–19. http://dx.doi.org/10.1016/j.cbd.2019.01.006.

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3

Esteve, M., and D. A. McLennan. "Spawning behavior of lenok, Brachymystax lenok (Salmoniformes) from the Uur River, Northern Mongolia." Journal of Ichthyology 48, no. 11 (2008): 1031–36. http://dx.doi.org/10.1134/s0032945208110040.

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4

Liu, Yang, Hongbai Liu, Wenhua Wu, Jiasheng Yin, Zhenbo Mou, and Fuhua Hao. "Effects of stocking density on growth performance and metabolism of juvenile Lenok (Brachymystax lenok)." Aquaculture 504 (April 2019): 107–13. http://dx.doi.org/10.1016/j.aquaculture.2019.01.058.

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5

Liu, Yang, Zhongjie Li, Tanglin Zhang, Jing Yuan, Zhenbo Mou, and Jiashou Liu. "Growth and energy budget of juvenile lenok Brachymystax lenok in relation to ration level." Chinese Journal of Oceanology and Limnology 33, no. 2 (2014): 347–55. http://dx.doi.org/10.1007/s00343-015-3349-x.

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6

Xia, Yingzhe1. "DNA sequence variation in the mitochondrial control region of lenok (Brachymystax lenok) populations in China." Biodiversity Science 14, no. 1 (2006): 48. http://dx.doi.org/10.1360/biodiv.050189.

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7

Liu, Y., X. Li, G. F. Xu, et al. "Effect of photoperiod manipulation on the growth performance of juvenile lenok, Brachymystax lenok (Pallas, 1773)." Journal of Applied Ichthyology 31, no. 1 (2014): 120–24. http://dx.doi.org/10.1111/jai.12632.

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8

SHI, Deliang, Qiwei WEI, Qingliang SUN, Luoxin LI, and Hao DU. "Early ontogenesis of Brachymystax lenok tsinlingensis." Journal of Fishery Sciences of China 19, no. 4 (2013): 557–67. http://dx.doi.org/10.3724/sp.j.1118.2012.00557.

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9

LIU, Yang, Hongbai LIU, Gefeng XU, Zhenbo MOU, and Jiasheng YIN. "Effects of water temperature on feeding and growth of the lenok Brachymystax lenok (Pallas) with different sizes." Journal of Fishery Sciences of China 25, no. 2 (2018): 286. http://dx.doi.org/10.3724/sp.j.1118.2018.17178.

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10

Balakirev, Evgeniy S., Nikolai S. Romanov, Pavel B. Mikheev, and Francisco J. Ayala. "Complete mitochondrial genome of Siberian taimen,Hucho taimennot introgressed by the lenok subspecies,Brachymystax lenokandB. lenok tsinlingensis." Mitochondrial DNA 27, no. 2 (2014): 815–16. http://dx.doi.org/10.3109/19401736.2014.919455.

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11

Matveev, A. N., V. P. Samusenok, A. L. Yuriev, A. I. Vokin, I. V. Samusenok, and S. S. Alekseyev. "Biology of Fishes of Lake Frolikha (Northern Baikal Region, East Siberia)." Bulletin of Irkutsk State University. Series Biology. Ecology 32 (2020): 50–82. http://dx.doi.org/10.26516/2073-3372.2020.32.50.

