Gotowa bibliografia na temat „Heterozygotes”
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Artykuły w czasopismach na temat "Heterozygotes"
Wicker, L. S., B. J. Miller, P. A. Fischer, A. Pressey i L. B. Peterson. "Genetic control of diabetes and insulitis in the nonobese diabetic mouse. Pedigree analysis of a diabetic H-2nod/b heterozygote." Journal of Immunology 142, nr 3 (1.02.1989): 781–84. http://dx.doi.org/10.4049/jimmunol.142.3.781.
Pełny tekst źródłaEverse, Stephen J., Thomas Orfeo, Kathleen E. Brummel-Ziedins, Matthew F. Hockin i Kenneth G. Mann. "Predicting Thrombosis in Factor VLeiden Heterozygotes." Blood 112, nr 11 (16.11.2008): 1818. http://dx.doi.org/10.1182/blood.v112.11.1818.1818.
Pełny tekst źródłaArora, Jatin, Federica Pierini, Paul J. McLaren, Mary Carrington, Jacques Fellay i Tobias L. Lenz. "HLA Heterozygote Advantage against HIV-1 Is Driven by Quantitative and Qualitative Differences in HLA Allele-Specific Peptide Presentation". Molecular Biology and Evolution 37, nr 3 (22.10.2019): 639–50. http://dx.doi.org/10.1093/molbev/msz249.
Pełny tekst źródłaFalchetti, Alberto, Annamaria Morelli, Andrea Amorosi, Francesco Tonelli, Silvia Fabiani, Valentina Martineti, Roberto Castello, Lino Furlani i Maria Luisa Brandi. "Allelic Loss in Parathyroid Tumors from Individuals Homozygous for Multiple Endocrine Neoplasia Type 11". Journal of Clinical Endocrinology & Metabolism 82, nr 7 (1.07.1997): 2278–82. http://dx.doi.org/10.1210/jcem.82.7.4042.
Pełny tekst źródłaDai, K., C. B. Gillies i A. E. Dollin. "Synaptonemal complex analysis of domestic sheep (Ovis aries) with Robertsonian translocations. II. Trivalent and pairing abnormalities in Massey I and Massey II heterozygotes". Genome 37, nr 4 (1.08.1994): 679–89. http://dx.doi.org/10.1139/g94-096.
Pełny tekst źródłaNg, Kevin, Erron W. Titus, Krystien V. Lieve, Thomas M. Roston, Andrea Mazzanti, Frederick H. Deiter, Isabelle Denjoy i in. "An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2 -Catecholaminergic Polymorphic Ventricular Tachycardia". Circulation 142, nr 10 (8.09.2020): 932–47. http://dx.doi.org/10.1161/circulationaha.120.045723.
Pełny tekst źródłaBonvicino, Cibele R., Paulo S. D'Andrea i Pavel M. Borodin. "Pericentric inversion in natural populations of Oligoryzomys nigripes (Rodentia: Sigmodontinae)". Genome 44, nr 5 (1.10.2001): 791–96. http://dx.doi.org/10.1139/g01-080.
Pełny tekst źródłaRossi, Enrico, Max K. Bulsara, John K. Olynyk, Digby J. Cullen, Lesa Summerville i Lawrie W. Powell. "Effect of Hemochromatosis Genotype and Lifestyle Factors on Iron and Red Cell Indices in a Community Population". Clinical Chemistry 47, nr 2 (1.02.2001): 202–8. http://dx.doi.org/10.1093/clinchem/47.2.202.
Pełny tekst źródłaGirolami, Antonio, Elisabetta Cosi, Silvia Ferrari, Bruno Girolami i Maria L. Randi. "Thrombotic Events in Homozygotes with a Proven or Highly Probable Arg304Gln Factor VII Mutation (FVII Padua)1): Only Limited Replacement Therapy is Needed in Case of Surgery". Cardiovascular & Hematological Disorders-Drug Targets 19, nr 3 (21.10.2019): 233–38. http://dx.doi.org/10.2174/1871529x19666190308114842.
Pełny tekst źródłaMcClelland, Erin E., Dustin J. Penn i Wayne K. Potts. "Major Histocompatibility Complex Heterozygote Superiority during Coinfection". Infection and Immunity 71, nr 4 (kwiecień 2003): 2079–86. http://dx.doi.org/10.1128/iai.71.4.2079-2086.2003.
Pełny tekst źródłaRozprawy doktorskie na temat "Heterozygotes"
GAY, PHILIPPE. "Etude de l'erythropoietine au cours des thalassemies heterozygotes". Aix-Marseille 2, 1992. http://www.theses.fr/1992AIX20193.
