Results 21 to 30 of about 342,848 (311)

Resultants in genetic linkage analysis

Journal of Symbolic Computation, 2006
Statistical models for genetic linkage analysis of k-locus diseases are k-dimensional subvarieties of a (3^k-1)-dimensional probability simplex. We determine the algebraic invariants of these models with general characteristics for k=1, in particular we recover, and generalize, the Hardy-Weinberg curve.
Ingileif B. Hallgrímsdóttir, Bernd Sturmfels   +1 more
openaire   +2 more sources

Construction of Genetic Linkage Map of Plum (Prunus salicina L.) with ISSR and SRAP Markers

Guangdong nongye kexue, 2022
【Objective】Plum (Prunus salicina L.) is a tree species with great economic prospect in northeast China, and it has important social and economic values. Genetic linkage maps of plum were constructed by molecular markers to provide a theoretical basis for
Lili SUN, Lina PENG, Zheng LI, Ruining HOU, Yunhui MOU   +4 more
doaj   +1 more source

Genetic linkage analysis supports the presence of two susceptibility loci for alcoholism and heavy drinking on chromosome 1p22.1-11.2 and 1q21.3-24.2 [PDF]

, 2005
Background: In order to confirm a previous finding of linkage to alcoholism on chromosome 1 we have carried out a genetic linkage study.Methods: DNA from eighteen families, densely affected by alcoholism, was used to genotype a set of polymorphic ...
Devitgh, Audrey, Kest, Wendy, Kest Wendy, Devitgh, A, McQuillin Andrew, Cook Christopher CH, McQuillin, Andrew, Gurling Hugh MD, Curtis, David, Gurling, Hugh M.D., Cook, Christopher C.H., Devitgh Audrey, Gurling, HMD, Guerrini, Irene, Curtis, D, Curtis David, McQuillin, A, Guerrini, I, Cook, CCH, Guerrini Irene, Kest, W   +20 more
core   +1 more source

A SNP based linkage map of the turkey genome reveals multiple intrachromosomal rearrangements between the Turkey and Chicken genomes [PDF]

, 2010
Background The turkey (Meleagris gallopavo) is an important agricultural species that is the second largest contributor to the world's poultry meat production.
Bastiaansen John WM, Vereijken, A., Martien AM Groenen, Aslam Muhammad L, Groenen, M.A.M., John WM Bastiaansen, Bastiaansen, J.W.M., Hendrik-Jan Megens, Muhammad L Aslam, Richard PMA Crooijmans, Addie Vereijken, Vereijken Addie, Crooijmans, R.P.M.A., Groenen Martien AM, Crooijmans Richard PMA, Megens, H.J.W.C., Aslam, M.L., Megens Hendrik-Jan   +17 more
core   +1 more source

An extremely rare association of Dyggve-Melchior-Clausen syndrome with mania: Coincidence or comorbidity

Indian Journal of Psychological Medicine, 2015
Dyggve-Melchior-Clausen syndrome is a progressive spondylo-epi-metaphyseal dysplasia associated with mental retardation, characterized by a triad of skeletal deformities (short trunk dwarfism, scoliosis, microcephaly, and limb deformities), facial ...
Sujita Kumar Kar, Shwetank Bansal, Deepak Kumar   +2 more
doaj   +1 more source

Linkage to chromosome 11p12 in two Maltese families with a highly penetrant form of osteoporosis [PDF]

, 2007
Osteoporosis is a metabolic bone disease with a strong genetic component. Family-based linkage studies were performed by a number of investigators to try to identify loci that might contain genes responsible for an increased susceptibility to ...
Brincat, Mark P., Raymond Galea, Angela Xuereb Anastasi, Mark Brincat, Galea, Raymond P., Vidal, Christopher, Xuereb-Anastasi, Angela, Christopher Vidal   +7 more
core   +1 more source

Novel SSR markers from BAC-end sequences, DArT arrays and a comprehensive genetic map with 1,291 marker loci for chickpea (Cicer arietinum L.) [PDF]

