Assignment of the human tyrosine hydroxylase gene to chromosome 11.

PubWeight™: 1.39‹?› | Rank: Top 5%

🔗 View Article (PMID 6148265)

Published in FEBS Lett on September 17, 1984

Authors

J F Powell, C Boni, A Lamouroux, I W Craig, J Mallet

Articles by these authors

Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer. J Clin Oncol (2000) 16.83

Hybridization and speciation. J Evol Biol (2013) 14.24

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nat Genet (2013) 9.46

Reproductive isolation caused by colour pattern mimicry. Nature (2001) 4.95

Altered ribosomal RNA genes in mitochondria from mammalian cells with chloramphenicol resistance. Nature (1981) 4.65

A common molecular basis for three inherited kidney stone diseases. Nature (1996) 4.26

MAOA, maltreatment, and gene-environment interaction predicting children's mental health: new evidence and a meta-analysis. Mol Psychiatry (2006) 4.16

Nicotine reinforcement and cognition restored by targeted expression of nicotinic receptors. Nature (2005) 4.15

Randomized trial of fenretinide to prevent second breast malignancy in women with early breast cancer. J Natl Cancer Inst (1999) 4.04

Superior efficacy of letrozole versus tamoxifen as first-line therapy for postmenopausal women with advanced breast cancer: results of a phase III study of the International Letrozole Breast Cancer Group. J Clin Oncol (2001) 3.92

The role of virus-specific CD8(+) cells in liver damage and viral control during persistent hepatitis B virus infection. J Exp Med (2000) 3.78

Phase III randomized trial comparing three platinum-based doublets in advanced non-small-cell lung cancer. J Clin Oncol (2002) 3.75

Gene-environment interaction analysis of serotonin system markers with adolescent depression. Mol Psychiatry (2004) 3.54

Diagnostic strategies in CADASIL. Neurology (2002) 3.52

DNA from buccal swabs recruited by mail: evaluation of storage effects on long-term stability and suitability for multiplex polymerase chain reaction genotyping. Behav Genet (2003) 3.42

Treatment of metastatic malignant melanoma with dacarbazine plus tamoxifen. N Engl J Med (1992) 3.11

The primary structure of human dopamine-beta-hydroxylase: insights into the relationship between the soluble and the membrane-bound forms of the enzyme. EMBO J (1987) 3.06

Oligodeoxyribonucleotide ligation to single-stranded cDNAs: a new tool for cloning 5' ends of mRNAs and for constructing cDNA libraries by in vitro amplification. Nucleic Acids Res (1991) 3.01

An adenovirus vector for gene transfer into neurons and glia in the brain. Science (1993) 2.79

Direct ex vivo analysis of hepatitis B virus-specific CD8(+) T cells associated with the control of infection. Gastroenterology (1999) 2.62

Different cytokine profiles of intraphepatic T cells in chronic hepatitis B and hepatitis C virus infections. Gastroenterology (1997) 2.61

Association between the tryptophan hydroxylase gene and manic-depressive illness. Arch Gen Psychiatry (1998) 2.55

Localization of the X inactivation centre on the human X chromosome in Xq13. Nature (1991) 2.48

Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome. J Mol Biol (1985) 2.39

The primary structure of human secretogranin I (chromogranin B): comparison with chromogranin A reveals homologous terminal domains and a large intervening variable region. EMBO J (1987) 2.33

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy. Nat Genet (1993) 2.23

Disruptive sexual selection against hybrids contributes to speciation between Heliconius cydno and Heliconius melpomene. Proc Biol Sci (2001) 2.16

Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays. Genes Brain Behav (2008) 2.08

Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Mol Psychiatry (2008) 2.07

Association of manic-depressive illness with tyrosine hydroxylase microsatellite marker. Lancet (1995) 2.07

Tyrosine hydroxylase-immunoreactive boutons in synaptic contact with identified striatonigral neurons, with particular reference to dendritic spines. Neuroscience (1984) 2.05

Complete coding sequence of rat tyrosine hydroxylase mRNA. Proc Natl Acad Sci U S A (1985) 2.01

Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: implications for Norrie disease. Genomics (1989) 1.93

A single human gene encoding multiple tyrosine hydroxylases with different predicted functional characteristics. Nature (1987) 1.91

Cloning and sequence analysis of the cDNA encoding a snake neurotoxin precursor. Biochimie (1985) 1.90

A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groups. Behav Genet (2001) 1.86

Amino acid sequence of rabbit kidney neutral endopeptidase 24.11 (enkephalinase) deduced from a complementary DNA. EMBO J (1987) 1.82

Dinucleotide repeat polymorphism at the MAOA locus. Nucleic Acids Res (1991) 1.77

Structural features of human monoamine oxidase A elucidated from cDNA and peptide sequences. J Neurochem (1988) 1.77

Molecular genetic evidence for heterogeneity in manic depression. Nature (1987) 1.76

Localization of the human tyrosine hydroxylase gene to 11p15: gene duplication and evolution of metabolic pathways. Cytogenet Cell Genet (1986) 1.76

Acute elevation of free fatty acid levels leads to hepatic insulin resistance in obese subjects. Metabolism (1987) 1.76

MRI hyperintensities of the temporal lobe and external capsule in patients with CADASIL. Neurology (2001) 1.75

Front-line chemotherapy with cisplatin and etoposide for patients with brain metastases from breast carcinoma, nonsmall cell lung carcinoma, or malignant melanoma: a prospective study. Cancer (1999) 1.75

