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10 results for “Hymenolepis”
Fig. 2 in Molecular confirmation of Hymenolepis hibernia in field mice (Apodemus sylvaticus) from St Kilda has potential to resolve a host-parasite relationship
Fig. 2. The Sanger sequence of 385 bp of mt-Cox-1 fragments of cyclophyllidean DNA generated from eggs recovered from mouse 9 and faeces X (6. H-HA25), aligned with 5 corresponding H. hibernia sequences published in the NCBI Genbank database. There are 12 intraspecific SNPs at positions 5, 60, 78, 84, 90, 156, 216, 219, 252, 262, 291 and 318. GeneBank submission ID: 2151861.
Fig. 1 in Molecular confirmation of Hymenolepis hibernia in field mice (Apodemus sylvaticus) from St Kilda has potential to resolve a host-parasite relationship
Fig. 1. Examples of cyclophyllidean tapeworms and eggs recovered from Apodemus sylvaticus viscera and faeces. A: Unarmed scolex of an intact tapeworm - mouse 5. B: Anoplocephalid tapeworm egg - mouse 8. C: Hymenolepidid egg cropped without changing dimensions from the same image as B, for comparison - mouse 8. D: Anoplocephalid tapeworm egg - mouse X (faeces from a cleat). E: Anoplocephalid onchosphere released after squashing an egg under a cover slip - mouse X (faeces from a cleat). F: Tapeworm from mouse 8 (scolex not intact). G: hymenolepidid tapeworm egg - mouse X (faeces from a cleat). H: Hexacanth onchosphere surrounded by an onchospheral membrane and inner zone of the embryophore, which has swollen, having been released from the egg shell by squashing under a cover slip - mouse 9. I: Hymenolepidid tapeworm egg - mouse 7. J: Hexacanth onchosphere surrounded by an intact onchospheral membrane and inner and outer zones of the embryophore, being released from a cracked egg shell by squashing under a cover slip - mouse 7. K: Hymenolepidid tapeworm egg - mouse 8. L: Hexacanth onchosphere surrounded by an onchospheral membrane and inner zone of the embryophore, which has swollen, having been released from the egg shell by squashing under a cover slip - mouse 8.
Fig. 3. Maximum Likelihood tree for the 35 haplotypes identified from 39 in Molecular confirmation of Hymenolepis hibernia in field mice (Apodemus sylvaticus) from St Kilda has potential to resolve a host-parasite relationship
Fig. 3. Maximum Likelihood tree for the 35 haplotypes identified from 39 mt-cox-1 sequences of Hymenolepis species. Of these, 19, 5, 2 and 8 haplotypes are identified in the Genbank database as H. diminuta, H. hibernia, H. microstoma and H. nana, respectively, and one haplotype (H-HA25) was identified here from the faeces of St Kilda mice 9 and X. Branches with bootstrap values (1000 replications) represented at the base of the nodes. The phylogeny is rooted with mt-cox-1 sequence of parasitic nematode H. contortus.
FIGURE 2 in Hymenolepis glabra (Anthemideae, Asteraceae), a new species from the Little Karoo (South Africa)
FIGURE 2. Known distribution of Hymenolepis glabra (stars), H. crithmifolia (circles) and H. indivisa (triangles).
FIGURE 1 in Hymenolepis glabra (Anthemideae, Asteraceae), a new species from the Little Karoo (South Africa)
FIGURE 1. General morphology of Hymenolepis glabra. (A) leaves 2- or 3-sect, sometimes entire towards the synflorescence. (B) Cypsela with pappus of scales and with prominent secretory cavities. (C) Synflorescence an open, doubly compound corymbs; note the terete ultimate leaf segments and glabrous stems and leaves. (D) Woody, much branched habit.
Figure 3 in Purification Of Adult Hymenolepis Diminuta (Cestoda) Mitochondrial Nadph Nad Transhydrogenase
Figure 3. Effects of non-immune and immune IgG on the activity of membrane-associated and purified Hymenolepis diminuta transhydrogenase. Preparations and treatments are indicated as follows: Broken line and closed circles, mitochondrial membranes plus non-immune IgG; solid line and open circles, purified enzyme plus non-immune IgG; broken line and closed squares, mitochondrial membranes plus immune IgG; and solid line open squares, plus immune IgG. The activity of untreated mitochondrial membranes and purified enzyme was 0.12 and 8.3 µmol/ min/mg, respectively. Incubations were performed as described in Materials and Methods.
Figure 1 in Purification Of Adult Hymenolepis Diminuta (Cestoda) Mitochondrial Nadph Nad Transhydrogenase
Figure 1. SDS-PAGE of the purification of Hymenolepis diminuta transhydrogenase. Lane designation and amount of protein used were as follows: lane A, mitochondrial membranes, 30 µg; lane B, NaCl-washed membranes, 30 µg; lane C, detergent extract, 25 µg; lane D, DEAE Sepharose I, 5 µg; lane E, DEAE Sepharose II, 5 µg; lane F, hydroxylapatite, 5 µg. Relative positions of protein markers are indicated at the left. Protein was visualized as described in Materials and Methods.
Figure 2 in Purification Of Adult Hymenolepis Diminuta (Cestoda) Mitochondrial Nadph Nad Transhydrogenase
Figure 2. Immunoblot of Hymenolepis diminuta transhydrogenase. Lane designation, amount of protein used, and treatment were as follows: lane A, mitochondrial membranes, 30 µg plus non-immune IgG; lane B, mitochondrial membranes, 30 µg plus immune IgG; lane C, purified enzyme, 5 µg plus non-immune protein, IgG; lane D, purified enzyme, 5 µg plus immune IgG. Relative positions of protein markers are indicated at the left. Immunoblots were performed as described in Materials and Methods.
FIGURE 1 in Valid publication of the name Anaphalis hymenolepis (Asteraceae)
FIGURE 1. Holotype of Anaphalis hymenolepis Y. Ling (PE barcode 00493318!).
Splenic B cells from Hymenolepis diminuta-infected mice ameliorate colitis independent of T cells and via cooperation with macrophages
GEO Series GSE61460. Mus musculus. 6 samples. Type: Expression profiling by array.
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