3.17 The accompanying pedigree and gel diagram that has multiple alleles. What are the possible show the phenotypes of the parents for an SSRP phenotypes of the progeny, and in what propor- show the phenotypes of the parents for an SSP tions are they expected? mon o boaOD 152 148 144 140 %3D king
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- W O () ENG 9:37 am O GENBIO-1ST-SEM-MIDTERN X 9 Schoology G karyotype of a certain huma x 6 BigBlueButton - GNBIO Messenger My Questions | bartleby + A app.schoology.com/common-assessment-delivery/start/5385424680?action=Donresume&submissionld=643190401 The diagram below shows a karyotype of a certain human. 8. 10 11 12 13 14 15 16 17 18 19 21 22 X Y Based on the karyotype, which of the following statements is most likely true? O The individual has a genetic condition caused by a nondisjunction event. The individual has a genetic condition caused by the X and Y chromosomes being different sizes. O The individual has a genetic condition caused by a chromosomal duplication. O The individual has a genetic condition caused chromosomes number one being different sizes. GENBIO-1ST-SEM-.pdf O 245180335_56899...jpg Show all ... TID N DAD × IDD . I ID.(19) WhatsApp 0 (542) H.E.R. - Changes X Why is it not possible X al%20School/OneDrive/Documents/Grade%2012%20variation%20and%20evolution%20 (D Page view A Read aloud V Draw Hig ii). iii). 13) 4. Sickle cell anemia is a favorable mutation. There is only one amino acid dillerent in Sickle hemoglobin (S) as compared with normal adult hemoglobin (A). Persons with sickle cell trait (AS) are able to survive in malarious areas. i) A couple each having sickle cell trait have five children. What is the probability thas they will have a child with sickle cell disease?Severe adverse effect of Tocilizumab and Dexamethasone in COVID19 ?
- 21:14 +4G KB/S LTED 41 96 09.00 Vo Microsoft Word - Assignment 02.docx Assignment 02 1. Groups of alleles associated with the lactose operon are as follows (in order of dominance for each allelic series): repressor, IS (superrepressor), I *(inducible), and I "(constitutive); operator, OC (constitutive, cis dominant) and 0+ (inducible, cis- dominant); structural, Z and Y. (a) Which of the following genotypes will produce B-galactosidase and B-galactoside permease if lactose is present: (1) 1*0* Z* Y*, (2) 1 *OCZ+ Y+, (3) OCZ+ Y+, (4) IS O+ Z+ Y+, and (5) 10+ Z+Y+? (b) Which of the above genotypes will produce ß-galactosidase and ß-galactoside permease if lactose is absent? Why? 2. By what mechanism does the presence of tryptophan in the medium in which E. coli cells are growing result in premature termination or attenuation of transcription of the trp operon? 3. Suppose that you used site-specific mutagenesis to modify the trpL sequence such that the two UGG Trp codons at positions…It has been found that blood types (ABO) affect the COVID-19 infection rate and the disease severity. Blood type A individuals are more likely to be infected and more likely to suffer from severe disease. Blood type O individuals seem to be less affected. Outline possible reasons for this. Note: So far, no studies have been published to conclusively answer this question, so there are no "wrong" answers here. The point is to come up with some ideas/hypotheses based on your knowledge about the molecular basis of blood types and what the consequences might be in relation to viral infections.Skin cancer carries a lifetime risk nearly equal to that of allother cancers combined. Following is a graph [modified fromK. H. Kraemer (1997). Proc. Natl. Acad. Sci. (USA) 94:11–14]depicting the age of onset of skin cancers in patients with orwithout XP, where the cumulative percentage of skin cancer is plotted against age. The non-XP curve is based on 29,757 cancerssurveyed by the National Cancer Institute, and the curverepresenting those with XP is based on 63 skin cancers from theXeroderma Pigmentosum Registry.
