Relevant bibliographies by topics / Gens candidats

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Gens candidats'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Gens candidats"

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Morin, Aurélie. "La participation politique au prisme de l’ethnicité : étude du discours des candidats issus de l’immigration maghrébine lors d’une échéance électorale en France." Notes de terrain 7, no. 1 (2007): 85–97. http://dx.doi.org/10.7202/016271ar.

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Résumé Lors des dernières élections françaises de 2004, la question de la place et du rôle des candidats d’origine maghrébine a été un enjeu controversé, relançant le débat sur le modèle universaliste français. Dans ce contexte, nous nous sommes interrogée sur l’importance accordée à l’ethnicité par les candidats d’origine maghrébine dans leur discours, à travers l’étude de leurs professions de foi et la réalisation d’entretiens. Trois types d’attitudes envers l’ethnicité ont ainsi été observés. Si la majorité des candidats ne mentionne aucun élément d’ordre ethnique, certains l’utilisent ponc
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Pelletier, Réjean. "Le personnel politique." Notes de recherche 25, no. 1 (2005): 83–102. http://dx.doi.org/10.7202/056072ar.

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Il est reconnu que, dans les grandes organisations à caractère bureaucratique, le pouvoir est détenu par une minorité. Il en est de même dans les régimes qui se définissent comme démocratiques où les représentants élus pour exercer le pouvoir politique ne constituent eux aussi qu'une minorité d'où est exclue d'une façon permanente la plus grande partie de la population. Bien plus, on a déjà montré qu'à chaque niveau politique — électeurs, adhérents, militants, cadres, députés, dirigeants nationaux — les caractéristiques sociales du groupe tendent à devenir moins « représentatives » de l'ensemb
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Zelenova, M. A., S. G. Vorsanova, and I. Y. Iourov. "Candidate processes for autism spectrum disorders revealed by copy number variation analysis." V.M. BEKHTEREV REVIEW OF PSYCHIATRY AND MEDICAL PSYCHOLOGY, no. 4-1 (December 9, 2019): 101–2. http://dx.doi.org/10.31363/2313-7053-2019-4-1-101-102.

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Despite the large number of candidate genes for mental disorders, molecular mechanisms of the majority remain unknown. To fill this gap, we have studied genomic networks-candidates (instead of genes) in a group of children with brain disorders. The identification of such processes seems to be more promising for developing therapeutic strategies in contrast to candidate gene identification.
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Chong, Veronica K., and John R. Stinchcombe. "Evaluating Population Genomic Candidate Genes Underlying Flowering Time in Arabidopsis thaliana Using T-DNA Insertion Lines." Journal of Heredity 110, no. 4 (2019): 445–54. http://dx.doi.org/10.1093/jhered/esz026.

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Abstract Population genomic scans have emerged as a powerful tool to detect regions of the genome that are potential targets of selection. Despite the success of genomic scans in identifying novel lists of loci potentially underlying adaptation, few studies proceed to validate the function of these candidate genes. In this study, we used transfer-DNA (T-DNA) insertion lines to evaluate the effects of 27 candidate genes on flowering time in North American accessions of Arabidopsis thaliana. We compared the flowering time of T-DNA insertion lines that knock out the function of a candidate gene o
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Thornblad, Tobias A., Kate S. Elliott, Jeremy Jowett, and Peter M. Visscher. "Prioritization of Positional Candidate Genes Using Multiple Web-Based Software Tools." Twin Research and Human Genetics 10, no. 6 (2007): 861–70. http://dx.doi.org/10.1375/twin.10.6.861.

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AbstractThe prioritization of genes within a candidate genomic region is an important step in the identification of causal gene variants affecting complex traits. Surprisingly, there have been very few reports of bioinformatics tools to perform such prioritization. The purpose of this article is to investigate the performance of 3 positional candidate gene software tools available, PosMed, GeneSniffer and SUSPECTS. The comparison was made for 40, 20 and 10 Mb regions in the human genome centred around known susceptibility genes for the common diseases breast cancer, Crohn's disease, age-relate
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Boultwood, Jacqueline, Carrie Fidler, Amanda J. Strickson, et al. "Narrowing and genomic annotation of the commonly deleted region of the 5q− syndrome." Blood 99, no. 12 (2002): 4638–41. http://dx.doi.org/10.1182/blood.v99.12.4638.