Pełny tekst źródłaRowe, Steven M., Cori Daines, Felix C. Ringshausen, Eitan Kerem, John Wilson, Elizabeth Tullis, Nitin Nair i in. "Tezacaftor–Ivacaftor in Residual-Function Heterozygotes with Cystic Fibrosis". MASSACHUSETTS MEDICAL SOC, 2017. http://hdl.handle.net/10150/626280.
Pełny tekst źródłaSousa, Ribeiro Maria Leticia de. "ß-Thalassemia and HB lepore heterozygotes: phenotype-genotype correlation". [Maastricht : Maastricht : Universiteit Maastricht] ; University Library, Maastricht University [Host], 1997. http://arno.unimaas.nl/show.cgi?fid=5822.
Pełny tekst źródłaLebea, Phiyani Justice 1974. "Molecular characterisation of suspected heterozygotes of trimethylaminuria / Phiyani Justice Lebea". Thesis, Potchefstroom University for Christian Higher Education, 2002. http://hdl.handle.net/10394/13595.
Pełny tekst źródłaThesis, MSc, Potchefstroom University for Christian Higher Education 2002.
Jansen, Natalie R. "Comparison of Health-Related Quality of Life Between Heterozygous Women with Fabry Disease, the General Population, and Patients with Chronic Disease". University of Cincinnati / OhioLINK, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1109182046.
Pełny tekst źródłaSkjönsberg, Åsa. "Hereditary susceptibility to inner ear stress agents studied in heterozygotes of the German waltzing guinea pig /". Stockholm, 2006. http://diss.kib.ki.se/2006/91-7140-817-7/.
Pełny tekst źródłaMARISSAL, CARBONNIER CATHERINE. "Depistage des heterozygotes pour le bloc de la 21 hydroxylase dans une population de femmes adultes hirsutes". Lille 2, 1988. http://www.theses.fr/1988LIL2M001.
Pełny tekst źródłaZhang, Mingcai. "The Role of New Mutations in Evolution: Identifying the Deleterious Effect of Heterozygotes and the Beneficial Effect on Adaptation to Salt-Stressed Environments in Drosophila Melanogaster". Bowling Green State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1276892040.
Pełny tekst źródłaYardin, Marie Roseline, of Western Sydney Hawkesbury University, Faculty of Science and Technology i School of Science. "Genetic variation in Anadara trapezia (Sydney cockle) : implications for the recruitment of marine organisms". THESIS_FST_SS_Yardin_M.xml, 1997. http://handle.uws.edu.au:8081/1959.7/56.
Pełny tekst źródłaDoctor of Philosophy (PhD)
HADJ, SAHRAOUI NADIA. "Processus involutifs affectant les cellules de purkinje au cours du vieillissement chez deux mutants neurologiques : les souris heterozygotes staggerer (+/sg) et reeler (+/rl)". Paris 6, 1996. http://www.theses.fr/1996PA066779.
Pełny tekst źródłaKsiążki na temat "Heterozygotes"
Tuckerman, Elizabeth M. Studies on the fragile x syndrome with special reference to X-inactivation in female heterozygotes. Birmingham: University of Birmingham, 1988.
Znajdź pełny tekst źródłaCallister, David Rooks. Heterozygosity retained in simulated composite breeds. 1993.
Znajdź pełny tekst źródłaBright-Thomas, Rowland J., i Andrew M. Jones. Cystic fibrosis. Redaktorzy Patrick Davey i David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0132.
Pełny tekst źródłaFrankham, Richard, Jonathan D. Ballou, Katherine Ralls, Mark D. B. Eldridge, Michele R. Dudash, Charles B. Fenster, Robert C. Lacy i Paul Sunnucks. Inbreeding reduces reproductive fitness. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780198783398.003.0003.
Pełny tekst źródłaHeidet, Laurence, Bertrand Knebelmann i Marie Claire Gubler. Alport syndrome. Redaktor Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0321.
Pełny tekst źródłaPearl, Phillip L., i William P. Welch. Pediatric Neurotransmitter Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0059.
Pełny tekst źródłaEhninger, Dan, i Alcino J. Silva. Tuberous Sclerosis and Autism. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199744312.003.0009.
Pełny tekst źródłaHeidet, Laurence, Bertrand Knebelmann i Marie Claire Gubler. Alport syndrome. Redaktor Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0322_update_001.
Pełny tekst źródłaPreconception and Prenatal Carrier Screening for Cystic Fibrosis: Clinical and Laboratory Guidelines. Amer College of Obstetricians &, 2001.
Znajdź pełny tekst źródłaKriemler, Susi. Exercise, physical activity, and cystic fibrosis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199232482.003.0033.
Pełny tekst źródłaCzęści książek na temat "Heterozygotes"
Scott, D., L. A. Jones, S. A. G. Elyan, A. Spreadborough, R. Cowan i G. Ribiero. "Identification of A-T heterozygotes". W Ataxia-Telangiectasia, 101–16. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-78278-7_9.
