Artykuły w czasopismach na temat „Heterozygotes”
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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 źródłaAghamohammadi, Asghar, Seyed M. Akrami, Marjan Yaghmaie, Nima Rezaei, Gholamreza Azizi, Mehdi Yaseri, Hassan Nosrati i Majid Zaki-Dizaji. "Individual Radiosensitivity Assessment of the Families of Ataxia-Telangiectasia Patients by G2-Checkpoint Abrogation". Sultan Qaboos University Medical Journal [SQUMJ] 18, nr 4 (28.03.2019): 440. http://dx.doi.org/10.18295/squmj.2018.18.04.003.
Pełny tekst źródłaYap, S., K. A. O’Donnell, C. O’Neill, P. D. Mayne, P. Thornton i E. Naughten. "Factor V Leiden (Arg506Gln), a Confounding Genetic Risk Factor but not Mandatory for the Occurrence of Venous Thromboembolism in Homozygotes and Obligate Heterozygotes for Cystathionine β-synthase Deficiency". Thrombosis and Haemostasis 81, nr 04 (1999): 502–5. http://dx.doi.org/10.1055/s-0037-1614513.
Pełny tekst źródłaJi, Yuanfu, Wayne A. Raska, Marcos De Donato, M. Nurul Islam-Faridi, H. James Price i David M. Stelly. "Identification and distinction among segmental duplication-deficiencies by fluorescence in situ hybridization (FISH)-adorned multivalent analysis". Genome 42, nr 4 (1.08.1999): 763–71. http://dx.doi.org/10.1139/g99-012.
Pełny tekst źródłaRo, Seungil, Sung Jin Hwang, Melodie Muto, William Keith Jewett i Nick J. Spencer. "Anatomic modifications in the enteric nervous system of piebald mice and physiological consequences to colonic motor activity". American Journal of Physiology-Gastrointestinal and Liver Physiology 290, nr 4 (kwiecień 2006): G710—G718. http://dx.doi.org/10.1152/ajpgi.00420.2005.
Pełny tekst źródłaPlöchl, E., J. P. Colombo, B. Wermuth i K. M. Gibson. "Increased plasma amylase in the family of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency". Clinical Chemistry 38, nr 2 (1.02.1992): 307–9. http://dx.doi.org/10.1093/clinchem/38.2.307.
Pełny tekst źródłaHo, PJ, J. Rochette, CA Fisher, B. Wonke, MK Jarvis, A. Yardumian i SL Thein. "Moderate reduction of beta-globin gene transcript by a novel mutation in the 5' untranslated region: a study of its interaction with other genotypes in two families". Blood 87, nr 3 (1.02.1996): 1170–78. http://dx.doi.org/10.1182/blood.v87.3.1170.bloodjournal8731170.
Pełny tekst źródłaLeebeek, F. W. G., J. Stibbe, E. A. R. Knot, C. Kluft, M. J. Gomes i M. Beudeker. "Mild Haemostatic Problems Associated with Congenital Heterozygous α2-Antiplasmin Deficiency". Thrombosis and Haemostasis 59, nr 01 (1988): 096–100. http://dx.doi.org/10.1055/s-0038-1646773.
Pełny tekst źródłaSuh, Ji Hyung, Ik Hee Ryu, Jin Pyo Hong, Ja Yoon Moon, Jin Seok Choi, Ikhyun Jun, Tae-Im Kim i Eung Kweon Kim. "Phenotypes of Granular Corneal Dystrophy Type 2 among Koreans in Their Twenties". Journal of the Korean Ophthalmological Society 63, nr 12 (15.12.2022): 965–72. http://dx.doi.org/10.3341/jkos.2022.63.12.965.
Pełny tekst źródłaSzatkowska, Iwona, Wilhelm Grzesiak, Magdalena Jędrzejczak, Andrzej Dybus, Daniel Zaborski i Dorota Jankowiak. "An analysis of CYP19, CYP21 and ER genotypes in Polish Holstein-Friesian cows with regard to the selected reproductive traits". Acta Veterinaria Brno 80, nr 1 (2011): 65–71. http://dx.doi.org/10.2754/avb201180010065.
