Marfan’s syndrome results from a mutation in the gene coding: (A) Collagen (B) Elastin (C) Fibrillin (D) Keratin

Marfan’s syndrome results from a mutation in the gene coding: (A) Collagen (B) Elastin (C) Fibrillin (D) Keratin
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Proteins that constitute keratin, collagen and elastin in body are (A) Protamines (B) Phosphol proteins (C) Scleroproteins (D) Metaproteins

Description : Proteins that constitute keratin, collagen and elastin in body are (A) Protamines (B) Phosphol proteins (C) Scleroproteins (D) Metaproteins

Last Answer : Answer : C

This major protein component of connective tissue in mammals comprises most of the organic matter of skin, tendons, bones, and teeth, and occurs as fibrous inclusions in most other body structures. Is this material: a) elastin b) collagen c) fatty acids d) keratin

Description : This major protein component of connective tissue in mammals comprises most of the organic matter of skin, tendons, bones, and teeth, and occurs as fibrous inclusions in most other body structures. Is this material: a) elastin b) collagen c) fatty acids d) keratin

Last Answer : ANSWER: B -- collagen 

The protein present in hair is (A) Elastin (B) Prolamine (C) Keratin (D) Gliadin

Description : The protein present in hair is (A) Elastin (B) Prolamine (C) Keratin (D) Gliadin

Last Answer : Answer : C

The protein present in hair is (A) Keratin (B) Elastin (C) Myosin (D) Tropocollagen

Description : The protein present in hair is (A) Keratin (B) Elastin (C) Myosin (D) Tropocollagen

Last Answer : Answer : A

Collagen and elastin have the following similarity: (A) Both are triple helices (B) Both have hydroxyproline residues (C) Both have hydrolysine residues (D) Both are glycoproteins

Description : Collagen and elastin have the following similarity: (A) Both are triple helices (B) Both have hydroxyproline residues (C) Both have hydrolysine residues (D) Both are glycoproteins

Last Answer : Answer : A

The most abundant protein in mammals is (A) Albumin (B) Haemoglobin (C) Collagen (D) Elastin

Description : The most abundant protein in mammals is (A) Albumin (B) Haemoglobin (C) Collagen (D) Elastin

Last Answer : Answer : C

Nondisjunction of a chromosome results in which of the following diagnoses? a) Down Syndrome When a pair of chromosomes fails to separate completely and creates a sperm or oocyte that contains two copies of a particular chromosome (nondisjunction) Down syndrome results from three number 21 chromosomes. b) Huntingon Disease Huntington disease is one example of a germ-line mutation. c) Duchenne Muscular Dystrophy Duchenne muscular dystrophy, an inherited form of muscular dystrophy, is an example of a genetic caused by structural gene mutations. d) Marphan Syndrome Marphan Syndrome is a genetic condition that may occur in a single family member as a result of spontaneous mutation.

Description : Nondisjunction of a chromosome results in which of the following diagnoses? a) Down Syndrome When a pair of chromosomes fails to separate completely and creates a sperm or oocyte that contains two ... genetic condition that may occur in a single family member as a result of spontaneous mutation.

Last Answer : a) Down Syndrome When a pair of chromosomes fails to separate completely and creates a sperm or oocyte that contains two copies of a particular chromosome (nondisjunction) Down syndrome results from three number 21 chromosomes.

Human nails are made up of - (1) Pigment (2) Elastin (3) Albumin (4) Keratin

Description : Human nails are made up of - (1) Pigment (2) Elastin (3) Albumin (4) Keratin

Last Answer : (4) Keratin Explanation: Keratin, a family of fibrous structural proteins, is the key structural component of hair and nails.

Collagen and elastin are formed by

Description : Collagen and elastin are formed by

Last Answer : Collagen and elastin are formed by A. Mocrophages B. Fibroblasts C. Mast cells D. Chondrocytes

Which of the following statements is correct? (a) Cornea consists of dense matrix of collagen and is the most sensitive portion of the eye. (b) Cornea is an external, transparent and protective proteinacious covering of the eye-ball. (c) Cornea consists of dense connective tissue of elastin and can repair itself. (d) Cornea is convex, transparent layer which is highly vascularised.