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The fish fauna of Lake Frolikha comprises 12 species confirmed by our recent studies: roach Rutilus rutilus (L.), minnow Phoxinus phonixus (L.), stone loach Barbatula toni (Dyb.), spine loach Cobitis melanoleuca Nichols, pike Esox lucius L. lenok Brachymystax lenok (Pallas), Arctic charr Salvelinus alpinus (L.), Baikal black grayling Thymallus baicalensis (Dyb.), burbot Lota lota (L.), sand sculpin Leocottus kesslerii (Dyb.), stone sculpin Paracottus knerii (Dyb.) and perch Perca fluviatilis L. Biological peculiarities of these fishes are determined by unique geographical position and limnic characteristics of Lake Frolikha. Being a typical glacial lake it is located at rather low altitude a.s.l. and is adjacent to the unparalleled ecosystem of Lake Baikal. An underdeveloped shallow coastal zone with sparse aquatic vegetation, which is characteristic of glacial lakes, determines some biological traits of Lake Frolikha cyprinids. As compared with other mountain lakes of Baikal Rift Zone (BRZ), roach and minnow have lower rates of linear and weight growth as well as unusual population sex ratios. Male to female ratio in roach is 2:1 and in minnow it is 1:1 whereas in other lakes it reaches 1:4 and 1:10 respectively. The presence of native Baikal species in Lake Frolikha provided abundant food for piscivores: sand sculpins are the dominant food item of lenok, Arctic charr and perch. Lenok and perch demonstrate prominent linear and weight growth rate in the lake. In other lakes of BRZ with less abundant prey fish species Arctic charr typically diverge into several trophic forms, but in Lake Frolikha they established a monomorphic mostly piscivorous population. Charr from Lake Frolikha are relatively small and short-lived representatives of the large form of Transbaikalian charr. Their unique feature is river spawning, which is not observed in any other charr population within BRZ. Due to special protection regime of the territory, which minimizes catch losses, several fish species maintain natural unaffected structure of their populations evidenced by the abundance of old fish. The population of lenok is represented by 19 age groups, the population of roach – by 15 groups and that of burbot – by 12 groups. Alternatively, populations of small-sized prey species such as minnow and sand sculpin, which are heavily influenced by numerous predators include fewer age groups than in other mountain lakes of BRZ.

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12

张, 立坤. "Observation of Embryonic Development of Brachymystax lenok." Open Journal of Fisheries Research 04, no. 03 (2017): 99–106. http://dx.doi.org/10.12677/ojfr.2017.43016.

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13

JIA, Z. Y., Y. Y. ZHANG, L. Y. SHI, Q. L. BAI, S. B. JIN, and Z. B. MOU. "Amplification of rainbow trout microsatellites inBrachymystax lenok." Molecular Ecology Resources 8, no. 6 (2008): 1520–21. http://dx.doi.org/10.1111/j.1755-0998.2008.02310.x.

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14

Gorlacheva, E. P. "FOOD LENOK BRACHYMYSTAX LENOK AND THE BAIKAL GRAYLING THYMALLUS BAICALENSIS MIDDLE REACHES OF THE RIVER CHIKOY (ZABAYKALSKY KRAI)." EurasianUnionScientists 1, no. 11(56) (2018): 12–16. http://dx.doi.org/10.31618/esu.2413-9335.2018.1.56.12-16.

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In 2017, we studied the composition of the bolus Lenka and chorusbridge reaches of the river Chikoy In the stomach, Lenka, grayling and discovered the pupa and imago of amphibiotic insects. The basis of the diet by mass of semimalignant and rucinski. Change of food components in different seasons of observations is established. The composition of the food lenok and grayling is the difference in the different watercourses. All this contributes to the divergence of fish in food niches and more complete use of food resources.

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15

Choi, E. J., D. H. Jin, and Y. C. Sohn. "Gonadotropins in the Manchurian trout, Brachymystax lenok tsinlingensis." Fish Physiology and Biochemistry 28, no. 1-4 (2003): 89–90. http://dx.doi.org/10.1023/b:fish.0000030483.11026.e5.

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16

Lee, Sang-Min, Kyoung-Duck Kim, Huem Gi Park, Chang Hwa Kim, and Kwan Eui Hong. "Protein requirement of juvenile Manchurian trout Brachymystax lenok." Fisheries Science 67, no. 1 (2001): 46–51. http://dx.doi.org/10.1046/j.1444-2906.2001.00197.x.

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17

Assylbekova, S., N. Badryzlova, and L. Kushnikova. "Analysis of the rates of development and growth of Brachymystax lenok Savinovi during artificial reproduction by the industrial method." Rybovodstvo i rybnoe hozjajstvo (Fish Breeding and Fisheries), no. 7 (July 1, 2020): 40–49. http://dx.doi.org/10.33920/sel-09-2007-04.

