Genes involved in ovulation rate and litter size in sheep
... since selection of breeding candidates is complicated. It is important to study genes associated with fertility so that breeding can include genotypic information from animals. This will increase the genetic improvements in reproduction traits since it will be easier to collect data and information ...
... since selection of breeding candidates is complicated. It is important to study genes associated with fertility so that breeding can include genotypic information from animals. This will increase the genetic improvements in reproduction traits since it will be easier to collect data and information ...
SHORT COMMUNICATION One-step multiplex RT-PCR
... The patient who was negative for BCR/ABL had clinical features and peripheral blood film suggestive of chronic myeloproliferative disease. Her condition was complicated by carcinoma of the breast that developed later. The use of conventional cytogenetic analysis has complemented PCR at initial diagn ...
... The patient who was negative for BCR/ABL had clinical features and peripheral blood film suggestive of chronic myeloproliferative disease. Her condition was complicated by carcinoma of the breast that developed later. The use of conventional cytogenetic analysis has complemented PCR at initial diagn ...
Post-Placental Hypoxia
... with a variety of morphological and functional foetal cardiac changes that aim either to compensate for the reduced oxygenation of vital organs or are the result of hypoxia-mediated foetal tissue damage ...
... with a variety of morphological and functional foetal cardiac changes that aim either to compensate for the reduced oxygenation of vital organs or are the result of hypoxia-mediated foetal tissue damage ...
CHAPTER 14 MENDEL AND THE GENE IDEA
... the phenotype in separate, distinguishable ways. For example, the M, N, and MN blood groups of humans are due to the presence of two specific molecules on the surface of red blood cells. People of group M (genotype MM) have one type of molecule on their red blood cells, people of group N (genoty ...
... the phenotype in separate, distinguishable ways. For example, the M, N, and MN blood groups of humans are due to the presence of two specific molecules on the surface of red blood cells. People of group M (genotype MM) have one type of molecule on their red blood cells, people of group N (genoty ...
Special Report on Genetics and: Gout 23 Selected Articles From 199
... Our purpose is to provide both general and focused information regarding the interplay between genetics, health, and the environment, including but not limited to nutrition. Genetics matter, but in most cases your lifestyle and environment matter even more. It’s often said, “Genetics loads the gun, ...
... Our purpose is to provide both general and focused information regarding the interplay between genetics, health, and the environment, including but not limited to nutrition. Genetics matter, but in most cases your lifestyle and environment matter even more. It’s often said, “Genetics loads the gun, ...
New techniques that could make germline genetic
... diabetes, heart disease and autism where a number of genes are involved, along with the environment. In the past a mouse with as few as three genes knocked out would have taken as many years to create; now it can be done in three weeks. CRISPR is also letting researchers get more out of other techno ...
... diabetes, heart disease and autism where a number of genes are involved, along with the environment. In the past a mouse with as few as three genes knocked out would have taken as many years to create; now it can be done in three weeks. CRISPR is also letting researchers get more out of other techno ...
The emergence of humanevolutionary medical genomics
... across the genome (e.g. Manolio and Collins 2009), has been the discovery and characterization of disease risk alleles, to account for heritable risk, infer the causes of polygenic disease at the levels of development, physiology, and pathways, and guide strategies for treatment and prevention. Vuln ...
... across the genome (e.g. Manolio and Collins 2009), has been the discovery and characterization of disease risk alleles, to account for heritable risk, infer the causes of polygenic disease at the levels of development, physiology, and pathways, and guide strategies for treatment and prevention. Vuln ...
Mutations in SIN4 and RGR1 Cause Constitutive Expression of MAL
... the maltose-binding sensor. Alternatively, other positive or negative regulators may be involved but may not have been identified as yet because they are encoded by repeated or essential genes. To identify possible additional players involved in regulating MAL gene expression, we designed a sensitiv ...
... the maltose-binding sensor. Alternatively, other positive or negative regulators may be involved but may not have been identified as yet because they are encoded by repeated or essential genes. To identify possible additional players involved in regulating MAL gene expression, we designed a sensitiv ...
Amplification of AML1 on a duplicated chromosome 21 in
... estimated the incidence of this abnormality to be 1.5%. Among adults over the age of 19 years, the incidence was o0.5% (one out of 229 patients). Patients with one or two additional signals corresponding to extra copies of chromosome 21 were excluded. The karyotypes, clinical details and follow-up d ...
