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... tomography scan was greater in  homozygous 
b3-adrenergic-receptor polymorphism: a genetic marker for visceral fat obesity and the insulin resistance syndrome
b3-adrenergic-receptor polymorphism: a genetic marker for visceral fat obesity and the insulin resistance syndrome
Sakane, N.; Yoshida, T.; Umekawa, T.; Kondo, M.; Sakai, Y.; Takahashi, T.
Arg64Arg (172 ± 17 cm2, n = 6) and ...
... heterozygous for the transgene. To create  homozygous 
Transgenic Animals as Bioreactors for Expression of Recombinant Proteins
Transgenic Animals as Bioreactors for Expression of Recombinant Proteins
Khillan, Jaspal S.
lines, heterozygous progeny are ...
... or impaired glucose tolerance, subjects  homozygous 
Association between Ala54Thr substitution of the fatty acid-binding protein 2 gene with insulin resistance and intra-abdominal fat thickness in Japanese men
Association between Ala54Thr substitution of the fatty acid-binding protein 2 gene with insulin resistance and intra-abdominal fat thickness in Japanese men
Yamada, K.; Yuan, X.; Ishiyama, S.; Koyama, K.; Ichikawa, F.; Koyanagi, A.; Koyama, W.; Nonaka, K.
for the Thr54 allele had higher basal ...
... phenotype, haemochromatosis patients  homozygous 
Phenotype-genotype correlation in haemochromatosis subjects
Phenotype-genotype correlation in haemochromatosis subjects
Mura, C.; Nousbaum, Jean-Baptiste; Verger, Paul; Moalic, Marie-Thèrèse; Raguenes, Odile; Mercier, Anne-Yvonne; Ferec, Claude
for the substitution (Tyr/Tyr) accounting ...
... mice, which were then used to produce mice  homozygous 
Cre-mediated generation of a VCAM-1 null allele in transgenic mice
Cre-mediated generation of a VCAM-1 null allele in transgenic mice
Terry, ROBERT W.; Kwee, LIA; Scott BALDWIN, H.; Labow, MARK A.
for the VCAM-1 conditional null, or floxed ...
... Three patients in two generations show  homozygous 
Different entities of proximal spinal muscular atrophy within one family
Different entities of proximal spinal muscular atrophy within one family
Wirth, B.; Tessarolo, D.; Hahnen, E.; Rudnik-Schöneborn, S.; Raschke, H.; Liguori, M.; Giacanelli, M.; Zerres, K.
deletions of exons 7 and 8 of the ...
... A  homozygous 
Peculiarities of the GSTM1 0/0 genotype in French heavy smokers with various types of chronic bronchitis
Peculiarities of the GSTM1 0/0 genotype in French heavy smokers with various types of chronic bronchitis
Baranova, H.; Perriot, J.; Albuisson, E.; Ivaschenko, T.; Baranov, V. S.; Hemery, B.; Mouraire, P.; Riol, N.; Malet, Paul
gene deletion of the glutathione ...
... CaMV 35S promoter is silenced in the T17  homozygous 
Silencing of a β-1,3-glucanase transgene is overcome during seed formation
Silencing of a β-1,3-glucanase transgene is overcome during seed formation
Balandin, Teresa; Castresana, Carmen
tobacco transgenic line. ...
... in vivo lipolysis in individuals  homozygous 
No effect of the Trp64Arg β3-adrenoceptor variant on in vivo lipolysis in subcutaneous adipose tissue
No effect of the Trp64Arg β3-adrenoceptor variant on in vivo lipolysis in subcutaneous adipose tissue
Snitker, S.; Odeleye, O. E.; Hellmér, J.; Boschmann, M.; Monroe, M. B.; Shuldiner, A. R.; Ravussin, E.
for the ’variant' allele coding for ...
... hyperandrogenic subjects suspected to be  homozygous 
Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic women
Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic women
Blanché, Hélène; Vexiau, Patrick; Clauin, Séverine; Le Gall, Isabelle; Fiet, Jean; Mornet, Etienne; Dausset, Jean; Bellanné-Chantelott, Christine
or heterozygous for NC 21-OH deficiency, ...
... was matched by sex and age to a patient  homozygous 
Genotype-phenotype correlation in cystic fibrosis patients compound heterozygous for the A455E mutation
Genotype-phenotype correlation in cystic fibrosis patients compound heterozygous for the A455E mutation
De Braekeleer, M.; Allard, Christian; Leblanc, Jean-Pierre; Simard, Fernand; Aubin, Gervais
for the ΔF508 mutation. ...
... dopaminergic neurons. Animals  homozygous 
In vitro evidence that the reduction in mesencepalic dopaminergic neurons in the weaver heterozygote is not due to a failure in target cell interaction
In vitro evidence that the reduction in mesencepalic dopaminergic neurons in the weaver heterozygote is not due to a failure in target cell interaction
Won, Lisa; Ghetti, Bernardino; Heller, Barbara; Heller, A.
for the wv gene exhibit marked deficits in ...
