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... to TH1-p.R202H). Whole brain extracts of  homozygous 
ICIEM Abstracts
ICIEM Abstracts
Th-ki/ki mice showed in the brain normal ...
... (FVL) and prothrombin mutation (PTM).  Homozygous 
Homozygous factor V Leiden and double heterozygosity for factor V Leiden and prothrombin mutation
Homozygous factor V Leiden and double heterozygosity for factor V Leiden and prothrombin mutation
Saemundsson, Ymir; Sveinsdottir, Signý Vala; Svantesson, Henrik; Svensson, Peter J.
FVL and PTM have long been feared ...
... approach to identify a subset of  homozygous 
An association-adjusted consensus deleterious scheme to classify homozygous Mis-sense mutations for personal genome interpretation
An association-adjusted consensus deleterious scheme to classify homozygous Mis-sense mutations for personal genome interpretation
Preeprem, Thanawadee; Gibson, Greg
non-synonymous single nucleotide ...
... used to lower lipid levels in adults with  homozygous 
Lomitapide: A Review of its Use in Adults with Homozygous Familial Hypercholesterolemia
Lomitapide: A Review of its Use in Adults with Homozygous Familial Hypercholesterolemia
Perry, Caroline M.
familial hypercholesterolemia, a rare, ...
... expressing the transgene in hemizygous and  homozygous 
Relative transgene expression frequencies in homozygous versus hemizygous transgenic mice
Relative transgene expression frequencies in homozygous versus hemizygous transgenic mice
Chang, Su-Ping; Opsahl, Margaret L.; Whitelaw, C. Bruce A.; Morley, Steven D.; West, John D.
mosaic 21OH/LacZ mouse adrenals and mosaic ...
... transgenic plants is the selection of  homozygous 
Fast-tracking development of homozygous transgenic cereal lines using a simple and highly flexible real-time PCR assay
Fast-tracking development of homozygous transgenic cereal lines using a simple and highly flexible real-time PCR assay
Mieog, Jos C; Howitt, Crispin A; Ral, Jean-Philippe
plants. ...
... eight cycles were done for couples with  homozygous 
Preimplation Diagnosis for Single-Gene Disorders
Preimplation Diagnosis for Single-Gene Disorders
Kuliev, Anver
or compound heterozygous male or female ...
... position is represented by "X” while a  homozygous 
iXora: exact haplotype inferencing and trait association
iXora: exact haplotype inferencing and trait association
Utro, Filippo; Haiminen, Niina; Livingstone, Donald, III; Cornejo, Omar E; Royaert, Stefan; Schnell, Raymond J; Motamayor, Juan Carlos; Kuhn, David N; Laxmi, Parida
position is chosen to be 0. ...
... markers to distinguish heterozygous from  homozygous 
Identification and fine-mapping of a QTL, qMrdd1, that confers recessive resistance to maize rough dwarf disease
Identification and fine-mapping of a QTL, qMrdd1, that confers recessive resistance to maize rough dwarf disease
Tao, Yongfu; Liu, Qingcai; Wang, Honghong; Zhang, Yanjun; Huang, Xinyi; Wang, Baobao; Lai, Jinsheng; Ye, Jianrong; Liu, Baoshen; Xu, Mingliang
genotypes at the six candidate regions. ...
... Heterozygous genotype 32.5–36.1 %, variant  homozygous 
Structural Genomic Variation in NOD-Like Receptors and Cancer
Structural Genomic Variation in NOD-Like Receptors and Cancer
Kutikhin, Anton G.; Yuzhalin, Arseniy E.
genotype 5.2–3.4 % 191 cases, 291 controls ...
... allele we call this site in the genotype  homozygous 
Maximum parsimony xor haplotyping by sparse dictionary selection
Maximum parsimony xor haplotyping by sparse dictionary selection
Elmas, Abdulkadir; Jajamovich, Guido H; Wang, Xiaodong
and denote it with the type of alleles in ...
... to the oocyte donor, or MHC-  homozygous 
Generation of Histocompatible Tissues via Parthenogenesis
Generation of Histocompatible Tissues via Parthenogenesis
Lampton, Paula W.; Newmark, Judith A.; Kiessling, Ann A.
and histocompatible to a significant ...
... Yeoh et al. [39]: Malays-  homozygous 
Current evidence for an inherited genetic basis of childhood acute lymphoblastic leukemia
Current evidence for an inherited genetic basis of childhood acute lymphoblastic leukemia
Urayama, Kevin Y.; Chokkalingam, Anand P.; Manabe, Atsushi; Mizutani, Shuki
, 0.65 (0.39–1.10); Chinese- ...
... constitution for LcyE5′TE. Genotypes with  homozygous 
Validation of the effects of molecular marker polymorphisms in LcyE and CrtRB1 on provitamin A concentrations for 26 tropical maize populations
Validation of the effects of molecular marker polymorphisms in LcyE and CrtRB1 on provitamin A concentrations for 26 tropical maize populations
Babu, Raman; Rojas, Natalia Palacios; Gao, Shibin; Yan, Jianbing; Pixley, Kevin
favorable CrtRB1-3′TE alleles had much ...