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The article presents the results of the first research on artificial reproduction in industrial conditions of the endemic, narrow-areal subspecies of Brachymystax lenok Savinovi, which lives in lake Markakol, East Kazakhstan region. The indicators of the heat sum characteristic for each stage of development, the rate of development and growth of the Markakolsky lenok from the moment of pre-breeding to late juveniles are described. To develop technological approaches for artificial fish reproduction, one of the most important points is to determine the optimal conditions for each stage and assess the risks (loss of fish products). At the stage of insemination and transportation of eggs to the place of incubation, the loss was 50 %. The largest losses of fish products were registered during the incubation stage. The most painlessly passed the period of holding and lifting on the float, where the loss was only 3 %. When growing pre-larvae and larvae in the pool, the daily waste did not exceed 1 %. Small-sized animals that were unable to adapt to artificial feeds fell into the waste. Losses during this period amounted to 15 % of the previous stage. In General, the yield of juveniles from the moment of fertilization to the end of the experiment was 16 %. The crucial factor in the development and growth of Lenok Markakolosky is the temperature regime. For the period of embryonic development, the most favorable water temperature is 7–8 °C. From the moment of hatching, the water temperature must be increased to 10–12 °C, and the optimal temperature for the cage growing of fingerlings varies from 12 to 14 °C.

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18

Zhengang, Wang, Bian Xinyu, Wang Maolin, et al. "Anesthetic effect of MS-222 on Brachymystax lenok Pallas." Advance in Agriculture Science 1, no. 1 (2019): 15–23. http://dx.doi.org/10.35534/aas.0101002.

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19

XUE, Chao, Qiwei WEI, Qingliang SUN, Jinming WU, and Luoxin LI. "Age and growth of Brachymystax lenok tsinlingensis." Journal of Fishery Sciences of China 20, no. 4 (2013): 743–49. http://dx.doi.org/10.3724/sp.j.1118.2013.00743.

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20

Xu, Gefeng, Feng Wang, Yang Liu, Yongfa Li, and Zhenbo Mou. "Threatened fishes of the world: Brachymystax lenok (Pallas 1773)." Environmental Biology of Fishes 85, no. 4 (2009): 299–300. http://dx.doi.org/10.1007/s10641-009-9501-8.

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21

Olson, Kirk W., Olaf P. Jensen, and Thomas R. Hrabik. "Feeding ecology and prey resource partitioning of lenok (Brachymystax lenok) and Baikal grayling (Thymallus arcticus baicalensis) in the Eg and Uur rivers, Mongolia." Ecology of Freshwater Fish 25, no. 4 (2015): 565–76. http://dx.doi.org/10.1111/eff.12234.

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22

Froufe, Elsa, Sergey Alekseyev, Paulo Alexandrino, and Steven Weiss. "The evolutionary history of sharp- and blunt-snouted lenok (Brachymystax lenok (Pallas, 1773)) and its implications for the paleo-hydrological history of Siberia." BMC Evolutionary Biology 8, no. 1 (2008): 40. http://dx.doi.org/10.1186/1471-2148-8-40.

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23

Ц, Өнөржаргал, Ганзориг Б, Жансагсодном М та Мэндсайхан Б. "ЭГ-СЭЛЭНГЭ МӨРНИЙ ЗЭВЭГ Brachymystax lenok, (Pallas,1773) ЗАГАСНЫ СУДАЛГААНЫ ДҮНГЭЭС". Mongolian Journal of Agricultural Sciences 20, № 01 (2017): 86–90. http://dx.doi.org/10.5564/mjas.v20i01.781.