... estimated the incidence of this abnormality to be 1.5%. Among adults over the age of 19 years, the incidence was o0.5% (one out of 229 patients). Patients with one or two additional signals corresponding to extra copies of chromosome 21 were excluded. The karyotypes, clinical details and follow-up d ...
07-050sr (Microsoft Word
... meaning given in Part 3 of that Schedule; non-vector system, for Schedule 2, has the meaning given in Part 3 of that Schedule; nucleic acid means either, or both, deoxyribonucleic acid (DNA), or ribonucleic acid (RNA), of any length; oncogenic modification means a genetic modification that is capabl ...
... meaning given in Part 3 of that Schedule; non-vector system, for Schedule 2, has the meaning given in Part 3 of that Schedule; nucleic acid means either, or both, deoxyribonucleic acid (DNA), or ribonucleic acid (RNA), of any length; oncogenic modification means a genetic modification that is capabl ...
Life 9e - Garvness
... Bloom’s Category: 2. Understanding 23. Restriction enzymes cleave DNA at specific sequences by hydrolyzing a. the 3´ hydroxyl of one nucleotide and the 5´ phosphate of the next one. b. at the 1´ carbons to cleave the nitrogenous bases. c. at the 2´ carbons to cleave hydroxyl groups. d. two phosphod ...
... Bloom’s Category: 2. Understanding 23. Restriction enzymes cleave DNA at specific sequences by hydrolyzing a. the 3´ hydroxyl of one nucleotide and the 5´ phosphate of the next one. b. at the 1´ carbons to cleave the nitrogenous bases. c. at the 2´ carbons to cleave hydroxyl groups. d. two phosphod ...
Gene Rearrangement Analysis and Ancestral Order Inference from
... the best tree returned by GRAPPA-IR. This six-genome dataset contains chloroplast genomes of land plants, green algae and a flagellate protist, which were separated by at least 450 million years of evolution [27]. The ancestral chloroplast genomes of land plants and algae contain inverted repeats, w ...
... the best tree returned by GRAPPA-IR. This six-genome dataset contains chloroplast genomes of land plants, green algae and a flagellate protist, which were separated by at least 450 million years of evolution [27]. The ancestral chloroplast genomes of land plants and algae contain inverted repeats, w ...
Glucose-6-Phosphate Dehydrogenase (GGPD) Mutations
... occurring at nt positions 95, 487, 493, 1024, 1360, and 1388 could a l r k derived from an ancient haplotype VI + VII. The 1376 mutation was found to be not only associated with haplo- ...
... occurring at nt positions 95, 487, 493, 1024, 1360, and 1388 could a l r k derived from an ancient haplotype VI + VII. The 1376 mutation was found to be not only associated with haplo- ...
Single-Gene Inheritance Single-Gene Inheritance
... crosses. The central components in this type of analysis are mutants, individual organisms having some altered form of a normal property. The normal form of any property of an organism is called the wild type, that which is found “in the wild,” or in nature. The genetic modus operandi is to mate an ...
... crosses. The central components in this type of analysis are mutants, individual organisms having some altered form of a normal property. The normal form of any property of an organism is called the wild type, that which is found “in the wild,” or in nature. The genetic modus operandi is to mate an ...
Molecular mapping of the rust resistance gene R4 to a large NBS
... Ó Springer-Verlag (outside the USA) 2011 This article is a U.S. government work, and is not subject to copyright in the United States. ...
... Ó Springer-Verlag (outside the USA) 2011 This article is a U.S. government work, and is not subject to copyright in the United States. ...
Host plant resistance – Importance – disease resistance, tolerance
... diseases as viruses, phytoplasmas wilts, and rusts etc. in which chemical control is very expensive and impractical. In crops of low cash value, chemical and other methods of control are often too expensive to be applied. In such crops development of varieties resistant to important diseases can be ...
... diseases as viruses, phytoplasmas wilts, and rusts etc. in which chemical control is very expensive and impractical. In crops of low cash value, chemical and other methods of control are often too expensive to be applied. In such crops development of varieties resistant to important diseases can be ...
University of Groningen Soft tissue sarcoma at the turn of the
... In the present study, chromosomal gain in 1q1 was the most important negative prognostic factor regarding survival. A relation between alterations at the long arm of chromosome 1 and human malignancies has been demonstrated in various tumor types, suggesting the existence of oncogenes (breast cancer ...
