Published in Biochem Genet on October 01, 1980
Nucleotide sequence, tissue-specific expression, and chromosome location of human carbonic anhydrase III: the human CAIII gene is located on the same chromosome as the closely linked CAI and CAII genes. Proc Natl Acad Sci U S A (1986) 1.16
Carbonic anhydrases in normal gastrointestinal tract and gastrointestinal tumours. World J Gastroenterol (2005) 1.06
Radioimmunoassay of carbonic anhydrase III in rat tissues. Biochem J (1984) 0.92
Expression of testosterone-dependent enzyme, carbonic anhydrase III, and oxidative stress in experimental alcoholic liver disease. Dig Dis Sci (1999) 0.87
Transport activity of the sodium bicarbonate cotransporter NBCe1 is enhanced by different isoforms of carbonic anhydrase. PLoS One (2011) 0.87
Circulating protein synthesis rates reveal skeletal muscle proteome dynamics. J Clin Invest (2015) 0.80
Induction of carbonic anhydrase III mRNA and protein by denervation of rat muscle. Biochem J (1988) 0.78
Isozyme patterns and protein profiles in neuromuscular disorders. J Med Genet (1982) 0.76
Decreased carbonic anhydrase III levels in the liver of the mouse mutant 'toxic milk' (tx) due to copper accumulation. Biochem J (1997) 0.75
Initial sequencing and analysis of the human genome. Nature (2001) 212.86
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet (2001) 6.96
A systematic, high-resolution linkage of the cytogenetic and physical maps of the human genome. Nat Genet (2000) 4.78
Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease). Lancet (2000) 4.54
Cloning and characterization of the major insulin-responsive glucose transporter expressed in human skeletal muscle and other insulin-responsive tissues. J Biol Chem (1989) 2.81
Transforming growth factor-beta1 gene polymorphisms and coronary artery disease. Clin Sci (Lond) (1998) 2.68
Intra-alveolar haemorrhage in sudden infant death syndrome: a cause for concern? J Clin Pathol (1999) 2.37
Interleukin-1 receptor antagonist gene polymorphism and coronary artery disease. Circulation (1999) 2.17
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2. Nat Genet (2000) 2.14
L-myo-inositol 1,4,5,6-tetrakisphosphate is present in both mammalian and avian cells. Biochem J (1988) 2.10
Evidence-based recommendations for the use of Negative Pressure Wound Therapy in traumatic wounds and reconstructive surgery: steps towards an international consensus. Injury (2011) 2.07
Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. J Med Genet (2002) 1.91
Prevalence of restless legs syndrome among men aged 18 to 64 years: an association with somatic disease and neuropsychiatric symptoms. Mov Disord (2001) 1.89
Are coroners' necropsies necessary? A prospective study examining whether a "view and grant" system of death certification could be introduced into England and Wales. J Clin Pathol (2001) 1.82
Angiotensin-converting enzyme gene deletion polymorphism. A new risk factor for lacunar stroke but not carotid atheroma. Stroke (1995) 1.77
Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein. Cell (1994) 1.65
Effect on patient management of a weekend 'on-call' nuclear medicine service. Nucl Med Commun (1994) 1.61
Mapping a gene for Noonan syndrome to the long arm of chromosome 12. Nat Genet (1994) 1.58
Role of snoring and daytime sleepiness in occupational accidents. Am J Respir Crit Care Med (2001) 1.50
Coupled chemical and mechanical reaction steps in a processive Neurospora kinesin. EMBO J (1999) 1.48
Angiotensin-converting enzyme gene polymorphism. What to do about all the confusion. Circulation (1996) 1.41
Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients. EMBO J (1987) 1.40
Unfairness for mouth cancer patients. Br Dent J (2012) 1.39
Evidence-based recommendations for negative pressure wound therapy: treatment variables (pressure levels, wound filler and contact layer)--steps towards an international consensus. J Plast Reconstr Aesthet Surg (2011) 1.33
