Evolution of the Vertebrate Genome as Reflected in Paralogous Chromosomal Regions in Man and the House Mouse von Lundin, Lars G.

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Gene duplications in early metazoan evolution von Lundin, Lars- G.

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Lampetra fluviatilis Neurotrophin Homolog, Descendant of a Neurotrophin Ancestor, Discloses the Early Molecular Evolution of Neurotrophins in the Vertebrate Subphylum von Hallbook, Finn, Lundin, Lars-Gustav, Kullander, Klas

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The human Hox-bearing chromosome regions did arise by block or chromosome (or even genome) duplications von Larhammar, Dan, Lundin, Lars-Gustav, Hallböök, Finn

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Val92Met variant of the melanocyte stimulating hormone receptor gene von Xu, Xiaolin, Thörnwall, Madeleine, Lundin, Lars-Gustav, Chhajlani, Vijay

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Evolution of the neuropeptide Y receptor family: gene and chromosome duplications deduced from the cloning and mapping of the five receptor subtype genes in pig von Wraith, A, Törnsten, A, Chardon, P, Harbitz, I, Chowdhary, B P, Andersson, L, Lundin, L G, Larhammar, D

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Origin of the prolactin-releasing hormone (PRLH) receptors: Evidence of coevolution between PRLH and a redundant neuropeptide Y receptor during vertebrate evolution von Lagerström, Malin C., Fredriksson, Robert, Bjarnadóttir, Thóra K., Fridmanis, Davids, Holmquist, Tomas, Andersson, Jan, Yan, Yi-Lin, Raudsepp, Terje, Zoorob, Rima, Kukkonen, Jyrki P., Lundin, Lars-Gustav, Klovins, Janis, Chowdhary, Bhanu P., Postlethwait, John H., Schiöth, Helgi B.

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The G-Protein-Coupled Receptors in the Human Genome Form Five Main Families. Phylogenetic Analysis, Paralogon Groups, and Fingerprints von Fredriksson, Robert, Lagerström, Malin C., Lundin, Lars-Gustav, Schiöth, Helgi B.

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Interferon-regulated influenza virus resistance gene Mx is localized on mouse chromosome 16 von STAEHELI, P, PRAVTCHEVA, D, LUNDIN, L.-G, ACKLIN, M, RUDDLE, F, LINDENMANN, J, HALLER, O

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Genetic variation of peptidase and pyrophosphatase in the chicken von Lundin, L.G. (Biomedical Center, Uppsala, Sweden), Wilhelmson, M

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Teratogenicity of 2,3,7,8-tetrachlorodibenzofuran in BXD recombinant inbred strains von Hassoun, Ezdihar, d'Argy, Roland, Dencker, Lennart, Lundin, Lars-Gustav, Borwell, Pavel

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Lysosomal mutations increase susceptibility to anaesthetics von Ahmed, F., Lundin, L. -G., Shire, J. G. M.

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Nerve growth factor in three neurologically deficient mouse mutants von Ebendal, Ted, Lundin, Lars-G.

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Pigment Mutations in the Mouse Which Also Affect Lysosomal Functions Lead to Suppressed Natural Killer Cell Activity von ÖRN, A., HÅKANSSON, E. M., GIDLUND, M., RAMSTEDT, U., AXBERG, I., WIGZELL, H., LUNDIN, L.‐G.

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A gene (Bmn) controlling β-mannosidase activity in the mouse is located in the distal part of chromosome 3 von LUNDIN, L.-G

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Conserved Synteny Between the Ciona Genome and Human Paralogons Identifies Large Duplication Events in the Molecular Evolution of the Insulin-Relaxin Gene Family von Olinski, Robert Piotr, Lundin, Lars-Gustav, Hallböök, Finn

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Localization of the gene for the vitamin B12 binding protein, transcobalamin II, near the centromere on mouse chromosome 11, linked with the hemoglobin alpha-chain locus von Frater-Schroder, M, Prochazka, M, Haller, O, Arwert, F, Porck, H.J, Skow, L.C, Lundin, L.G, Hilkens, J, Hilgers, J

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Genetic Variation in Number of Pituitary PAS-Purple Cells in the House Mouse von HÅKANSSON, E. M., LUNDIN, L.-G.

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Inheritance of type-III hyperlipoproteinemia. Lipoprotein patterns in first-degree relatives von Vessby, Bengt, Hedstrand, H., Lundin, L-G., Olsson, U.

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Acid phosphatases from different organs and animal forms compared by starch-gel electrophoresis von Lundin, L.-G., Allison, A.C.

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