Results 21 to 30 of about 2,465,783 (307)

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   +3 more sources

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

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

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

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

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

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   +2 more sources

A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development

Molecular Genetics & Genomic Medicine, 2014
Primary vesicoureteric reflux (VUR), the retrograde flow of urine from the bladder toward the kidneys, results from a developmental anomaly of the vesicoureteric valve mechanism, and is often associated with other urinary tract anomalies.
J. M. Darlow, M. G. Dobson, R. Darlay, C. M. Molony, M. Hunziker, A. J. Green, H. J. Cordell, P. Puri, D. E. Barton   +8 more
doaj   +1 more source

Annotated genetic linkage maps of Pinus pinaster Ait. from a Central Spain population using microsatellite and gene based markers

BMC Genomics, 2012
Background Pinus pinaster Ait. is a major resin producing species in Spain. Genetic linkage mapping can facilitate marker-assisted selection (MAS) through the identification of Quantitative Trait Loci and selection of allelic variants of interest in ...
de Miguel Marina, de Maria Nuria, Guevara M, Diaz Luis, Sáez-Laguna Enrique, Sánchez-Gómez David, Chancerel Emilie, Aranda Ismael, Collada Carmen, Plomion Christophe, Cabezas José-Antonio, Cervera María-Teresa   +11 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