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... of diabetic nephropathy, with individuals  homozygous 
ACE Gene Polymorphism and Diabetic Complications
ACE Gene Polymorphism and Diabetic Complications
Kennon, Brian; Connell, John M. C.
for the deletion allele (DD) having a ...
... mice are then mated to generate the  homozygous 
Tissue-Specific KO of ECM Proteins
Tissue-Specific KO of ECM Proteins
Hirsch, Emilio; Brancaccio, Mara; Altruda, Fiorella
offspring needed for phenotypic analysis. ...
... Syndrome or strain Heterozyous phenotype  Homozygous 
Pax3 and Vertebrate Development
Pax3 and Vertebrate Development
Epstein, Jonathan A.
phenotype Human Waardenburg syndrome ...
... us to produce isogenic, transgenic,  homozygous 
Isogenic Transgenic Homozygous Fish Induced by Artificial Parthenogenesis
Isogenic Transgenic Homozygous Fish Induced by Artificial Parthenogenesis
Nam, Yoon Kwon; Cho, Young Sun; Kim, Dong Soo
vertebrates by combining with ...
... into three groups that are heterozygous or  homozygous 
An allele of the 1-aminocyclopropane-1-carboxylate synthase gene (Md-ACS1) accounts for the low level of ethylene production in climacteric fruits of some apple cultivars
An allele of the 1-aminocyclopropane-1-carboxylate synthase gene (Md-ACS1) accounts for the low level of ethylene production in climacteric fruits of some apple cultivars
Harada, T.; Sunako, T.; Wakasa, Y.; Soejima, J.; Satoh, T.; Niizeki, M.
for the ACS1–1 and ACS1–2 alleles. ...
... by mutations in the LDL receptor [7].  Homozygous 
Gene therapy for lipid disorders
Gene therapy for lipid disorders
Kawashiri, Masa-aki; Rader, Daniel J
FH, owing to mutations in both LDL ...
... DNA of the following genotypes: (1)  Homozygous 
The Use of Immobilized Mismatch Binding Protein in Mutation/SNP Detection
The Use of Immobilized Mismatch Binding Protein in Mutation/SNP Detection
Wagner, Robert; Dean, Alan
wild-type (WT/WT); (2) ...
... polymorphism, 83 probands (76.1 %) were  homozygous 
The tumour necrosis factor alpha –238 G → A and –308 G → A promoter polymorphisms are not associated with insulin sensitivity and insulin secretion in young healthy relatives of Type II Diabetic patients
The tumour necrosis factor alpha –238 G → A and –308 G → A promoter polymorphisms are not associated with insulin sensitivity and insulin secretion in young healthy relatives of Type II Diabetic patients
Koch, M.; Rett, K.; Volk, A.; Maerker, E.; Haist, K.; Weisser, M.; Rettig, A.; Renn, W.; Häring, H. U.
for the G-allele, 25 probands (22.9 %) ...
... by Crithidia immunofluorescence. Of the 30  homozygous 
Autoimmunity in IgM-deficient mice
Autoimmunity in IgM-deficient mice
Putterman, Chaim
sIgM knockout mice, 9 developed ...
... phase following the selection of  homozygous 
Strategies to optimize marker-assisted introgression of multiple unlinked QTL
Strategies to optimize marker-assisted introgression of multiple unlinked QTL
Koudandé, O. Delphin; Iraqi, Fuad; Thomson, Peter C.; Teale, Alan J.; van Arendonk, Johan A.M.
animals at the three QTL as an intercross ...
... phenotype and molecular analysis, several  homozygous 
Field performance of Xa21 transgenic indica rice (Oryza sativa L.), IR72
Field performance of Xa21 transgenic indica rice (Oryza sativa L.), IR72
Tu, J.; Datta, K.; Khush, G. S.; Zhang, Q.; Datta, S.K.
lines carrying Xa21 against the bacterial ...
... parotid, kidney and small intestine RNA in  homozygous 
SLE and Dnase1-deficient mice
SLE and Dnase1-deficient mice
Pickering, Matthew
mice and reduced to 50% normal in ...
... form and in one patient in the  homozygous 
Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations
Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations
Yang, X.; Aoki, Y.; Li, X.; Sakamoto, O.; Hiratsuka, M.; Gibson, K. M.; Kure, S.; Narisawa, K.; Matsubara, Y.; Suzuki, Y.
form, respectively. ...
