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... conditions. When polyploid plants have an odd number of sets, they are typically seedless. This can be a desirable trait for certain fruit-producing crops such as bananas. C30. The turtles are two distinct species that appear phenotypically identical. The turtles with 48 chromosomes are polyploid re ...
The role of Cdx genes in the mammalian gut
The role of Cdx genes in the mammalian gut

... single layered epithelium at 14 days post coitum (dpc).6 Cdx4 is expressed in the earliest hindgut invagination7 but little is known of its distribution after 10 dpc. It is important to note that in addition to their role in the gut, Cdx genes are active at multiple other sites during early developm ...
C1. Duplications and deficiencies involve a change in the total
C1. Duplications and deficiencies involve a change in the total

... conditions. When polyploid plants have an odd number of sets, they are typically seedless. This can be a desirable trait for certain fruit-producing crops such as bananas. C30. The turtles are two distinct species that appear phenotypically identical. The turtles with 48 chromosomes are polyploid re ...
Fc RIIIB Gene Duplication: Evidence for Presence and Expression of
Fc RIIIB Gene Duplication: Evidence for Presence and Expression of

... fragment of the NA2-FcgRIIIB gene from gDNA by an allelespecific primer-annealing (ASPA) PCR. As shown in Fig 2A to C, direct sequencing of these products showed that the individuals were heterozygous at nucleotide position 266. At this position, a C as well as an A were detected, suggesting that tw ...
Chapter 6 - whsbaumanbiology
Chapter 6 - whsbaumanbiology

...  Mendel drew three ...
A defense-offense multi-layered regulatory switch in a pathogenic
A defense-offense multi-layered regulatory switch in a pathogenic

... governing this switch by deterministic and stochastic computational methods, as well as experimentally. This module, termed here Double Selector Switch (DSS), comprises the RNA regulator RNAIII and the transcription factor Rot, defining a doublelayered switch involving both transcriptional and post- ...
View PDF
View PDF

... independently of each other during gamete formation (meiosis). ...
Female Sterile Mutations on the Second Chromosome of
Female Sterile Mutations on the Second Chromosome of

... ensure the production of a normal egg capable of supportingthedevelopment of anormalembryo (GARCIA-BELLIDO and ROBBINS1983; PERRIMON, ENCSTROM and MAHOWALD1984). These genes can be grouped in several classes. On the one hand, all cells involved in oogenesis require thenormal complement of household ...
Genetic Analysis: the Terminology *
Genetic Analysis: the Terminology *

... --Specific: loss of dopaminergic neurons at 5 dpf with no other defects --Non-specific: loss of dopaminergic neurons with loss of gut, liver, jaw differentiation; if it were examined, all late organ development arrests. Type of gene mutant: e.g. DNA polymerase subunit etc. ...
The Endocrine System
The Endocrine System

... Endocrine glands usually release their secretions (hormones) directly into the blood, which transports the secretions throughout the body. This figure shows the location of the major endocrine glands in the human body. ...
IV. Chromosome Number Anomalies
IV. Chromosome Number Anomalies

... a) The extra X chromosome becomes inactivated. b) Characteristics: testes and prostate gland are underdeveloped, facial hair is lacking, may be breast development, large hands and feet, very long arms and legs, slow to learn How Life Changes 9B Hope for Down Syndrome A. Chris Burke was born with Dow ...
Point mutations in BCL6 DNA-binding domain reveal distinct
Point mutations in BCL6 DNA-binding domain reveal distinct

... all the mutants. Incorporation of the mutations was confirmed by automated DNA sequencing. The following mutants were constructed: pcDNA-BCL6 mut1 (C/G520-523, cysteine 520 and 523 replaced by glycine), mut2 (C/G548-551), mut3 (C/G576-579), mut4 (C/G604-607), mut5 (C/G 632-635), and mut6 (C/G660-663 ...
nuclear structure (2): the nucleolus
nuclear structure (2): the nucleolus

... proteins that will remain associated with the rRNA; proteins (enzymes) that cut the RNA transcript to form the 5.8S, 18S, and 28S ribosomal RNA molecules; and proteins that help the assembly of the ribosomal subunits (such as nucleolin). ...
Light and an exogenous transcription factor
Light and an exogenous transcription factor