- 30*_SP23 - General Biology I (for majo us page Ö A 3:1 phenotypic ratio will occur when which of the following crosses is done? Select one: O a. Ttx Tt O b. O c. O d. O e. O f. GgTt x GgTt GGtt x ggTT GGTT x ggtt TT x tt tt x Tt tt x tt Oh. TT x Tt Oi. TT x TT g. O g. 000 MacBook AirSome people have a genetic predisposition for developing priondiseases. Examples are described in Table 25.6. In the case ofGerstmann-Straüssler-Scheinker disease, the age of onset istypically 30–50 years, and the duration of the disease (whichleads to death) is about 5 years. Suggest a possible explanationwhy someone can live for a relatively long time withoutsymptoms and then succumb to the disease in a relativelyshort time.Trivla Game Show _Make Your Own Tri ngston.schoology.com/common-assessment-delivery/start/4789189591?action=onresume&submissionld=463322566 Dillon WF g Aa v Done In guinea pigs, black hair (B) is dominant to white hair (b) and rough hair (R) is dominant to smooth hair (r). What are all the possible genotypes of a guinea pig that has black, rough hair? (Select all that apply.) O BBRR BBRr BBrr BBRR BbRr O bbRR O bbRr O bbrr O Black O White O Rough OSmooth O Rough O Smooth
- . Mutations in an autosomal gene in humans cause aform of hemophilia called von Willebrand disease(vWD). This gene specifies a blood plasma proteincleverly called von Willebrand factor (vWF). vWFstabilizes factor VIII, a blood plasma protein specified by the wild-type hemophilia A gene. Factor VIIIis needed to form blood clots. Thus, factor VIII is rapidly destroyed in the absence of vWF.Which of the following might successfully be employed in the treatment of bleeding episodes in hemophiliac patients? Would the treatments workimmediately or only after some delay needed forprotein synthesis? Would the treatments have only ashort-term or a prolonged effect? Assume that allmutations are null (that is, the mutations result in thecomplete absence of the protein encoded by the gene)and that the plasma is cell-free.a. transfusion of plasma from normal blood into avWD patientb. transfusion of plasma from a vWD patient into adifferent vWD patientc. transfusion of plasma from a hemophilia A…2. 235O 4) Q7. Haemophiliacs possess a non-functional form of the gene responsible for the production of blood clotting factors. Shown below is the occurrence of haemophilia in one family. = male = female = male haemophiliac 7. 8. 5. 9. 3. 11 12 Usingthe following symbols: H = dominant allele h = recessive allele 1) State the genotypes of the following individuals. Individual Genotype 1. 6. 2) On the basis of the information provided, is the inheritance of haemophilia: (i) autosomal or sex-linked? (ii) dominant or recessive? 3) State the probability of individual 8 being a carrier of haemophilia. 4) Explain why only females can be carriers of haemophilia.9:31 Dh O N ll 97% 20220331_200252.jpg Phoblims 84 In Drovphila a chros was made buetween females ell enprening the 3X- linkage, recuesive thaits, Slut bristus (sc), Scale body (5) and vermillion eye (v) and wild type males. On the FI, ell femalis cuere wild type whil all mals enprunid ell the matonttraits. The Chos was labrid to the F2 generation Ond 1000 offspring were countid arith resalt shoued beloo: Phonatype Se S V Set st yt. Set s v- Sc st v+ Sc st v Sct s vt. s vt. 314 280 156 46 30 10 14 Sc sct st v- To00 Uing the nommelature, detumine genatyps of Pond Fl patnt. D Osder f genes ond mapdistonce. 9 Aru there moto or fuver double crou thon onfectid D aleulate the Caeffeicint of Coincidence. 62 Femole hutrazygous for ehony le/e), searlit (st"/st) end spineles sst/ss) were itest chomud ord the following F praginy wrere olitainid:- Preginy Phenolypt Wild type e st ss - et st ss.- 67 8. 68 347 Spiniless - e st sst Scarlt fineles - e st so Ebony Ebony seorlet- ct set ss Ehgrny…