... In the present study, chromosomal gain in 1q1 was the most important negative prognostic factor regarding survival. A relation between alterations at the long arm of chromosome 1 and human malignancies has been demonstrated in various tumor types, suggesting the existence of oncogenes (breast cancer ...
Spinal Muscular Atrophy
... SMA has a continuous spectrum of symptoms that ranges from very severe to mild across the four classifications of SMA types SMA experts recommend that medical care for patients should be tailored to their current level of function. Please see for more information the Consensus Statement for Standard ...
... SMA has a continuous spectrum of symptoms that ranges from very severe to mild across the four classifications of SMA types SMA experts recommend that medical care for patients should be tailored to their current level of function. Please see for more information the Consensus Statement for Standard ...
Phenotypic overlap in the contribution of individual genes to CNV
... candidates through manual searches of the literature and on-line resources. We describe here the development of a computational framework to comprehensively search phenotypic information from model organisms and single-gene human hereditary disorders and thus speed the interpretation of the complex ...
... candidates through manual searches of the literature and on-line resources. We describe here the development of a computational framework to comprehensively search phenotypic information from model organisms and single-gene human hereditary disorders and thus speed the interpretation of the complex ...
Gene Nomenclature System for Rice
... Genes with approved names and symbols will all be associated with a gene function or phenotype and, where possible, at the time of registration, researchers will be asked to identify a systematic locus identifier for the new gene from the RAP annotation database. Links to systematic_locus_IDs in oth ...
... Genes with approved names and symbols will all be associated with a gene function or phenotype and, where possible, at the time of registration, researchers will be asked to identify a systematic locus identifier for the new gene from the RAP annotation database. Links to systematic_locus_IDs in oth ...
BIOMARKERS What do they tell us that we don*t already
... BIOMARKERS What do they tell us that we don’t already know? ...
... BIOMARKERS What do they tell us that we don’t already know? ...
Association of functionally significant Melanocortin
... North American adults was 2.25% (CI95%: 1.44– 3.47) compared with a prevalence of 0.64% (CI95%: 0.26 – 1.43) in lean controls (P ¼ 0.005) (OR ¼ 4.3). In addition, a total of 41 subjects carried the common variant Val103Ile and 12 subjects carried the common variant Leu251Ile (Table 2). The frequency ...
... North American adults was 2.25% (CI95%: 1.44– 3.47) compared with a prevalence of 0.64% (CI95%: 0.26 – 1.43) in lean controls (P ¼ 0.005) (OR ¼ 4.3). In addition, a total of 41 subjects carried the common variant Val103Ile and 12 subjects carried the common variant Leu251Ile (Table 2). The frequency ...
Reconstruction of a Functional Human Gene Network, with an
... contributing only weak effects to the disease. Pinpointing these disease genes within the myriad of susceptibility loci identified in linkage studies is difficult because these loci may contain hundreds of genes. However, in any disorder, most of the disease genes will be involved in only a few diff ...
... contributing only weak effects to the disease. Pinpointing these disease genes within the myriad of susceptibility loci identified in linkage studies is difficult because these loci may contain hundreds of genes. However, in any disorder, most of the disease genes will be involved in only a few diff ...
No correlation between phenotype and genotype in boys with a
... Key points • Rett syndrome (RS) used to be considered as affecting girls only. However, 17 males with a mutation in MECP2 have been reported so far. Six of these had the karyotype 47,XXY or were mosaics for the mutation. The remaining cases can be divided into two groups, a severe type, who die with ...
... Key points • Rett syndrome (RS) used to be considered as affecting girls only. However, 17 males with a mutation in MECP2 have been reported so far. Six of these had the karyotype 47,XXY or were mosaics for the mutation. The remaining cases can be divided into two groups, a severe type, who die with ...
BMC Genomics - LCBB
... the best tree returned by GRAPPA-IR. This six-genome dataset contains chloroplast genomes of land plants, green algae and a flagellate protist, which were separated by at least 450 million years of evolution [27]. The ancestral chloroplast genomes of land plants and algae contain inverted repeats, w ...
... the best tree returned by GRAPPA-IR. This six-genome dataset contains chloroplast genomes of land plants, green algae and a flagellate protist, which were separated by at least 450 million years of evolution [27]. The ancestral chloroplast genomes of land plants and algae contain inverted repeats, w ...