A gene for lymphedema-distichiasis maps to 16q24.3. Am J Hum Genet (1999) 1.32
Is telomere length in peripheral blood lymphocytes correlated with cancer susceptibility or radiosensitivity? Br J Cancer (2007) 1.32
The natural history of Noonan syndrome: a long-term follow-up study. Arch Dis Child (2006) 1.29
Chromosome specific paints from a high resolution flow karyotype of the mouse. Nat Genet (1995) 1.28
Epilepsy monitoring and advice recorded: general practitioners' views, current practice and patients' preferences. Br J Gen Pract (1996) 1.25
Does a Th1 over Th2 dominancy really exist in the early stages of Mycobacterium avium subspecies paratuberculosis infections? Immunobiology (2010) 1.25
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene. Am J Hum Genet (2000) 1.23
General practitioner's knowledge of when to refer deaths to a coroner. Br J Gen Pract (1995) 1.22
Effect of hemorrhagic shock on transmembrane potential. Surgery (1969) 1.20
Isolation of a cDNA probe for a human jejunal brush-border hydrolase, sucrase-isomaltase, and assignment of the gene locus to chromosome 3. Gene (1987) 1.20
Adverse health effects among women living with heavy snorers. Health Care Women Int (2000) 1.16
Vitamin D receptor gene polymorphisms are associated with breast cancer risk in a UK Caucasian population. Br J Cancer (2001) 1.16
Excessive daytime sleepiness at work and subjective work performance in the general population and among heavy snorers and patients with obstructive sleep apnea. Chest (1996) 1.16
Sequence and transcriptional analysis of clpX, a class-III heat-shock gene of Bacillus subtilis. Gene (1996) 1.14
Sequence of the complete cDNA and the 5' structure of the human sucrase-isomaltase gene. Possible homology with a yeast glucoamylase. Biochem J (1992) 1.14
The dnaB-pheA (256 degrees-240 degrees) region of the Bacillus subtilis chromosome containing genes responsible for stress responses, the utilization of plant cell walls and primary metabolism. Microbiology (1996) 1.13
QT interval in twins. J Hum Hypertens (2000) 1.12
Radioimmunoassay of human muscle carbonic anhydrase III in dystrophic states. Clin Chim Acta (1982) 1.11
Prenatal diagnosis of autosomal dominant polycystic kidney disease (PKD1) presenting in utero and prognosis for very early onset disease. J Med Genet (1998) 1.10
The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings. Clin Genet (2013) 1.10
Milroy disease and the VEGFR-3 mutation phenotype. J Med Genet (2005) 1.10
Sleep-disordered breathing and occupational accidents. Scand J Work Environ Health (2000) 1.09
CD14 and toll-like receptor 4: a link between infection and acute coronary events? Heart (2004) 1.08
Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene. Hum Genet (2001) 1.07
The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype. Am J Hum Genet (2001) 1.06
Characterization of human carbonic anhydrase III from skeletal muscle. Biochem Genet (1979) 1.05
Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions. J Med Genet (2001) 1.03
Air weapon fatalities. J Clin Pathol (1998) 1.02
A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH. Oncogene (2006) 1.01
Splicing mutations in KCNQ1: a mutation hot spot at codon 344 that produces in frame transcripts. Circulation (1999) 1.00
Sexual differentiation of rat liver carbonic anhydrase III. Biochim Biophys Acta (1983) 0.99
Angiotensin converting enzyme insertion/deletion polymorphism: association with ethnic origin. J Hypertens (1994) 0.99
Evidence-based recommendations for the use of negative pressure wound therapy in chronic wounds: steps towards an international consensus. J Tissue Viability (2011) 0.98
Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema. J Med Genet (2003) 0.98
Location of mutations within the PKD2 gene influences clinical outcome. Kidney Int (2000) 0.97
Haemochromatosis gene mutations in idiopathic dilated cardiomyopathy. Heart (2000) 0.97
