Published in Exp Eye Res on December 01, 2001
Lens gap junctions in growth, differentiation, and homeostasis. Physiol Rev (2010) 1.70
On the mechanism of organelle degradation in the vertebrate lens. Exp Eye Res (2008) 1.67
Oxidative stress, lens gap junctions, and cataracts. Antioxid Redox Signal (2009) 1.49
Discovering the molecular components of intercellular junctions--a historical view. Cold Spring Harb Perspect Biol (2009) 1.39
Development of a macromolecular diffusion pathway in the lens. J Cell Sci (2003) 1.18
Connexin mutants and cataracts. Front Pharmacol (2013) 1.11
A novel GJA8 mutation causing a recessive triangular cataract. Mol Vis (2008) 1.06
The cataract causing Cx50-S50P mutant inhibits Cx43 and intercellular communication in the lens epithelium. Exp Cell Res (2009) 1.04
Cataracts are caused by alterations of a critical N-terminal positive charge in connexin50. Invest Ophthalmol Vis Sci (2008) 1.01
Homeostasis in the vertebrate lens: mechanisms of solute exchange. Philos Trans R Soc Lond B Biol Sci (2011) 0.93
Phosphorylation and truncation sites of bovine lens connexin 46 and connexin 50. Exp Eye Res (2009) 0.91
A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene. Mol Vis (2007) 0.90
Connexin50D47A decreases levels of fiber cell connexins and impairs lens fiber cell differentiation. Invest Ophthalmol Vis Sci (2013) 0.89
Proteomics and phosphoproteomics analysis of human lens fiber cell membranes. Invest Ophthalmol Vis Sci (2013) 0.85
Microphthalmia and cataract in rats with a novel point mutation in connexin 50 - L7Q. Mol Vis (2008) 0.83
Connexin46fs380 causes progressive cataracts. Invest Ophthalmol Vis Sci (2014) 0.81
Roles and regulation of lens epithelial cell connexins. FEBS Lett (2014) 0.80
Quantitative proteomics analysis with iTRAQ in human lenses with nuclear cataracts of different axial lengths. Mol Vis (2016) 0.78
Age-related retention of fiber cell nuclei and nuclear fragments in the lens cortices of multiple species. Mol Vis (2011) 0.77
Focus on lens connexins. BMC Cell Biol (2017) 0.75
Ethylnitrosourea-induced base pair substitution affects splicing of the mouse gammaE-crystallin encoding gene leading to the expression of a hybrid protein and to a cataract. Genetics (2002) 0.75
Comment on 'characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract' by J.C. Graw et al., Experimental Eye Research, Vol. 73 (2001) pp 867-876. Exp Eye Res (2002) 0.75
Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. N Engl J Med (2001) 44.67
CCR7 coordinates the primary immune response by establishing functional microenvironments in secondary lymphoid organs. Cell (1999) 12.50
Autoregulation and function of a repressor in bacteriophage lambda. Science (1976) 6.83
A putative chemokine receptor, BLR1, directs B cell migration to defined lymphoid organs and specific anatomic compartments of the spleen. Cell (1996) 5.97
Predicting coiled coils by use of pairwise residue correlations. Proc Natl Acad Sci U S A (1995) 5.94
Oblique stepwise rise and growth of the Tibet plateau. Science (2001) 5.38
Hippocampal long-term potentiation is impaired in mice lacking brain-derived neurotrophic factor. Proc Natl Acad Sci U S A (1995) 5.25
Assays for laboratory confirmation of novel human coronavirus (hCoV-EMC) infections. Euro Surveill (2012) 4.95
The origin of the major cystic fibrosis mutation (delta F508) in European populations. Nat Genet (1994) 4.94
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B. Nat Genet (1998) 4.91
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell (1998) 4.72
Specific Constants for Visual Excitation. Proc Natl Acad Sci U S A (1937) 4.60
A family of octamer-specific proteins present during mouse embryogenesis: evidence for germline-specific expression of an Oct factor. EMBO J (1989) 4.47
Oct-4: a germline-specific transcription factor mapping to the mouse t-complex. EMBO J (1990) 4.42
Trial of low-dose aspirin plus dipyridamole versus anticoagulants for prevention of aortocoronary vein graft occlusion. Lancet (1989) 4.04
A five-step "microskills" model of clinical teaching. J Am Board Fam Pract (1992) 3.94
Genome-wide, large-scale production of mutant mice by ENU mutagenesis. Nat Genet (2000) 3.92
