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... with SLE or lupus-like manifestations: (a)  homozygous 
Fetal and Neonatal Illnesses Caused or Influenced by Maternal Transplacental IgG and/or Therapeutic Antibodies Applied During Pregnancy
Fetal and Neonatal Illnesses Caused or Influenced by Maternal Transplacental IgG and/or Therapeutic Antibodies Applied During Pregnancy
Berencsi, György, III; Szomor, Katalin N.
deficiencies of the early components of ...
... the first year of life, infants with the  homozygous 
Cholestatic Syndromes in Childhood and Catch-Up Growth
Cholestatic Syndromes in Childhood and Catch-Up Growth
Pawlowska, Joanna; Socha, Piotr; Jankowska, Irena
Pi ZZ phenotype may temporarily show ...
... offsprings were crossed to generate  homozygous 
Lipocalin 2 alleviates iron toxicity by facilitating hypoferremia of inflammation and limiting catalytic iron generation
Lipocalin 2 alleviates iron toxicity by facilitating hypoferremia of inflammation and limiting catalytic iron generation
Xiao, Xia; Yeoh, Beng San; Saha, Piu; Olvera, Rodrigo Aguilera; Singh, Vishal; Vijay-Kumar, Matam
Lcn2KO mice and their WT littermates. ...
... described pronounced ALS-like features in  homozygous 
Metal-deficient SOD1 in amyotrophic lateral sclerosis
Metal-deficient SOD1 in amyotrophic lateral sclerosis
Hilton, James B.; White, Anthony R.; Crouch, Peter J.
, wild-type SOD1-overexpressing mice ...
... Vietnamese (Fukao et al. 2010). Patients  homozygous 
Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency
Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency
Abdelkreem, Elsayed; Akella, Radha Rama Devi; Dave, Usha; Sane, Sudhir; Otsuka, Hiroki; Sasai, Hideo; Aoyama, Yuka; Nakama, Mina; Ohnishi, Hidenori; Mahmoud, Shaimaa; Abd El Aal, Mohamed; Fukao, Toshiyuki
for p.Met193Arg have, in general, typical ...
... analysis on two glioma cell lines having  homozygous 
Glioblastoma Multiforme: Role of Polycomb Group Proteins
Glioblastoma Multiforme: Role of Polycomb Group Proteins
Facchino, Sabrina; Abdouh, Mohamed; Bernier, Gilbert
deletions of the INK4A/ARF locus. ...
... htt gene in mouse is lethal and embryos  homozygous 
Mitochondrial Dynamics and Huntington’s Disease: A Dance of Fate
Mitochondrial Dynamics and Huntington’s Disease: A Dance of Fate
Wang, Hongmin; Karbowski, Mariusz; Monteiro, Mervyn J.
for the deletion die by embryonic day 8.5 ...
... All three parents were shown to be highly  homozygous 
The abundance of homoeologue transcripts is disrupted by hybridization and is partially restored by genome doubling in synthetic hexaploid wheat
The abundance of homoeologue transcripts is disrupted by hybridization and is partially restored by genome doubling in synthetic hexaploid wheat
Hao, Ming; Li, Aili; Shi, Tongwei; Luo, Jiangtao; Zhang, Lianquan; Zhang, Xuechuan; Ning, Shunzong; Yuan, Zhongwei; Zeng, Deying; Kong, Xingchen; Li, Xiaolong; Zheng, Hongkun; Lan, Xiujin; Zhang, Huaigang; Zheng, Youliang; Mao, Long; Liu, Dengcai
on the basis of genotyping at 160 ...
... to be exceedingly high (77% inclusive of  homozygous 
Impact of Antiplatelet Therapy and Platelet Reactivity Testing on Cardiovascular Outcomes in Patients with Chronic Kidney Disease
Impact of Antiplatelet Therapy and Platelet Reactivity Testing on Cardiovascular Outcomes in Patients with Chronic Kidney Disease
Nathan, Sandeep; Conway, Brian
and heterozygous carriers) in elderly ...
... equal effect and two parental strains are  homozygous 
Genetic analysis of resistance to late leaf spot in interspecific groundnuts
Genetic analysis of resistance to late leaf spot in interspecific groundnuts
Pasupuleti, Janila; Ramaiah, Venuprasad; Rathore, Abhishek; Rupakula, Aruna; Reddy, R. Kanaka; Waliyar, Farid; Nigam, Shyam Narayan
for alternative alleles at all loci ...
... and Southard 1970). This mouse is  homozygous 
Differential Expression of Genes Involved in the Degeneration and Regeneration Pathways in Mouse Models for Muscular Dystrophies
Differential Expression of Genes Involved in the Degeneration and Regeneration Pathways in Mouse Models for Muscular Dystrophies
Onofre-Oliveira, P. C. G.; Santos, A. L. F.; Martins, P. M.; Ayub-Guerrieri, D.; Vainzof, M.
for the dystrophia-muscularis spontaneous ...
... between heterozygous and dominant  homozygous 
Genetic Divergence Detected by ISSR Markers and Characterization of Microsatellite Regions in Mytilus Mussels
Genetic Divergence Detected by ISSR Markers and Characterization of Microsatellite Regions in Mytilus Mussels
Varela, Miguel A.; González-Tizón, Ana; Mariñas, Luis; Martínez-Lage, Andrés
. ...
