'Humans and other animals'-on the scope of brain science.

Abstract:

:Abstract: This essay is dedicated to Obaid on the occasion of his 80th birthday. We both worked on the behavior of Drosophila and on what underlies behavior in the fly brain. Is that the fly's mind? The essay is about some limitations of brain science. It is just a little piece of writing. It is meant to honor Obaid for his contributions to Drosophila neurogenetics in 40 years and to science in India. I hope he takes it instead of a bowl of flowers-adding to the praise.

journal_name

J Neurogenet

journal_title

Journal of neurogenetics

authors

Heisenberg M

doi

10.3109/01677063.2012.687796

subject

Has Abstract

pub_date

2012-09-01 00:00:00

pages

267-70

issue

3-4

eissn

0167-7063

issn

1563-5260

journal_volume

26

pub_type

历史文章,杂志文章
  • Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.

    abstract::To date, less than 10 pedigrees have been reported with ZNF335 mutations since it was discovered in 2012 and little is known about ZNF335-related clinical spectrum. We describe a 12 years old male patient who is only child of nonconsanguineous Turkish parents. Trio whole genome sequencing identified previously unrepor...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2020.1833006

    authors: Caglayan AO,Yaghouti K,Kockaya T,Kemer D,Cankaya T,Ameziane N,Cogulu O,Coker M,Yalcinkaya C

    更新日期:2020-11-20 00:00:00

  • The early years of Drosophila chemosensory genetics in Mumbai's Tata Institute of Fundamental Research.

    abstract::Some of the very first chemosensory mutants in Drosophila were generated in screens done in the 1970s at Obaid Siddiqi's lab in Tata Institute of Fundamental Research (TIFR), Mumbai. This is a personal account of some of the early work with these mutants, which led to their physiological and molecular characterization...

    journal_title:Journal of neurogenetics

    pub_type: 历史文章,杂志文章

    doi:10.3109/01677063.2012.677880

    authors: Hasan G

    更新日期:2012-09-01 00:00:00

  • A novel mutation in the gene encoding noggin is not causative in human neural tube defects.

    abstract::Neural tube defects (NTD) are a common birth defect, with both genetic and environmental contributions to their etiology. In mouse, null mutations in Noggin result in fully-penetrant NTDs. We investigated Noggin for mutations that may predispose to human NTDs in 202 NTD cases. One variant allele was identified in a ma...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:

    authors: Bauer KA,George TM,Enterline DS,Stottmann RW,Melvin EC,Siegel D,Samal S,Hauser MA,Klingensmith J,Nye JS,Speer MC,Neural Tube Defects Collaborative Group.

    更新日期:2002-01-01 00:00:00

  • C. elegans: a sensible model for sensory biology.

    abstract::From Sydney Brenner's backyard to hundreds of labs across the globe, inspiring six Nobel Prize winners along the way, Caenorhabditis elegans research has come far in the past half century. The journey is not over. The virtues of C. elegans research are numerous and have been recounted extensively. Here, we focus on th...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2020.1823386

    authors: Iliff AJ,Xu XZS

    更新日期:2020-09-01 00:00:00

  • Helmsman is expressed in both trachea and photoreceptor development: partial inactivation alters tracheal morphology and visually guided behavior.

    abstract::We have identified helmsman (hlm), which is expressed in the fruit fly photoreceptor cells during neural network development. Hlm is also expressed in the elongating cells of the embryonic trachea. Both photoreceptor neurons and embryonic trachea cells elongate in precise, targeted growth for cell-to-cell specific rec...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677060801893276

    authors: McKay JP,Nightingale B,Pollock JA

    更新日期:2008-01-01 00:00:00

  • Dopamine modulates female sexual receptivity in Drosophila melanogaster.

    abstract::Newly eclosed Drosophila melanogaster flies were systemically depleted of dopamine by feeding an inhibitor of the biosynthetic enzyme, tyrosine hydroxylase, and analyzed for abnormalities in courtship behavior. Dopamine-depleted females were significantly less receptive to males than were control females, although mal...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677069809167259

    authors: Neckameyer WS

    更新日期:1998-03-01 00:00:00

  • From form to function: the ways to know a neuron.

