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... test, the exploratory activity of the  homozygous 
Targeted mutation of CCK2 receptor gene modifies the behavioural effects of diazepam in female mice
Targeted mutation of CCK2 receptor gene modifies the behavioural effects of diazepam in female mice
Raud, Sirli; Rünkorg, Kertu; Veraksitš, Alar; Reimets, Ain; Nelovkov, Aleksei; Abramov, Urho; Matsui, Toshimitsu; Bourin, Michel; Volke, Vallo; Kõks, Sulev; Vasar, Eero
(−/−) mice was significantly higher ...
... 10.5/F/W t(8;21) (AML-M2) t(11;16) 0/18/  homozygous 
Polymorphisms in the MLL breakpoint cluster region (BCR)
Polymorphisms in the MLL breakpoint cluster region (BCR)
Echlin-Bell, Deborah R.; Smith, Lydia L.; Li, Loretta; Strissel, Pamela L.; Strick, Reiner; Gupta, Vandana; Banerjee, Jhula; Larson, Richard; Relling, Mary V.; Raimondi, Susan C.; Hayashi, Yasuhide; Taki, Tomohiko; Zeleznik-Le, Nancy; Rowley, Janet D.
-(GAA)5/5 UC-2 17/F/B Hodgkin's disease ...
... 202T>C (2); Heterozygous 59T>G/202T>C (3);  Homozygous 
Lewis enzyme (α1–3/4 fucosyltransferase) polymorphisms do not explain the Lewis phenotype in the gastric mucosa of a Portuguese population
Lewis enzyme (α1–3/4 fucosyltransferase) polymorphisms do not explain the Lewis phenotype in the gastric mucosa of a Portuguese population
Serpa, Jacinta; Almeida, Raquel; Oliveira, Carla; Silva, Filipe Santos; Silva, Elisabete; Reis, Celso; Le Pendu, Jacques; Oliveira, Graça; Ribeiro, Luís Manuel Cunha; David, Leonor
59T>G (4); ...
... of the carotid artery system in Hoxa3  homozygous 
Disruption of the Hoxa3 homeobox gene results in anomalies of the carotid artery system and the arterial baroreceptors
Disruption of the Hoxa3 homeobox gene results in anomalies of the carotid artery system and the arterial baroreceptors
Kameda, Yoko; Watari-Goshima, Natsuko; Nishimaki, Toshiyuki; Chisaka, Osamu
mutant mice, in comparison with wild-type ...
... and also prevent the viability of animals  homozygous 
Analyzing the Function of Tumor Suppressor Genes Using a Drosophila Model
Analyzing the Function of Tumor Suppressor Genes Using a Drosophila Model
Pagliarini, Raymond A.; Quiñones, Ana T.; Xu, Tian
for the balancer chromosome. ...
... pain sensitivity in heterozygous (+/−) and  homozygous 
Altered pain sensitivity and morphine-induced anti-nociception in mice lacking CCK2 receptors
Altered pain sensitivity and morphine-induced anti-nociception in mice lacking CCK2 receptors
Veraksitš, Alar; Rünkorg, Kertu; Kurrikoff, Kaido; Raud, Sirli; Abramov, Urho; Matsui, Toshimitsu; Bourin, Michel; Kõks, Sulev; Vasar, Eero
(−/−) mice. ...
... GTGCGAGGTGAACAGG 3′. Genomic DNA from Pdt  homozygous 
A new mouse limb mutation identifies a Twist allele that requires interacting loci on Chromosome 4 for its phenotypic expression
A new mouse limb mutation identifies a Twist allele that requires interacting loci on Chromosome 4 for its phenotypic expression
Blanc, Isabelle; Bach, Antoine; Lallemand, Yvan; Perrin-Schmitt, Fabienne; Guénet, Jean-Louis; Robert, Benoît
mutant embryos was amplified. ...
