![]() | H Maurice GoodmanUniversity of California, Berkeley | Department of Psychology, University of Massachusetts Medical School | Department of Molecular Biology, Massachusetts General Hospital, ... |
KOL Resume for H Maurice Goodman
Year | |
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2020 | University of California, Berkeley |
2009 | Department of Psychology, University of Massachusetts Medical School |
2006 | Department of Molecular Biology, Massachusetts General Hospital, 02114, Boston, MA, USA |
2005 | Department of Genetics, Harvard Medical School and Department of Molecular Biology, Massachusetts General Hospital, 02114, Boston, MA, USA |
2004 | Department of Physiology, University of Massachusetts Medical School, Worcester, Massachusetts 02155 |
2003 | Department of Physiology, University of Massachusetts Medical School (L.D., G.P.F., L.-R.T., H.M.G.), Worcester, Massachusetts 01655; |
2002 | Department of Genetics, Harvard Medical School, Boston, MA 02115, USA |
2001 | Department of Physiology, University of Massachusetts Medical School, Worcester, Massachusetts 01655 |
2000 | Department of Molecular Biology, Massachusetts General Hospital, Wellman Building 11, 02114, Boston, MA, USA |
1999 | Department of Genetics, Harvard Medical School, and Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114 |
1998 | Department of Physiology (S.M., M.U., O.U., H.M.G., H.Y.), University of Massachusetts Medical School, Worcester, Massachusetts 01655, and 2Sepracor, Inc. (J.R.M.), Marlborough, Massachusetts 01752 |
1997 | Department of Genetics, Harvard Medical School, Boston, MA 02114, USA |
1996 | Department of Genetics, Haward Medical School and Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114 |
1995 | Department of Genetics, Harvard Medical School, Massachusetts General Hospital, Boston, MA 02114, USA. Faculdade de Medicina de Ribeirao Preto-Universidade de Sao Paulo, Brazil. |
1994 | Department of Biological Sciences, University of Iowa, Iowa City, Iowa 52242 (H.-B.K., S.-C.P, H.-P.P., M.-C. S.) |
1993 | Department of Physiology, University of Massachusetts Medical School, Worcester, Massachusetts |
1992 | Department of Genetics, Harvard Medical School, and Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114. Laboratorium voor Genetica, Universiteit Ghent, Belgium |
1991 | Department of Genetics, Harvard Medical School, Massachusetts 02114 Department of Molecular Biology, Massachusetts General Hospital Boston, Massachusetts 02114 Department of Genetics, North Carolina State University, Raleigh, North Carolina 27695 Department of Botany, The University of Iowa, Iowa City, Iowa 52242 Department of Biology, The University of Iowa, Iowa City, Iowa 52242 Laboratorium voor Genetica, Rijksuniversiteit Gent, Belgium |
1990 | Department of Genetics, Harvard Medical School and Department of Molecular Biology, Massachusetts General HospitalBoston, MA 02114, USA Laboratorium voor Genetica, Rijksuniversiteit Ghent, Belgium |
1989 | Department of Genetics, Harvard Medical School and Department of Molecular Biology, Massachusetts General Hospital, Boston |
1988 | Department of Physiology, University of Massachusetts Medical School, 01605, Worcester, MA, USA |
1987 | Department of Physiology, University of Massachusetts Medical School, Worcester, Mass., USA |
1986 | Department of Molecular Biology Massachusetts General Hospital Boston, Massachusetts 02114 USA |
1985 | Dept. of Molecular Biology, Massachusetts General Hospital USA Department of Genetics Harvard Medical School, Massachusetts General Hospital Boston, MA 02114, U.S.A. |
1984 | Departments of Medicine and Genetics, Harvard Medical School, 02114, Boston, Massachusetts |
1983 | Department of Molecular Biology, Massachusetts General Hospital, 02114, Boston, Massachusetts |
1982 | Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, and The Howard Hughes Medical Institute Laboratory, University of California, 94143, San Francisco, CA, USA |