    abstract::The shape of a neuron, its morphological signature, dictates the neuron's function by establishing its synaptic partnerships. Here, we review various anatomical methods used to reveal neuron shape and the contributions these have made to our current understanding of neural function in the Drosophila brain, especially ...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.1080/01677060802610604

    authors: Meinertzhagen IA,Takemura SY,Lu Z,Huang S,Gao S,Ting CY,Lee CH

    更新日期:2009-01-01 00:00:00

  • Kinase-mediated signaling cascades in mood disorders and antidepressant treatment.

    abstract::Kinase-mediated signaling cascades regulate a number of different molecular mechanisms involved in cellular homeostasis, and are viewed as one of the most common intracellular processes that are robustly dysregulated in the pathophysiology of mood disorders such as depression. Newly emerged, rapid acting antidepressan...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.1080/01677063.2016.1245303

    authors: Yuan LL,Wauson E,Duric V

    更新日期:2016-01-01 00:00:00

  • Mapping neural circuits with activity-dependent nuclear import of a transcription factor.

    abstract::Abstract: Nuclear factor of activated T cells (NFAT) is a calcium-responsive transcription factor. We describe here an NFAT-based neural tracing method-CaLexA (calcium-dependent nuclear import of LexA)-for labeling active neurons in behaving animals. In this system, sustained neural activity induces nuclear import of ...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2011.642910

    authors: Masuyama K,Zhang Y,Rao Y,Wang JW

    更新日期:2012-03-01 00:00:00

  • Role of hippocampal Met-enkephalin in the genotype-dependent regulation of exploratory behavior in mice.

    abstract::Intrahippocampal microinjections with anti-Met-enkephalin antiserum enhanced novelty-induced vertically oriented exploratory acts and horizontal locomotor activity in inbred mouse strain DBA/2 and reduced these behaviors in C57BL/6 so that strain differences originally present between the normal serum controls were el...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068609106848

    authors: van Abeelen JH,Gerads HJ

    更新日期:1986-05-01 00:00:00

  • The murine mutation trembler-J: proof of semidominant expression by use of the linked vestigial tail marker.

    abstract::Trembler-J, TrJ, is a peripheral hypomyelinating murine mutant. In intercrosses (TrJ/ + X TrJ/ +) there are severely affected (behaviorally and pathologically), mildly affected, and normal offspring, while backcrosses (TrJ/ + X + / +) produce only mildly affected and normal offspring. We used the closely linked marker...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068309107071

    authors: Henry EW,Sidman RL

    更新日期:1983-09-01 00:00:00

  • Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphisms.

    abstract::A search for the defective gene causing torsion dystonia has been carried out in a family manifesting an autosomal dominant mode of inheritance of this movement disorder. Complete neurologic examination and establishment of lymphoblast lines have been carried out for over 50 members. Linkage analysis, using cloned DNA...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068609106846

    authors: Breakefield XO,Bressman SB,Kramer PL,Ozelius L,Moskowitz C,Tanzi R,Brin MF,Hobbs W,Kaufman D,Tobin A

    更新日期:1986-05-01 00:00:00

  • The role of human-specific gene duplications during brain development and evolution.

    abstract::One of the most fascinating questions in evolutionary biology is how traits unique to humans, such as their high cognitive abilities, erect bipedalism, and hairless skin, are encoded in the genome. Recent advances in genomics have begun to reveal differences between the genomes of the great apes. It has become evident...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2013.789512

    authors: Sassa T

    更新日期:2013-09-01 00:00:00

  • Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomy.

    abstract::Myoclonic status in nonprogressive encephalopathy (MSNE) is an early-onset, drug-resistant epileptic syndrome characterized by occurrence of continuous diffuse epileptiform abnormalities, associated with positive and/or negative phenomena and accompanied by transient and recurring motor, cognitive, and behavioral impa...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2015.1091452

    authors: Nicita F,Garone G,Papetti L,Consoli F,Magliozzi M,De Luca A,Spalice A

    更新日期:2015-01-01 00:00:00

  • Identification of a Drosophila presenilin homologue: evidence of alternatively spliced forms.