... siblings of two heterozygous carriers were  homozygous 
Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family
Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family
Leal, Alejandro; Berghoff, Corinna; Berghoff, Martin; Del Valle, Gerardo; Contreras, Carlos; Montoya, Olga; Hernández, Erick; Barrantes, Ramiro; Schlötzer-Schrehardt, Ursula; Neundörfer, Bernhard; Reis, André; Rautenstrauss, Bernd; Heuss, Dieter
for this mutation. ...
... expression in advancing populations. The  homozygous 
Additive transgene expression and genetic introgression in multiple green-fluorescent protein transgenic crop × weed hybrid generations
Additive transgene expression and genetic introgression in multiple green-fluorescent protein transgenic crop × weed hybrid generations
Halfhill, M. D.; Millwood, R. J.; Weissinger, A. K.; Warwick, S. I.; Stewart, C. N., Jr
T1 single-locus insert GFP/Bacillus ...
... from Italy with NSHI, all of whom were  homozygous 
Connexin 26 35delG does not represent a mutational hotspot
Connexin 26 35delG does not represent a mutational hotspot
Rothrock, Caryn R.; Murgia, Alessandra; Sartorato, Edi L.; Leonardi, Emanuela; Wei, Sainan; Lebeis, Sarah L.; Yu, Laura E.; Elfenbein, Jill L.; Fisher, Rachel A.; Friderici, Karen H.
for the 35delG mutation, and 100 DNA ...
... all the other chromosomal regions were  homozygous 
Fine linkage mapping enables dissection of closely linked quantitative trait loci for seed dormancy and heading in rice
Fine linkage mapping enables dissection of closely linked quantitative trait loci for seed dormancy and heading in rice
Takeuchi, Y.; Lin, S. Y.; Sasaki, T.; Yano, M.
for Nipponbare. ...
... [4, 5, 6, 8, 15, 16], 9 appeared in the  homozygous 
Relations between molecular and biological abnormalities in 11 families from siblings affected with methylenetetrahydrofolate reductase deficiency
Relations between molecular and biological abnormalities in 11 families from siblings affected with methylenetetrahydrofolate reductase deficiency
Tonetti, Carole; Saudubray, Jean-Marie; Echenne, Bernard; Landrieu, Pierre; Giraudier, Stéphane; Zittoun, Jacqueline
state and the others were either in a ...
... exon 2 of MURR1 in our collection of 2-2  homozygous 
New haplotypes in the Bedlington terrier indicate complexity in copper toxicosis
New haplotypes in the Bedlington terrier indicate complexity in copper toxicosis
Coronado, Veronica A.; Damaraju, Deepti; Kohijoki, Ritva; Cox, Diane W.
affected terriers. ...
... alterations [mutation, hypermethylation,  homozygous 
Differential alterations of the genes in the CDKN2A-CCND1-CDK4-RB1 pathway are associated with the development of head and neck squamous cell carcinoma in Indian patients
Differential alterations of the genes in the CDKN2A-CCND1-CDK4-RB1 pathway are associated with the development of head and neck squamous cell carcinoma in Indian patients
Tripathi (Bhar), Anusri; Banerjee, Soma; Chunder, Neelanjana; Roy, Anup; Sengupta, Arunava; Roy, Bidyut; Roychowdhury, Susanta; Panda, Chinmay Kumar
deletion and loss of ...
... from five families) and crosses with  homozygous 
Inheritance of self-compatibility in almond: breeding strategies to assure self-compatibility in the progeny
Inheritance of self-compatibility in almond: breeding strategies to assure self-compatibility in the progeny
Ortega, E.; Dicenta, F.
self-compatible parents (62 descendants ...
... a 55–65°C temperature scan. To detect  homozygous 
Evaluation of Temperature Gradient Capillary Electrophoresis for Detection of the Factor V Leiden Mutation
Evaluation of Temperature Gradient Capillary Electrophoresis for Detection of the Factor V Leiden Mutation
Murphy, Kathleen M.; Hafez, Michael J.; Philips, Juliet; Yarnell, Kellie; Gutshall, Kevin R.; Berg, Karin D.
mutations, ...
