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... expression of YWHAQ (14-3-3-theta).  Homozygous 
Tiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumors
Tiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumors
Heidenblad, Markus; Lindgren, David; Jonson, Tord; Liedberg, Fredrik; Veerla, Srinivas; Chebil, Gunilla; Gudjonsson, Sigurdur; Borg, Åke; Månsson, Wiking; Höglund, Mattias
deletions were identified at 10 different ...
... progeny (and thereby ignored or considered  homozygous 
Microsatellite allele dose and configuration establishment (MADCE): an integrated approach for genetic studies in allopolyploids
Microsatellite allele dose and configuration establishment (MADCE): an integrated approach for genetic studies in allopolyploids
van Dijk, Thijs; Noordijk, Yolanda; Dubos, Tiphaine; Bink, Marco CAM; Meulenbroek, Bert J; Visser, Richard GF; van de Weg, Eric
when using conventional approaches), six ...
... carrying the restorer gene cassettes in  homozygous 
Intron hairpin and transitive RNAi mediated silencing of orfH522 transcripts restores male fertility in transgenic male sterile tobacco plants expressing orfH522
Intron hairpin and transitive RNAi mediated silencing of orfH522 transcripts restores male fertility in transgenic male sterile tobacco plants expressing orfH522
Nizampatnam, Narasimha Rao; Dinesh Kumar, Viswanathaswamy
condition were identified and crossed with ...
... individuals by increasing the frequency of  homozygous 
Identification of genomic regions associated with inbreeding depression in Holstein and Jersey dairy cattle
Identification of genomic regions associated with inbreeding depression in Holstein and Jersey dairy cattle
Pryce, Jennie E; Haile-Mariam, Mekonnen; Goddard, Michael E; Hayes, Ben J
deleterious recessive alleles. ...
... apparent), 8 of 50 dogs were found to be  homozygous 
A retrospective study of the prevalence of the canine degenerative myelopathy associated superoxide dismutase 1 mutation (SOD1:c.118G > A) in a referral population of German Shepherd dogs from the UK
A retrospective study of the prevalence of the canine degenerative myelopathy associated superoxide dismutase 1 mutation (SOD1:c.118G > A) in a referral population of German Shepherd dogs from the UK
Holder, Angela L; Price, James A; Adams, Jamie P; Volk, Holger A; Catchpole, Brian
and a further 19 were heterozygous for the ...
... status of a specific DNA fragment may be  homozygous 
On-chip HA/SSCP for the detection of hereditary haemochromatosis
On-chip HA/SSCP for the detection of hereditary haemochromatosis
Manage, Dammika P.; Zheng, Yao; Somerville, Martin J.; Backhouse, Christopher J.
mutant (both strands have the same ...
... for three times. Identification of  homozygous 
Accumulation of the azelaic acid-induced protein AZI1 affects lignin synthesis and deposition in Arabidopsis thaliana
Accumulation of the azelaic acid-induced protein AZI1 affects lignin synthesis and deposition in Arabidopsis thaliana
Gao, Hang; Wang, Xiao-Yan; Han, Yao-Yao; Du, Gai-Liang; Feng, Huan; Xu, Zi-Qin
T-DNA knockout, overexpressing and RNAi ...
... impairment of MTHFR activity for  homozygous 
Polymorphisms in the Methylenetetrahydrofolate Reductase Gene
Polymorphisms in the Methylenetetrahydrofolate Reductase Gene
Schwahn, Bernd; Rozen, Rima
mutant individuals. ...
... AS11 seed vs WT. Co-incident  homozygous 
Triacylglycerol synthesis by PDAT1 in the absence of DGAT1 activity is dependent on re-acylation of LPC by LPCAT2
Triacylglycerol synthesis by PDAT1 in the absence of DGAT1 activity is dependent on re-acylation of LPC by LPCAT2
Xu, Jingyu; Carlsson, Anders S; Francis, Tammy; Zhang, Meng; Hoffman, Travis; Giblin, Michael E; Taylor, David C
knockout lines of dgat1/lpcat2 exhibited ...
... 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. ...
... 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. ...
... 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 ...
... atherosclerosis. Methods Participants  Homozygous 
Monocytes of patients with familial hypercholesterolemia show alterations in cholesterol metabolism
Monocytes of patients with familial hypercholesterolemia show alterations in cholesterol metabolism
Mosig, Sandy; Rennert, Knut; Büttner, Petra; Krause, Siegfried; Lütjohann, Dieter; Soufi, Muhidien; Heller, Regine; Funke, Harald
and heterozygous FH patients with ...
... of the lung. Some studies suggest that  homozygous 
Prevalence of Variants in Methylenetetrahydrofolate Reductase and the Severity of Pulmonary Vascular Disease
Prevalence of Variants in Methylenetetrahydrofolate Reductase and the Severity of Pulmonary Vascular Disease
Day, R. W.; Mack, G. K.; Barker, A. M.; Rees, T. Q.; Jorgensen, L. O.; Botto, L. D.
