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... and impaired panicle development in the  homozygous 
Agrobacterium T-DNA insertion in the rice DWARF SHOOT AND DEFECTIVE PANICLE1 (DSDP1) gene causes a severe dwarf phenotype, reduces plant vigour, and affects seed germination
Agrobacterium T-DNA insertion in the rice DWARF SHOOT AND DEFECTIVE PANICLE1 (DSDP1) gene causes a severe dwarf phenotype, reduces plant vigour, and affects seed germination
Basu, Debjani; Majhi, Bharat Bhusan; Sripriya, Rajasekaran; Veluthambi, Karuppannan
state. ...
... pure or complicated HSP resulting from  homozygous 
Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks
Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks
Souza, Paulo Victor Sgobbi; Rezende Pinto, Wladimir Bocca Vieira; Rezende Batistella, Gabriel Novaes; Bortholin, Thiago; Oliveira, Acary Souza Bulle
or compound heterozygous mutations in the ...
... 2,676,067 SNVs and 463,158 INDELs were  homozygous 
Whole genome sequencing of Guzerá cattle reveals genetic variants in candidate genes for production, disease resistance, and heat tolerance
Whole genome sequencing of Guzerá cattle reveals genetic variants in candidate genes for production, disease resistance, and heat tolerance
Rosse, Izinara C.; Assis, Juliana G.; Oliveira, Francislon S.; Leite, Laura R.; Araujo, Flávio; Zerlotini, Adhemar; Volpini, Angela; Dominitini, Anderson J.; Lopes, Beatriz C.; Arbex, Wagner A.; Machado, Marco A.; Peixoto, Maria G. C. D.; Verneque, Rui S.; Martins, Marta F.; Coimbra, Roney S.; Silva, Marcos V. G. B.; Oliveira, Guilherme; Carvalho, Maria Raquel S.
, not found in any database searched, and ...
... into the T2 generation when Cas9-free  homozygous 
CRISPR-Cas9 and CRISPR-Cpf1 mediated targeting of a stomatal developmental gene EPFL9 in rice
CRISPR-Cas9 and CRISPR-Cpf1 mediated targeting of a stomatal developmental gene EPFL9 in rice
Yin, Xiaojia; Biswal, Akshaya K.; Dionora, Jacqueline; Perdigon, Kristel M.; Balahadia, Christian P.; Mazumdar, Shamik; Chater, Caspar; Lin, Hsiang-Chun; Coe, Robert A.; Kretzschmar, Tobias; Gray, Julie E.; Quick, Paul W.; Bandyopadhyay, Anindya
mutants were obtained. ...
... (AC) for rs2283261; 14 % of patients were  homozygous 
ABCC8 Single Nucleotide Polymorphisms are Associated with Cerebral Edema in Severe TBI
ABCC8 Single Nucleotide Polymorphisms are Associated with Cerebral Edema in Severe TBI
Jha, Ruchira M.; Puccio, Ava M.; Okonkwo, David O.; Zusman, Benjamin E.; Park, Seo-Young; Wallisch, Jessica; Empey, Philip E.; Shutter, Lori A.; Clark, Robert S. B.; Kochanek, Patrick M.; Conley, Yvette P.
for the minor allele (CC, Table 2). ...
... between the lamina and leaf sheath of  homozygous 
Novel rice mutants overexpressing the brassinosteroid catabolic gene CYP734A4
Novel rice mutants overexpressing the brassinosteroid catabolic gene CYP734A4
Qian, Wenjing; Wu, Chao; Fu, Yaping; Hu, Guocheng; He, Zhengquan; Liu, Wenzhen
brd3-D, the wild type and d1. ...
... we identify 27 genes that have  homozygous 
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing
Jansen, Iris E.; Ye, Hui; Heetveld, Sasja; Lechler, Marie C.; Michels, Helen; Seinstra, Renée I.; Lubbe, Steven J.; Drouet, Valérie; Lesage, Suzanne; Majounie, Elisa; Gibbs, J. Raphael; Nalls, Mike A.; Ryten, Mina; Botia, Juan A.; Vandrovcova, Jana; Simon-Sanchez, Javier; Castillo-Lizardo, Melissa; Rizzu, Patrizia; Blauwendraat, Cornelis; Chouhan, Amit K.; Li, Yarong; Yogi, Puja; Amin, Najaf; van Duijn, Cornelia M.; Morris, Huw R.; Brice, Alexis; Singleton, Andrew B.; David, Della C.; Nollen, Ellen A.; Jain, Shushant; Shulman, Joshua M.; Heutink, Peter; International Parkinson’s Disease Genetics Consortium (IPGDC)
or compound heterozygous loss-of-function ...
