Phenylalanine PowerPoint Presentations - PPT

Phenylalanine Malonate Broth is used for the differentiation of member
Phenylalanine Malonate Broth is used for the differentiation - pdf

luanne-sto

Ingredients Gms / Litre Yeast extract 1.000 Sodium malonate 3.000 DL-Phenylalanine 2.000 Ammonium sulphate 2.000 Dipotassium phosphate 0.600 Monopotassium phosphate 0.400 Sodium chloride 2.000 Bromo t

Faculdade de Medicina da Universidade de Coimbra
Faculdade de Medicina da Universidade de Coimbra - presentation

faustina-d

Biologia Celular e Molecular II. 2012/2013. Work done by:. Cátia Ferreira (T5). Isa Costa (T6) . Jéssica Vasconcelos (T5). Sara Ferreira (T6). Cellular and Molecular . M. echanisms in Phenylketonuria.

Phenylketonuria (PKU)
Phenylketonuria (PKU) - presentation

trish-goza

By: Adrienne Gebele. What is PKU?. 1. Inherited disorder. Occurrence varied due to ethnicity and geography. About 1 and 10,000 to 15,000 infants are born with in the U.S.. People born with PKU have an inactive liver enzyme which causes a dangerous build up of phenylalanine in the blood.

Chemistry and Biology Interface
Chemistry and Biology Interface - presentation

trish-goza

Summer Institute – Sept. 11, 2011. Teachable Unit. Title: Proteins. Context. A one-week series in a 100-level course for biology majors given early in the semester. Class is 50-100 students. Learning Goals of Teachable Unit- .

7-5 Phenylketonuria Report
7-5 Phenylketonuria Report - presentation

liane-varn

By Kevin Zhu, Walter Chen, and. Sachin Patro. Definition. Phenylketonuria (PKU) is a genetic disorder that is described by an lack of ability of the body to use the necessary amino acid called phenylalanine. Amino acids are the building blocks for body’s proteins. 'Essential' amino acids can only be attained from the food that we eat. Our body does not normally produce them. The 'classic PKU', the enzyme that breaks down phenylalanine hydroxylase, is absolutely or almost completely lacking. This enzyme normally turns phenylalanine to another amino acid called tyrosine. Without this ‘Classic PKU', phenylalanine and it’s other breakdown chemicals from other enzyme method, build up in the blood and body tissues. .

Aromatic amino acid metabolism
Aromatic amino acid metabolism - presentation

phoebe-cli

Aromatic amino acid contains aromatic . ring. . They . are:. Phenylalanine(Benzene . ring or phenyl. ).. Tyrosine(phenol).. Tryptophan(indole).. Phenylalanine and Tryptophan are essential amino acids..

L-Phenylalanine
L-Phenylalanine - pdf

lindy-duni

Mol. Wt. 165.19 (S) 5.46.0 (1.0 g, water 100 ml). (4) Chloride Not more than 0.021% as Cl (0.50 g, Control solution 0.01 mol/l (5)

Arginine 490 (R) and glutamic acid 508 (E), phenylalanine 480 (F) and
Arginine 490 (R) and glutamic acid 508 (E), phenylalanine 48 - pdf

tatiana-do

102 * Figure 4.2: Band 3 Transmembrane Region 542 490 508 480 479 4.4.1 Clinical Severity Proband A (R490H) has mild anaemia and a normal reticulocyte count. This contrasts with the patients exa

PKU  By Taylor Brady If this child eats any protein she risks severe  brain damage. Find out why..
PKU By Taylor Brady If this child eats any protein she risk - presentation

celsa-spra

What is PKU?. PKU is an inherited disorder that is an error of metabolism that increases the levels of a substance in the blood called phenylalanine hydroxylase.. Phenylalanine is an important amino acid and the body needs it for health; you get it from food. It is a building block for proteins in the body..

Examples of  Life  Course
Examples of Life Course - presentation

olivia-mor

Development. PKU. : A Life Course . Development . Perspective. PKU & Life Course Development:. Birth to Two Years. Issues. :. Brain . is particularly sensitive to elevated phenylalanine . levels.

Metabolic medications
Metabolic medications - presentation

debby-jeon

Dr. . Nawal. . Makhseed. . MBBS, FAAP, FRCPC, DABMGG, FCCMG. Pediatric Metabolic Consultant. Metabolic drugs group . Emergency . Hyperammonemia. medications . Maintenance . hyperammonemia. medications .

Metabolic medications
Metabolic medications - presentation

pasty-tole

Dr. . Nawal. . Makhseed. . MBBS, FAAP, FRCPC, DABMGG, FCCMG. Pediatric Metabolic Consultant. Metabolic drugs group . Emergency . Hyperammonemia. medications . Maintenance . hyperammonemia. medications .

Single Nucleotide Polymorphisms
Single Nucleotide Polymorphisms - presentation

luanne-sto

Arthur M. . Lesk. Bologna Winter School 2011. 1. What are SNPs and why are they important?. SNP = Single nucleotide polymorphism, an . isolated. change in a single nucleotide. SNPs are one type of mutation .

AMINO
AMINO - presentation

kittie-lec

ACID. A protein molecule consists of one or more long . unbranched. polymer chains composed of numerous small subunits or monomers is called amino acids .. There are 20 amino acids from which 18 have same structure..

SEVEN AMINO ACIDS DEGRADED TO ACETYL COA
SEVEN AMINO ACIDS DEGRADED TO ACETYL COA - presentation

kittie-lec

THE EXCRETION OF AMMONIUM IONS. A part of NH4+ that is formed in the degradation of amino acids is used for the biosynthesis of nitrogen compounds. In most of the land living vertebrates the excess NH4+ is converted in urea and in that form is excreted. In birds and reptiles it is converted into uric acid and in aquatic animals it is directly excreted as urea..

Amino Acid Metabolism (day-2)
Amino Acid Metabolism (day-2) - presentation

luanne-sto

What to Know. What is the Metabolic Fate of Ammonium?. How is Escherichia coli Glutamine Synthetase regulated?. Understand general ways that organisms synthesize amino acids. Know the definition of essential versus nonessential amino acids.

24.9  Synthesis of Amino Acids
24.9 Synthesis of Amino Acids - presentation

stefany-ba

Plants and bacteria produce all of their amino acids using NH. 4. +. and NO. 3. –. .. Humans can synthesize 9 of the 20 amino acids found in their proteins.. Nonessential amino acids are synthesized in the body, while essential amino acids must be obtained from diet..

GLUCOGENIC & KETOGENIC AMINO ACIDS
GLUCOGENIC & KETOGENIC AMINO ACIDS - presentation

phoebe-cli

DR AMINA . BIOCHEMISTRY. All tissues have some capability for synthesis of:. The non-essential amino acids,. Amino acid remodeling, . and Conversion of non-amino acid carbon skeletons into amino acids and other derivatives that contain nitrogen. .

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