    abstract::Some cases of Alzheimer's disease are inherited as a dominant trait in humans. To date, mutations in three genes account for some of them: the amyloid precursor protein (APP) and presenilins 1 and 2 (PS-1 and PS-2, respectively). The function of the presenilins is still unclear, although they belong to a transmembrane...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677069809108554

    authors: Marfany G,Del-Favero J,Valero R,De Jonghe C,Woodrow S,Hendriks L,Van Broeckhoven C,Gonzàlez-Duarte R

    更新日期:1998-01-01 00:00:00

  • High frequency of mutations in the PIK3CA gene helical and kinase coding regions in a group of Iranian patients with high-grade glioblastomas: five novel mutations.

    abstract::Glioblastoma multiform (GBM; World Health Organization (WHO) grade IV) and anaplastic astrocytomas (AA; WHO grade III) are highly aggressive and lethal astrocytic brain tumors. To detect cancer-specific somatic mutations in two hot-spot regions of PIK3CA gene, the helical and kinase domains (encoded by exons 9 and 20,...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2011.623202

    authors: Derakhshandeh-Peykar P,Alivi J,Hossein-nezhad A,Rautenstrauss B,Vesal RE,Doriani A

    更新日期:2011-12-01 00:00:00

  • Dopamine DRD2 polymorphism (DRD2/ANNK1-Taq1A) is not a significant risk factor in writer's cramp.

    abstract::Writers' cramp is a movement disorder with dystonic co-contraction of fingers and hand during writing and is part of the clinical spectrum of focal dystonias. Previous studies showed reduced striatal dopamine receptor D2 (DRD2) availability in dystonia. The expression of D2 receptors is modulated by a DRD2/ANKK1-Taq1A...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2016.1238916

    authors: Zeuner KE,Acewicz A,Knutzen A,Dressler D,Lohmann K,Witt K

    更新日期:2016-01-01 00:00:00

  • Optomotor-blind in the development of the Drosophila HS and VS lobula plate tangential cells.

    abstract::The horizontal system and vertical system cells of the dipteran optic lobes are well understood regarding their physiology and role in visually guided behavior. Little is known, however, about their development. Drosophila optomotor-blind (omb) is required for the development of the HS/VS cells which are lacking in th...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2014.917645

    authors: Sen A,Grimm S,Hofmeyer K,Pflugfelder GO

    更新日期:2014-09-01 00:00:00

  • The irre cell recognition module (IRM) protein Kirre is required to form the reciprocal synaptic network of L4 neurons in the Drosophila lamina.

    abstract::Each neuropil module, or cartridge, in the fly's lamina has a fixed complement of cells. Of five types of monopolar cell interneurons, only L4 has collaterals that invade neighboring cartridges. In the proximal lamina, these collaterals form reciprocal synapses with both the L2 of their own cartridge and the L4 collat...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2014.883390

    authors: Lüthy K,Ahrens B,Rawal S,Lu Z,Tarnogorska D,Meinertzhagen IA,Fischbach KF

    更新日期:2014-09-01 00:00:00

  • Behavioral Plasticity in the C. elegans Mechanosensory Circuit.

    abstract::This review outlines research into the cellular and molecular mechanisms underlying a simple behavior in the soil-dwelling nematode, C. elegans. A tap administered to the side of a petri plate acts as a nonlocalized mechanical stimulus to the worms within. Most adult worms respond to this tap stimulus with backward lo...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.1080/01677060802298509

    authors: Ardiel EL,Rankin CH

    更新日期:2008-01-01 00:00:00

  • Strong stimulation triggers full fusion exocytosis and very slow endocytosis of the small dense core granules in carotid glomus cells.

    abstract::Chemosensory glomus cells of the carotid bodies release transmitters, including ATP and dopamine mainly via the exocytosis of small dense core granules (SDCGs, vesicular diameter of ∼100 nm). Using carbon-fiber amperometry, we showed previously that with a modest uniform elevation in cytosolic Ca2+ concentration ([Ca2...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2018.1497629

    authors: Tse A,Lee AK,Takahashi N,Gong A,Kasai H,Tse FW

    更新日期:2018-09-01 00:00:00

  • Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.