Pełny tekst źródłaGr�nfeld, J. P., O. Lidove i F. Barbey. "Heterozygotes with Fabry�s Disease". W Contributions to Nephrology, 208–10. Basel: KARGER, 2001. http://dx.doi.org/10.1159/000060188.
Pełny tekst źródłaDallapiccola, B., i B. Porfirio. "Chromosomal Studies in Fanconi Anemia Heterozygotes". W Fanconi Anemia, 145–58. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74179-1_12.
Pełny tekst źródłaNorman, Amos, i H. Rodney Withers. "Mammography Screening for A-T Heterozygotes". W Ataxia-Telangiectasia, 137–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-78278-7_12.
Pełny tekst źródłaKamatani, Naoyuki, Hisashi Yamanaka, Kusuki Nishioka, Yutaro Nishida i Kiyonobu Mikanagi. "Diagnosis of Lesch-Nyhan Heterozygotes by Peripheral Blood". W Purine and Pyrimidine Metabolism in Man V, 157–62. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5104-7_24.
Pełny tekst źródłaSahota, Amrik, Steve Bye, Ju Chen, Nada H. Khattar, Mitchell S. Turker, Fernando Moro, H. Anne Simmonds, Brian T. Emmerson, Ross B. Gordon i J. A. Tischfield. "Molecular Characterization of a Novel Mutation in APRT Heterozygotes". W Purine and Pyrimidine Metabolism in Man VIII, 675–78. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-2584-4_140.
Pełny tekst źródłaJordan, G., i J. D. Mollon. "Unique hues in heterozygotes for protan and deutan deficiencies". W Documenta Ophthalmologica Proceedings Series, 67–76. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5408-6_6.
Pełny tekst źródłaPaeratakul, Umnarj, i Milton W. Taylor. "Selection and Characterization of APRT Heterozygotes of Mouse L-5178Y Cells". W Purine and Pyrimidine Metabolism in Man V, 253–58. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5104-7_40.
Pełny tekst źródłaShin, Y. S., H. Steigüber, P. Klemm, W. Endres, O. Schwab i G. Wolff. "Branching Enzyme in Erythrocytes. Detection of Type IV Glycogenosis Homozygotes and Heterozygotes". W Studies in Inherited Metabolic Disease, 252–54. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1259-5_46.
Pełny tekst źródłaArnemann, J. "Heterozygotie". W Springer Reference Medizin, 1107–8. Berlin, Heidelberg: Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_3499.
Pełny tekst źródłaStreszczenia konferencji na temat "Heterozygotes"
Hassan, H. J., L. Cianetti, P. M. Mannucci, V. Vicente, R. Cortese i C. Peschle. "HEREDITARY THROMBOPHILIA CAUSED BY MISSENSE MUTATION IN PROTEIN C GENE". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642944.
Pełny tekst źródłaBounameaux, H., Ph de Moerloose, J. Vogel, G. Reber, B. Krahenbuhl i C. Bouvier. "NORMAL PREGNANCY AND DELIVERY IN A PATIENT WITH SEVERE PROTEIN C DEFICIENCY AND PREVIOUS DEEP-VEIN THROMBOSIS". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644312.
Pełny tekst źródłaBorg, J. Y., M. C. Owen, C. Soria, J. Caen i R. W. Carrell. "ANTITHROMBIN ROUEN-I(47 ARG→HIS) AND ROUEN-II (47SER) : TWO NEW VARIANTS WITH DECREASED HEPARIN AFFINITY". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643679.
Pełny tekst źródłaWautier, J. L., B. Boi zard, Y. Gruel i J. P. Caen. "IMMUNOLOGICAL STUDY OF GLYCOPROTEINS AND ANTIGENS IN GLANZMANN'S THROMBASTHENIA HETEROZYGOTES". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644742.
Pełny tekst źródłaCastaman, G., F. Rodeghiero i M. Ruggeri. "HOMOZYGOUS FACTOR XII CONGENITAL DEFICIENCY: STUDY OF 10 NEW FAMILIES." W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643300.
Pełny tekst źródłaErenso, D., R. Solomon, J. Cooper, G. Welker, E. Aguilar, B. Flanagan, C. Pennycuff i in. "Heterozygotes and Homozygotes Genotypes Human Red Blood Cells Response to Trap and Drag Force". W Bio-Optics: Design and Application. Washington, D.C.: OSA, 2013. http://dx.doi.org/10.1364/boda.2013.jt2a.25.