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The 5q− syndrome is the most distinct of the myelodysplastic syndromes, and the molecular basis for this disorder remains unknown. We describe the narrowing of the common deleted region (CDR) of the 5q− syndrome to the approximately 1.5-megabases interval at 5q32 flanked by D5S413 and theGLRA1 gene. The Ensembl gene prediction program has been used for the complete genomic annotation of the CDR. The CDR is gene rich and contains 24 known genes and 16 novel (predicted) genes. Of 40 genes in the CDR, 33 are expressed in CD34+ cells and, therefore, represent candidate genes since they are express
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Talwar, Puneet, Renu Gupta, Suman Kushwaha, et al. "Viral Induced Oxidative and Inflammatory Response in Alzheimer’s Disease Pathogenesis with Identification of Potential Drug Candidates: A Systematic Review using Systems Biology Approach." Current Neuropharmacology 17, no. 4 (2019): 352–65. http://dx.doi.org/10.2174/1570159x16666180419124508.

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Alzheimer’s disease (AD) is genetically complex with multifactorial etiology. Here, we aim to identify the potential viral pathogens leading to aberrant inflammatory and oxidative stress response in AD along with potential drug candidates using systems biology approach. We retrieved protein interactions of amyloid precursor protein (APP) and tau protein (MAPT) from NCBI and genes for oxidative stress from NetAge, for inflammation from NetAge and InnateDB databases. Genes implicated in aging were retrieved from GenAge database and two GEO expression datasets. These genes were individually used
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Díaz-Gay, Marcos, Sebastià Franch-Expósito, Coral Arnau-Collell, et al. "Integrated Analysis of Germline and Tumor DNA Identifies New Candidate Genes Involved in Familial Colorectal Cancer." Cancers 11, no. 3 (2019): 362. http://dx.doi.org/10.3390/cancers11030362.

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Colorectal cancer (CRC) shows aggregation in some families but no alterations in the known hereditary CRC genes. We aimed to identify new candidate genes which are potentially involved in germline predisposition to familial CRC. An integrated analysis of germline and tumor whole-exome sequencing data was performed in 18 unrelated CRC families. Deleterious single nucleotide variants (SNV), short insertions and deletions (indels), copy number variants (CNVs) and loss of heterozygosity (LOH) were assessed as candidates for first germline or second somatic hits. Candidate tumor suppressor genes we
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Blackwell, J. M., G. F. Black, C. S. Peacock, et al. "Immunogenetics of leishmanial and mycobacterial infections: the Belem Family Study." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 352, no. 1359 (1997): 1331–45. http://dx.doi.org/10.1098/rstb.1997.0118.

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In the 1970s and 1980s, analysis of recombinant inbred, congenic and recombinant haplotype mouse strains permitted us to effectively ‘scan’ the murine genome for genes controlling resistance and susceptibility to leishmanial infections. Five major regions of the genome were implicated in the control of infections caused by different Leishmania species which, because they show conserved synteny with regions of the human genome, immediately provides candidate gene regions for human disease susceptibility genes. A common intramacrophage niche for leishmanial and mycobacterial pathogens, and a sim
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Song, Long, Jing Qin Wu, Chong Mei Dong, and Robert F. Park. "Integrated Analysis of Gene Expression, SNP, InDel, and CNV Identifies Candidate Avirulence Genes in Australian Isolates of the Wheat Leaf Rust Pathogen Puccinia triticina." Genes 11, no. 9 (2020): 1107. http://dx.doi.org/10.3390/genes11091107.

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The leaf rust pathogen, Puccinia triticina (Pt), threatens global wheat production. The deployment of leaf rust (Lr) resistance (R) genes in wheat varieties is often followed by the development of matching virulence in Pt due to presumed changes in avirulence (Avr) genes in Pt. Identifying such Avr genes is a crucial step to understand the mechanisms of wheat-rust interactions. This study is the first to develop and apply an integrated framework of gene expression, single nucleotide polymorphism (SNP), insertion/deletion (InDel), and copy number variation (CNV) analysis in a rust fungus and id
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Dissertations / Theses on the topic "Gens candidats"

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Bustamante, Pineda Mariona. "Estudis d'associació i funcionals en gens candidats per a l'osteoporosi." Doctoral thesis, Universitat de Barcelona, 2007. http://hdl.handle.net/10803/1887.