... synthesis, the so-called ‘early genes’ (Martin et al., 1991; Martin and Gerats, 1993; Pellettier et al., 1997); other terminal steps of the pathway (‘late genes’) lead to the synthesis of the final compounds. The characterization of mutants defective in anthocyanin accumulation in petunia flowers (a ...
Salmonella typhi mutants defective in anaerobic respiration are
Salmonella typhi mutants defective in anaerobic respiration are

... oxygen availability (Lee & Falkow, 1990), for which enteric bacteria have developed adaptive responses. Facultative anaerobes, such as Escherichia coli and Salmonella typhimurium, can grow under aerobic or anaerobic conditions, deriving energy from a variety of respiratory or fermentative processes. ...
Comparisons of Maize pericarp color1 Alleles
Comparisons of Maize pericarp color1 Alleles

... of P1-rr4B2 (e.g., it has a single coding sequence flanked by two long [6.3 kb] direct repeats). However, the P1-rw1077 coding sequence is chimeric, consisting of a p1-like 59 UTR followed by p2-like exons and introns. Farther downstream, the P1-rw1077 allele has a region similar to the Ji retroelem ...
Higher Biology - Unit 1 Cell Biology
Higher Biology - Unit 1 Cell Biology

... Explain what a carrier is. Explain what genetic counselling is. Describe a situation when a couple may need genetic counselling. ...
Abstract - BioMed Central
Abstract - BioMed Central

RNA-Seq Tutorial - Gene Codes Corporation
RNA-Seq Tutorial - Gene Codes Corporation

... What  you  see  in  this  plot  is  the  expression  profile  for  each  of  these  genes,  in  your  cell   lines.  If  you  click  on  a  specific  gene  in  the  Gene  list,  its  plot  line  is  emphasized  and  the   variation  in  expression  of  that  gene  across  all  the  cell  lines  is   ...
PPT - Bioinformatics.ca
PPT - Bioinformatics.ca

... – TF binding sites, gene structure (intron/exon), SNPs ...
Patients - HAL
Patients - HAL

... protein with unknown function, is specifically expressed in apical retinal pigment epithelium microvilli. Since rhodopsin and RGR, another opsin-like protein, cause retinitis pigmentosa, we screened by D-HPLC the peropsin gene RRH in 331 patients (288 retinitis pigmentosa and 82 other retinal dystro ...
Free PDF
Free PDF

... active secretory organ, sending out and responding to signals that modulate appetite, insulin sensitivity, energy expenditure, inflammation and immunity1-10. The fatty acid (FA) binding protein 2(FABP2) gene codes for intestinal FABP, which is a member of a family of small intracellular lipid-bindin ...
5 BLY 122 Lecture Notes (O`Brien) 2009 II. Protists
5 BLY 122 Lecture Notes (O`Brien) 2009 II. Protists

... (b) Results: Infective children (with gametocytes) attracted 2X as many mosquitoes as the 2 other groups Picture Slide showing results (2) Experiment 2 (a) Cured parasitized children and repeated the experiment (b) Results: Children whose blood was cleared of infective stages no longer attracted mos ...
Vertical and horizontal gene transfer in lichens
Vertical and horizontal gene transfer in lichens

... The evolution of MAT genes is very fast, even though in certain species they need to remain conserved (1). MAT 1-1 is coding for a protein containing a conserved alpha-box motif. MAT 1-2 is coding for a protein containing conserved DNA-binding domain called HMG box. It was shown that those two domai ...
LP - Columbia University
LP - Columbia University

... C. Reminder: all eukaryotic DNA is in double helix, supercoiled, AND associated with special proteins called histones at all times -- it's super-supercoiling and association with additional proteins that changes. (More details next term.) ...
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NEDD9

Neural precursor cell expressed developmentally down-regulated protein 9 (NEDD-9) is a protein that in humans is encoded by the NEDD9 gene. NEDD-9 is also known as enhancer of filamentation 1 (EF1), CRK-associated substrate-related protein (CAS-L), and Cas scaffolding protein family member 2 (CASS2). An important paralog of this gene is BCAR1.
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