... and PEX26 c.292C>T mutation in its  homozygous 
Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthood
Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthood
Berendse, Kevin; Engelen, Marc; Ferdinandusse, Sacha; Majoie, Charles B. L. M.; Waterham, Hans R.; Vaz, Frédéric M.; Koelman, Johannes H. T. M.; Barth, Peter G.; Wanders, Ronald J. A.; Poll-The, Bwee Tien
form versus the more severe compound ...
... i is the frequency at SNP i for which the  homozygous 
A comparison of principal component regression and genomic REML for genomic prediction across populations
A comparison of principal component regression and genomic REML for genomic prediction across populations
Dadousis, Christos; Veerkamp, Roel F; Heringstad, Bjørg; Pszczola, Marcin; Calus, Mario PL
genotype is coded 2, calculated across all ...
... The CRH-KO mice were obtained by mating of  homozygous 
Corticotropin-Releasing Hormone Affects Short Immobilization Stress-Induced Changes in Lung Cytosolic and Membrane Glucocorticoid Binding Sites
Corticotropin-Releasing Hormone Affects Short Immobilization Stress-Induced Changes in Lung Cytosolic and Membrane Glucocorticoid Binding Sites
Benes, Jan; Tomankova, Hana; Novakova, Martina; Rohan, Zdeněk; Kvetnansky, Richard; Myslivecek, Jaromir
mice and the CRH–/– genotype was confirmed ...
... participants [48]. They suggested that a  homozygous 
Single nucleotide polymorphisms modify the transporter activity of ABCG2
Single nucleotide polymorphisms modify the transporter activity of ABCG2
Morisaki, Kuniaki; Robey, Robert W.; Özvegy-Laczka, Csilla; Honjo, Yasumasa; Polgar, Orsolya; Steadman, Kenneth; Sarkadi, Balázs; Bates, Susan E.
variant allele at this position may result ...
... visualize Rec7 and Rad51 foci. The  homozygous 
Meiotic recombination proteins localize to linear elements in Schizosaccharomyces pombe
Meiotic recombination proteins localize to linear elements in Schizosaccharomyces pombe
Lorenz, Alexander; Estreicher, Anna; Kohli, Jürg; Loidl, Josef
rec7::GFP strain was not like the wild ...
... patterns of inheritance [18]. Recently,  homozygous 
Multiple System Atrophy
Multiple System Atrophy
Levin, Johannes; Maaß, Sylvia; Schuberth, Madeleine; Höglinger, Günter
and compound heterozygous mutations in the ...
... The ‘ZUBajh97-01A’ line is the  homozygous 
BcMF13, a new reproductive organ-specific gene from Brassica rapa. ssp. chinensis, affects pollen development
BcMF13, a new reproductive organ-specific gene from Brassica rapa. ssp. chinensis, affects pollen development
Li, Yanyan; Cao, Jiashu; Huang, Li; Yu, Xiaolin; Xiang, Xun
(msms) male meiotic cytokinesis (mmc) ...
... 894G > T SNP) as compared to those who had  homozygous 
Endothelial nitric oxide synthase gene haplotypes and diabetic nephropathy among Asian Indians
Endothelial nitric oxide synthase gene haplotypes and diabetic nephropathy among Asian Indians
Ahluwalia, Tarunveer Singh; Ahuja, Monica; Rai, Taranjit Singh; Kohli, Harbir Singh; Sud, Kamal; Bhansali, Anil; Khullar, Madhu
wild-type alleles (P < 0.05, Table 7). ...
... c.1980A>G; p.Val660Val) in family 2 (  homozygous 
Identification of a Novel Deletion Mutation (c.1780delG) and a Novel Splice-Site Mutation (c.1412-1G>A) in the CCM1/KRIT1 Gene Associated with Familial Cerebral Cavernous Malformation in the Chinese Population
Identification of a Novel Deletion Mutation (c.1780delG) and a Novel Splice-Site Mutation (c.1412-1G>A) in the CCM1/KRIT1 Gene Associated with Familial Cerebral Cavernous Malformation in the Chinese Population
Yang, Chenlong; Zhao, Jizong; Wu, Bingquan; Zhong, Haohao; Li, Yan; Xu, Yulun
) and family 4 (heterozygous). ...
... co-workers has shown that a male subject  homozygous 
Gender-specific effect of physical training on AQP7 protein expression in human adipose tissue
Gender-specific effect of physical training on AQP7 protein expression in human adipose tissue
Lebeck, Janne; Østergård, Torben; Rojek, Aleksandra; Füchtbauer, Ernst-Martin; Lund, Sten; Nielsen, Søren; Praetorius, Jeppe
for a mutation in AQP7, which gives a ...
... inverted repeat (IR) into tobacco lines  homozygous 
Advances in Plant Gene Silencing Methods
Advances in Plant Gene Silencing Methods
Pandey, Prachi; Senthil-Kumar, Muthappa; Mysore, Kirankumar S.
for NOSpro-npt II gene lead to the ...
... This mutation was backcrossed and made  homozygous 
Natural and experimental evolution of sexual conflict within Caenorhabditis nematodes
Natural and experimental evolution of sexual conflict within Caenorhabditis nematodes
Palopoli, Michael F.; Peden, Colin; Woo, Caitlin; Akiha, Ken; Ary, Megan; Cruze, Lori; Anderson, Jennifer L.; Phillips, Patrick C.
into 12 different C. elegans natural ...
... genome contains many non-gene-family,  homozygous 
Chromosome level assembly of the hybrid Trypanosoma cruzi genome
Chromosome level assembly of the hybrid Trypanosoma cruzi genome
Weatherly, D Brent; Boehlke, Courtney; Tarleton, Rick L
genes (i.e. with only a single annotated ...