A computationally directed screen identifying interacting coiled coils from Saccharomyces cerevisiae. Proc Natl Acad Sci U S A (2000) 3.92
Gene regulation at the right operator (OR) bacteriophage lambda. I. OR3 and autogenous negative control by repressor. J Mol Biol (1980) 3.64
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Nature (1992) 3.63
Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities. Genes Dev (1998) 3.49
Group epitope mapping by saturation transfer difference NMR to identify segments of a ligand in direct contact with a protein receptor. J Am Chem Soc (2001) 3.47
Conservation of methylation reprogramming in mammalian development: aberrant reprogramming in cloned embryos. Proc Natl Acad Sci U S A (2001) 3.25
Antagonistic interactions between FGF and BMP signaling pathways: a mechanism for positioning the sites of tooth formation. Cell (1997) 3.08
Middle East Respiratory Syndrome coronavirus (MERS-CoV) serology in major livestock species in an affected region in Jordan, June to September 2013. Euro Surveill (2013) 2.97
The Notch intracellular domain is ubiquitinated and negatively regulated by the mammalian Sel-10 homolog. J Biol Chem (2001) 2.89
Octamer binding proteins confer transcriptional activity in early mouse embryogenesis. EMBO J (1989) 2.70
Pax: a murine multigene family of paired box-containing genes. Genomics (1991) 2.60
Sequence interpretation. Functional annotation of mouse genome sequences. Science (2001) 2.54
Degree of methylation of transgenes is dependent on gamete of origin. Nature (1987) 2.52
Efficacy and safety of short-term administration of aerosolised recombinant human DNase I in adults with stable stage cystic fibrosis. Lancet (1993) 2.50
Contact investigation of a case of human novel coronavirus infection treated in a German hospital, October-November 2012. Euro Surveill (2013) 2.39
Simulations of the static and dynamic molecular conformations of xyloglucan. The role of the fucosylated sidechain in surface-specific sidechain folding. Plant J (1991) 2.34
A role for mel-18, a Polycomb group-related vertebrate gene, during theanteroposterior specification of the axial skeleton. Development (1996) 2.33
On the Duplexity Theory of Visual Response in Vertebrates. Proc Natl Acad Sci U S A (1938) 2.22
Disruption of the CNTF gene results in motor neuron degeneration. Nature (1993) 2.22
Social support and the course of bipolar disorder. J Abnorm Psychol (1999) 2.08
Oral mucositis and the clinical and economic outcomes of hematopoietic stem-cell transplantation. J Clin Oncol (2001) 2.05
Genetic and immunologic factors in microvascular disease in type I insulin-dependent diabetes. Diabetes (1982) 2.05
Impaired glucose tolerance in HIV-positive patients receiving and those not receiving protease inhibitors. Ann Intern Med (1999) 2.05
The genetic susceptibility to type 1 (insulin-dependent) diabetes: analysis of the HLA-DR association. Diabetologia (1983) 2.04
A fluorometric method for the differentiation of algal populations in vivo and in situ. Photosynth Res (2002) 2.03
Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus. Mol Psychiatry (2002) 2.01
A genome-wide search for linkage to asthma. German Asthma Genetics Group. Genomics (1999) 2.00
Pax genes and organogenesis. Bioessays (1997) 1.98
Genital chlamydial infections in patients attending a gynaecological outpatient clinic. Br J Vener Dis (1978) 1.97
Molecular karyotyping using an SNP array for genomewide genotyping. J Med Genet (2004) 1.95
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B. Nat Genet (1999) 1.93
Insulin-like growth factor-I is an autocrine regulator of chromogranin A secretion and growth in human neuroendocrine tumor cells. Cancer Res (2000) 1.90
Langerhans cells transport Leishmania major from the infected skin to the draining lymph node for presentation to antigen-specific T cells. Eur J Immunol (1993) 1.88
Characterization and developmental expression of Pax9, a paired-box-containing gene related to Pax1. Dev Biol (1995) 1.87
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis. Am J Hum Genet (1998) 1.87
Increases in manic symptoms after life events involving goal attainment. J Abnorm Psychol (2000) 1.85
