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Harold Gainer

Researcher at National Institutes of Health

Publications -  216
Citations -  13780

Harold Gainer is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Vasopressin & Supraoptic nucleus. The author has an hindex of 61, co-authored 216 publications receiving 13532 citations. Previous affiliations of Harold Gainer include Utrecht University & University of Pennsylvania.

Papers
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Journal ArticleDOI

Multiple-rate components of axonally transported proteins in the hypothalamo-neurohypophysial system of the rat

TL;DR: The transport of labeled proteins from the hypothalamus to the neurohypophysis following 35S-methionine injection into the rat supraoptic nucleus was studied using a unique approach adapted for the study of short-axon systems.
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The -216- to -100-bp Sequence in the 5'-Flanking Region of the Oxytocin Gene Contains a Cell-Type Specific Regulatory Element for its Selective Expression in Oxytocin Magnocellular Neurones

TL;DR: Testing the coupled hypotheses that the −216‐ to −100‐bp sequence is responsible for the selective expression of the OXT gene in OXT‐MNCs and its selective repression in vasopressin (AVP)‐MCNs shows that these and other data demonstrate that the 5′‐flanking region of the oxytocin gene contains only an activator of transcription operating in the OXMNs.
Book

Molecular Neuroendocrinology: From Genome to Physiology

TL;DR: The 19 chapters are divided into four sectors and presents a range of case studies that exemplify the state-of-the-art application of genomic technologies in physiological and behavioural experiments that seek to better understand complex biological processes.
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Bcl-xL and caspase inhibition increase the survival of rat oxytocin and vasopressin magnocellular neurons in organotypic culture.

TL;DR: It is found that the novel, membrane permeant form of Bcl-xL that was employed in these studies protected both OT and VP MCNs from degeneration as long as the Bcl -xL was present in the medium.
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Effects of ciliary neurotrophic factor and leukemia inhibiting factor on oxytocin and vasopressin magnocellular neuron survival in rat and mouse hypothalamic organotypic cultures

TL;DR: The use of the neurotrophic factors, leukemia inhibiting factor (LIF) and ciliary neurotrophic factor (CNTF) to rescue rat vasopressin (Avp)- and oxytocin (Oxt)-MCNs from axotomy-induced, programmed cell death in vitro is described.