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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Molecular biological aspects of nitrogen starvation in cyanobacteria

Alley, M. R. K. January 1987 (has links)
No description available.
2

Immunogenetics of rheumatoid arthritis

Thomson, W. January 1987 (has links)
No description available.
3

Synaptonemal complex formation in Avena

Jones, Marion January 1987 (has links)
No description available.
4

Pea seed lipoxygenase variants

North, Helen Mary January 1990 (has links)
No description available.
5

Structure and function of the methylenomycin A resistance gene of Streptomyces coelicolor A3(2)

Neal, R. J. January 1987 (has links)
No description available.
6

Arginine and proline catabolism in Schizosaccharomyces pombe

Walters, Nicola Jane January 1988 (has links)
No description available.
7

A study of the myc gene in feline leukaemias

Forrest, D. January 1987 (has links)
No description available.
8

A Genetic Study of Linkage and Inheritance in Barley

Oldham, Jerald Dean 01 January 1962 (has links)
No description available.
9

Estudio del gen del canal de sodio (SCN5A) en una población de pacientes con diagnóstico de síndrome de Brugada

García-Molina Sáez, Esperanza 27 July 2011 (has links)
El Síndrome de Brugada (SB) se caracteriza por una elevación del segmento ST en las derivaciones precordiales derechas del ECG. Tiene una base genética estando ligado a mutaciones en el canal de Na+ del corazón (SCN5A) y otros genes recientemente relacionados. El estudio de secuenciación directa del gen SCN5A en nuestra población llevó a la identificación de mutaciones causales o probablemente causales en un 10% de los casos, inferior al publicado en la literatura. En los casos índice en los que no se detectó una variante en su secuencia se realizó el estudio de grandes reordenamientos génicos sin identificarse ninguno mediante la técnica de Multiplex Ligation Probe Amplification. Los pacientes de nuestra cohorte portadores de mutación presentan con mayor frecuencia ECG tipo I espontáneo y más casos de muerte súbita familiar que los pacientes de SB con genotipo negativo. El estudio genético de las familias de los portadores de mutación ha permitido identificar a un grupo significativo de portadores sin expresión fenotípica.
10

Molecular genetic study of vulval morphogenesis in C. elegans and related nematode species

Panyala, Sujatha 29 June 2017 (has links)
<p> Caenorhabditis elegans (C. elegans) is a model organism which is known for its transparent body, small body size, high reproductivity and short lifecycle. Several important genes and signal transduction pathways are well conserved in C. elegans. lin//, a LIM homeobox family member, plays a crucial role in the development of the vulva in C. elegans. LIM homeobox genes are a subgroup of Homeobox family that play fundemental role in animal development. In C. elegans lin-If mutant animals fail to form a functional vulva and vulval-uterine connection and consequently exhibit egg-laying defective phenotype. The cell lineage and marker gene expression studies have shown that lin-// is required for the patterning of all primary and secondary lineage vulval cells. lin- II also functions in the nervous system. </p> <p> lin-// expression is mainly observed in the developing vulval cells and in the pi cells which are involved in the formation of vulval-uterine connection. lin-If expression is also seen in VCs and in some of the head and tail neurons. The completed genome sequences of closely related species in Caenorhabditis genus serve as a power tool to do systematic comparative studies. The lin-If regulatory sequences from these species have been compared along with the expression patterns. </p> <p> We looked at the regulation of lin-// in closely related nematode species like C. elegans, C. briggsae, C. remanei and Caenorhabditis n species. </p> <p> Consistent with this. expression of lin-11 is observed in the developing vulval cells. We are interested in understanding evolutionary changes in the regulation and function of lin-II in reproductive system </p> <p> /in-11 is a LIM homeodomain family member which IS involved in several developmental events. lin-11 role is documented in the thermoregulatory circuit specifying AIY interneuron, in chemosensory neurons like A W A and olfactory neurons A WS. During vulval development lin-II expression is dynamically expressed in subset of secondary lineage cells and is broadly expressed in all the cells indicating its role in cell identity and cell fusion of the vulval cells. lin-II is also required for the formation of vulval uterine connection which is the passage to lay eggs in the hermaphrodite. linllloss of function hermaphrodites have change in the axis of the secondary lineage cells during vulval development, uterine Jt cell migration defect, defects in the AIY, A W A and A WS interneurons resulting in egg-laying defect and protruding vulva and neuronal defects and reduced mating efficiency. </p> <p> The expression pattern of lin-If in closely related species is highly similar but not identical. From the sequence comparison of lin-If regulatory sequences a 1 kb conserved block of sequences have been identified which includes the regulatory sequences responsible for the expression of lin-If in vulva and Jt cells. We propose that cisregulatory elements controlling lin-If gene expression are slowly evolving though there is no change in the function which indicates that lin-If plays critical role during the development of the vulva and other tissues. </p> / Thesis / Master of Science (MSc)

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