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L'osteoporosi, una malaltia complexa determinada tant per factors genètics com ambientals, està caracteritzada per una reduïda densitat mineral òssia (DMO), un deteriorament de la microarquitectura òssia i un augment del risc de patir fractures osteoporòtiques. En el present treball ens vam plantejar estudiar les causes genètiques que determinen l'aparició de l'osteoporosi mitjançant la realització d'estudis d'associació i estudis funcionals. <br/>Els gens candidats clàssics per a l'osteoporosi que hem analitzat han estat el gen <i>COL1A1</i>, el gen <i>ESR1</i>, el gen <i>VDR</i> i el gen <i>
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Zhang, Yu. "Identification and characterization of candidate genes for peach fruit shape." Doctoral thesis, Universitat Autònoma de Barcelona, 2018. http://hdl.handle.net/10803/666885.

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El fruit del préssec deriva de l'ovari madur, que es converteix en drupa. La seva forma pot variar entre rodona i plana, adquirint algunes formes intermèdies com la forma aplanada. En el préssec, el fruit pla (anomenat paraguaià) és causat per un al·lel parcialment dominant que ha d'estar en heterocigosis (Ss), mentre que els fruits d'arbres homozigots (SS) avorten poques setmanes després del quallat del fruit. Investigacions anteriors han identificat un marcador SSR (UDP98-412) altament associat al caràcter i que és adequat per a la seva utilització en selecció assistida per marcadors (SAM).
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Illa, Berenguer Eudald. "Mapatge de gens candidats implicats en la qualitat del fruit al presseguer." Doctoral thesis, Universitat de Barcelona, 2010. http://hdl.handle.net/10803/966.

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En els darrers anys, la important reconversió varietal ha permès una millor qualitat, més adaptada tan a les exigències de la producció com de la distribució i del consumidor. La primera generació de milloradors van posar tot el seu èmfasi en millorar les característiques comercials de la fruita com el color, la fermesa i el sabor. Tanmateix el mercat actual exigeix altres atributs de tipus organolèptic i nutricional, addicionals als anteriors. Entendre la base genètica que controla cadascun dels caràcters determinarà la nostra capacitat per obtenir uns fruits més atractius i sans per al consu
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Jodar, Bifet Meritxell. "Anàlisi del contingut de RNA i estudi mutacional de gens candidats en iinfertilitat masculina." Doctoral thesis, Universitat de Barcelona, 2012. http://hdl.handle.net/10803/119732.

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La infertilitat és un problema que cada cop és més comú en la població actual. S’ha definit que la meitat dels casos de la infertilitat es deu a un factor masculí, no obstant, la gran majoria segueix sent d’etiologia desconeguda. Els grans objectius d’aquesta tesi es poden dividir en dos camps: (i) la cerca de factors genètics que puguin ser causa de la infertilitat masculina i (ii) la cerca de nous factors, com els RNAs i miRNAs, que puguin aclarir la patogenicitat de tipus determinats de infertilitat i el seu futur ús com a biomarcadors de la fertilitat. Vam utilitzar tres estratègies per
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López, Girona Elena. "Genetic architecture of agronomic traits in peach [Prunus persica (L.) Batsch]: subacid, flat shape and nectarine." Doctoral thesis, Universitat Autònoma de Barcelona, 2014. http://hdl.handle.net/10803/285555.

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L'objectiu dels programes de millora genètica del préssec és generar varietats adaptats a les condicions agronòmiques locals i satisfer els requeriments del consumidor. Això últim implica millorar la qualitat del fruit. L'estratègia seguida per molts milloradors es basa en la selección de descendents de creuaments on s’espera segregació per a caràcters fenotípics. Es tracta d’un mètode costós tant en temps com en diners a causa del período de juvenilitad del presseguer (2-3 anys) i també als recursos que suposa el mantener les plàntules en el camp durant el procés d’avaluació i selecció. L'obj
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Castro, i. Català Marta de. "Candidate genes for psychosis and their interaction with environmental factors: impact on psychosis-proneness = Gens candidats per psicosi i la seva interacció amb factors ambientals: impacte sobre la vulnerabilitat per a psicosi." Doctoral thesis, Universitat de Barcelona, 2017. http://hdl.handle.net/10803/456371.

