
John D. Gearhart - US grants
Affiliations: | Johns Hopkins University, Baltimore, MD |
Area:
Cell Biology, Molecular Biology, Neuroscience BiologyWebsite:
https://hss.sas.upenn.edu/people/john-d-gearhartWe are testing a new system for linking grants to scientists.
The funding information displayed below comes from the NIH Research Portfolio Online Reporting Tools and the NSF Award Database.The grant data on this page is limited to grants awarded in the United States and is thus partial. It can nonetheless be used to understand how funding patterns influence mentorship networks and vice-versa, which has deep implications on how research is done.
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High-probability grants
According to our matching algorithm, John D. Gearhart is the likely recipient of the following grants.Years | Recipients | Code | Title / Keywords | Matching score |
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1989 — 1991 | Gearhart, John D | R01Activity Code Description: To support a discrete, specified, circumscribed project to be performed by the named investigator(s) in an area representing his or her specific interest and competencies. |
Differential Gene Expression in Early Mouse Embryos @ Johns Hopkins University The objective of this proposal is to identify genes whose expression is regulated differentially during the blastocyst, egg cylinder, and primitive streak stages of mouse embryogenesis. One commonly used strategy for the identification and subsequent characterization of important gene transcripts is the construction and analyses of cDNA libraries. The principal limitation to this approach in early mammalian embryogenesis is the amount of tissue (and thus RNA) per embryo. We have modified standard procedures for cDNA cloning, and have developed a new procedure using polymerase chain reaction to efficiently clone small amounts of RNA. We have constructed and characterized a large cDNA library from blastocysts which has a proportional representation of RNA species. We are currently generating libraries to inner cell mass, early egg cylinders, and primitive streak embryos. We propose in this application to identify sets of genes that show stage specificity and tissue-specific expression with the ultimate goal of determining how the expression of these sets is regulated. cDNAs will be identified by differential screens, partially sequenced, and homologies sought. In situ hybridization will be used to examine the spatial distribution of gene expression within embryos. Additionally, the libraries will be probed for conserved sequences that appear to regulate transcription during development (such as homeobox, paired box, and "zinc finger" protein domains), and for oncogenes and growth factors that influence morphogenesis and cell differentiation (TGF-alpha, TGf-beta EGF receptor and insulin-like growth factor). The abundance and tissue distribution of transcripts of these genes will be determined. |
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1989 — 2000 | Gearhart, John D | P01Activity Code Description: For the support of a broadly based, multidisciplinary, often long-term research program which has a specific major objective or a basic theme. A program project generally involves the organized efforts of relatively large groups, members of which are conducting research projects designed to elucidate the various aspects or components of this objective. Each research project is usually under the leadership of an established investigator. The grant can provide support for certain basic resources used by these groups in the program, including clinical components, the sharing of which facilitates the total research effort. A program project is directed toward a range of problems having a central research focus, in contrast to the usually narrower thrust of the traditional research project. Each project supported through this mechanism should contribute or be directly related to the common theme of the total research effort. These scientifically meritorious projects should demonstrate an essential element of unity and interdependence, i.e., a system of research activities and projects directed toward a well-defined research program goal. |
Genes, Aneuploidy, and Mammalian Development @ Johns Hopkins University |
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1994 — 1998 | Gearhart, John D | P01Activity Code Description: For the support of a broadly based, multidisciplinary, often long-term research program which has a specific major objective or a basic theme. A program project generally involves the organized efforts of relatively large groups, members of which are conducting research projects designed to elucidate the various aspects or components of this objective. Each research project is usually under the leadership of an established investigator. The grant can provide support for certain basic resources used by these groups in the program, including clinical components, the sharing of which facilitates the total research effort. A program project is directed toward a range of problems having a central research focus, in contrast to the usually narrower thrust of the traditional research project. Each project supported through this mechanism should contribute or be directly related to the common theme of the total research effort. These scientifically meritorious projects should demonstrate an essential element of unity and interdependence, i.e., a system of research activities and projects directed toward a well-defined research program goal. |
Utilization of Transgenics in the Study of Down Syndrome @ Johns Hopkins University The objective of the proposed research is to identify the genetic and biological bases for features of the Down Syndrome (DS) phenotype. This will be accomplished through the use of large segments of human chromosome 21 (HSA21) cloned as yeast artificial chromosomes, or YACs, and introduced into the germ line of the mouse. These YAC transgenics will be analyzed for the neurobiological and other features of the DS phenotype. The Specific Aims of the project are: 1) To determine if the overexpression of the amyloid precursor protein (APP) gene in transgenic mice leads to the neuropathology seen in DS. A principal pathologic hallmark of DS is deposition of B-amyloid protein (ABeta) forming plaques in the parenchyma of amygdala, hippocampus, and neocortex. ABeta is a small peptide derived from the amyloid precursor protein, an integral membrane glycoproteins encoded by a large gene (400kb) on HSA21. Possible mechanisms involved in the production of ABeta and the formation of the amyloid-containing plaques include the overexpression of APP. We will analyze several lines of APP YAC transgenics as they age, including lines with different levels of APP overexpression, as well as line carrying a mutation in the APP gene, which in humans results in Alzheimer's disease. 