1981 | Department of Biochemistry and Biophysics, University of California, 94143, San Francisco, California, USA |
1980 | Department of Biochemistry and Biophysics, University of California, San Francisco (UCSF) 94143; Howard Hughes Medical Institute, University of California, 94143, San Francisco, California |
H Maurice Goodman: Influence Statistics
Concept | World rank |
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growthhormone expression variety | #1 |
data dibutyryl cyclic | #1 |
nr2 nitrate induction | #1 |
ca2i okadaic | #1 |
psclol plasmid | #1 |
hydrogenbonded loop | #1 |
monocistronic hn mrna | #1 |
akr expression | #1 |
10−5–10−3 activity | #1 |
aataataa | #1 |
growth hormone12 | #1 |
position116 and135 | #1 |
highly specific cytotoxins | #1 |
sse1 mutant embryos | #1 |
tumor nonpancreatic tissue | #1 |
messengers synthesis | #1 |
transgenic plants position | #1 |
cytosolic gapdhs | #1 |
enzyme initiation | #1 |
refractoriness growth hormone | #1 |
joining cohesive ends | #1 |
unusual kinaselike domain | #1 |
pyruvate dehydrogenase data | #1 |
adipocytes 4 | #1 |
turnover glycosylation | #1 |
pr1 pseudogenes tobacco | #1 |
yeast proteasome subunits | #1 |
species specificity hghr | #1 |
alpha2 16k | #1 |
ligation linear concatemers | #1 |
growth hormone messenger | #1 |
mutant hy1 | #1 |
oxidation dibutyryl cyclic | #1 |
phorbol esters cgtca | #1 |
ability glucose oxidation | #1 |
aft1 1433 proteins | #1 |
16k pellets | #1 |
ecori substrate order | #1 |
molecular analysis polypeptides | #1 |
activity relationship tritium | #1 |
glucose metabolism segments | #1 |
seeds λatgsr2 hybridizes | #1 |
alternative splicing sr1 | #1 |
ta28 | #1 |
analyses regulation | #1 |
enhancer dna elements | #1 |
pr1 pseudogenes | #1 |
nuclear extracts leaves | #1 |
protein ankyrin repeats | #1 |
morphological genetic markers | #1 |
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Prominent publications by H Maurice Goodman
Characterization of dna complementary to nucleotide sequences at the 5′-terminus of the avian sarcoma virus genome
[ PUBLICATION ]
The 5′-end of the genome of avian sarcoma virus (ASV) contains a sequence of nucleotides which is the initial template for transcription by RNA-directed DNA polymerase. We have prepared DNA complementary to this sequence (cDNA5,) and have characterized the sequence by chemical analysis and molecular hybridization. The length of cDNA5, (00 nucleotides) provides an estimate of the distance from the primer for DNA synthesis (tRNAtrp) to the 5′-terminus of the genome. As reported previously ...
Known for Dna Complementary | Nucleotide Sequence | Sarcoma Virus | Viral Transcription | Asv Genome |
Comparative genome studies are important contributors to our understanding of genome evolution. Most comparative genome studies in plants have been based on genetic mapping of homologous DNA loci in different genomes. Large-scale comparative physical mapping has been hindered by the lack of efficient and affordable techniques. We report here the adaptation of fluorescence in situ hybridization (FISH) techniques for comparative physical mapping between Arabidopsis thaliana and Brassica ...
Known for Situ Hybridization | Rapa Genome | Bacterial Artificial | Comparative Fluorescence | Arabidopsis Thaliana |
Proteins bound at adjacent DNA elements act synergistically to regulate human proenkephalin cAMP inducible transcription.
[ PUBLICATION ]
Synthesis of the endogenous opioid precursor, proenkephalin, is regulated by neurotransmitters and membrane depolarization. These events act through second messenger dependent signal transduction pathways via a short inducible DNA enhancer to regulate transcription of the proenkephalin gene. Two DNA elements located within this enhancer are essential for the transcriptional response to cAMP and phorbol ester. Inactivation of either element by mutation or by alteration of their ...