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Schizophrenia is a severe and complex mental disorder that results in an inability to cope with life’s ordinary demands and routines. Normally, it appears in late adolescence, more frequently and developing earlier in males. It seems that disruption of the factors and pathways involved in brain development may cause modifications in neural structure, function or connectivity, leading to a final brain more susceptible to develop psychotic symptoms. The high diversity of symptoms intra- and inter-patient, makes the exploration of the aetiology and biological pathways underlying this illness, as
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Castro, Miró Marta de. "Metodologies d'alt rendiment per a la identificació de noves mutacions i gens causants de distròfies de retina: estudi funcional de nous candidats." Doctoral thesis, Universitat de Barcelona, 2017. http://hdl.handle.net/10803/456372.

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Les distròfies de retina (DR) formen un ampli grup dins les patologies hereditàries de la visió que es caracteritza perquè cursen amb afectació retinal i per la seva elevada heterogeneïtat clínica i genètica. A nivell clínic les DR es classifiquen entre formes estacionàries o progressives i formes maculars o generalitzades i, en general, són difícils de diagnosticar. A nivell genètic s’han identificat més de 260 gens causals, associats a formes sindròmiques i no sindròmiques, que s’hereten seguint els patrons coneguts d’herència mendeliana. A més, algunes DR, particularment les que afecten el
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Vidal, i. Fàbrega Oriol. "Anàlisi de quantitative trait loci i de gens candidats relacionats amb la qualitat de la carn i de la canal en una població Landrace." Doctoral thesis, Universitat Autònoma de Barcelona, 2004. http://hdl.handle.net/10803/5654.

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Els treballs que inclou aquest compendi s'han desenvolupat dins del projecte FEDER 2FD97-0916-C02-02, que té com a objectiu principal confirmar l'existència, en una població comercial Landrace altament seleccionada, de quantitative trait loci (QTL) prèviament descrits en encreuaments de races divergents. Els caràcters analitzats en aquest projecte inclouen tant mesures de la qualitat de la carn com de conformació i de qualitat de la canal.<br/>Mitjançant la segregació de marcadors moleculars tipus microsatèl·lits en un pedigrí de dues generacions d'una població Landrace es van analitzar 10 re
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Saus, Martínez Ester. "Study of genomic variability in the genetic susceptibility to psychiatric disorders: SNPs, CNVs and miRNAs." Doctoral thesis, Universitat Pompeu Fabra, 2010. http://hdl.handle.net/10803/7221.

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In this thesis we have studied genetic elements potentially contributing to the pathophysiology of psychiatric disorders, focusing on different sources of human genome variability, including SNPs and CNVs, which can affect not only coding genes but also RNA regulatory elements, such as miRNAs. First, we have interrogated different candidate genes for psychiatric disorders overlapping with known CNVs, finding 14 different genes variable in copy number in psychiatric disorders but not in control individuals. Then, narrowing the analysis on mood disorders, we explored GSK3&#946; gene considering
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Jacq, Laurent. "Recherche de gènes de susceptibilité à la polyarthrite rhumatoïde et aux syndromes coronaires aigus." Thesis, Evry-Val d'Essonne, 2010. http://www.theses.fr/2010EVRY0014.

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La polyarthrite rhumatoïde (PR) et la maladie coronaire (MC) sont deux maladies touchant l'adulte comportant une susceptibilité génétique et partageant plusieurs chapitres physiopathologiques. Nous avons recherché des gènes de susceptibilité à la PR en employant une approche gène-candidat dans des loci suggerés par les données d'études de criblage du genome. Nous avons mis au point une étude originale (Genescaf) d'approche des gènes impliqués dans la MC<br>Rhumatoid arthritis (RA) and coronary artery disease (CAD) are two adult diseases involving some genetic susceptibility genes and sharing m
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Books on the topic "Gens candidats"

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Bennett, Philip. Parkinson's disease: A molecular investigation of potential candidate genes. University of Birmingham, 1995.

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Ramsden, James Daniel. Angiopoietins in goitre: Candidates for anti-angiogenic gene therapy? University of Birmingham, 2002.

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Shieh, Jia-Ching. Isolation and characterisation of candida albicans cell cycle genes. University of Manchester, 1994.

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Nolan, Tania. Molecular analysis of cell cycle genes in Candida albicans. University of Manchester, 1996.

