Results 251 to 260 of about 2,721,776 (301)

Evaluation of multi-environment adaptability of flour quality traits in spring wheat varieties and screening of high-quality genotypes using AMMI and GGE models. [PDF]

Front Plant Sci
Sun N, Huang Q, Yang H, Zhang Z, Wang W, Zhang X, Ma L, Tuerxunbai D, Zou H, Madiyaer J, Geng H.   +10 more
europepmc   +1 more source

HIV-V3Augur: A Novel Machine Learning Model for Predicting HIV-1 Tropism in Sub-Subtype A6 and CRF63_02A6, Predominant Variants in Russia and Countries of the Former Soviet Union. [PDF]

Viruses
Elfimov K, Gotfrid L, Nokhova A, Gashnikova M, Ekushov V, Halikov M, Osipova I, Baboshko D, Murzin A, Kondeikin I, Kiryakina A, Totmenin A, Agaphonov A, Gashnikova N.   +13 more
europepmc   +1 more source

Scalable medium-density genotyping platforms for cultivar identification, pedigree authentication, marker-assisted and genomic selection, and other applications in strawberry. [PDF]

G3 (Bethesda)
Pincot DDA, Sleper JA, Famula RA, Lopéz CM, Velasco D, Al Rwahnih M, Krill-Brown A, Whitaker VM, Knapp SJ, Feldmann MJ.   +9 more
europepmc   +1 more source

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Genotype-phenotype correlations in phenylketonuria

Clinica Chimica Acta, 1993
Genotyping of the phenylalanine hydroxylating system offers a new way of characterizing patients with phenylalanine hydroxylase (PAH) deficiency. This paper investigates the power of genotyping as a parameter for differential diagnosis and as a measure of the risk factor of brain damage in well-treated patients with phenylketonuria (PKU).
F K, Trefz, P, Burgard, T, König, B, Goebel-Schreiner, U, Lichter-Konecki, D, Konecki, E, Schmidt, H, Schmidt, H, Bickel   +8 more
openaire   +2 more sources

Genotype/phenotype correlations in aniridia

American Journal of Ophthalmology, 1998
To detect and characterize mutations in cases of familial and sporadic aniridia in Maritime Canada, and to look for indications of genotype/phenotype correlation within the cohort.Twelve consecutive and unrelated patients (probands) who had total or nearly complete absence of irides, and four affected relatives, were recruited from Maritime Canada ...
S K, Gupta, I, De Becker, F, Tremblay, D L, Guernsey, P E, Neumann   +4 more
openaire   +2 more sources

Genotype-environment correlation and IQ

Behavior Genetics, 1987
The estimation of various forms of genotype-environment (GE) correlation is considered. Two methods of estimating “passive” GE correlation from adoption studies are presented and illustrated with IQ data from five adoption studies. One method involves comparison of variances in adoptive and nonadoptive families, whereas the other compares parent-child ...
J C, Loehlin, J C, DeFries
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DUOXS defects: Genotype-phenotype correlations

Annales d'Endocrinologie, 2011
Congenital hypothyroidism (CH) is the most common congenital endocrine disorder, accounting for up to 1:1500 newborns per year. CH can be related to defects in either formation and migration of the thyroid gland (dysgenesis) or thyroid hormone synthesis. The pathogenesis of dysgenetic CH is still largely unknown. On the contrary, several mutations have
L. Fugazzola, M. Muzza, G. Weber, P. Beck Peccoz, L. Persani   +4 more
openaire   +3 more sources

The genotype–phenotype correlation in Pompe disease

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2012
AbstractPompe disease is an autosomal recessive lysosomal glycogen storage disorder that is caused by acid α‐glucosidase (GAA) deficiency and is due to pathogenic sequence variations in the corresponding GAA gene. The correlation between genotypes and phenotypes is strict, in that patients with the most severe phenotype, classic infantile Pompe disease,
Haan, Marian, Hoogeveen - Westerveld, Marianne, van der Ploeg, Ans, Reuser, Arnold   +3 more
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Genotype-phenotype correlation in myotonic dystrophy

Clinical Genetics, 1998
Myotonic dystrophy (DM) is caused by a mutation in the length of a trinucleotide (CTG) repeat in the 3' untranslated region of the my‐otonin protein kinase gene located on chromosome 19q13.3. The normal gene has between 5 and 36 CTG trinucleotide repeats, whereas minimally affected individuals have 50 copies and severely affected DM‐patients have ...
E B, Gharehbaghi-Schnell, J, Finsterer, I, Korschineck, B, Mamoli, B R, Binder   +4 more
openaire   +2 more sources

Genotype–phenotype correlation in colorectal polyposis

Clinical Genetics, 2011
Newton KF, Mallinson EKL, Bowen J, Lalloo F, Clancy T, Hill J, Evans DGR. Genotype–phenotype correlation in colorectal polyposis.Familial adenomatous polyposis (FAP) has been divided into three clinical subtypes: mild, classical and severe. This study aimed to investigate for a correlation between genotype and phenotype.
Newton, K. F., Mallinson, E. K.L., Bowen, J., Lalloo, F., Clancy, T., Hill, J., Evans, D. G.R.   +6 more
openaire   +3 more sources