Overexpression of activin A in the skin of transgenic mice reveals new activities of activin in epidermal morphogenesis, dermal fibrosis and wound repair. EMBO J (1999) 1.84
Novel mutations in the gamma-crystallin genes cause autosomal dominant congenital cataracts. J Med Genet (2002) 1.84
Variations of cervical vertebrae after expression of a Hox-1.1 transgene in mice. Cell (1990) 1.79
The role of Pax-1 in axial skeleton development. Development (1994) 1.79
Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity. Am J Hum Genet (1999) 1.77
Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL). Cancer Res (2001) 1.75
Effects of ENU dosage on mouse strains. Mamm Genome (2000) 1.69
A mouse gene homologous to the Drosophila gene caudal is expressed in epithelial cells from the embryonic intestine. Genes Dev (1988) 1.68
The biogenetic anatomy of vitamin B6. A 13C NMR investigation of the biosynthesis of pyridoxol in Escherichia coli. J Biol Chem (1996) 1.68
Primary prevention of diabetes mellitus. Diabetes Care (1987) 1.67
The function of the soluble interleukin 6 (IL-6) receptor in vivo: sensitization of human soluble IL-6 receptor transgenic mice towards IL-6 and prolongation of the plasma half-life of IL-6. J Exp Med (1996) 1.65
Teeth. Where and how to make them. Trends Genet (1999) 1.64
The Notch ligand Jagged1 is required for inner ear sensory development. Proc Natl Acad Sci U S A (2001) 1.64
Survival of AIDS patients with primary central nervous system lymphoma is dramatically improved by HAART-induced immune recovery. AIDS (2001) 1.63
Genome search for susceptibility loci of common idiopathic generalised epilepsies. Hum Mol Genet (2000) 1.61
Functional limitations to daily living tasks in the aged: a focus group analysis. Hum Factors (1998) 1.60
Insulin-like growth factor-binding protein 2 in tumorigenesis: protector or promoter? Cancer Res (2001) 1.60
Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster. Hum Mol Genet (1996) 1.59
DHFR/MSH3 amplification in methotrexate-resistant cells alters the hMutSalpha/hMutSbeta ratio and reduces the efficiency of base-base mismatch repair. Proc Natl Acad Sci U S A (1997) 1.58
Expression of Delta1 and Serrate1 (Jagged1) in the mouse inner ear. Mech Dev (1999) 1.56
Geometry-controlled kinetics. Nat Chem (2010) 1.54
Pax1 and Pax9 synergistically regulate vertebral column development. Development (1999) 1.53
Optimal excitation wavelengths for in vivo detection of oral neoplasia using fluorescence spectroscopy. Photochem Photobiol (2000) 1.53
A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36. Nat Genet (1995) 1.52
The Ca2+-binding proteins S100A8 and S100A9 are encoded by novel injury-regulated genes. J Biol Chem (2001) 1.52
A novel mutation and novel features in Nijmegen breakage syndrome. J Med Genet (2001) 1.50
Electronic structure of spatially aligned graphene nanoribbons on Au(788). Phys Rev Lett (2012) 1.49
Parasitism of epidermal Langerhans cells in experimental cutaneous leishmaniasis with Leishmania major. J Infect Dis (1993) 1.47
A gene for familial hemiplegic migraine maps to chromosome 19. Nat Genet (1993) 1.46
Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis. EMBO J (2001) 1.46
IGF-binding protein-5: flexible player in the IGF system and effector on its own. J Endocrinol (2002) 1.45
Interleukin-6 stimulates clonogenic growth of primary and metastatic human colon carcinoma cells. Cancer Lett (2000) 1.45
A clinical and laboratory study to compare the addition of 0.2 mg of morphine, 0.2 mg of epinephrine, or their combination to hyperbaric bupivacaine for spinal anesthesia in cesarean section. Anesth Analg (1993) 1.43
The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. Am J Hum Genet (1997) 1.41
Linking disease-associated genes to regulatory networks via promoter organization. Nucleic Acids Res (2005) 1.41
Intrinsic tumors of the insula: a prospective surgical study of 30 patients. J Neurosurg (1996) 1.41
Oligosaccharins--oligosaccharides that regulate growth, development and defence responses in plants. Glycobiology (1992) 1.41
Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree. Am J Hum Genet (2000) 1.41
The solution conformation of sialyl-alpha (2----6)-lactose studied by modern NMR techniques and Monte Carlo simulations. J Biomol NMR (1992) 1.41