... Among the 765 siblings, 20 (11 boys) were  homozygous 
The HLA-DR phenotype modulates the humoral immune response to enterovirus antigens
The HLA-DR phenotype modulates the humoral immune response to enterovirus antigens
Sadeharju, K.; Knip, M.; Hiltunen, M.; Åkerblom, H. K.; Hyöty, H.
for HLA-DR3, 9 (3 boys) for HLA-DR2, and ...
... These three groups represented clones  homozygous 
A fluorogenic 5′ nuclease (TaqMan) assay to assess dosage of a marker tightly linked to red skin color in autotetraploid potato
A fluorogenic 5′ nuclease (TaqMan) assay to assess dosage of a marker tightly linked to red skin color in autotetraploid potato
De Jong, W. S.; De Jong, D. M.; Bodis, M.
for the red allele, heterozygous for the ...
... exotic parent. At these marker loci the  homozygous 
Advanced backcross QTL analysis in barley (Hordeum vulgare L.)
Advanced backcross QTL analysis in barley (Hordeum vulgare L.)
Pillen, K.; Zacharias, A.; Léon, J.
Hsp genotype was associated with an ...
... that compound heterozygous (SAO/G701D) and  homozygous 
Anion exchanger 1 mutations associated with distal renal tubular acidosis in the Thai population
Anion exchanger 1 mutations associated with distal renal tubular acidosis in the Thai population
Yenchitsomanus, Pa-thai; Sawasdee, Nunghathai; Paemanee, Atchara; Keskanokwong, Thitima; Vasuvattakul, Somkiat; Bejrachandra, Sasitorn; Kunachiwa, Warunee; Fucharoen, Supan; Jittphakdee, Prapaporn; Yindee, Wanwimon; Promwong, Charupon
(G701D/G701D) mutations of the anion ...
... lanes 1 and 2 contained genomic DNA target  homozygous 
High accuracy genotyping directly from genomic DNA using a rolling circle amplification based assay
High accuracy genotyping directly from genomic DNA using a rolling circle amplification based assay
Alsmadi, Osama A; Bornarth, Carole J; Song, Wanmin; Wisniewski, Michele; Du, Jing; Brockman, Joel P; Faruqi, A Fawad; Hosono, Seiyu; Sun, Zhenyu; Du, Yuefen; Wu, Xiaohong; Egholm, Michael; Abarzúa, Patricio; Lasken, Roger S; Driscoll, Mark D
for the Factor V Leiden mutation (M), ...
... of 1,031 Atlantic salmon with 64 animals  homozygous 
MHC polymorphism and disease resistance in Atlantic salmon (Salmo salar); facing pathogens with single expressed major histocompatibility class I and class II loci
MHC polymorphism and disease resistance in Atlantic salmon (Salmo salar); facing pathogens with single expressed major histocompatibility class I and class II loci
Grimholt, Unni; Larsen, Stig; Nordmo, Rolf; Midtlyng, Paul; Kjoeglum, Sissel; Storset, Arne; Saebø, Solve; Stet, René J. M.
for Sasa-UBA and 373 ...
... high levels of γ, the SAD transgene became  homozygous 
Transgenic Mice and Hemoglobinopathies
Transgenic Mice and Hemoglobinopathies
Fabry, Mary E.; Bouhassira, Eric E.; Suzuka, Sandra M.; Nagel, Ronald L.
, suggesting that competition with γ had ...
... in all patients. One patient who was  homozygous 
Identification of pathogenic mutations in the human rapsyn gene
Identification of pathogenic mutations in the human rapsyn gene
Dunne, Vanessa; Maselli, Ricardo A.
for N88K was only mildly affected, while ...
... and yet no phenotype was observed in mice  homozygous 
Gene trap mutagenesis of hnRNP A2/B1: a cryptic 3' splice site in the neomycin resistance gene allows continued expression of the disrupted cellular gene
Gene trap mutagenesis of hnRNP A2/B1: a cryptic 3' splice site in the neomycin resistance gene allows continued expression of the disrupted cellular gene
Roshon, Michael; DeGregori, James V; Ruley, H Earl
for the provirus. ...