Description : Which of the following statements is correct? (a) Cornea consists of dense matrix of collagen and is the most sensitive portion of the eye. (b) Cornea is an external, transparent and protective ... elastin and can repair itself. (d) Cornea is convex, transparent layer which is highly vascularised.

Last Answer : (a) Cornea consists of dense matrix of collagen and is the most sensitive portion of the eye.

Which of the following protein is rich in cysteine? (A) Elastine (B) Collagen (C) Fibrin (D) Keratin

Description : Which of the following protein is rich in cysteine? (A) Elastine (B) Collagen (C) Fibrin (D) Keratin

Last Answer : Answer : D

A protein rich in cysteine is (A) Collagen (B) Keratin (C) Haemoglobin (D) Gelatin

Description : A protein rich in cysteine is (A) Collagen (B) Keratin (C) Haemoglobin (D) Gelatin

Last Answer : Answer : B

I have a few Marfan's Syndrome symptoms, Can i really have it even if not classic?

Description : I have a few Marfan's Syndrome symptoms, Can i really have it even if not classic?

Last Answer : Get off of Fluther and make an appointment with a psychotherapist. You are not a well man, and no one here can help you.

The individual who demonstrates displacement of the sternum is described as having a a) pigeon chest. Pigeon chest may occur with rickets, Marfan’s syndrome, or severe kyphoscoliosis. b) barrel chest. A barrel chest is seen in patients with emphysema as a result of overinflation of the lungs. c) funnel chest. A funnel chest occurs when there is a depression in the lower portion of the sternum. d) kyphoscoliosis. Kyphoscoliosis is characterized by elevation of the scapula and a corresponding S-shaped spine.

Description : The individual who demonstrates displacement of the sternum is described as having a a) pigeon chest. Pigeon chest may occur with rickets, Marfan's syndrome, or severe kyphoscoliosis. ... kyphoscoliosis. Kyphoscoliosis is characterized by elevation of the scapula and a corresponding S-shaped spine.

Last Answer : a) pigeon chest. Pigeon chest may occur with rickets, Marfan’s syndrome, or severe kyphoscoliosis.

The brown-black pigment of the skin that is transferred to other epidermal cells and gives the skin its color is called A. albumin B. collagen C. keratin D. melanin

Description : The brown-black pigment of the skin that is transferred to other epidermal cells and gives the skin its color is called A. albumin B. collagen C. keratin D. melanin

Last Answer : Ans: D

Which of the following makes the skin layer impervious to water? (1) Collagen (2) Melanin (3) Keratin (4) Chitin

Description : Which of the following makes the skin layer impervious to water? (1) Collagen (2) Melanin (3) Keratin (4) Chitin

Last Answer : (3) Keratin Explanation: Keratin is a family of fibrous structural proteins. Keratin is the key structural material making up the outer layer of human skin. It is also the key structural component ... layer of the skin almost waterproof, and along with collagen and elastin, gives skin its strength.

Which of the following makes the skin layer impervious to water ? (1) Collagen (2) Melanin (3) Keratin (4) Chitin

Description : Which of the following makes the skin layer impervious to water ? (1) Collagen (2) Melanin (3) Keratin (4) Chitin 

Last Answer : Keratin

Which type of Mendelian inherited condition results in both genders being affected equally in a vertical pattern? a) Automosomal dominant inheritance An individual who has an autosomal dominant inherited condition carries a gene mutation for that condition on one chromosome of a pair. b) Automosomal recessive inheritance The pattern of inheritance in autosomal recessive inherited conditions is different from that of autosomal dominant inherited conditions in that it is more horizontal than vertical, with relatives of a single generation tending to have the condition. c) X-linked inheritance X-linked conditions may be inherited in families in recessive or dominant patterns.

Description : Which type of Mendelian inherited condition results in both genders being affected equally in a vertical pattern? a) Automosomal dominant inheritance An individual who has an autosomal dominant ... that combine during early embryonic development leading to incomplete closure of the neural tube.

Last Answer : a) Automosomal dominant inheritance An individual who has an autosomal dominant inherited condition carries a gene mutation for that condition on one chromosome of a pair.