2) To determine if the overexpression of superoxide dismutase 1 (SOD1) in transgenic mice results in features of DA. The overexpression of SOD1 has been reported in transgenic mice to result in abnormal neuromuscular junctions. The transgene used in those experiments did not have the regulatory sequences responsible for tissue-appropriate expression. We will repeat these studies with YAC transgenics that carry significantly more upstream sequences of the SOD1 gene. We will also examine the effects of SOD1 overexpression as a result of a mutation in the human SOD1 gene. 3) To determine if the dosage imbalance of genes on several selected YACs carrying HSA21 sequences from he 21q22 region (and more distally) results in features of DS in transgenic mice. We will select stable, nonchimeric YACs with known markers or genes and will introduce these into the germ line of mice. If features of the DS phenotype are observe in the transgenic mice, the sequence responsible will be defined through YAC fragmentation and hybridization gene cloning strategies. |
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1997 | Gearhart, John D | R13Activity Code Description: To support recipient sponsored and directed international, national or regional meetings, conferences and workshops. |
Exstrophy/Epispadias Urological Conference @ Johns Hopkins University Bladder exstrophy, cloacal exstrophy, and epispadias are all variants of the exstrophy-epispadias complex. Although the incidence of this complex is not common, its effects on the child are life-long. Although recently, better ways of managing these conditions have been developed, there is still a need for more basic science research to understand how exstrophic bladder smooth muscle and its matrix components develop in the pre-natal and newborn period and how they can be optimized to yield better functional results. Meanwhile, the surgical reconstructive techniques for patients with this spectrum of conditions continues to be debated within the literature. This conference will bring together major clinical investigators who care for patients born with the exstrophy-epispadias complex as well as scientific investigators who study the morphologic and functional bladder changes seen in this condition as well as in normal bladder development. An international field of 29 speakers (most of whom have been working with the exstrophy-epispadias complex for at least 5 years) will present their work on a particular subtopic in a 15 or 20 minute talk. Subtopics will be clustered together and followed by open panel discussions. We hope to assemble speakers with diverse views to prompt a vigorous exchange of ideas. There will also be an opportunity for young investigators to present their work in a moderated poster session. Presenters will also submit their work for publication in a conference manuscript. This conference will be unique for several reasons. There has never been an international conference of this magnitude which has been dedicated solely to the topic of the exstrophy-epispadias complex. Second, it will combine the expertise of both clinical and laboratory investigators most of whom have spent many years studying the changes in bladder composition and function which occur with this clinical spectrum, and will allow them a format for presenting their most recent findings. Lastly, there will be time for in-depth discussion to insure that everyone will benefit from this experience. Our goal is to not only disseminate important new information, but also to encourage further collaboration between clinicians and basic scientists. |
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2000 — 2002 | Gearhart, John D | P01Activity Code Description: For the support of a broadly based, multidisciplinary, often long-term research program which has a specific major objective or a basic theme. A program project generally involves the organized efforts of relatively large groups, members of which are conducting research projects designed to elucidate the various aspects or components of this objective. Each research project is usually under the leadership of an established investigator. The grant can provide support for certain basic resources used by these groups in the program, including clinical components, the sharing of which facilitates the total research effort. A program project is directed toward a range of problems having a central research focus, in contrast to the usually narrower thrust of the traditional research project. Each project supported through this mechanism should contribute or be directly related to the common theme of the total research effort. These scientifically meritorious projects should demonstrate an essential element of unity and interdependence, i.e., a system of research activities and projects directed toward a well-defined research program goal. |
Transgenesis in the Study of Down Syndrome @ Johns Hopkins University The objective of the proposed research is to identify the genetic and biological bases for features of the Down Syndrome phenotype. This will be accomplished through the transfer of genes and chromosomal segments (cloned as YACs, BACs, and/or PACs) from human chromosome 21 through transgenic procedures into the mouse germline, producing dosage imbalance for the transferred sequences. Attempts will be made to generate mice carrying chromosome 21 through physical transfer of the chromosome into mouse embryonic stem cells. The transgenic animals will be analyzed for neurobiological and other features of the of the DS phenotype. Analysis will also be performed on tissues from transgenic animals to determine those genes whose expression changes in response to the presence of extra copies of genes or chromosomal segments. |
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2001 | Gearhart, John P | R13Activity Code Description: To support recipient sponsored and directed international, national or regional meetings, conferences and workshops. |