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Улс орон хөгжихийн хирээр эрчим хүчний хэрэглээ ихэсч усны барилга байгууламжуудыг барих ажил эрчимтэй явагдаж байгаагаас шалтгаалан тэдгээр нь загасны нүүдэл, шилжилт хөдөлгөөн, идэш тэжээл, популяцийн төлөв байдалд хэрхэн нөлөөлөхийг судлах зорилгоор Эг-Сэлэнгэ мөрний загасны судалгааг 2014-2015 онд явуулсан. Эгийн голоос судалгаанд 2+-8+ насны 206-500 (326±77.9) мм урттай, 88-1321 (582±436.4) гр жинтэй, Сэлэнгэ мөрнөөс 2+-9+ насны 205-563 (378±73.1) мм урттай, 83-1768 (599±381.2) гр жинтэй зэвэг загас хамрагдсан бөгөөд 2+-5+ насны өсвөр насны загас 73.3%-79.1%-ийг эзэлж байна. Түүний идэш тэжээлийн бүрэлдэхүүнд сээрнуруугүйтэн амьтад хуурай массын 97%-ийг эзэлж, загас 1.9-2.3%-ийг эзэлж байна. Зэвэг загасны шилжилт хөдөлгөөнийн тогтоох зорилгоор анх удаа тусгай зориулалтын дохиолол дамжуулагчийг мэс заслын аргаар хэвлийд суулган тракин хийн 2 км шилжилт хөдөлгөөн хийж байгааг тогтоолоо.

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24

XU, Gefeng, Yang LIU, Zhenbo MOU, and Yongfa LI. "Ontogeny of immune organs during early developmental stages of Brachymystax lenok." Journal of Fishery Sciences of China 19, no. 4 (2013): 568–76. http://dx.doi.org/10.3724/sp.j.1118.2012.00568.

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25

Zhao, Yahui, and Chunguang Zhang. "Threatened fishes of the world: Brachymystax lenok tsinlingensis Li, 1966 (Salmonidae)." Environmental Biology of Fishes 86, no. 1 (2008): 11–12. http://dx.doi.org/10.1007/s10641-008-9337-7.

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26

Lee, Seungki, and Goro Yoshizaki. "Successful cryopreservation of spermatogonia in critically endangered Manchurian trout (Brachymystax lenok)." Cryobiology 72, no. 2 (2016): 165–68. http://dx.doi.org/10.1016/j.cryobiol.2016.01.004.

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27

Liu, Yang, Zhenbo Mou, Gefeng Xu, Yongfa Li, and Changan Wang. "The effect of light intensity on the growth ofBrachymystax lenok(Pallas, 1773)." Aquaculture Research 43, no. 12 (2011): 1838–44. http://dx.doi.org/10.1111/j.1365-2109.2011.02993.x.

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28

Di, Wang, Li Shao-Wu, Xu Ge-Feng, Liu Yang, Mou Zhen-Bo, and Lu Tong-Yan. "Assessing genetic diversity in three wild Brachymystax lenok populations using AFLP markers." Chinese Journal of Agricultural Biotechnology 6, no. 3 (2009): 241–47. http://dx.doi.org/10.1017/s1479236209990106.

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AbstractThe genetic diversities of 72 individuals from three wild Lenok populations of Mudanjiang River (MD), Yalujiang River (YL) and Wusulijiang River (WSL) in the northeast of China were analysed using amplified fragment length polymorphism (AFLP) markers. The results showed that 541 polymorphic loci out of 559 were amplified by 12 primer pairs and the percentage of polymorphic loci was 96.78%. Shannon indices for the MD, YL and WSL populations were 0.3988±0.2913, 0.3254±0.3037, 0.2125±0.2862, respectively, and Nei's gene diversity indices were 0.2737±0.2062, 0.2229±0.2129, 0.1446±0.1985, respectively. The average total genetic diversity (Ht) was 0.3512±0.0.0208 and the average genetic diversity within populations (Hs) was 0.2137±0.0152. Among the three populations, the average genetic distance (Dst) was 0.1375 and the gene differentiation coefficient (Gst) was 0.3914. The genetic diversity was 60.85% within populations and 39.15% among populations. The gene flow index (Nm) was 0.7776. The analysis of molecular variance (AMOVA) indicated that the average fixation index (Fst) was 0.55336. The variance was 55.16% within populations and 44.84% among populations. The highest polymorphism ratio was in the MD group and the lowest in the WSL group.

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29

Nakano, Shigeru. "Diet differentiation in polymorphicBrachymystax lenok in streams of southern primor′e, Russia." Ichthyological Research 46, no. 1 (1999): 100–102. http://dx.doi.org/10.1007/bf02674953.