... for the plasma of a heterozygous or a  homozygous 
Evaluation of a highly specific functional test for the detection of factor V Leiden
Evaluation of a highly specific functional test for the detection of factor V Leiden
Quehenberger, P.; Handler, S.; Mannhalter, C.; Pabinger-Fasching, I.; Speiser, W.
carrier of the factor V Leiden mutation, ...
... DNA (T) sequence and may be present in the  homozygous 
Use of Uracil DNA Glycosylase in Scanning for Unknown DNA Mutations and Polymorphisms
Use of Uracil DNA Glycosylase in Scanning for Unknown DNA Mutations and Polymorphisms
Vaughan, Pat
or heterozygous state. ...
... of AS was 10.4 and 6.7 mL/min per kg for  homozygous 
Disposition of acetaminophen and indocyanine green in cystic fibrosis-knockout mice
Disposition of acetaminophen and indocyanine green in cystic fibrosis-knockout mice
Kulkarni, Swarupa G.; Pegram, Anita A.; Smith, Philip C.
and heterozygous males, respectively, ...
... of the founder fish. Generation of  Homozygous 
Transgenic Zebrafish
Transgenic Zebrafish
Lin, Shuo
Transgenic Fish The founder transgenic ...
... or secretion.[9] With the exception of  homozygous 
Role of Lipid-Lowering Pharmacotherapy in Children
Role of Lipid-Lowering Pharmacotherapy in Children
Tonstad, Serena
familial hypercholesterolaemia involving ...
... concentration in tumors that presented a  homozygous 
Breast cancer prognostic significance of a single nucleotide polymorphism in the proximal androgen response element of the prostate specific antigen gene promoter
Breast cancer prognostic significance of a single nucleotide polymorphism in the proximal androgen response element of the prostate specific antigen gene promoter
Bharaj, Bhupinder; Scorilas, Andreas; Diamandis, Eleftherios P.; Giai, Maurizia; Levesque, Michael A.; Sutherland, Donald J.A.; Hoffman, Barry R.
G as opposed to ...
... and 13 of 47 atypical patients were either  homozygous 
Typical Friedreich's ataxia without GAA expansions and GAA expansions without typical Friedreich's ataxia
Typical Friedreich's ataxia without GAA expansions and GAA expansions without typical Friedreich's ataxia
McCabe, D.J.H.; Ryan, F.; Moore, D.P.; McQuaid, S.; King, M.D.; Kelly, A.; Daly, K.; Barton, D.E.; Murphy, R.P.
or heterozygous for the GAA expansion. ...
... 10 and 11 of the Brca2 gene. Mice that are  homozygous 
Mammary-specific targeting of the murine BRCA2 breast cancer susceptibility gene in mice
Mammary-specific targeting of the murine BRCA2 breast cancer susceptibility gene in mice
Collins, NK; McAllister, KA; Bennett, LM; Wagner, K-U; Ward, T; Malphurs, J; Goulding, G; Eddy, EM; Davis, BJ; Wiseman, RW
for this mutation exhibit an embryonic ...
... of genomic integrity. Both BRCA2 and BRCA1  homozygous 
Role of BRCAgene dysfunction in breast and ovarian cancer predisposition
Role of BRCAgene dysfunction in breast and ovarian cancer predisposition
Scully, Ralph
mutant cells exhibit ionizing radiation ...
... failure in a significant percentage of  homozygous 
Homeobox genes in mammary gland development and neoplasia
Homeobox genes in mammary gland development and neoplasia
Lewis, Michael T
mutant animals ([39]; Lewis Mt, Daniel CW, ...
... PiZ mutation and to determine hetero- and  homozygous 
Rapid analysis of α1-antitrypsin PiZ genotype by a real-time PCR approach
Rapid analysis of α1-antitrypsin PiZ genotype by a real-time PCR approach
Ortiz-Pallardó, M. Elena; Zhou, Hui; Fischer, Hans-Peter; Neuhaus, Thomas; Sachinidis, Agapios; Vetter, Hans; Brüning, Thomas; Ko, Yon
carrier status from whole blood and from ...