Pełny tekst źródłaJones, G., S. Zammit, N. Norton, M. L. Hamshere, S. J. Jones, C. Milham, R. D. Sanders i in. "Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype". British Journal of Psychiatry 179, nr 4 (październik 2001): 351–55. http://dx.doi.org/10.1192/bjp.179.4.351.
Pełny tekst źródłaHerrmann, Mark G., Jacob D. Durtschi, Carl T. Wittwer i Karl V. Voelkerding. "Expanded Instrument Comparison of Amplicon DNA Melting Analysis for Mutation Scanning and Genotyping". Clinical Chemistry 53, nr 8 (1.08.2007): 1544–48. http://dx.doi.org/10.1373/clinchem.2007.088120.
Pełny tekst źródłaRosendaal, Frits, Marco Cattaneo, Maurizio Margaglione, Valerio De Stefano, Tony Cumming, Valder Arruda, Andreas Hillarp, Jean-Luc Reny i Joseph Emmerich. "Combined Effect of Factor V Leiden and Prothrombin 20210A on the Risk of Venous Thromboembolism". Thrombosis and Haemostasis 86, nr 09 (2001): 809–16. http://dx.doi.org/10.1055/s-0037-1616136.
Pełny tekst źródłaShanmugam, V., K. W. Sell i B. K. Saha. "Mistyping ACE heterozygotes." Genome Research 3, nr 2 (1.10.1993): 120–21. http://dx.doi.org/10.1101/gr.3.2.120.
Pełny tekst źródłaPowell, Lawrie W., i Elizabeth C. Jazwinska. "Hemochromatosis in Heterozygotes". New England Journal of Medicine 335, nr 24 (12.12.1996): 1837–39. http://dx.doi.org/10.1056/nejm199612123352410.
Pełny tekst źródłaSwift, Michael. "Manifestations in heterozygotes". American Journal of Medical Genetics 39, nr 4 (15.06.1991): 501. http://dx.doi.org/10.1002/ajmg.1320390431.
Pełny tekst źródłaKatoh, Masaya, i David W. Foltz. "Biochemical evidence for the existence of a null allele at the leucine aminopeptidase-2 (Lap-2) locus in the oyster Crassostrea virginica (Gmelin)". Genome 32, nr 4 (1.08.1989): 687–90. http://dx.doi.org/10.1139/g89-499.
Pełny tekst źródłaZhang, Jianning, Daniel G. Fuster, Mary Ann Cameron, Henry Quiñones, Carolyn Griffith, Xiao-Song Xie i Orson W. Moe. "Incomplete distal renal tubular acidosis from a heterozygous mutation of the V-ATPase B1 subunit". American Journal of Physiology-Renal Physiology 307, nr 9 (1.11.2014): F1063—F1071. http://dx.doi.org/10.1152/ajprenal.00408.2014.
Pełny tekst źródłaGundry, Cameron N., Joshua G. Vandersteen, Gudrun H. Reed, Robert J. Pryor, Jian Chen i Carl T. Wittwer. "Amplicon Melting Analysis with Labeled Primers: A Closed-Tube Method for Differentiating Homozygotes and Heterozygotes". Clinical Chemistry 49, nr 3 (1.03.2003): 396–406. http://dx.doi.org/10.1373/49.3.396.
Pełny tekst źródłaBombardier, Chris, Linda J. Jacobson, Marilyn J. Manco-Johnson i Neil A. Goldenberg. "Evidence of Increased Plasma Coagulative Capacity by CloFAL Assay among Pediatric Factor V Leiden and Prothrombin G20210A Heterozygotes with, Versus without, a First-or Second-Degree Family History of Venous Thromboembolism". Blood 112, nr 11 (16.11.2008): 5345. http://dx.doi.org/10.1182/blood.v112.11.5345.5345.
Pełny tekst źródłaWebb, A. J., P. Imlah i A. E. Carden. "Succinylcholine and halothane as a field test for the heterozygote at the halothane locus in pigs". Animal Science 42, nr 2 (kwiecień 1986): 275–79. http://dx.doi.org/10.1017/s0003356100017992.
