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... study, the methods to identify non-  homozygous 
Assessment of wheat variety stability using SSR markers
Assessment of wheat variety stability using SSR markers
Wang, Li Xin; Li, Hong Bo; Gu, Tie Cheng; Liu, Li Hua; Pang, Bin Shuang; Qiu, Jun; Zhao, Chang Ping
SSR loci and calculate the ...
... from TLR2 and TLR4. These individuals are  homozygous 
ESID 2014 ORAL PRESENTATIONS
ESID 2014 ORAL PRESENTATIONS
for a loss-of-function TIRAP allele. ...
... and osteopenia were revealed in the  homozygous 
Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice
Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice
Kemter, Elisabeth; Rathkolb, Birgit; Becker, Lore; Bolle, Ines; Busch, Dirk H; Dalke, Claudia; Elvert, Ralf; Favor, Jack; Graw, Jochen; Hans, Wolfgang; Ivandic, Boris; Kalaydjiev, Svetoslav; Klopstock, Thomas; Rácz, Ildikó; Rozman, Jan; Schrewe, Anja; Schulz, Holger; Zimmer, Andreas; Fuchs, Helmut; Gailus-Durner, Valérie; de Angelis, Martin Hrabé; Wolf, Eckhard; Aigner, Bernhard
mutant mice which were also described in ...
... of the mutated GmKASIIIA gene. Lines  homozygous 
Mapping the low palmitate fap1 mutation and validation of its effects in soybean oil and agronomic traits in three soybean populations
Mapping the low palmitate fap1 mutation and validation of its effects in soybean oil and agronomic traits in three soybean populations
Cardinal, Andrea J.; Whetten, Rebecca; Wang, Sanbao; Auclair, Jérôme; Hyten, David; Cregan, Perry; Bachlava, Eleni; Gillman, Jason; Ramirez, Martha; Dewey, Ralph; Upchurch, Greg; Miranda, Lilian; Burton, Joseph W.
for the GmKASIIIA mutation (fap1) had a ...
... peripheral and central auditory pathways.  Homozygous 
Hearing Loss is an Early Consequence of Npc1 Gene Deletion in the Mouse Model of Niemann–Pick Disease, Type C
Hearing Loss is an Early Consequence of Npc1 Gene Deletion in the Mouse Model of Niemann–Pick Disease, Type C
King, Kelly A.; Gordon-Salant, Sandra; Pawlowski, Karen S.; Taylor, Anna M.; Griffith, Andrew J.; Houser, Ari; Kurima, Kiyoto; Wassif, Christopher A.; Wright, Charles G.; Porter, Forbes D.; Repa, Joyce J.; Brewer, Carmen C.
mutant Npc1 nih mice on a Balb/c ...
... displayed male sterile phenotype in the  homozygous 
A novel T-DNA integration in rice involving two interchromosomal translocations
A novel T-DNA integration in rice involving two interchromosomal translocations
Majhi, Bharat Bhusan; Shah, Jasmine M.; Veluthambi, Karuppannan
condition. ...
... deletions. Average stearic acid in lines  homozygous 
Effect of Δ9-stearoyl-ACP-desaturase-C mutants in a high oleic background on soybean seed oil composition
Effect of Δ9-stearoyl-ACP-desaturase-C mutants in a high oleic background on soybean seed oil composition
Ruddle, Paul, II; Whetten, Rebecca; Cardinal, Andrea; Upchurch, Robert G.; Miranda, Lilian
for the deletions was 12.2 %. ...
... and ApoE ε4/ε4 homozygosity an ApoE ε4/ε4  homozygous 
A large ApoE ε4/ε4 homozygous cohort reveals no association with Parkinson’s disease
A large ApoE ε4/ε4 homozygous cohort reveals no association with Parkinson’s disease
Multhammer, Manuel; Michels, Andreas; Zintl, Maria; Mendoza, Maria Cristina; Klünemann, Hans-Hermann
cohort was compared with an ApoE ε3/ε3 ...
... resistant genetic background, in either  homozygous 
The plant genetic background affects the efficiency of the pepper major nematode resistance genes Me1 and Me3
The plant genetic background affects the efficiency of the pepper major nematode resistance genes Me1 and Me3
Barbary, A.; Palloix, A.; Fazari, A.; Marteu, N.; Castagnone-Sereno, P.; Djian-Caporalino, C.
or heterozygous allelic status. ...
... 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 ...
... (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 ...
... 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; ...
... pharmacotherapy with disulfiram, while CC  homozygous 
Pharmacogenetics of Addiction Therapy
Pharmacogenetics of Addiction Therapy
Nielsen, David A.; Nielsen, Ellen M.; Dasari, Teja; Spellicy, Catherine J.
individuals, those carrying two copies of ...
... form of the disease (Table 1). Thus, while  homozygous 
Towards the targeted management of Chediak-Higashi syndrome
Towards the targeted management of Chediak-Higashi syndrome
Lozano, Maria L; Rivera, Jose; Sánchez-Guiu, Isabel; Vicente, Vicente
or bi-allelic missense mutations are ...