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30

LIU, QIAO, YANG LI, HONGWEI LIANG, and XIAOLIN LIU. "Isolation and characterization of fourteen novel microsatellite loci from Brachymystax lenok tsinlingensi." Journal of Genetics 94, S1 (2014): 35–37. http://dx.doi.org/10.1007/s12041-014-0359-y.

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31

Xu, Gefeng, Tianqing Huang, Wei Gu, et al. "Characterization, expression, and functional analysis of the hepcidin gene from Brachymystax lenok." Developmental & Comparative Immunology 89 (December 2018): 131–40. http://dx.doi.org/10.1016/j.dci.2018.08.013.

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32

Ko, Myeong-Hun, Kwang-Seek Choi, and Mee-Sook Han. "Distribution status, habitat characteristics and extinction threat evaluation of the endangered species, Brachymystax lenok tsinlingensis (Pisces: Salmonidae)." Korean Journal of Ichthyology 33, no. 2 (2021): 74–83. http://dx.doi.org/10.35399/isk.33.2.4.

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33

Shao, J., W. Luo, Q. Wei, et al. "Assignment of parentage by microsatellite analysis in the endangered Brachymystax lenok tsinlingensis (Salmonidae)." Aquatic Biology 26 (June 19, 2017): 69–73. http://dx.doi.org/10.3354/ab00675.

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34

XU, Gefeng, Yang LIU, Yongfa LI, and Zhenbo MOU. "Organogenesis of the digestive system in Brachymystax lenok during early development." Journal of Fishery Sciences of China 20, no. 4 (2013): 733–42. http://dx.doi.org/10.3724/sp.j.1118.2013.00733.

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35

高, 晓田. "The Growth Characters of F₂ Brachymystax lenok Culturing in Ponds." Open Journal of Fisheries Research 04, no. 02 (2017): 58–64. http://dx.doi.org/10.12677/ojfr.2017.42010.

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36

Li, Ping, Feng Wang, Sien Wen, Hongbao Shen, and Xiaoyan Du. "Genetic diversity and population structure of Brachymystax lenok tsinlingensis using mitochondrial DNA sequences." Mitochondrial DNA Part B 2, no. 2 (2017): 408–10. http://dx.doi.org/10.1080/23802359.2017.1347897.

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37

Zhang, Hui, Zhenbo Mu, LiangMei Xu, Gefeng Xu, Min Liu, and Anshan Shan. "Dietary Lipid Level Induced Antioxidant Response in Manchurian Trout, Brachymystax lenok (Pallas) Larvae." Lipids 44, no. 7 (2009): 643–54. http://dx.doi.org/10.1007/s11745-009-3313-7.

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38

XU, Ge-Feng, Zhen-Bo MU, Shu-Qun XUE, et al. "ANALYSIS ON GENETIC POLYMORPHISM OF CHROMOSOME OF BRACHYMYSTAX LENOK IN DIFFERENT VALLEYS." Acta Hydrobiologica Sinica 33, no. 5 (2010): 975–79. http://dx.doi.org/10.3724/sp.j.1035.2009.50975.

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39

Guo, Wei, Jian Shao, Ping Li, Jinming Wu, and Qiwei Wei. "Morphology and ultrastructure of Brachymystax lenok tsinlingensis spermatozoa by scanning and transmission electron microscopy." Tissue and Cell 48, no. 4 (2016): 321–27. http://dx.doi.org/10.1016/j.tice.2016.05.009.

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40

Hartman, Kyle J., and Olaf P. Jensen. "Anticipating climate change impacts on Mongolian salmonids: bioenergetics models for lenok and Baikal grayling." Ecology of Freshwater Fish 26, no. 3 (2016): 383–96. http://dx.doi.org/10.1111/eff.12282.

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41

CHOI, Eunju, Hyeyeon KO, Jihye SHIN, Mi-Ae KIM, and Young Chang SOHN. "Expression of gonadotropin genes in Manchurian trout Brachymystax lenok and production of recombinant gonadotropins." Fisheries Science 71, no. 6 (2005): 1193–200. http://dx.doi.org/10.1111/j.1444-2906.2005.01083.x.