Pełny tekst źródłaSimioni, Paolo, Elisabetta Castoldi, Barbara Lunghi, Daniela Tormene, Jan Rosing i Francesco Bernardi. "An underestimated combination of opposites resulting in enhanced thrombotic tendency". Blood 106, nr 7 (1.10.2005): 2363–65. http://dx.doi.org/10.1182/blood-2005-04-1461.
Pełny tekst źródłaPrence, Elizabeth M., Cheryl A. Jerome, Barbara L. Triggs-Raine i Marvin R. Natwicz. "Heterozygosity for Tay-Sachs and Sandhoff Diseases among Massachusetts Residents with French Canadian Background". Journal of Medical Screening 4, nr 3 (wrzesień 1997): 133–36. http://dx.doi.org/10.1177/096914139700400304.
Pełny tekst źródłaPhillips, R. B., M. P. Matsuoka, W. W. Smoker i A. J. Gharrett. "Inheritance of a chromosomal polymorphism in odd-year pink salmon from southeastern Alaska". Genome 42, nr 5 (1.10.1999): 816–20. http://dx.doi.org/10.1139/g99-010.
Pełny tekst źródłaChiang, Y. Jeffrey, Michael T. Hemann, Karen S. Hathcock, Lino Tessarollo, Lionel Feigenbaum, William C. Hahn i Richard J. Hodes. "Expression of Telomerase RNA Template, but Not Telomerase Reverse Transcriptase, Is Limiting for Telomere Length Maintenance In Vivo". Molecular and Cellular Biology 24, nr 16 (15.08.2004): 7024–31. http://dx.doi.org/10.1128/mcb.24.16.7024-7031.2004.
Pełny tekst źródłaFairbrother, J. E., i A. R. Beaumont. "Heterozygote deficiencies in a cohort of newly settled Mytilus edulis spat". Journal of the Marine Biological Association of the United Kingdom 73, nr 3 (sierpień 1993): 647–53. http://dx.doi.org/10.1017/s002531540003318x.
Pełny tekst źródłaDooner, H. K., i J. L. Kermicle. "THE TRANSPOSABLE ELEMENT Ds AFFECTS THE PATTERN OF INTRAGENIC RECOMBINATION AT THE bz AND R LOCI IN MAIZE". Genetics 113, nr 1 (1.05.1986): 135–43. http://dx.doi.org/10.1093/genetics/113.1.135.
Pełny tekst źródłaMotojima, Masaru, Sho Tanimoto, Masato Ohtsuka, Taiji Matsusaka, Tsutomu Kume i Koichiro Abe. "Characterization of Kidney and Skeleton Phenotypes of Mice Double Heterozygous for Foxc1 and Foxc2". Cells Tissues Organs 201, nr 5 (2016): 380–89. http://dx.doi.org/10.1159/000445027.
Pełny tekst źródłaTorpy, David J., Anthony W. Bachmann, Jeffrey E. Grice, Stephen P. Fitzgerald, Patrick J. Phillips, Judith A. Whitworth i Richard V. Jackson. "Familial Corticosteroid-Binding Globulin Deficiency Due to a Novel Null Mutation: Association with Fatigue and Relative Hypotension". Journal of Clinical Endocrinology & Metabolism 86, nr 8 (1.08.2001): 3692–700. http://dx.doi.org/10.1210/jcem.86.8.7724.
Pełny tekst źródłaAlcalay, R. N., A. Siderowf, R. Ottman, E. Caccappolo, H. Mejia-Santana, M. X. Tang, L. Rosado i in. "Olfaction in Parkin heterozygotes and compound heterozygotes: The CORE-PD study". Neurology 76, nr 4 (29.12.2010): 319–26. http://dx.doi.org/10.1212/wnl.0b013e31820882aa.
Pełny tekst źródłaYing, Ying, Xiao-Ming Liu, Amy Marble, Kirstie A. Lawson i Guang-Quan Zhao. "Requirement of Bmp8b for the Generation of Primordial Germ Cells in the Mouse". Molecular Endocrinology 14, nr 7 (1.07.2000): 1053–63. http://dx.doi.org/10.1210/mend.14.7.0479.