... active cTBS in participants that were  homozygous 
Is prepulse modification altered by continuous theta burst stimulation? DAT1 genotype and motor threshold interact on prepulse modification following brain stimulation
Is prepulse modification altered by continuous theta burst stimulation? DAT1 genotype and motor threshold interact on prepulse modification following brain stimulation
Notzon, S.; Vennewald, N.; Gajewska, A.; Klahn, A. L.; Diemer, J.; Winter, B.; Fohrbeck, I.; Arolt, V.; Pauli, P.; Domschke, K.; Zwanzger, P.
carriers of the 10-repeat-allele of the ...
... PACAP weighed significantly less than  homozygous 
Early Neurobehavioral Development of Mice Lacking Endogenous PACAP
Early Neurobehavioral Development of Mice Lacking Endogenous PACAP
Farkas, Jozsef; Sandor, Balazs; Tamas, Andrea; Kiss, Peter; Hashimoto, Hitoshi; Nagy, Andras D.; Fulop, Balazs D.; Juhasz, Tamas; Manavalan, Sridharan; Reglodi, Dora
mice. ...
... yielded six single-copy transgenic lines.  Homozygous 
Enhancement of sheath blight tolerance in transgenic rice by combined expression of tobacco osmotin (ap24) and rice chitinase (chi11) genes
Enhancement of sheath blight tolerance in transgenic rice by combined expression of tobacco osmotin (ap24) and rice chitinase (chi11) genes
Sripriya, Rajasekaran; Parameswari, Chidambaram; Veluthambi, Karuppannan
T2 plants of all lines accumulated high ...
... immunodeficiency was reported to have a  homozygous 
Combined T- and B-Cell Immunodeficiencies
Combined T- and B-Cell Immunodeficiencies
Deist, Françoise; Moshous, Despina; Villa, Anna; Al-Herz, Waleed; Roifman, Chaim M.; Fischer, Alain; Notarangelo, Luigi D.
germ-line mutation of the gene encoding ...
... isolated from lymphocytes of eight ELA  homozygous 
Polymorphism at expressed DQ and DR loci in five common equine MHC haplotypes
Polymorphism at expressed DQ and DR loci in five common equine MHC haplotypes
Miller, Donald; Tallmadge, Rebecca L.; Binns, Matthew; Zhu, Baoli; Mohamoud, Yasmin Ali; Ahmed, Ayeda; Brooks, Samantha A.; Antczak, Douglas F.
horses. ...
... to investigate whether the sample was  homozygous 
Diversity of MHC class I alleles in Spheniscus humboldti
Diversity of MHC class I alleles in Spheniscus humboldti
Kikkawa, Eri; Tanaka, Masafumi; Naruse, Taeko K.; Tsuda, Tomi T.; Tsuda, Michio; Murata, Koichi; Kimura, Akinori
or heterozygous for the MHC class I ...
... A single copy, GFP-expressing line (  homozygous 
CRISPR/Cas9-mediated targeted mutagenesis in upland cotton (Gossypium hirsutum L.)
CRISPR/Cas9-mediated targeted mutagenesis in upland cotton (Gossypium hirsutum L.)
Janga, Madhusudhana R.; Campbell, LeAnne M.; Rathore, Keerti S.
, T3 generation) was used to test the ...
... chaperone in multicellular organisms. The  homozygous 
Sublethal endoplasmic reticulum stress caused by the mutation of immunoglobulin heavy chain-binding protein induces the synthesis of a mitochondrial protein, pyrroline-5-carboxylate reductase 1
Sublethal endoplasmic reticulum stress caused by the mutation of immunoglobulin heavy chain-binding protein induces the synthesis of a mitochondrial protein, pyrroline-5-carboxylate reductase 1
Jin, Hisayo; Komita, Mari; Koseki, Haruhiko; Aoe, Tomohiko
mutant BiP mice died within several hours ...
... selected resistant germplasm derived from  homozygous 
Discovery and introgression of the wild sunflower-derived novel downy mildew resistance gene Pl19 in confection sunflower (Helianthus annuus L.)
Discovery and introgression of the wild sunflower-derived novel downy mildew resistance gene Pl19 in confection sunflower (Helianthus annuus L.)
Zhang, Z. W.; Ma, G. J.; Zhao, J.; Markell, S. G.; Qi, L. L.
BC2F3 progeny provides a novel gene for ...