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Nicholl, David J. A study of candidate genes in Parkinson's disease and related neurodegenerative disorders. University of Birmingham, 1998.

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Stoldt, Volker R. Morphogenese des humanpathogenen Pilzes Candida albicans: Isolierung und Charakterisierung der Gene EFGI und RFGI. J. Cramer, 1995.

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Dyer, Philip Henry. Investigation of the genetics of nephropathy in type 1 diabetes mellitus: Candidate gene studies. University of Birmingham, 2000.

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Thompson, Miles. Mutation screening of dopamine and serotonin candidate genes in Tourette's syndrome and alcohol-dependent patients. National Library of Canada = Bibliothèque nationale du Canada, 1999.

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Oelbaum, Raymond Stuart. An analysis of four candidate genes for non-insulin-dependent diabetes using restriction fragment length polymorphism markers. University of Manchester, 1994.

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Crowley, J. Isolation of candida albican genes involved in cAMP metabolism by the rescue of caffeine sensitive saccharomyces cerevisiae mutants. UMIST, 1996.

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Book chapters on the topic "Gens candidats"

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Giri, Prerna, and Bhagyalaxmi Mohapatra. "Candidate Gene." In Encyclopedia of Animal Cognition and Behavior. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-47829-6_1-1.

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Teare, M. Dawn. "Candidate Gene Association Studies." In Methods in Molecular Biology. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60327-416-6_8.

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Singer, Jonathan B. "Candidate Gene Association Analysis." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60761-247-6_13.

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Song, Youeun, and Abha R. Gupta. "Candidate Genes in Autism." In Encyclopedia of Autism Spectrum Disorders. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-1698-3_1317.

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Song, Youeun, and Abha R. Gupta. "Candidate Genes in Autism." In Encyclopedia of Autism Spectrum Disorders. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-319-91280-6_1317.

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Sturtevant, Joy. "Reporter Gene Assays in Candida albicans." In Candida albicans. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_15.

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Rihet, Pascal. "Innate Immunity Genes as Candidate Genes." In Innate Immunity. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-570-1_2.

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Nobile, Clarissa J., and Aaron P. Mitchell. "Large-Scale Gene Disruption Using the UAU1 Cassette." In Candida albicans. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_17.

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Zhu, Meng-Jin, Xiang Li, and Shu-Hong Zhao. "Digital Candidate Gene Approach (DigiCGA) for Identification of Cancer Genes." In Methods in Molecular Biology. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-759-4_7.

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David, Anna L., and Simon N. Waddington. "Candidate Diseases for Prenatal Gene Therapy." In Prenatal Gene Therapy. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-873-3_2.

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Conference papers on the topic "Gens candidats"

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Huber, P., J. Dalmon, M. Laurent, G. Courtois, D. Thevenon та G. Marguerie. "CHARACTERIZATION OFTHE 5’FLANKING REGION FOR THE HUMAN FIBRINOGEN β GENE". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642889.

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Fibrinogen is coded by three separate genes located in a 50kb region of chromosome 4 and organized in a α - β - γ orientation with an inversion of the gene 3- A human genomic library was constructed using the EMBL4 phage and screened with cDNA probes coding for human fibrinogen Aα, Bβ and γ chains. Clones, covering the fibrinogen locus,were identified, and their organization was analyzed by means of hybridization and restriction mapping. Among these clones one recombinant phage containing the β gene and large 5’ and 3’ -flanking sequences was isolated.To identify the regulatory sequences Dpstr
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DO, Quan, and Pierre LARMANDE. "Candidate gene prioritization using graph embedding." In 2020 RIVF International Conference on Computing and Communication Technologies (RIVF). IEEE, 2020. http://dx.doi.org/10.1109/rivf48685.2020.9140776.

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de Oliveira Littiere, Thayssa, Gustavo Henrique de Frias Castro, Maria Del Pilar Rodriguez Rodriguez, et al. "IDENTIFICAÇÃO DE GENES CANDIDATOS RELACIONADOS A PERFORMANCE EM EQUINOS ATRAVÉS DE REDE GENE-FATOR DE TRANSCRIÇÃO." In SIMCAV 2021. Even3, 2021. http://dx.doi.org/10.29327/simcav2021.330039.