... population was created using selected  homozygous 
Fine mapping of a preharvest sprouting QTL interval on chromosome 2B in white wheat
Fine mapping of a preharvest sprouting QTL interval on chromosome 2B in white wheat
Somyong, Suthasinee; Ishikawa, Goro; Munkvold, Jesse D.; Tanaka, James; Benscher, David; Cho, Yong-Gu; Sorrells, Mark E.
recombinant BC1F4 and BC1F5 lines (Fig. 1; ...
... higher risks of SRNS in individuals  homozygous 
The p.R229Q variant of the NPHS2 (podocin) gene in focal segmental glomerulosclerosis and steroid-resistant nephrotic syndrome: a meta-analysis
The p.R229Q variant of the NPHS2 (podocin) gene in focal segmental glomerulosclerosis and steroid-resistant nephrotic syndrome: a meta-analysis
Lu, Lu; Wan, Heng; Yin, Yi; Feng, Wen-Jun; Wang, Ming; Zou, Yu-Cong; Huang, Bo; Wang, Dong-Tao; Shi, Yin; Zhao, Yan; Wei, Lian-Bo
for the variant allele (OR 7.411, 95 % ...
... increase in root system biomass in  homozygous 
The effect of altered dosage of a mutant allele of Teosinte branched 1 (tb1-ref) on the root system of modern maize
The effect of altered dosage of a mutant allele of Teosinte branched 1 (tb1-ref) on the root system of modern maize
Gaudin, Amelie CM; McClymont, Sarah A; Soliman, Sameh SM; Raizada, Manish N
tb1-ref mutants balanced the increase in ...
... unclear. Methods and results We found a  homozygous 
Homozygous deletion of the activin A receptor, type IB gene is associated with an aggressive cancer phenotype in pancreatic cancer
Homozygous deletion of the activin A receptor, type IB gene is associated with an aggressive cancer phenotype in pancreatic cancer
Togashi, Yosuke; Sakamoto, Hiroki; Hayashi, Hidetoshi; Terashima, Masato; de Velasco, Marco A; Fujita, Yoshihiko; Kodera, Yasuo; Sakai, Kazuko; Tomida, Shuta; Kitano, Masayuki; Ito, Akihiko; Kudo, Masatoshi; Nishio, Kazuto
deletion of the activin A receptor, type ...
... were 23,767 germline mutations (9,067 in  homozygous 
Whole exome sequencing of a single osteosarcoma case—integrative analysis with whole transcriptome RNA-seq data
Whole exome sequencing of a single osteosarcoma case—integrative analysis with whole transcriptome RNA-seq data
Reimann, Ene; Kõks, Sulev; Ho, Xuan Dung; Maasalu, Katre; Märtson, Aare
form and 14,700 in heterozygous form) and ...
... or -6-bp/+6-bp; High expression:TS,  homozygous 
Polymorphisms in Genes of Drug Targets and Metabolism
Polymorphisms in Genes of Drug Targets and Metabolism
Bohanes, Pierre; Lenz, Heinz-Josef
3R with any 3’-UTR genotype and 2R/3R with ...
... disease course in patients with a  homozygous 
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations
Eggens, Veerle RC; Barth, Peter G; Niermeijer, Jikke-Mien F; Berg, Jonathan N; Darin, Niklas; Dixit, Abhijit; Fluss, Joel; Foulds, Nicola; Fowler, Darren; Hortobágyi, Tibor; Jacques, Thomas; King, Mary D; Makrythanasis, Periklis; Máté, Adrienn; Nicoll, James AR; O’Rourke, Declan; Price, Sue; Williams, Andrew N; Wilson, Louise; Suri, Mohnish; Sztriha, Laszlo; Dijns-de Wissel, Marit B; van Meegen, Mia T; van Ruissen, Fred; Aronica, Eleonora; Troost, Dirk; Majoie, Charles BLM; Marquering, Henk A; Poll-Thé, Bwee Tien; Baas, Frank
p.D132A mutation. ...
... lines (IL) are near-isogenic lines  homozygous 
Characterization and mapping of a QTL derived from Solanum habrochaites associated with elevated rutin content (quercetin-3-rutinoside) in tomato
Characterization and mapping of a QTL derived from Solanum habrochaites associated with elevated rutin content (quercetin-3-rutinoside) in tomato
Hanson, Peter; Schafleitner, Roland; Huang, Shu-Mei; Tan, Chee-Wee; Ledesma, Dolores; Yang, Ray-Yu
for one or several mapped wild DNA ...
... breeds. None of the unaffected animals was  homozygous 
A nonsense mutation in PLD4 is associated with a zinc deficiency-like syndrome in Fleckvieh cattle
A nonsense mutation in PLD4 is associated with a zinc deficiency-like syndrome in Fleckvieh cattle
Jung, Simone; Pausch, Hubert; Langenmayer, Martin C; Schwarzenbacher, Hermann; Majzoub-Altweck, Monir; Gollnick, Nicole S; Fries, Ruedi
for the defect allele, while all eight ...
... as to the Ala499Val polymorphism in the  homozygous 
XPC gene polymorphisms contribute to bladder cancer susceptibility: a meta-analysis
XPC gene polymorphisms contribute to bladder cancer susceptibility: a meta-analysis
Dai, Qiang-Sheng; Hua, Rui-Xi; Zeng, Rui-Fang; Long, Jian-Ting; Peng, Zhen-Wei
and recessive models. ...