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Showing results 150 to 169 of 372 < previous   next >
PreviewIssue DateTitleAuthor(s)
1997Genetic and physical mapping of the Aspergillus nidulans pyruvate decarboxylase encoding gene, pdcA, allowing the anchoring of a small floating contig in the ordered cosmid libraryLockington, R.; Kelly, J.
2014Genetic bottlenecks in time and space: reconstructing invasions from contemporary and historical collectionsDormontt, E.; Gardner, M.; Breed, M.; Rodger, J.; Prentis, P.; Lowe, A.
2016Genetic consequences of forest fragmentation by agricultural land in an arboreal marsupialLancaster, M.; Cooper, S.; Carthew, S.
2015Genetic heritage of the balto-slavic speaking populations: a synthesis of autosomal, mitochondrial and Y-chromosomal dataKushniarevich, A.; Utevska, O.; Chuhryaeva, M.; Agdzhoyan, A.; Dibirova, K.; Uktveryte, I.; Möls, M.; Mulahasanovic, L.; Pshenichnov, A.; Frolova, S.; Shanko, A.; Metspalu, E.; Reidla, M.; Tambets, K.; Tamm, E.; Koshel, S.; Zaporozhchenko, V.; Atramentova, L.; Kučinskas, V.; Davydenko, O.; et al.
2016The genetic history of Ice Age EuropeFu, Q.; Posth, C.; Hajdinjak, M.; Petr, M.; Mallick, S.; Fernandes, D.; Furtwängler, A.; Haak, W.; Meyer, M.; Mittnik, A.; Nickel, B.; Peltzer, A.; Rohland, N.; Slon, V.; Talamo, S.; Lazaridis, I.; Lipson, M.; Mathieson, I.; Schiffels, S.; Skoglund, P.; et al.
2016The genetic history of Peruvian Quechua-Lamistas and Chankas: uniparental DNA Patterns among autochthonous Amazonian and Andean populationsSandoval, J.; Lacerda, D.; Acosta, O.; Jota, M.; Robles-Ruiz, P.; Salazar-Granara, A.; Vieira, P.; Paz-y-Miño, C.; Fujita, R.; Santos, F.; Jin, L.; Li, H.; Li, S.; Swamikrishnan, P.; Javed, A.; Parida, L.; Royyuru, A.; Mitchell, R.; Zalloua, P.; Adhikarla, S.; et al.
1996Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardationGedeon, A.; Glass, I.; Connor, J.; Mulley, J.
1997Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2Horwitz, M.; Benson, K.; Li, F.; Wolff, J.; Leppert, M.; Hobson, L.; Mangelsdorf, M.; Yu, S.; Hewett, D.; Richards, R.; Raskind, W.
1997The genome organisation of the Fanconi Anemia Group A (FAA) GeneIanzano, L.; d'Apolito, M.; Centra, M.; Savino, M.; Levran, O.; Auerbach, A.; Cleton-Jansen, A.; Doggett, N.; Pronk, J.; Tipping, A.; Gibson, R.; Mathew, C.; Whitmore, S.; Apostolou, S.; Callen, D.; Zelante, L.; Savoia, A.
2018Genome-wide gene-environment interaction in depression: a systematic evaluation of candidate genes: the childhood trauma working-group of PGC-MDDVan der Auwera, S.; Peyrot, W.; Milaneschi, Y.; Hertel, J.; Baune, B.; Breen, G.; Byrne, E.; Dunn, E.; Fisher, H.; Homuth, G.; Levinson, D.; Lewis, C.; Mills, N.; Mullins, N.; Nauck, M.; Pistis, G.; Preisig, M.; Rietschel, M.; Ripke, S.; Sullivan, P.; et al.
2018A genome-wide scan for signatures of selection in Azeri and Khuzestani buffalo breedsMokhber, M.; Moradi-Shahrbabak, M.; Sadeghi, M.; Moradi-Shahrbabak, H.; Stella, A.; Nicolzzi, E.; Rahmaninia, J.; Williams, J.
2011A Genome-Wide survey of imprinted genes in rice seeds reveals imprinting primarily occurs in the endospermLuo, M.; Taylor, J.; Spriggs, A.; Zhang, H.; Wu, X.; Russell, S.; Singh, M.; Koltunow, A.
2018The genomic history of southeastern EuropeMathieson, I.; Alpaslan-Roodenberg, S.; Posth, C.; Szécsényi-Nagy, A.; Rohland, N.; Mallick, S.; Olalde, I.; Broomandkhoshbacht, N.; Candilio, F.; Cheronet, O.; Fernandes, D.; Ferry, M.; Gamarra, B.; Fortes, G.; Haak, W.; Harney, E.; Jones, E.; Keating, D.; Krause-Kyora, B.; Kucukkalipci, I.; et al.
1997Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3Mitchison, H.; Munroe, P.; O'Rawe, A.; Taschner, P.; De Vos, N.; Kremmidiotis, G.; Lensink, I.; Munk, A.; D'Arigo, K.; Anderson, J.; Lerner, T.; Moyzis, R.; Callen, D.; Breuning, M.; Doggett, N.; Gardiner, R.; Mole, S.
1999Genomic structure and expression analysis of the spastic paraplegia gene, SPG7Settasatian, C.; Whitmore, S.; Crawford, J.; Bilton, R.; Cleton-Jansen, A.; Sutherland, G.; Callen, D.
2018A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiencyJansen, S.; Hoischen, A.; Coe, B.; Carvill, G.; van Esch, H.; Bosch, D.; Andersen, U.; Baker, C.; Bauters, M.; Bernier, R.; van Bon, B.; Claahsen-van der Grinten, H.; Gecz, J.; Gilissen, C.; Grillo, L.; Hackett, A.; Kleefstra, T.; Koolen, D.; Kvarnung, M.; Larsen, M.; et al.
1999Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromesMcDermott, M.; Aksentijevich, I.; Galon, J.; McDermott, E.; Ogunkolade, B.; Centola, M.; Mansfield, E.; Gadina, M.; Karenko, L.; Petterson, T.; McCarthy, J.; Frucht, D.; Aringer, M.; Torosyan, Y.; Teppo, A.; Wilson, M.; Karaarslan, H.; Wan, Y.; Todd, I.; Wood, G.; et al.
2016Getting a head in hard soils: convergent skull evolution and divergent allometric patterns explain shape variation in a highly diverse genus of pocket gophers (Thomomys)Marcy, A.; Hadly, E.; Sherratt, E.; Garland, K.; Weisbecker, V.
2017Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsyEwans, L.; Field, M.; Zhu, Y.; Turner, G.; Leffler, M.; Dinger, M.; Cowley, M.; Buckley, M.; Scheffer, I.; Jackson, M.; Roscioli, T.; Shoubridge, C.
2010Great expectations: using massively parallel sequencing to solve inherited disordersCorbett, M.; Gecz, J.