677TT variants and compound heterozygous ...
... against the sheath blight disease. The  homozygous 
Transgene stacking and marker elimination in transgenic rice by sequential Agrobacterium-mediated co-transformation with the same selectable marker gene
Transgene stacking and marker elimination in transgenic rice by sequential Agrobacterium-mediated co-transformation with the same selectable marker gene
Ramana Rao, Mangu Venkata; Parameswari, Chidambaram; Sripriya, Rajasekaran; Veluthambi, Karuppannan
marker-free transgenic rice line CoT23 ...
... (75.9%). Of the PRA controls none are  homozygous 
A novel mutation in TTC8 is associated with progressive retinal atrophy in the golden retriever
A novel mutation in TTC8 is associated with progressive retinal atrophy in the golden retriever
Downs, Louise M; Wallin-Håkansson, Berit; Bergström, Tomas; Mellersh, Cathryn S
for the mutation, only 3.5% carry the ...
... affected and unaffected individuals were  homozygous 
Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation
Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation
Chograni, Manèl; Chaabouni, Myriam; Mâazoul, Faouzi; Bouzid, Hedi; Kraiem, Abdelhafid; Chaabouni, Habiba B Bouhamed
for the modified alleles. ...
... Reserve University. For the all alleles,  homozygous 
Progression of Inner Ear Pathology in Ames Waltzer Mice and the Role of Protocadherin 15 in Hair Cell Development
Progression of Inner Ear Pathology in Ames Waltzer Mice and the Role of Protocadherin 15 in Hair Cell Development
Pawlowski, Karen S.; Kikkawa, Yayoi S.; Wright, Charles G.; Alagramam, Kumar N.
males were crossed to heterozygous ...
... Tl st320 – Gp – – – – K Tl All lines were  homozygous 
Inheritance and genetic mapping of two nuclear genes involved in nuclear–cytoplasmic incompatibility in peas (Pisum sativum L.)
Inheritance and genetic mapping of two nuclear genes involved in nuclear–cytoplasmic incompatibility in peas (Pisum sativum L.)
Bogdanova, Vera S.; Galieva, Elvira R.; Yadrikhinskiy, Arseniy K.; Kosterin, Oleg E.
for the alleles indicated – not determined ...
... model: OR = 1.10, 95 % CI = 1.05–1.15;  homozygous 
Association between the XPD/ERCC2 Lys751Gln polymorphism and risk of cancer: evidence from 224 case–control studies
Association between the XPD/ERCC2 Lys751Gln polymorphism and risk of cancer: evidence from 224 case–control studies
Wu, Kai-Ge; He, Xiao-Feng; Li, Yun-Hui; Xie, Wei-Bin; Huang, Xi
model: OR = 1.14, 95 % CI = 1.08–1.21; ...
... augmented contractile response in humans  homozygous 
The Arg389Gly β1-adrenoceptor gene polymorphism influences the acute effects of β-adrenoceptor blockade on contractility in the human heart
The Arg389Gly β1-adrenoceptor gene polymorphism influences the acute effects of β-adrenoceptor blockade on contractility in the human heart
Huntgeburth, Michael; La Rosée, Karl; ten Freyhaus, Henrik; Böhm, Michael; Schnabel, Petra; Hellmich, Martin; Rosenkranz, Stephan
for the Arg389 allele. ...
... Case report Spastic diplegia 1 – –  Homozygous 
The genomic basis of cerebral palsy: a HuGE systematic literature review
The genomic basis of cerebral palsy: a HuGE systematic literature review
O’Callaghan, M. E.; MacLennan, A. H.; Haan, E. A.; Dekker, G.; The South Australian Cerebral Palsy Research Group
, severe acute chorioamnionitis FVL – – – ...
... in T 2 and T 3 generations, respectively.  Homozygous 
Establishment of homozygous transgenic rice lines after elimination of unlinked albino traits from transgenic events through segregation
Establishment of homozygous transgenic rice lines after elimination of unlinked albino traits from transgenic events through segregation
Parameswari, Chidambaram; Sripriya, Rajasekaran; Veluthambi, Karuppannan
transgenic plants free from the albino ...
... peritonitis are the most frequent signs of  homozygous 
The report of sequence analysis on familial Mediterranean fever gene (MEFV) in South-eastern Mediterranean region (Kahramanmaraş) of Turkey
The report of sequence analysis on familial Mediterranean fever gene (MEFV) in South-eastern Mediterranean region (Kahramanmaraş) of Turkey
Kilinc, Metin; Ganiyusufoglu, Eda; Sager, Hatice; Celik, Ahmet; Olgar, Seref; Cetin, Gozde Yildirim; Davutoglu, Mehmet; Altunoren, Orcun
M694V and combine heterozygous mutations. ...
... 68% of the SCD patients in the UAE were  homozygous 
Genetic Disorders in the United Arab Emirates
Genetic Disorders in the United Arab Emirates
Al-Gazali, Lihadh; Ali, Bassam R.
for the Saudi Arabian/Indian haplotype ...