... Summary We report a  homozygous 
A homozygous kinase-defective mutation in the insulin receptor gene in a patient with leprechaunism
A homozygous kinase-defective mutation in the insulin receptor gene in a patient with leprechaunism
Takahashi, Y.; Kadowaki, H.; Momomura, K.; Fukushima, Y.; Orban, T.; Okai, T.; Taketani, Y.; Akanuma, Y.; Yazaki, Y.; Kadowaki, T.
missense mutation at position 1092 ...
... anaemia. In addition, the patient is  homozygous 
Methionine synthase deficiency without megaloblastic anaemia
Methionine synthase deficiency without megaloblastic anaemia
Kvittingen, E. A.; Spangen, S.; Lindemans, J.; Fowler, B.
for the C677T polymorphism in the 5,10 ...
... respectively. Results: Ten subjects were  homozygous 
Genetic polymorphism of CYP2C19 and lansoprazole pharmacokinetics in Japanese subjects
Genetic polymorphism of CYP2C19 and lansoprazole pharmacokinetics in Japanese subjects
Katsuki, H.; Nakamura, C.; Arimori, K.; Fujiyama, S.; Nakano, M.
(wt/wt subjects) for the wt allele in both ...
... or crosses with non-transformed plants of  homozygous 
Occasional loss of expression of phosphinothricin tolerance in sexual offspring of transgenic oilseed rape (Brassica napus L.)
Occasional loss of expression of phosphinothricin tolerance in sexual offspring of transgenic oilseed rape (Brassica napus L.)
Metz, Peter L.J.; Jacobsen, Evert; Stiekema, Willem J.
transgenic oilseed rape plants if the ...
... sites in transplantable organs. Currently,  homozygous 
Analysis of transgene integration sites in transgenic pigs by fluorescence in situ hybridization
Analysis of transgene integration sites in transgenic pigs by fluorescence in situ hybridization
Kuipers, Henriette W.; Langford, Gillian A.; White, David J.G.
lines have been produced as well as lines ...
... and three adult galactosemic subjects,  homozygous 
Quantitative assessment of whole body galactose metabolism in galactosemic patients
Quantitative assessment of whole body galactose metabolism in galactosemic patients
Berry, G. T.; Nissim, I.; Gibson, J. B.; Mazur, A. T.; Lin, Z.; Elsas, L. J.; Singh, R. H.; Klein, P. D.; Segal, S.
for the most common GALT gene defect, the ...
...  Homozygous 
Manganese metabolism is impaired in the Belgrade laboratory rat
Manganese metabolism is impaired in the Belgrade laboratory rat
Chua, Anita C. G.; Morgan, Evan H.
Belgrade rats have a hypochromic anaemia ...
... heterozygous Pax6 Sey-Neu /Pax6 Sey and  homozygous 
Genetic background effects on dental and other craniofacial abnormalities in homozygous small eye (Pax6Sey/Pax6Sey) mice
Genetic background effects on dental and other craniofacial abnormalities in homozygous small eye (Pax6Sey/Pax6Sey) mice
Quinn, Jane C.; West, John D.; Kaufman, M. H.
Pax6 Sey /Pax6 Sey fetuses from several ...
... of their disease fully explained: 7 were  homozygous 
Primary hyperoxaluria type 1: Diagnostic relevance of mutations and polymorphisms in the alanine:glyoxylate aminotransferase gene (AGXT)
Primary hyperoxaluria type 1: Diagnostic relevance of mutations and polymorphisms in the alanine:glyoxylate aminotransferase gene (AGXT)
Tarn, A. C.; von Schnakenburg, C.; Rumsby, G.
for the G630A mutation, 5 were ...
... all three genotypes measured at 20 s: for  homozygous 
The intrinsic Clconductance of mouse kidney cortex brush-border membrane vesicles is not related to CFTR
The intrinsic Clconductance of mouse kidney cortex brush-border membrane vesicles is not related to CFTR
King, N.; Colledge, W. H.; Ratcliff, R.; Evans, M. J.; Simmons, N. L.
–/– animals [14C]glucose uptake was ...
... The  homozygous 
Development of cerebellar hypoplasia in jaundiced Gunn rats: a quantitative light microscopic analysis
Development of cerebellar hypoplasia in jaundiced Gunn rats: a quantitative light microscopic analysis
Conlee, John W.; Shapiro, S. M.
(jj) Gunn rat provides a model for ...
... chromosomes. Almost all the patients  homozygous 
Mutation and haplotype analyses of the Werner’s syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population
Mutation and haplotype analyses of the Werner’s syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population
Matsumoto, Takehisa; Imamura, Osamu; Yamabe, Yukako; Kuromitsu, Junro; Tokutake, Yoshiki; Shimamoto, Akira; Suzuki, Noriyuki; Satoh, Misako; Kitao, Saori; Ichikawa, Koji; Kataoka, Hiroshi; Sugawara, Kahori; Thomas, Winston; Mason, Brian; Tsuchihashi, Zenta; Drayna, D.; Sugawara, Minoru; Sugimoto, Masanobu; Furuichi, Y.; Goto, Makoto
for mutation 4 shared a haplotype around ...
... reductase (MTHFR) is a  homozygous 
Thermolabile Methylenetetrahydrofolate Reductase
Thermolabile Methylenetetrahydrofolate Reductase
Kang, Soo-Sang; Passen, Edward L.; Kim, Myunghee H.; Ruggie, Neal
genetic defect that is defined by its in ...