Known for Proenkephalin Camp | Dna Elements | Enkcre1 Enkcre2 | Transcription Factors | Genetic Humans |
The glutamine synthetase gene family of Arabidopsis thaliana light-regulation and differential expression in leaves, roots and seeds
[ PUBLICATION ]
Glutamine synthetase (GS) plays an important role in the assimilation of nitrogen by higher plants. We present here a molecular analysis of the GS polypeptides, mRNAs, and genes of Arabidopsis thaliana. Western blot analysis of leaf and root protein extracts revealed at least two distinct GS polypeptides; 43 kDa and 39 kDa GS polypeptides were present in leaves, while only a 39 kDa GS was detected in roots. The 43 kDa GS polypeptide is light-inducible. In etiolated seedlings only the 39 ...
Known for Arabidopsis Thaliana | Northern Blotting | Leaves Roots | Glutamine Synthetase | 39 Kda |
Transcription of DNA from the RNA genome of avian sarcoma virus by RNA-directed DNA polymerase in vitro initiates on a primer (tRNATrp) located near the 5'-terminus of the viral genome. One of the major products of transcription is a single-stranded DNA chain complementary to a sequence of 101 nucleotides immediately distal to the site of initiation of DNA synthesis. We have determined the complete nucleotide sequence of this transcribed chain for the Prague strain of avian sarcoma ...
Known for Avian Sarcoma Virus | Nucleotide Sequence | Viral Rna | Initiation Dna Synthesis | Directed Dna |
We report here the identification of a cis-acting region involved in light regulation of the nuclear gene (GapB) encoding the B subunit of chloroplast glyceraldehyde 3-phosphate dehydrogenase from Arabidopsis thaliana. Our results show that a 664-bp GapB promoter fragment is sufficient to confer light induction and organ-specific expression of the Escherichia coli beta-glucuronidase reporter gene (Gus) in transgenic tobacco (Nicotiana tabacum) plants. Deletion analysis indicates that the ...
Known for Nuclear Gene | Arabidopsis Thaliana | Gap Boxes | Light Induction | Phosphate Dehydrogenase |
Molecular cloning and characterization of avian sarcoma virus circular DNA molecules.
[ PUBLICATION ]
Supercoiled DNA molecules were used for the molecular cloning of full-length avian sarcoma virus (ASV) DNA. Viral DNA produced by the Schmidt-Ruppin A (SR-A) strain of ASV was isolated from acutely infected transformed quail cells. Supercoiled DNA was separated from linear and open circular DNA by acid phenol extraction, opened into a full-length linear form by cleavage with the restriction endonuclease SacI, and cloned into lambda gtWES x lambda B. Four different cloned viral DNA ...
Known for Molecular Cloning | Circular Dna | Terminal Redundancy | Avian Sarcoma | Src Gene |
Growth hormone (GH) produces insulin-like effects in rat adipocytes that have been deprived of GH for at least 3 h. The effect of a saturating concentration of GH is qualitatively and quantitatively similar to that produced by 2-4 ng/ml insulin but differs from that of insulin in the respect that adipocytes become refractory to prolonged or repeated stimulation with GH. Since activation of tyrosine kinase is an early event in the action of both hormones, we investigated the possibility ...
Known for Tyrosine Phosphorylation | Insulin Receptor | Growth Hormone | Data Irs1 | Beta Subunit |
The fusion protein (F) gene of mumps virus was cloned from a cDNA library constructed from infected cell mRNA. The F-specific plasmids were identified by hybridization to a degenerate oligonucleotide probe whose sequence was deduced from the N-terminal amino acid sequence of the F2 protein. The complete nucleotide sequence of the F gene was determined. The gene is 1786 nucleotides long and encodes one long open reading frame of 538 amino acids. The F protein has a 19-amino acid signal ...