Cancer cells may become resistant to amethopterin by (A) Developing mechanisms to destroy amethopterin (B) Amplification of dihydrofolate reducatse gene (C) Mutation in the dihydrofolate reductase gene so that the enzyme is no longer inhibited by amethopterin (D) Developing alternate pathway of thymidylate synthesis

Description : Cancer cells may become resistant to amethopterin by (A) Developing mechanisms to destroy amethopterin (B) Amplification of dihydrofolate reducatse gene (C) Mutation in the dihydrofolate reductase ... is no longer inhibited by amethopterin (D) Developing alternate pathway of thymidylate synthesis

Last Answer : Answer : B

All the following statements about retino blastoma are true except (A) At least two mutations are required for its development (B) One mutation can be inherited from a parent (C) Children who have inherited one mutation develop retinoblastoma at a younger age (D) RB 1 gene promotes the development of retinoblastoma

Description : All the following statements about retino blastoma are true except (A) At least two mutations are required for its development (B) One mutation can be inherited from a parent (C) Children ... mutation develop retinoblastoma at a younger age (D) RB 1 gene promotes the development of retinoblastoma

Last Answer : Answer : D

Retinoblastoma can result from a mutation in (A) ras proto-oncogene (B) erbB proto-oncogene (C) p 53 gene (D) RB 1 gene

Description : Retinoblastoma can result from a mutation in (A) ras proto-oncogene (B) erbB proto-oncogene (C) p 53 gene (D) RB 1 gene

Last Answer : Answer : D

Ras proto-oncogene is converted into oncogene by (A) A point mutation (B) Chromosomal translocation (C) Insertion of a viral promoter upstream of the gene (D) Gene amplification

Description : Ras proto-oncogene is converted into oncogene by (A) A point mutation (B) Chromosomal translocation (C) Insertion of a viral promoter upstream of the gene (D) Gene amplification

Last Answer : Answer : A

The coding sequences in lac operon include (A) i gene (B) i gene, operator locus and promoter (C) z, y and a genes (D) i, z, y and a genes

Description : The coding sequences in lac operon include (A) i gene (B) i gene, operator locus and promoter (C) z, y and a genes (D) i, z, y and a genes

Last Answer : Answer : D

Non-coding sequences in a gene are known as (A) Cistrons (B) Nonsense codons (C) Introns (D) Exons

Description : Non-coding sequences in a gene are known as (A) Cistrons (B) Nonsense codons (C) Introns (D) Exons

Last Answer : Answer : C

The smallest unit of DNA capable of coding for the synthesis of a polypeptide is (A) Operon (B) Repressor gene (C) Cistron (D) Replicon

Description : The smallest unit of DNA capable of coding for the synthesis of a polypeptide is (A) Operon (B) Repressor gene (C) Cistron (D) Replicon

Last Answer : Answer : C

The example of metalloproteins: (A) Siderophilin (B) OREES mucoid (C) Elastin (D) All of these

Description : The example of metalloproteins: (A) Siderophilin (B) OREES mucoid (C) Elastin (D) All of these

Last Answer : Answer : A

The example of scleroproteins: (A) Glutamin (B) Giladin (C) Salmine (D) Elastin

Description : The example of scleroproteins: (A) Glutamin (B) Giladin (C) Salmine (D) Elastin

Last Answer : Answer : D

A point mutation results from (A) Substitution of a base (B) Insertion of a base (C) Deletion of a base (D) All of these

Description : A point mutation results from (A) Substitution of a base (B) Insertion of a base (C) Deletion of a base (D) All of these

Last Answer : Answer : A

In the following partial sequence of mRNA, a mutation of the template DNA results in a change in codon 91 to UAA. The type of mutation is 88 89 90 91 92 93 94 GUC GAC CAG UAG GGC UAA CCG (A) Missene (B) Silent (C) Nonsense (D) Frame shit

Description : In the following partial sequence of mRNA, a mutation of the template DNA results in a change in codon 91 to UAA. The type of mutation is 88 89 90 91 92 93 94 GUC GAC CAG UAG GGC UAA CCG (A) Missene (B) Silent (C) Nonsense (D) Frame shit