... disease signs when compared to mice  homozygous 
Spir2; a novel QTL on chromosome 4 contributes to susceptibility to pneumococcal infection in mice
Spir2; a novel QTL on chromosome 4 contributes to susceptibility to pneumococcal infection in mice
Wisby, Laura; Fernandes, Vitor E; Neill, Daniel R; Kadioglu, Aras; Andrew, Peter W; Denny, Paul
for BALB/c (p = 0.01) or CBA/Ca (p = ...
... revealed an overall mortality of 77.6%.  Homozygous 
Detection of the V1016G mutation in the voltage-gated sodium channel gene of Aedes aegypti (Diptera: Culicidae) by allele-specific PCR assay, and its distribution and effect on deltamethrin resistance in Thailand
Detection of the V1016G mutation in the voltage-gated sodium channel gene of Aedes aegypti (Diptera: Culicidae) by allele-specific PCR assay, and its distribution and effect on deltamethrin resistance in Thailand
Stenhouse, Steven A; Plernsub, Suriya; Yanola, Jintana; Lumjuan, Nongkran; Dantrakool, Anchalee; Choochote, Wej; Somboon, Pradya
1016G individuals survived at higher rates ...
... objective of this study was to analyze the  homozygous 
Biased Homozygous Haplotypes Across the Human Caveolin 1 Upstream Purine Complex in Parkinson’s Disease
Biased Homozygous Haplotypes Across the Human Caveolin 1 Upstream Purine Complex in Parkinson’s Disease
Darvish, Hossein; Heidari, Abolfazl; Hosseinkhani, Saman; Movafagh, Abolfazl; Khaligh, Ali; Jamshidi, Javad; Noorollahi-Moghaddam, Hamid; Heidari-Rostami, Hamid Reza; Karkheiran, Siamak; Shahidi, Gholam-Ali; Togha, Mansoureh; Paknejad, Seyed Mohammad Hassan; Ashrafian, Hossein; Abdi, Siamak; Firouzabadi, Saghar Ghasemi; Jamaldini, Seyed Hamid; Ohadi, Mina
haplotype compartment of the human ...
... the accurate determination of all the  homozygous 
Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC)
Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC)
Benigni, Michele; Battistini, Stefania; Ricci, Claudia
and heterozygous genotypes in 350 DNA ...
... five reads identified only a single novel  homozygous 
A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome
A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome
Pohl, Esther; Aykut, Ayca; Beleggia, Filippo; Karaca, Emin; Durmaz, Burak; Keupp, Katharina; Arslan, Esra; Onay, Melis Palamar; Yigit, Gökhan; Özkinay, Ferda; Wollnik, Bernd
variant, c.497G>T, located in PAX1 that ...
... greater risk of SRLV infection than those  homozygous 
Small ruminant lentivirus genetic subgroups associate with sheep TMEM154 genotypes
Small ruminant lentivirus genetic subgroups associate with sheep TMEM154 genotypes
Sider, Lucia H; Heaton, Michael P; Chitko-McKown, Carol G; Harhay, Greg P; Smith, Timothy PL; Leymaster, Kreg A; Laegreid, William W; Clawson, Michael L
with a lysine (K35) haplotype. ...
... We now report the first description of a  homozygous 
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia
Fratta, Pietro; Poulter, Mark; Lashley, Tammaryn; Rohrer, Jonathan D.; Polke, James M.; Beck, Jon; Ryan, Natalie; Hensman, Davina; Mizielinska, Sarah; Waite, Adrian J.; Lai, Mang-Ching; Gendron, Tania F.; Petrucelli, Leonard; Fisher, Elizabeth M. C.; Revesz, Tamas; Warren, Jason D.; Collinge, John; Isaacs, Adrian M.; Mead, Simon
patient and compare it to a series of ...
... Background The pathogenicity of the NPHS2  homozygous 
NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis
NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis
Kerti, Andrea; Csohány, Rózsa; Wagner, László; Jávorszky, Eszter; Maka, Erika; Tory, Kálmán
p.R229Q variant in steroid-resistant ...
... background, we first selected plants  homozygous 
Increased copy number at the HvFT1 locus is associated with accelerated flowering time in barley
Increased copy number at the HvFT1 locus is associated with accelerated flowering time in barley
Nitcher, Rebecca; Distelfeld, Assaf; Tan, ChorTee; Yan, Liuling; Dubcovsky, Jorge
for vrn-H1 and ...
... wild-type strain and a panel of strains  homozygous 
Assembly of a phased diploid Candida albicansgenome facilitates allele-specific measurements and provides a simple model for repeat and indel structure
Assembly of a phased diploid Candida albicansgenome facilitates allele-specific measurements and provides a simple model for repeat and indel structure
Muzzey, Dale; Schwartz, Katja; Weissman, Jonathan S; Sherlock, Gavin
for particular chromosomes. ...
... population carried an average of 1.35  homozygous 
Development of a next-generation NIL library in Arabidopsis thaliana for dissecting complex traits
Development of a next-generation NIL library in Arabidopsis thaliana for dissecting complex traits
Fletcher, Richard S; Mullen, Jack L; Yoder, Seth; Bauerle, William L; Reuning, Gretchen; Sen, Saunak; Meyer, Eli; Juenger, Thomas E; McKay, John K
and 2.49 heterozygous introgressions per ...