Known for Fusion Protein Gene | Mumps Virus | Messenger Rna | Viral Sequence Homology | Sequence Protein |
The major capsid protein (VP1) of simian virus 40 (SV40) has been analyzed by two-dimensional electrophoresis. This system separates protein according to isoelectric point by isoelectric-focusing, and according to molecular weight by sodium dodecylsulphate electrophoresis (O'Farrell, 1975). VP1 synthesis in infected CV-1 cells can be monitored directly by analysis of unfractionated whole cell extracts; the resolution of VP1 from cellular proteins allows its detection as early as 13 hr ...
Known for Simian Virus | Major Capsid Protein | Dimensional Electrophoresis | Molecular Weight | Isoelectric Point |
Transcription of DNA from the 70S RNA of Rous sarcoma virus. I. Identification of a specific 4S RNA which serves as primer.
[ PUBLICATION ]
The enzymatic transcription of DNA from the 70S RNA of Rous sarcoma virus (RSV) is initiated on the 3' terminus of a molecule of 4S RNA which is hydrogen bonded to the viral genome. We labeled this primer with radioactive deoxynucleotides, and demonstrated that its release from 70S RNA by thermal denaturation was accompanied by a reduction in the template activity of the viral RNA. Two-dimensional electrophoresis in polyacrylamide gels separated the 4S RNAs associated with the 70S RNA of ...
Known for 70s Rna | Rous Sarcoma Virus | Genetic Transcription | Dna Synthesis | Viral Genome |
Ligation of EcoRI endonuclease-generated DNA fragments into linear and circular structures
[ PUBLICATION ]
Double-stranded DNA fragments terminated at their 5′-ends by the singlestranded sequence pA-A-T-T-, generated by digestion of DNA with EcoRI restriction endonuclease, were ligated with Escherichia coli polynucleotide ligase under various conditions of temperature, concentration and time. The linear and circular products of ligation were separated by electrophoresis in agarose gel and quantitated by densitometry. The rate of ligation of (EcoRI-cleaved) simian virus (SV40) DNA at a ...
Known for Dna Fragment | Viral Electrophoresis | Circular Structures | Ecori Endonuclease | Linear Concatemers |
The two nonallelic genes, insulin I and II of the rat, are separated by at least 7 kb of DNA. There is no obvious similarity in the sequence organization surrounding each gene, although the coding regions of the genes themselves share extensive homology. In three strains of rat, the insulin II gene lies predominantly on a 4.0 kb Eco RI restriction fragment, whereas the insulin I gene is located on a 9.4 kb Eco RI fragment in the Hooded strain, on a 7.2 kb Eco RI fragment in the ...
Known for Insulin Gene | Cloned Rat | Intervening Sequences | Dna Sequence | Coding Region |
A common trans-acting factor is involved in transcriptional regulation of neurotransmitter genes by cyclic AMP.
[ PUBLICATION ]
Activation of neurotransmitter receptors can regulate transcription in postsynaptic cells through the actions of second messengers. Trans-synaptic regulation of transcription appears to be an important mechanism controlling the synthesis of molecules involved in neuronal signaling, especially neuropeptides. Proenkephalin, vasoactive intestinal polypeptide, and somatostatin have been shown to be transcriptionally regulated by the second messenger, cyclic AMP (cAMP), as has the ...
Known for Transcriptional Regulation | Cyclic Camp | Enkcre1 Enkcre2 | Vasoactive Intestinal | Transcription Factors |
Key People For Growth Hormone
H Maurice Goodman:Expert Impact
Concepts for whichH Maurice Goodmanhas direct influence:Growth hormone, Adipose tissue, Rat adipocytes, Okadaic acid, Nucleotide sequence, Arabidopsis thaliana, Arabidopsis genome, Gene expression.
H Maurice Goodman:KOL impact
Concepts related to the work of other authors for whichfor which H Maurice Goodman has influence:Growth hormone, Gene expression, Arabidopsis thaliana, Escherichia coli, Amino acid, Nucleotide sequence, Protein kinase.
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