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42

Yu, Jeong-Nam, and Myounghai Kwak. "The complete mitochondrial genome of Brachymystax lenok tsinlingensis (Salmoninae, Salmonidae) and its intraspecific variation." Gene 573, no. 2 (2015): 246–53. http://dx.doi.org/10.1016/j.gene.2015.07.049.

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43

Li, Ping, Qigen Liu, Jiale Li, Feng Wang, Sien Wen, and Ning Li. "Transcriptomic responses to heat stress in gill and liver of endangered Brachymystax lenok tsinlingensis." Comparative Biochemistry and Physiology Part D: Genomics and Proteomics 38 (June 2021): 100791. http://dx.doi.org/10.1016/j.cbd.2021.100791.

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44

Romeo, Azzurra Anna, Anna Chierichini, Diana Giannarelli, et al. "Standard Versus High Dose Lenograstim in Adults with Hematological Malignancies for Peripheral Blood Progenitor Cell Mobilization: Results of a Retrospective Study on Behalf of Rome Transplant Network." Blood 112, no. 11 (2008): 2302. http://dx.doi.org/10.1182/blood.v112.11.2302.2302.

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Abstract PURPOSE: The aim of this retrospective study was to compare 5 vs 10 mcg/kg/day of lenograstim (Leno) (Myelostim 34®) in collecting target dose of CD34+ peripheral blood progenitor cells (PBPC) in adults candidate to autologous transplant. Univariate and multivariate analysis were carried out in order to identify factors predicting for satisfactory procedures. Material and Methods: From 01/’04 to 06/’08, 166 consecutive patients from 2 Institutions participating to the Rome Transplant Network with acute leukemias in complete remission (AL, #28), lymphomas (#77) and multiple myeloma (MM, #61) underwent 182 CD34+ PBPC mobilization procedures with Leno following standardized regimens. Only the 1st procedure for each patient was considered for the analysis. The target dose of CD34+ cells was ≥ 2 x106/kg for AL, ≥ 4 for lymphomas and ≥ 8 for MM with Leno starting at day +19, +1 and +5 from the end of chemotherapy, respectively. Eighty-seven patients received 5 mcg/kg Leno subcutaneously once a day (Leno5 cohort), while 79 patients were given Leno twice a day for a total dose of 10 mcg/kg (Leno10 cohort). Quantitative variables were compared by using analysis of variance (ANOVA); for qualitative parameters we used the chi-square test. A multivariate logistic model was used to analyze associations between some baseline characteristics and effectiveness to reach the required CD34+ cell target dose. Linear analysis was used to determine the relative significance of the same characteristics as predictive variables for stimulation length. Enter and remove limits were p=0.10 and 0.15, respectively. The SPSS (13.0) statistical program was used for analysis. Results: Age, sex, diagnosis and relative target dose, previous therapy including fludarabine, radiotherapy, number of previous chemotherapy regimens were not significantly different between the 2 cohorts. No statistically significant difference was observed in terms of number of apheresis performed, amount of blood processed, total number of CD34+ PBPC x103/mL mobilized and CD34+ cells x106/kg collected between the 2 cohorts. Reaching of the target dose and stimulation length are reported in table by Leno dose administered. # reaching the target Mean days ±SD Diagnosis CD34 + cell target x106/kg Leno5 Leno10 p Leno5 Leno10 p AL ≥ 2 14/19 (74%) 5/9 (56%) ns 11.2 ±6.4 6.2 ±3.1 0.035 Lymphomas ≥ 4 25/37 (68%) 33/40 (83%) ns 9.3 ±2.4 9.7 ±1.8 ns MM ≥ 8 21/31 (68%) 27/30 (90%) 0.034 8.7 ±2 7.6 ±1.8 0.033 Total 60/87 (69%) 65/79 (82%) 0.047 9.5 ±3.6 8.5 ±2.3 0.038 Forty-one patients did not reach the cell target. Of these, 16 underwent in any case PBPC transplant with the CD34+ cell dose collected. Of the remaining 25 patients, 9 were excluded from further attempts of PBPC mobilization, while 16 underwent 1 or 2 additional procedures and 10 of them were later transplanted. Overall, of 166 patients, 151 [Leno5 #76 (87%), Leno10 #75 (95%); p=ns] were able to be submitted to transplant. No Leno-related adverse event was observed in both the patient cohorts. In multivariate analysis, factors predicting for reaching the required CD34+ cell target dose were sex, with a negative impact of female sex (p=0.028), and Leno dose, with a positive impact of high dose, although exclusively restricted to MM patients (p=0.05). Finally, the multivariate analysis identified previous therapy not including fludarabine as the only factor significantly correlated with a shorter stimulation length (p=0.002). Conclusion: High dose Leno showed a higher capacity of harvesting only in MM patients for whom the CD34+ cell target was the highest to be collected. Leno dose did not impact on the CD34+ cell collection for AL and lymphoma patients as well as on the proportion of autologous transplants finally performed. As previously reported in healthy donors, in our study patient sex was an independent predictive factor for reaching the required CD34+ cell dose. Finally, fludarabine negatively influenced the length of Leno administration.