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Permyakova, M. D., S. V. Osipova, A. V. Permyakov, et al. "CANDIDATE GENES FOR REGULATION OF LIPOXYGENASE ACTIVITY." In The All-Russian Scientific Conference with International Participation and Schools of Young Scientists "Mechanisms of resistance of plants and microorganisms to unfavorable environmental". SIPPB SB RAS, 2018. http://dx.doi.org/10.31255/978-5-94797-319-8-970-974.

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Braun, Terry A., Todd Scheetz, Gregg L. Webster, and Thomas L. Casavant. "Mining biological databases for candidate disease genes." In ITCom 2001: International Symposium on the Convergence of IT and Communications, edited by Howard J. Siegel. SPIE, 2001. http://dx.doi.org/10.1117/12.434869.

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Xie, Bingqing, Gady Agam, Natalia Maltsev, and Conrad Gilliam. "Conditional Random Field for Candidate Gene Prioritization." In BCB'13: ACM-BCB2013. ACM, 2013. http://dx.doi.org/10.1145/2506583.2512374.

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El-fadl, Rihab, Nasser Rizk, Amena Fadel, and Abdelrahman El Gamal. "The Profile of Hepatic Gene Expression of Glucose Metabolism in Mice on High Fat Diet." In Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2020. http://dx.doi.org/10.29117/quarfe.2020.0213.

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Obesity is a growing problem worldwide, and recent data indicated that 20% of the populations would be obese. Obesity arises as a multifactorial disease caused by inherited traits that interact with lifestyle factors such as diet and physical activity. The liver plays an essential role in the gluco-regulation via regulating glucose, lipid and protein metabolism. The process of glucose metabolism is controlled by a range of molecular mechanisms and genes which affect the metabolism of the liver during intake of high fat diet (HFD). The objective of this research is to investigate the profile of
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Dong, Guiying, Zhi-Ping Liu, Rui Gao, and Yuqing Zhao. "Identification of candidate genes for Rituximab response in rheumatoid arthritis with weighted gene co-expression network analysis." In 2017 Chinese Automation Congress (CAC). IEEE, 2017. http://dx.doi.org/10.1109/cac.2017.8243817.

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Borland, Shona, Gennadiy Tenin, Simon Williams, et al. "BS9 KMT2C- a tetralogy of fallot candidate gene." In British Cardiovascular Society Annual Conference ‘Digital Health Revolution’ 3–5 June 2019. BMJ Publishing Group Ltd and British Cardiovascular Society, 2019. http://dx.doi.org/10.1136/heartjnl-2019-bcs.173.

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Wang, Ran. "Candidate chemosensory protein genes in whiteflyBemisiatabaci by transcriptome analysis." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.114182.

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Reports on the topic "Gens candidats"

1

Lee, Cheng-Chi. Cloning Human Chromosome 17 Genes: Candidate Genes for BRCA1. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada361576.

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Zhao, Xia, Kim Glenn, Zhiqiang Du, and Max F. Rothschild. Candidate Gene Discovery for Dog Cryptorchidism. Iowa State University, 2008. http://dx.doi.org/10.31274/ans_air-180814-932.

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Liu, Wanguo. CHK2, A Candidate Prostate Cancer Susceptibility Gene. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada443052.

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Liu, Wanguo. CHK2, A Candidate Prostate Cancer Susceptibility Gene. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada423213.

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Liu, Wanguo. CHK2, A Candidate Prostate Cancer Susceptibility Gene. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada413554.

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Zhao, Xia, Zhiqiang Du, Kim Glenn, and Max F. Rothschild. Candidate Gene Discovery for Retained Testicles in Dogs. Iowa State University, 2009. http://dx.doi.org/10.31274/ans_air-180814-911.

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Srivastava, Meera. Novel Role of Candidate Tumor Suppressor ANX7 Gene in Prostate Cancer. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada485782.

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Eaves, Connie, and Yun Zhao. Identification of Novel Genes and Candidate Targets in CML Stem Cells. Defense Technical Information Center, 2009. http://dx.doi.org/10.21236/ada502095.

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Dai, Wei, Qi Wang, and Suqing Xie. Investigation of the Candidate Tumor Suppressor Gene prk in Prostate Cancer. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada413339.

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Dai, Wei. Investigation of the Candidate Tumor Suppressor Gene prk in Prostate Cancer. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada405508.

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