... recessive (AR) immunodeficiency caused by  homozygous 
Defects in Intrinsic and Innate Immunity: Receptors and Signaling Components
Defects in Intrinsic and Innate Immunity: Receptors and Signaling Components
Parvaneh, Nima; Lilic, Desa; Roesler, Joachim; Niehues, Tim; Casanova, Jean-Laurent; Picard, Capucine
or compound heterozygous mutation in HOIL1 ...
... folate deficient states [22]. Individuals  homozygous 
The impact of MTHFR 677 C/T genotypes on folate status markers: a meta-analysis of folic acid intervention studies
The impact of MTHFR 677 C/T genotypes on folate status markers: a meta-analysis of folic acid intervention studies
Colson, Natalie J.; Naug, Helen L.; Nikbakht, Elham; Zhang, Ping; McCormack, Joanna
for the mutation have significantly ...
... we found that the survival rate of  homozygous 
Important Roles of Ring Finger Protein 112 in Embryonic Vascular Development and Brain Functions
Important Roles of Ring Finger Protein 112 in Embryonic Vascular Development and Brain Functions
Tsou, Jen-Hui; Yang, Ying-Chen; Pao, Ping-Chieh; Lin, Hui-Ching; Huang, Nai-Kuei; Lin, Shih-Ting; Hsu, Kuei-Sen; Yeh, Che-Ming; Lee, Kuen-Haur; Kuo, Chu-Jen; Yang, De-Ming; Lin, Jiann-Her; Chang, Wen-Chang; Lee, Yi-Chao
Rnf112 knockout mice in 129/sv and C57BL/6 ...
... individuals. It was heterozygous in 64 and  homozygous 
Frequency of a natural truncated allele of MdMLO19 in the germplasm of Malus domestica
Frequency of a natural truncated allele of MdMLO19 in the germplasm of Malus domestica
Pessina, Stefano; Palmieri, Luisa; Bianco, Luca; Gassmann, Jennifer; van de Weg, Eric; Visser, Richard G. F.; Magnago, Pierluigi; Schouten, Henk J.; Bai, Yuling; Riccardo Velasco, R.; Malnoy, Mickael
in 25. ...
... in wild type mice and its absence in  homozygous 
Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice
Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice
Martinez-Garay, Isabel; Guidi, Luiz G.; Holloway, Zoe G.; Bailey, Melissa A. G.; Lyngholm, Daniel; Schneider, Tomasz; Donnison, Timothy; Butt, Simon J. B.; Monaco, Anthony P.; Molnár, Zoltán; Velayos-Baeza, Antonio
KO1 animals. ...
... state, included *28 (20 heterozygous, 8  homozygous 
Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory
Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory
Moyer, Ann M.; Skierka, Jennifer M.; Kotzer, Katrina E.; Kluge, Michelle L.; Black, John L.; Baudhuin, Linnea M.
), *16 (1 heterozygous), *3 (1 ...
... that have been currently identified in 172  homozygous 
Netherton Syndrome: A Genotype-Phenotype Review
Netherton Syndrome: A Genotype-Phenotype Review
Sarri, Constantina A.; Roussaki-Schulze, Angeliki; Vasilopoulos, Yiannis; Zafiriou, Efterpi; Patsatsi, Aikaterini; Stamatis, Costas; Gidarokosta, Polyxeni; Sotiriadis, Dimitrios; Sarafidou, Theologia; Mamuris, Zissis
or compound heterozygous patients from 144 ...
... dominant, recessive, heterozygous and  homozygous 
Associations between single-nucleotide polymorphisms and inflammatory bowel disease-associated colorectal cancers in inflammatory bowel disease patients: a meta-analysis
Associations between single-nucleotide polymorphisms and inflammatory bowel disease-associated colorectal cancers in inflammatory bowel disease patients: a meta-analysis
Li, H.; Jin, Z.; Li, X.; Wu, L.; Jin, J.
models) were used to analyze the ...
... significantly increased in carriers of  homozygous 
Driver mutations (JAK2V617F, MPLW515L/K or CALR), pentraxin-3 and C-reactive protein in essential thrombocythemia and polycythemia vera
Driver mutations (JAK2V617F, MPLW515L/K or CALR), pentraxin-3 and C-reactive protein in essential thrombocythemia and polycythemia vera
Lussana, Federico; Carobbio, Alessandra; Salmoiraghi, Silvia; Guglielmelli, Paola; Vannucchi, Alessandro Maria; Bottazzi, Barbara; Leone, Roberto; Mantovani, Alberto; Barbui, Tiziano; Rambaldi, Alessandro
JAK2V617F mutation compared to all the ...