Last Answer : Answer : B

All the following statements about restriction fragment length polymorphism are true except (A) It results from mutations in restriction sites (B) Mutations in restriction sites can occur in coding or non-coding regions of DNA (C) It is inherited in Mendelian fashion (D) It can be used to diagnose any genetic disease

Description : All the following statements about restriction fragment length polymorphism are true except (A) It results from mutations in restriction sites (B) Mutations in restriction sites can occur in coding or non- ... It is inherited in Mendelian fashion (D) It can be used to diagnose any genetic disease

Last Answer : Answer : D

Trials for gene therapy in human beings were first carried out, with considerable success, in a genetic disease called (A) Cystic fibrosis (B) Thalassemia (C) Adenosine deaminase deficiency (D) Lesch-Nyhan syndrome

Description : Trials for gene therapy in human beings were first carried out, with considerable success, in a genetic disease called (A) Cystic fibrosis (B) Thalassemia (C) Adenosine deaminase deficiency (D) Lesch-Nyhan syndrome

Last Answer : Answer : C

Ehlers-Danlos syndrome characterized by hypermobile joints and skin abnormalities is due to (A) Abnormality in gene for procollagen (B) Deficiency of lysyl oxidase (C) Deficiency of prolyl hydroxylase (D) Deficiency of lysyl hydroxylase

Description : Ehlers-Danlos syndrome characterized by hypermobile joints and skin abnormalities is due to (A) Abnormality in gene for procollagen (B) Deficiency of lysyl oxidase (C) Deficiency of prolyl hydroxylase (D) Deficiency of lysyl hydroxylase

Last Answer : Answer : A

The most striking example of point mutation is found in a disease called (a) Down’s syndrome (b) sickle cell anaemia (c) thalassaemia (d) night blindness.

Description : The most striking example of point mutation is found in a disease called (a) Down’s syndrome (b) sickle cell anaemia (c) thalassaemia (d) night blindness.

Last Answer : (b) sickle cell anaemia

Anyone take collagen supplement and actually see some results?

Description : Anyone take collagen supplement and actually see some results?

Last Answer : I took them for about a year and saw no discernible results.

What is gene mutation? -Biology

Description : What is gene mutation? -Biology

Last Answer : answer:

A point mutation occurs in a sex cell of an adult chimpanzee. The mutation is located on a gene responsible for the development of the eye. Which describes the most likely effect of this mutation?

Description : A point mutation occurs in a sex cell of an adult chimpanzee. The mutation is located on a gene responsible for the development of the eye. Which describes the most likely effect of this mutation?

Last Answer : The chimpanzee's offspring will have abnormal eyes.

How does a mutation in a gene affect the order of DNA based?

Description : How does a mutation in a gene affect the order of DNA based?

Last Answer : A mutation in a gene can happen by addition, deletion orsubstitution of base pairs. This means that the order of the baseswill change- a new base may be added, a base may be lost, or onebase ... occurs in a sex cell, themutation can be passed on to an offspring and affect theoffspring's phenotype.

How is it possible for a point mutation to have no effect on the function of the gene TAC CG?

Description : How is it possible for a point mutation to have no effect on the function of the gene TAC CG?

Last Answer : Feel Free to Answer

When one gene pair hides the effect of the other unit, the phenomenon is referred to as: (1) Epistasis (2) Mutation (3) None of the options (4) Dominance

Description : When one gene pair hides the effect of the other unit, the phenomenon is referred to as: (1) Epistasis (2) Mutation (3) None of the options (4) Dominance

Last Answer : (1) Epistasis Explanation: Epistasis refers to the phenomenon in which one gene hides the effect of the other. In other word, it does not allow the other gene to express itself. This is counterpart of ... may be in one direction only meaning that ei-ther A hides the effect of B or vice versa.

Gamma rays can cause – (1) gene mutation (2) sneezing (3) burning (4) fever

Description : Gamma rays can cause – (1) gene mutation (2) sneezing (3) burning (4) fever

Last Answer : (1) gene mutation Explanation: In molecular biology and genetics, mutations are accidental changes in a genomic sequence of DNA: the DNA sequence of a cell's genome or the DNA or RNA ... viruses, transposons and mutagenic chemicals, as well as errors that, occur during meiosis or DNA replication.