International Symposium On Exstrophy-Epispadias Complex @ Johns Hopkins University DESCRIPTION (Adapted from applicant's description): Bladder exstrophy, cloacal exstrophy and epispadias are all variants of the exstrophy-epispadias complex. Although this is an uncommon congenital anomaly, its effects on the child and family are life-long. Significant strides have been made in improving the functional and cosmetic results of surgical reconstruction, however an understanding of the embryological development of the anomaly and the resultant changes in the bladder and related organs of the body in this congenital anomaly continue to be elucidated. This Second Symposium will again bring together researchers and surgeons from around the world to share and develop consensus on the latest research efforts in the field as well as showcasing the latest surgical advances. Fifteen to twenty minute talks will be presented by individuals with considerable expertise in the field of exstrophy and epispadias (minimum 5 years of experience in this area). This will be followed by open panel discussions in which audience participation will be permitted. Fielding a panel of speakers with diverse views on the various aspects of research and management will permit a vigorous exchange of ideas. There will also be the opportunity for young researchers in the field to present their continuing work. Presenters will have their material submitted for publication in the conference proceedings. The First Symposium was well attended and the reviews were universally positive. The Proceedings have been published in the form of a text. It is hoped that the continued rapport generated by conferences of this nature will permit greater collaboration between researchers in the field from all parts of the world and further improve the understanding of this complex set of malformations. |
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2001 — 2002 | Gearhart, John D | P01Activity Code Description: For the support of a broadly based, multidisciplinary, often long-term research program which has a specific major objective or a basic theme. A program project generally involves the organized efforts of relatively large groups, members of which are conducting research projects designed to elucidate the various aspects or components of this objective. Each research project is usually under the leadership of an established investigator. The grant can provide support for certain basic resources used by these groups in the program, including clinical components, the sharing of which facilitates the total research effort. A program project is directed toward a range of problems having a central research focus, in contrast to the usually narrower thrust of the traditional research project. Each project supported through this mechanism should contribute or be directly related to the common theme of the total research effort. These scientifically meritorious projects should demonstrate an essential element of unity and interdependence, i.e., a system of research activities and projects directed toward a well-defined research program goal. |
Genes, Aneuploidy and Mammalian Development @ Johns Hopkins University Down Syndrome is the most common known genetic cause of mental retardation. The major goal of this program is to understand the genetic and biologic bases of mental retardation in Down Syndrome. Building on the increasing large body of information on Down Syndrome, from the genetics to the clinical features, this program utilizes recombinant DNA technology, comparative genetics, and animal models in attempts to identify and characterize the genes involved in the Syndrome, particularly those producing the neurobiological and cognitive deficits. Also, utilizing some of the animal models, neuropharmacological interventions are proposed in attempts to ameliorate the learning and memory deficits that have been demonstrated in these animals. These animal-based efforts will ultimately lead to therapies for the neurobiological and cognitive deficits characteristic of Down Syndrome. Finally, we propose a new study combining cytogenetic, molecular and epidemiological approaches to address factors that may predispose to non-dysfunction of chromosome 21 and the genetic basis of the phenotypic consequences of an additional chromosome 21. |
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2009 | Gearhart, John P | R13Activity Code Description: To support recipient sponsored and directed international, national or regional meetings, conferences and workshops. |
3rd International Symposium On the Exstrophy - Epispadias Complex @ Johns Hopkins University DESCRIPTION (provided by applicant): Bladder exstrophy, cloacal exstrophy, and epispadias are all variants of the exstrophyepispadias complex. Although this is an uncommon congenital anomaly, its effects on the child and family are life-long. Over the last 50 years, slow, incremental refinements in the medical and surgical management of these conditions have permitted most children to lead productive lives with good renal outcomes. Yet, while significant gains have been made, the etiology for the development of the complex and the mechanisms that do not permit complete success in all children still remain to be determined. There is still much to be learned in areas of such as incontinence management, detrusor physiology, genital reconstruction, and fertility as they relate to exstrophy, epispadias, and cloacal exstrophy. This symposium intends to concentrate on those areas. The 3rd International Symposium on the Exstrophy - Epispadias Complex is the only academic forum dedicated solely to the exchange of ideas in the management of these conditions and again brings together recognized international experts in the field and allows for their cross talk with junior investigators and young clinicians, setting the stage for continued advancement. Fifteen to twenty minute talks will be presented by individuals with considerable expertise in the field of exstrophy and epispadias. These sessions will then be followed by open panel discussions in which audience participation is permitted. Fielding a panel of speakers with diverse views on the various aspects of research and management will permit a vigorous exchange of ideas. There will also be opportunities for young researchers in the field to present their continuing work. Presenters will have their material submitted for publication in the conference proceedings. Our two previous symposiums were well attended and reviews were universally positive. It is hoped that the continued rapport generated by conferences of this nature will permit greater collaboration between researchers in the field from all parts of the world and further improve our understanding of this complex set of malformations. While bladder exstrophy, epispadias, and cloacal exstrophy doomed children to dismal outcomes fifty years ago, slow, incremental refinements in the medical and surgical management of these conditions have permitted most children to lead productive lives with good renal outcomes. Yet, while significant gains have been made, the etiology for the development of the complex and the mechanisms that do not permit complete success in all children still remain to be determined. The 3rd International Symposium on the Exstrophy - Epispadias Complex is the only academic forum dedicated solely to the exchange of ideas in the management of these conditions and brings together recognized international experts in the field and allows for their cross talk with junior investigators and young clinicians, setting the stage for continued advancement. |
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