Pełny tekst źródłaChun, Sehwan, So-Young Bang, Hye-Soon Lee, Sang-Cheol Bae i Kwangwoo Kim. "267 Relative expression strength of HLA-DRB1 in heterozygotes is associated with rheumatic diseases". W 13th International Congress on Systemic Lupus Erythematosus (LUPUS 2019), San Francisco, California, USA, April 5–8, 2019, Abstract Presentations. Lupus Foundation of America, 2019. http://dx.doi.org/10.1136/lupus-2019-lsm.267.
Pełny tekst źródłaZikan, M., O. Dubova, V. Student, P. Koliba, T. Brtnicky i P. Kabele. "824 Double heterozygotes for high penetrance susceptibility genes are not rare and require special care". W ESGO 2021 Congress. BMJ Publishing Group Ltd, 2021. http://dx.doi.org/10.1136/ijgc-2021-esgo.556.
Pełny tekst źródła"Chromosome synapsis and recombination in intraspecific and interspecific heterozygotes for chromosomal rearrangements in voles of the genus Alexandromys". W Bioinformatics of Genome Regulation and Structure/Systems Biology (BGRS/SB-2022) :. Institute of Cytology and Genetics, the Siberian Branch of the Russian Academy of Sciences, 2022. http://dx.doi.org/10.18699/sbb-2022-384.
Pełny tekst źródłaPloos van Amstel, J. K., A. L. van der Zanden, P. H. Reitsma i R. M. Bertina. "RESTRICTION ANALYSIS AND SOUTHERN BLOTTING OF TOTAL HUMAN DNA REVEALS THE EXISTENCE OF MORE THAN ONE GENE HOMOLOGOUS WITH PROTEIN S cDNA". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644639.
Pełny tekst źródłaRaporty organizacyjne na temat "Heterozygotes"
Moll, Ute M. Risk for Sporadic Breast Cancer in Ataxia Telangiectasia Heterozygotes. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2000. http://dx.doi.org/10.21236/ada395438.
Pełny tekst źródłaMoll, Ute M. Risk for Sporadic Breast Cancer in Ataxia Telangiectasia Heterozygotes. Fort Belvoir, VA: Defense Technical Information Center, sierpień 1999. http://dx.doi.org/10.21236/ada393435.
Pełny tekst źródłaGao, Qingshen. Susceptibility of BRCA2 Heterozygous Normal Mammary Epithelial Cells to Radiation-Induced Transformation. Fort Belvoir, VA: Defense Technical Information Center, październik 2005. http://dx.doi.org/10.21236/ada455086.
Pełny tekst źródłaGao, Quingshen. Susceptibility of BRCA2 Heterozygous Normal Mammary Epithelial Cells to Radiation Induced Transformation. Fort Belvoir, VA: Defense Technical Information Center, październik 2002. http://dx.doi.org/10.21236/ada412997.
Pełny tekst źródłaRichmond, Robert C. Cell and Molecular Biology of Ataxia Telangiectasia Heterozygous Human Mammary Epithelial Cells Irradiated in Culture. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 2002. http://dx.doi.org/10.21236/ada412826.
Pełny tekst źródłaSmith, Adrian P., John A. Lee i Steven I. Reed. Breast Tumor Kinetics in Mice Overexpressing Cyclin E and Heterozygous for Tumor Suppressor p53 or Rb. Fort Belvoir, VA: Defense Technical Information Center, maj 2001. http://dx.doi.org/10.21236/ada395709.
Pełny tekst źródłaSmith, Adrian P., Steven I. Reed i John A. Lee. Breast Tumor Kinetics in Mice Overexpressing Cyclin E and Heterozygous for Tumor Suppressor p53 or Rb. Fort Belvoir, VA: Defense Technical Information Center, maj 2002. http://dx.doi.org/10.21236/ada407356.
Pełny tekst źródłaSmith, Adrian P., Steven I. Reed i John A. Lee. Breast Tumor Kinetics in Mice Overexpressing Cyclin E and Heterozygous for Tumor Suppressor p53 or Rb. Fort Belvoir, VA: Defense Technical Information Center, maj 2003. http://dx.doi.org/10.21236/ada416982.
Pełny tekst źródłaKurimasa, Akihiro, Sandeep Burma, Melinda Henrie, Honghai Ouyang, Mitsuhiko Osaki, Hisao Ito, Hatsumi Nagasawa i in. Disruption of NBS1 gene leads to early embryonic lethality in homozygous null mice and induces specific cancer in heterozygous mice. Office of Scientific and Technical Information (OSTI), kwiecień 2002. http://dx.doi.org/10.2172/943450.
Pełny tekst źródłaGinzberg, Idit, Richard E. Veilleux i James G. Tokuhisa. Identification and Allelic Variation of Genes Involved in the Potato Glycoalkaloid Biosynthetic Pathway. United States Department of Agriculture, sierpień 2012. http://dx.doi.org/10.32747/2012.7593386.bard.
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