Which enzyme will be produced in a cell if there is a nonsense mutation in the lac Y gene? (a) Transacetylase (b) Lactose permease and transacetylase (c) β-galactosidase (d) Lactose permease

Description : Which enzyme will be produced in a cell if there is a nonsense mutation in the lac Y gene? (a) Transacetylase (b) Lactose permease and transacetylase (c) β-galactosidase (d) Lactose permease

Last Answer : β-galactosidase

A gene pair hides the effect of another gene. The phenomenon is called (a) dominance (b) segregation (c) epistasis (d) mutation

Description : A gene pair hides the effect of another gene. The phenomenon is called (a) dominance (b) segregation (c) epistasis (d) mutation

Last Answer : (c) epistasis

A heritable change in DNA is called a ______. a. mistake b. mutation c. gene d. pathogen

Description : A heritable change in DNA is called a ______. a. mistake b. mutation c. gene d. pathogen

Last Answer : b. mutation

A specific BRCA1 cancer-predisposing gene mutation seems to occur more frequently among women of which descent? a) Ashkanazi Jewish Expression of the BRCA1 gene is an example of inheritance in the development of breast cancer. b) Mediterranean Glucose-6-phosphate dehydrogenase deficiency (G6PD) is a common enzyme abnormality that affects millions of people throughout the world, especially those of Mediterranean, South East Asian, African, Middle Eastern, and Near Eastern origin.

Description : A specific BRCA1 cancer-predisposing gene mutation seems to occur more frequently among women of which descent? a) Ashkanazi Jewish Expression of the BRCA1 gene is an example of ... of treatment for tuberculosis) are at significantly increased risk for developing isoniazid-induced hepatitis.

Last Answer : a) Ashkanazi Jewish Expression of the BRCA1 gene is an example of inheritance in the development of breast cancer.

27. A ‘single step-large mutation’ is known as ... b) Branching descent b) Natural Selection c) Saltation d) Gene Migration

Description : 27. A ‘single step-large mutation’ is known as ... b) Branching descent b) Natural Selection c) Saltation d) Gene Migration

Last Answer : c) Saltation

7. A ‘single step-large mutation’ is known as ... a) Branching descent b) Natural Selection c) Saltation d) Gene Migration

Description : 7. A ‘single step-large mutation’ is known as ... a) Branching descent b) Natural Selection c) Saltation d) Gene Migration

Last Answer : c) Saltation

_______________ acts to inhibit reproductive isolation. A) Mutation B) Natural selection C) Genetic drift D) Gene flow

Description : _______________ acts to inhibit reproductive isolation. A) Mutation B) Natural selection C) Genetic drift D) Gene flow

Last Answer : D) Gene flow

The origin of a new species first requires A) reduced gene flow. B) increased gene flow. C) reduced mutation rates. D) increased mutation rates.

Description : The origin of a new species first requires A) reduced gene flow. B) increased gene flow. C) reduced mutation rates. D) increased mutation rates.

Last Answer : A) reduced gene flow.

If a gene mutation prevents formation of an enzyme normally used by a lysosomes, a disease may result known as (A) Lysosomal abstracted disease (B) Lysosomal secretory disease (C) Lysosomal storage disease (D) All A, B and C

Description : If a gene mutation prevents formation of an enzyme normally used by a lysosomes, a disease may result known as (A) Lysosomal abstracted disease (B) Lysosomal secretory disease (C) Lysosomal storage disease (D) All A, B and C

Last Answer : (C) Lysosomal storage disease

The type of gene interaction in which the effects of one gene override or mask the effects of other entirely different genes is called: a) linkage b) mutation c) pleitropy (pron: ply-ah-tropy) d) epistasis (pron: eh-pis-te-sis)

Description : The type of gene interaction in which the effects of one gene override or mask the effects of other entirely different genes is called: a) linkage b) mutation c) pleitropy (pron: ply-ah-tropy) d) epistasis (pron: eh-pis-te-sis)

Last Answer : ANSWER: D -- EPISTASIS