    abstract::Autosomal recessive cerebellar ataxias are a group of clinically and genetically heterogeneous neurodegenerative disorders. Growing data have shown that there is difficulty with genetic counseling in a deeply consanguineous population because of the presence of genetic heterogeneity in patients sharing similar phenoty...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677060802025233

    authors: Bouhlal Y,Zouari M,Kefi M,Ben Hamida C,Hentati F,Amouri R

    更新日期:2008-01-01 00:00:00

  • A qualitative and quantitative light microscopic study of the inferior olivary complex in the adult staggerer mutant mouse.

    abstract::In the homozygous staggerer (sg/sg) mutant mouse, most of the Purkinje cells (the primary targets for olivocerebellar climbing fibers) are missing or ectopic. In this study, the organization and cell number of the inferior olivary complex in sg/sg were determined and compared to the inferior olive of the wildtype (+/+...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068509100143

    authors: Blatt GJ,Eisenman LM

    更新日期:1985-02-01 00:00:00

  • The pattern of early neuronal differentiation in Drosophila melanogaster.

    abstract::Based on the staining of Drosophila embryos with neuron-specific monoclonal antibodies we describe the differentiation of the earliest neurons in the central nervous system. The metameric array undergoes a number of changes during development that distinguish several morphological units: metameres, neuromeres and gang...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068609106856

    authors: Canal I,Ferrús A

    更新日期:1986-09-01 00:00:00

  • Adaptive adjustment of the generalization-discrimination balance in larval Drosophila.

    abstract::Learnt predictive behavior faces a dilemma: predictive stimuli will never 'replay' exactly as during the learning event, requiring generalization. In turn, minute differences can become meaningful, prompting discrimination. To provide a study case for an adaptive adjustment of this generalization-discrimination balanc...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2010.498066

    authors: Mishra D,Louis M,Gerber B

    更新日期:2010-09-01 00:00:00

  • The rdgB gene of Drosophila: a link between vision and olfaction.

    abstract::otal (ota=olfactory trap abnormal), an X-linked mutation of Drosophila isolated by virtue of abnormal olfactory behavior, is shown to be an allele of rdgB (retinal degeneration B), a gene required for normal visual system physiology. rdgB function is shown to be necessary for olfactory response of both adult files and...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677060701695441

    authors: Woodard C,Alcorta E,Carlson J

    更新日期:2007-10-01 00:00:00

  • Karl-Friedrich Fischbach's first publications and their impact in the biological sciences.

    abstract::Predictions from the theory of transfection, Karl-Friedrich Fischbach's first paper, were confirmed 20 years later. Also a model, proposed already in 1977 by Karl-Friedrich and colleagues, to explain the nonmonotonous dependence on light intensity of phototaxis in Drosophila, finds support in recent studies of functio...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2013.873430

    authors: Spatz HC

    更新日期:2014-09-01 00:00:00

  • FOXO regulates cell fate specification of Drosophila ventral olfactory projection neurons.

    abstract::Diverse types of neurons must be specified in the developing brain to form the functional neural circuits that are necessary for the execution of daily tasks. Here, we describe the participation of Forkhead box class O (FOXO) in cell fate specification of a small subset of Drosophila ventral olfactory projection neuro...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2018.1556651

    authors: Wei JY,Chung PC,Chu SY,Yu HH

    更新日期:2019-03-01 00:00:00

  • RNA editing in the Drosophila DMCA1A calcium-channel alpha 1 subunit transcript.

    abstract::Messenger RNA editing of transcripts encoding voltage-sensitive ion channels has not been extensively analyzed--least of all in Drosophila, for which several channel-encoding genes are known. Previous sequence studies of D. melanogaster's cacophony gene, which encodes an alpha 1 calcium-channel subunit called Dmca1A, ...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677069809108560

    authors: Smith LA,Peixoto AA,Hall JC

    更新日期:1998-11-01 00:00:00

  • Temperature signaling underlying thermotaxis and cold tolerance in Caenorhabditis elegans.

    abstract::Caenorhabditis elegans has a simple nervous system of 302 neurons. It however senses environmental cues incredibly precisely and produces various behaviors by processing information in the neural circuit. In addition to classical genetic analysis, fluorescent proteins and calcium indicators enable in vivo monitoring o...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2020.1734001

    authors: Takeishi A,Takagaki N,Kuhara A

    更新日期:2020-09-01 00:00:00