Pełny tekst źródłaKropp, Peter A., Jennifer C. Dunn, Bethany A. Carboneau, Doris A. Stoffers i Maureen Gannon. "Cooperative function of Pdx1 and Oc1 in multipotent pancreatic progenitors impacts postnatal islet maturation and adaptability". American Journal of Physiology-Endocrinology and Metabolism 314, nr 4 (1.04.2018): E308—E321. http://dx.doi.org/10.1152/ajpendo.00260.2017.
Pełny tekst źródłaKotchetkoff, Elaine Cristina de Almeida, Fabíola Isabel Suano de Souza, Fernando Luiz Affonso Fonseca, Sonia Hix, Sergio Aron Ajzen, David Carlos Shigueoka, Beatriz Tavares Costa Carvalho i Roseli Oselka Saccardo Sarni. "Assessing cardiovascular risk in ATM heterozygotes". Revista da Associação Médica Brasileira 64, nr 2 (luty 2018): 148–53. http://dx.doi.org/10.1590/1806-9282.64.02.148.
Pełny tekst źródłaMarx, Stephen J., i Ninet Sinaii. "Neonatal Severe Hyperparathyroidism: Novel Insights From Calcium, PTH, and the CASR Gene". Journal of Clinical Endocrinology & Metabolism 105, nr 4 (28.11.2019): 1061–78. http://dx.doi.org/10.1210/clinem/dgz233.
Pełny tekst źródłaGallant, E. M., J. R. Mickelson, B. D. Roggow, S. K. Donaldson, C. F. Louis i W. E. Rempel. "Halothane-sensitivity gene and muscle contractile properties in malignant hyperthermia". American Journal of Physiology-Cell Physiology 257, nr 4 (1.10.1989): C781—C786. http://dx.doi.org/10.1152/ajpcell.1989.257.4.c781.
Pełny tekst źródłaFelice, Alexander, Joseph Borg, Wilma Cassar, Ruth Galdies, Monica Pizzuto, Maryrose Caruana i Christian Scerri. "Hb F Malta I in Association with Hb F Sardinia (AyT) and Hb Valletta in Heterozygotes: Quantification of the Six Globins Suggests Developmental Control of the XMN-I Site and Interplay with the (AT)xTy Sequence in Connection with Globin Gene Switching." Blood 108, nr 11 (16.11.2006): 3830. http://dx.doi.org/10.1182/blood.v108.11.3830.3830.
Pełny tekst źródłaLozano, R., C. Ruiz Rejón i M. Ruiz Rejón. "Interchange polymorphism in natural populations of Allium paniculatum L. (Liliaceae): nature, frequency, effects, and mechanism of maintenance". Canadian Journal of Genetics and Cytology 28, nr 3 (1.06.1986): 348–57. http://dx.doi.org/10.1139/g86-052.
Pełny tekst źródłaWest, John D., i Jean H. Flockhart. "Non-additive inheritance of glucose phosphate isomerase activity in mice heterozygous at the Gpi-1s structural locus". Genetical Research 54, nr 1 (sierpień 1989): 27–36. http://dx.doi.org/10.1017/s0016672300028342.
Pełny tekst źródłaPittschieler, Klaus. "Heterozygotes and liver involvement". Acta Paediatrica 83, s393 (luty 1994): 21–23. http://dx.doi.org/10.1111/j.1651-2227.1994.tb13202.x.
Pełny tekst źródłaMitchell, SC. "Trimethylaminuria: susceptibility of heterozygotes". Lancet 354, nr 9196 (grudzień 1999): 2164–65. http://dx.doi.org/10.1016/s0140-6736(05)77067-7.
Pełny tekst źródłaDechant, Michael, Thomas Poellot, Ulrich Kunzendorf i Thomas Valerius. "Heterogeneous Expression of the 158V and 158F Alleles in FcγRIIIA Heterozygous Donors." Blood 104, nr 11 (16.11.2004): 1362. http://dx.doi.org/10.1182/blood.v104.11.1362.1362.
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