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Kaygorodova, Irina A., Elena V. Dzyuba, and Nikolay M. Pronin. "Leech-Like Parasites (Clitellata, Acanthobdellida) Infecting Native and Endemic Eastern Siberian Salmon Fishes." Scientific World Journal 2012 (2012): 1–8. http://dx.doi.org/10.1100/2012/652827.

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Salmonoid fish bdellosis is caused by leech-like ectoparasites in the monogenetic order Acanthobdellida. AlthoughAcanthobdellaspecies have been known to infect several threatened species in Eurasia, little is known about their ecology and epidemiology. In this paper, we report on the mass affection (up to 70.7%) of fish in lower course of the Chechuj River, a right tributary of the Lena and provide information on findingAcanthobdella peledinaon two of six salmonoid fish species inhabiting there: lenok and grayling. New and more specific data on morphological peculiarities and feeding strategy were obtained. The ratio of body length to width in studied acanthobdellid collection is significantly less than one provided for theA. livanowiand the restA. peledinafrom other water systems of Eurasia. Biology and lifestyle of the parasite population are revealed for the first time.

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Li, Zheng, Songyan Zhang, Jiuxiang Gao, et al. "Structural and functional characterization of CATH_BRALE, the defense molecule in the ancient salmonoid, Brachymystax lenok." Fish & Shellfish Immunology 34, no. 1 (2013): 1–7. http://dx.doi.org/10.1016/j.fsi.2012.07.004.

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Zhang, Y.-Y., Z.-Y. Jia, F. Ji, and Z.-B. Mou. "Effects of stocking density on survival, growth and size variation of juvenile Brachymystax lenok (Pallas, 1773)." Journal of Applied Ichthyology 24, no. 6 (2008): 685–89. http://dx.doi.org/10.1111/j.1439-0426.2008.01158.x.

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Wen, Sien, Ping Li, Feng Wang, Jiale Li, Haixia Liu, and Ning Li. "De novo assembly and microsatellite marker development of the transcriptome of the endangered Brachymystax lenok tsinlingensis." Genes & Genomics 42, no. 7 (2020): 727–34. http://dx.doi.org/10.1007/s13258-020-00939-3.

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Yoon, Ju-Duk, Jeong-Hui Kim, Hyun-Bin Jo, et al. "Seasonal habitat utilization and movement patterns of the threatened Brachymystax lenok tsinlingensis in a Korean river." Environmental Biology of Fishes 98, no. 1 (2014): 225–36. http://dx.doi.org/10.1007/s10641-014-0254-7.

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Liu, Haixia, Yang Li, Xiaolin Liu, et al. "Phylogeographic structure ofBrachymystax lenok tsinlingensis(Salmonidae) populations in the Qinling Mountains, Shaanxi, based on mtDNA control region." Mitochondrial DNA 26, no. 4 (2014): 532–37. http://dx.doi.org/10.3109/19401736.2013.865168.

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