, 2011
Chickpea (Cicer arietinum L.) is the third most important cool season food legume, cultivated in arid and semi-arid regions of the world. The goal of this study was to develop novel molecular markers such as microsatellite or simple sequence repeat (SSR)
Varghese, Nicy, Nayak Spurthi N., Polavarapu B Kavikishor, Upadhyaya, Hari D., Town, C D, Gudipati, Srivani, Bohra, Abhishek, Thirunavukkarasu, Nepolean, Nayak, S N, Kulwal, P L, Winter, P, Nayak, Spurthi N., Peter Winter, Varghese, N., Pawan L. Kulwal, Pooran M. Gaur, Upadhyaya Hari D., Penmetsa, R.V., Kilian, Andrzej, Kavikishor, P.B., Gudipati Srivani, Thudi, M, Thudi, M., Rajeev K Varshney, Bohra Abhishek, Varshney Rajeev K., Nicy Varghese, Varshney, R.K., R Varma Penmetsa, Shah, Trushar M., Bohra, A., Kahl Günter, KaviKishor Polavarapu B., Mahendar Thudi, Kilian Andrzej, Gaur, P M, Gaur, P., Abhishek Bohra, Nayak, S.N., Kilian, A, Cook, D.R., Trushar M Shah, Shah, T.M., Cook, D., Nepolean Thirunavukkarasu, Christopher D Town, Kahl, Günter, Hari D. Upadhyaya, Shah, T M, Cook, D R, Upadhyaya, H D, Hansson, Bengt, Town, Christopher D., Spurthi N. Nayak, Kulwal, P.L., Winter, P., Hansson, B., Günter Kahl, Polavarapu B. KaviKishor, Town Christopher D., Srivani Gudipati, Kahl, G., Spurthi N Nayak, Winter, Peter, Gaur, P.M., Cook, Douglas R., Cook Douglas R., Christopher D. Town, Pawan L Kulwal, Gaur, Pooran M., Trushar M. Shah, Thudi Mahendar, Varghese, N, Andrzej Kilian, Thudi, Mahendar, Varshney, Rajeev K., Winter Peter, Gaur Pooran M., Varshney, R K, Kilian, A., Upadhyaya, H.D., Thirunavukkarasu, N., Rajeev K. Varshney, KaviKishor, Polavarapu B., Kulwal, Pawan L., Varghese Nicy, Pooran M Gaur, Thirunavukkarasu Nepolean, Town, C.D., Bohra, A, R. Varma Penmetsa, Douglas R Cook, Penmetsa, R. Varma, Kulwal Pawan L., Penmetsa, R V, Penmetsa R. Varma, Douglas R. Cook, Kavi Kishor, P B, Gudipati, S, Thirunavukkarasu, N, Hari D Upadhyaya, Gudipati, S., Shah, T., Shah Trushar M., Kahl, G   +104 more
core   +1 more source

Quantitative trait loci influencing low density lipoprotein particle size in African Americans

Journal of Lipid Research, 2006
Genomic regions that influence LDL particle size in African Americans are not known. We performed family-based linkage analyses to identify genomic regions that influence LDL particle size and also exert pleiotropic effects on two closely related lipid ...
Iftikhar J. Kullo, Keyue Ding, Eric Boerwinkle, Stephen T. Turner, Mariza de Andrade   +4 more
doaj   +1 more source

Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14 [PDF]

, 2009
Childhood absence epilepsy (CAE) is an idiopathic generalised epilepsy (IGE) characterised by typical absence seizures manifested by transitory loss of awareness with 2.5–4 Hz spike-wave complexes on ictal EEG.
Sander, Thomas, Eeg-Olofsson, O, Everett, KV, Everett, Kate V., Friis, Mogens Laue, Dulac, Olivier, Siren, Auli, Dooley, Joseph M, Aschauer, H, Kjeldsen, MJ, Dulac, O, Wirrell, Elaine, Covanis, Athanasios, Brouwer, Oebele, Covanis, A, Sirén, A, Aicardi, Jean, Gardiner, RM, Durner, Martina, Robinson, R, Nabbout, Rima, Gardiner, R. Mark, McKeigue, Paul, Sander, T, Dooley, JM, Gardiner, R Mark, McKeigue, Paul; id_orcid, Chioza, BA, Aschauer, Harald, Everett, Kate V, Eeg-Olofsson, Orvar, Brouwer, O, Nabbout, R, McKeigue, P, Robinson, Robert, Chioza, Barry A., Dooley, Joseph M., Nashef, L, Feucht, Martha, Feucht, M, Guerrini, R, Aicardi, J, Durner, M, Nashef, Lina, Wirrell, E, Callenbach, P, Guerrini, Renzo, Callenbach, Petra, Chioza, Barry A, Friis, ML, Kjeldsen, Marianne Juel, Eeg-Olofsson, Orvar,   +51 more
core   +1 more source

New technologies for delineating and characterizing the lipid exome: prospects for understanding familial combined hyperlipidemia

Journal of Lipid Research, 2009
This review summarizes the progress made in cutting through the biological and genetic complexity of the Gordian knot that is familial combined hyperlipidemia. We particularly focus on how the application of new genomic technologies, especially massively
Stuart D. Horswell, Helen E. Ringham, Carol C. Shoulders   +2 more
doaj   +1 more source