Argentaffinoma Is Characterized By Excess Excretion Of______
Argentaffinoma Is Characterized By Excess Excretion Of______
5- Hydroxy Indole Acetate | |
Phenyl Acetate | |
Phenyl Lactate | |
3- Hydroxy Phenyl Pyruvate |
پاک اسٹڈی لائبریری اپنی خدمات کو بہتر کرنے کے لئے نئے سوفٹ وئیر انسٹال کررہی ہے ۔ اس لئے آئندہ کچھ دن آپ کو کچھ صفحات تک رسائی میں مشکلات کا سامنا ہوسکتا ہے ۔ جس کے لئے ہم معذرت خواہ ہیں۔
Pak Study Library is installing new software to improve its services. herefore, in the next few days, you may face difficulties in accessing some pages. sorry for the inconvenience.
Argentaffinoma Is Characterized By Excess Excretion Of______
5- Hydroxy Indole Acetate | |
Phenyl Acetate | |
Phenyl Lactate | |
3- Hydroxy Phenyl Pyruvate |
Aniacinosis Results In______
Pellagra | |
Nyctalopia | |
Perleche | |
Beri Beri |
Angular Cheilosis Is Frequently Associated With Deficiency Of______
Niacin | |
Thiamine | |
Folic Acid | |
Riboflavin |
An Example Of Layses Is______
Glutamine Synthetase | |
Fumarase | |
Amylase | |
Cholinesterase |
An Essential For The Conversion Of Glucose To Glycogen In Liver Is______
Pyruvate Kinase | |
Utp | |
Gtp | |
Guanosine |
An Enzyme That Makes A Double Stranded Dna Copy From A Single Stranded Rna Template Molecule Is Known As______
Rna Polymerase | |
Reverse Transcriptase | |
Dna Polymerase | |
Phospho Kinase |
An Enzyme Not Involved In Glycolysis Is______
Aldolase | |
Enolase | |
Glycerophosphate Dehydrogenase | |
Phosphoglycero Mutase |
Ammonia Produced By Brain Is Trapped As______
Urea | |
Creatinine | |
Uric Acid | |
Glutamine |
Ammonia Is Detoxified In Liver To Form______
Creatinine | |
Uric Acid | |
Urea | |
Glutamine |
Amino Acids Excreted In The Urine In Cystinosis______
Cystine | |
Ornithine | |
Arginine | |
All Of The Above |
All These Reactions Take Place Inside The Mitochondria Except______
Krebs Cylce | |
Electron Transfer | |
Emp Pathway | |
Urea Cycle |
All Of The Following Are True About Manifestations Of Vitamin E Deficiency Except______
Cerebellar Ataxia | |
Hemolytic Anemia | |
Autonomic Dysfunctions | |
Posterior Column Abnormalities |
All Of The Following Are Substrates For Gluconeogenesis Except______
Tryptophan | |
Oleic Acid | |
Glycerol | |
Alanine |
All Of The Following Are Globular Proteins Except______
Prolamines | |
Myosin | |
Albumin | |
Globulin |
All Are True Regarding Glucose 6 Phosphate Deficiency Except______
Hyperglycemia | |
Hyperuricemia | |
Defective Cori Cycle | |
Increased Mobilization Of Glycogen From Liver |
All Are True Of The Genetic Code Except______
Universal | |
Degenerate | |
Punctuation | |
Non Overlapping |
All Are True About Glutathione Except ?
It Converts Hemoglobin To Methemoglobin | |
It Scavenges Free Radicals And Superoxide Ions | |
It Conjugates Xenobiotics | |
It Is A Tripetide |
All Are Genetic Amino Acid Deficiency Disease Except______
Homocystinuria | |
Alkaptonuria | |
Phenyl Ketonuria | |
6Alactosemia |
All Are Derived Of Cholesterol Except______
Glycocholic Acid | |
Testosterone | |
Chenodeoxy Cholic Acid | |
Cholecystokinin |
All Are Components Of Basement Membrane Except______
Eutactin | |
Laminin | |
Rhodopsin | |
Nidogen |
Alkaptonuria, An Inherited Metabolic Disorder Of L0tyrosine Metabolism Is Due To Lack Of______
Tyrosine Oxidase | |
Parahydroxy Phenyl Pyruvate Hydroxylase | |
Tyrosine Transaminase | |
Homogentisate Oxidase |
Alkaptonuria An Inherited Metabolic Disorder Is Due To The Deficiency Of______
Tyrosine Transaminase | |
Cystathionase | |
Homogentisate Oxidase | |
Pheylalanine Hydroxylase |
Albumins And Globulins Are ______ Proteins?
Peptones | |
Simple | |
Prolamines | |
Lactalbumin |
Albumin Is Synthesized By______
Muscle | |
Liver | |
Kidney | |
Spleen |
Albinism Is A Genetic Disease That Results In Incomplete Metabolism Of______
Cystine | |
Tyrosine | |
Alanine | |
Histidine |