Angiotensin converting enzyme gene I/D polymorphism, blood pressure and the renin-angiotensin system in Caucasian and Afro-Caribbean peoples. J Hum Hypertens (1996) 0.97
Prenatal diagnosis of a double bisatellited marker with an unusual copy number ratio. Prenat Diagn (1990) 0.97
Reversal of experimental allergic encephalomyelitis with non-mitogenic, non-depleting anti-CD3 mAb therapy with a preferential effect on T(h)1 cells that is augmented by IL-4. Int Immunol (2001) 0.96
Expression from the proximal promoter of the carbonic anhydrase 1 gene as a marker for differentiation in colon epithelia. Differentiation (1993) 0.96
Immunoassay of carbonic anhydrase III in rat tissues. FEBS Lett (1982) 0.96
Changes in skeletal muscle gene transcription induced by chronic stimulation. Muscle Nerve (1988) 0.95
The adenosine transporter of Toxoplasma gondii. Identification by insertional mutagenesis, cloning, and recombinant expression. J Biol Chem (1999) 0.95
Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types. Mamm Genome (2001) 0.95
Restless Legs Syndrome among working-aged women. Eur Neurol (2001) 0.94
Energy dissipation in atomic force microscopy and atomic loss processes. Phys Rev Lett (2001) 0.94
Brooke-Spiegler syndrome locus assigned to 16q12-q13. J Invest Dermatol (2000) 0.94
Large-scale molecular analysis of a 34 Mb interval on chromosome 6q: major refinement of the RP25 interval. Ann Hum Genet (2007) 0.93
The 3'-untranslated sequence of human skeletal muscle alpha-actin mRNA. J Muscle Res Cell Motil (1984) 0.93
Xanthine phosphoribosyltransferase from Leishmania donovani. Molecular cloning, biochemical characterization, and genetic analysis. J Biol Chem (1999) 0.93
Carbonic anhydrase (CA)-related proteins (CA-RPs), and transmembrane proteins with CA or CA-RP domains. EXS (2000) 0.92
Are abundant proteins less variable? Nature (1980) 0.92
Radioimmunoassay of carbonic anhydrase III in rat tissues. Biochem J (1984) 0.92
A new classification system for primary lymphatic dysplasias based on phenotype. Clin Genet (2010) 0.92
Susceptibility to ankylosing spondylitis. Rheumatology (Oxford) (2000) 0.92
Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci. Am J Med Genet (2001) 0.91
Epilepsy in general practice: patients' psychological symptoms and their perception of stigma. Br J Gen Pract (1996) 0.91
Evidence for reflex adrenergic inhibition of acid secretion in the conscious rat. Am J Physiol (1986) 0.91
Lurching, reeling, waddling and staggering in mice--is carbonic anhydrase (CA) VIII a candidate gene? Biochem Soc Trans (1994) 0.90
The embryonic RNA helicase gene (ERH): a new member of the DEAD box family of RNA helicases. Biochem J (1995) 0.90
Heritability of DNA-damage-induced apoptosis and its relationship with age in lymphocytes from female twins. Br J Cancer (2006) 0.90
Carbonic anhydrase III in obese Zucker rats. Am J Physiol (1993) 0.89
Three children with Milroy disease and de novo mutations in VEGFR3. Clin Genet (2007) 0.89
Soluble bovine galactose-binding lectin. cDNA cloning reveals the complete amino acid sequence and an antigenic relationship with the major encephalitogenic domain of myelin basic protein. Biochem J (1989) 0.88
The expression of carbonic anhydrases II and IV in the human pancreatic cancer cell line (Capan 1) is associated with bicarbonate ion channels. Biol Cell (1994) 0.88
Effects of hypophysectomy and growth hormone infusion on rat hepatic carbonic anhydrases. J Endocrinol (1986) 0.88
Nucleotide sequence and chromosomal assignment of a cDNA encoding the large isoform of human glutamate decarboxylase. Ann Hum Genet (1992) 0.88
Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs. J Med Genet (2005) 0.88
Headache, snoring and sleep apnoea. J Neurol (1996) 0.88
Similar prevalence of enteroviral genome within the myocardium from patients with idiopathic dilated cardiomyopathy and controls by the polymerase chain reaction. Br Heart J (1992) 0.87