1 – Mitosis and Meiosis 1. A certain species has three pairs of chromosomes: an acrocentric pair‚ a metacentric pair‚ and a telocentric pair. Draw a cell of this species as it would appear in metaphase of mitosis. (BAP 2.18) 2. A cell in G1 of interphase has 12 chromosomes. How many chromosomes and DNA molecules will be found per cell when this original cell progresses to the following stages? (BAP 2.20) a) G2 of interphase b) Metaphase I of meiosis c) Prophase of mitosis d) Anaphase I of meiosis
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MEMBERS OF TEACHING STAFF College of Basic Science and Humanities‚ OUAT‚ Bhubaneswar-03 Sl. No 1 Department Name of the Teacher/ Designation Scientist Dr. Simadri Misra Director Specialization Solid state physics Tel. / Mob. No e-mail ID M-8895730684 Tel/Fax - 0674-2397029 directorbasicscience@gmail.com Mob. 9776353573 2 Physics Dr.(Mrs.) G. Das Prof &Head 3 4 5 6 7 8 9 10 11 12 13 14 15 Chemistry Dr. M. R. Acharya Assoc.Prof Assoc.Prof Asst. Prof Asst. Prof Asst. Prof Asst
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Clinical Laboratory Scientist What They Are and What They Do A clinical laboratory scientist can have a few different names such as “Medical Laboratory Scientist” or “Medical Laboratory Technician/Technologist”. A clinical laboratory scientist‚ or CLS‚ works in a laboratory testing different samples—bodily fluids‚ tissue samples‚ and cultures‚ to name some—to identify diseases and treatments for said diseases. What it Takes and Training To become a CLS‚ one must have a background of high school
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Mild Mental Retardation Speech and Language Disorders Introduction: Mild mental retardation is a lifelong disability that limits both the intellectual function and the adaptive behavior during the period of development. It first appears in children under the age of 18 and occurs in 2.5-3% of the population. There are a number of factors that cause mental retardation and most of the causes are chromosomal‚ metabolic and environmental. Symptoms appear once the child is born and later in childhood
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can be detected in one of the parents. A person having the CHARGE Syndrome has a risk of 50% to pass on the CHD7 mutation. But infertility is common in CHARGE Syndrome. So‚ a result of parent-to-child transmission is rare. Location of CHD7 Cytogenetic Location: 8q12.2 Molecular Location on chromosome 8: base pairs 61‚591‚323 to 61‚780‚586 The CHD7 gene is located on the long (q) arm of chromosome 8 at position 12.2. More precisely‚ the CHD7 gene is located from base pair 61‚591‚323 to base
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Cate Lee 5th Period Honors Biology Mrs. Presley Tay Sachs Disease A mutation (or mutating) is changing a structure of a gene. Tay Sachs disease is a lethal mutation inherited as an autosomal recessive disorder‚ it is also known as Hexosaminidase A deficiency‚ GM2-Gangliosidosis‚ or TSD. Tay Sachs is an extremely tragic disease that has no cure. Tay Sachs was named after and discovered by english ophthalmologist Warren Tay and Jewish-American neurologist Bernard Sachs. Tay and Sach’s development
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Klinefelter syndrome is an additional X chromosome in the cells affecting males. Meiotic nondisjunction is the major result of this syndrome. There are differences in the degree of severity of physical‚ language‚ and behavioral development symptoms between affected individuals. Klinefelter syndrome is not passed from parent to child; even though‚ women who have pregnancies after the age of 35 may have an increased chance of having a boy with the presence of extra sex chromosome. Tests for chromosome
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PATHOLOGY LABORATORY UNIT The pathology laboratory unit is an important part of the hospital services. This unit help to support cancer research and treatment for accurate diagnosis and effective cancer care to patients. The pathology unit had received an accreditation for laboratory from the Royal College of Pathologists of Thailand on June 30‚ 2011. Personnel This unit consists of 12 personnel; 2 consultant pathologists‚ 1 pathologist‚ 5 scientists‚ 2 administrative officers‚ and 2 operation staffs
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Cited: Zuckerman‚ B. “Cytogenetic‚ Host – Parasite Interactions‚ and Physiology”. (2012): 3-10. Frederic‚ Chalmel. “The Conserved Transcriptome in Human and Rodent Male Gametogenesis”. 104‚No.20 (2007): 8346-8351. Jagiello‚ David. “Bio regulators of Reproduction” (2012): 122-125
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and this was all based on morphological and cytochemical findings (Bennett et al.‚ 1976). This WHO classification system (WHO‚ 1999) further expended the parameters used when diagnosing AML they based their classification on the immunological‚ cytogenetic‚ morphological and clinical findings (Moe et al.‚ 2008). The revised (2008) World Health Organization classification system develops and improves the FAB system. According to the WHO classification‚ acute myeloid leukaemias are grouped into four
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