The HIV-1 DNA flap stimulates HIV vector-mediated cell transduction in the brain. Nat Biotechnol (2001) 1.75

[Obstetrical paralysis of the brachial plexus. II. Therapeutics. Treatment of sequelae. Priority for the treatment of the shoulder. Method for the expression of results]. Rev Chir Orthop Reparatrice Appar Mot (1972) 1.72

Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. Am J Hum Genet (2000) 1.68

Psychiatric genetics: search for phenotypes. Trends Neurosci (1998) 1.68

Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain. Nat Genet (1993) 1.68

Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children. Mol Psychiatry (2007) 1.68

What initiates speciation in passion-vine butterflies? Proc Natl Acad Sci U S A (1997) 1.65

Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) Group. Lancet (1996) 1.64

Sequence of two mRNAs encoding active rat tryptophan hydroxylase. J Neurochem (1988) 1.61

Apolipoprotein E: non-cognitive symptoms and cognitive decline in late onset Alzheimer's disease. J Neurol Neurosurg Psychiatry (1996) 1.60

Predominant T-helper 1 cytokine profile of hepatitis B virus nucleocapsid-specific T cells in acute self-limited hepatitis B. Hepatology (1997) 1.58

Inulin and perabrodil clearance after alimentary haemorrhage in man. J Physiol (1941) 1.57

Gonadotropin-releasing hormone (GnRH) in ancient teleosts, the bonytongue fishes: putative origin of salmon GnRH. Gen Comp Endocrinol (1998) 1.55

Sorafenib in patients with advanced biliary tract carcinoma: a phase II trial. Br J Cancer (2009) 1.54

Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis. Hum Mol Genet (1999) 1.54

An application of the Theory of Planned Behaviour to blood donation: the importance of self-efficacy. Health Educ Res (2004) 1.54

Quantitative effects on gene silencing by allelic variation at a tetranucleotide microsatellite. Hum Mol Genet (2001) 1.54

Adjuvant chemotherapy in the treatment of colon cancer: randomized multicenter trial of the Italian National Intergroup of Adjuvant Chemotherapy in Colon Cancer (INTACC). Ann Oncol (2003) 1.52

The primary structure of bovine chromogranin A: a representative of a class of acidic secretory proteins common to a variety of peptidergic cells. EMBO J (1986) 1.52

Early kinetics of innate and adaptive immune responses during hepatitis B virus infection. Gut (2009) 1.49

Characterization of the genomic organization of human carcinoembryonic antigen (CEA): comparison with other family members and sequence analysis of 5' controlling region. Genomics (1990) 1.47

Oxaliplatin as single agent in previously untreated colorectal carcinoma patients: a phase II multicentric study. Ann Oncol (1998) 1.47

Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms. Mol Psychiatry (2005) 1.46

Localization of the human dopamine beta hydroxylase (DBH) gene to chromosome 9q34. Cytogenet Cell Genet (1988) 1.44

Cotranscription and intergenic splicing of human galactose-1-phosphate uridylyltransferase and interleukin-11 receptor alpha-chain genes generate a fusion mRNA in normal cells. Implication for the production of multidomain proteins during evolution. J Biol Chem (1998) 1.42

Mutations in all five exons of SOD-1 may cause ALS. Ann Neurol (1998) 1.40

Operation of Randle's cycle in patients with NIDDM. Diabetes (1990) 1.40

Suicidal behaviors and the tryptophan hydroxylase gene. Arch Gen Psychiatry (1995) 1.40

Autism and genetics: clinical approach and association study with two markers of HRAS gene. Am J Med Genet (1995) 1.40

Conserved hepatitis C virus sequences are highly immunogenic for CD4(+) T cells: implications for vaccine development. Hepatology (1999) 1.39

Sex-linked hybrid sterility in a butterfly. Evolution (2001) 1.38

Induction of serotonin transporter by hypoxia in pulmonary vascular smooth muscle cells. Relationship with the mitogenic action of serotonin. Circ Res (1999) 1.37

Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255]. Nucleic Acids Res (1987) 1.36

The acute effects of synthetic intravenous Delta9-tetrahydrocannabinol on psychosis, mood and cognitive functioning. Psychol Med (2009) 1.36

Familial amyotrophic lateral sclerosis. Molecular pathology of a patient with a SOD1 mutation. Neurology (1997) 1.35

Neuromuscular function impairment is not caused by motor neurone loss in FALS mice: an electromyographic study. Neuroreport (1996) 1.33

Selective bird predation on the peppered moth: the last experiment of Michael Majerus. Biol Lett (2012) 1.33

Genomic organization of human centromeric alpha satellite DNA: characterization of a chromosome 17 alpha satellite sequence. DNA (1987) 1.33

Human monoamine oxidase gene (MAOA): chromosome position (Xp21-p11) and DNA polymorphism. Genomics (1988) 1.30

Absorption of haemoglobin iron. Biochem J (1942) 1.29

Monoamine oxidase A gene and bipolar affective disorder. Am J Hum Genet (1994) 1.28

Studies with deoxyribonucleic acid from blue-green algae. Arch Mikrobiol (1969) 1.28

Placental lactogens induce serotonin biosynthesis in a subset of mouse beta cells during pregnancy. Diabetologia (2010) 1.28

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders. Hum Mol Genet (1997) 1.27

Isolation and characterization of a candidate gene for Norrie disease. Nat Genet (1992) 1.27