Published in Biochemistry on February 12, 1991
The gelatin-binding site of human 72 kDa type IV collagenase (gelatinase A). Biochem J (1994) 1.00
Origin of fibronectin type II (FN2) modules: structural analyses of distantly-related members of the kringle family idey the kringle domain of neurotrypsin as a potential link between FN2 domains and kringles. Protein Sci (2001) 0.87
1H-n.m.r. studies of the fibronectin 13 kDa collagen-binding fragment. Evidence for autonomous conserved type I and type II domain folds. Biochem J (1992) 0.75
Shape, size, and distribution of Ca(2+) release units and couplons in skeletal and cardiac muscles. Biophys J (1999) 5.37
A prospective study of prevalence and association of peripheral neuropathy in Indian patients with newly diagnosed type 2 diabetes mellitus. J Postgrad Med (2014) 3.53
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel. Lancet (2001) 3.39
The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane. Trends Biochem Sci (1998) 3.24
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. Brain (2006) 3.16
Worldwide DNA sequence variation in a 10-kilobase noncoding region on human chromosome 22. Proc Natl Acad Sci U S A (2000) 2.67
Global patterns of human DNA sequence variation in a 10-kb region on chromosome 1. Mol Biol Evol (2001) 2.64
Reversible modification of arginine residues. Application to sequence studies by restriction of tryptic hydrolysis to lysine residues. J Biol Chem (1975) 2.63
Preparation and characterization of Ng-mono-, di- and trimethylated arginines. Acta Biochim Biophys Acad Sci Hung (1977) 2.62
Evolution of the proteases of blood coagulation and fibrinolysis by assembly from modules. Cell (1985) 2.59
Regulation of Ca2+ signaling in transgenic mouse cardiac myocytes overexpressing calsequestrin. J Clin Invest (1998) 2.29
Development of a species-specific PCR assay for detection of Leishmania donovani in clinical samples from patients with kala-azar and post-kala-azar dermal leishmaniasis. J Clin Microbiol (2001) 2.23
Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cord. Neurology (2006) 2.19
Cutaneous signs. Skinmed (2003) 2.04
Anaphylaxis secondary to levobupivacaine. Anaesthesia (2011) 2.02
Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells. Hum Mol Genet (2000) 1.90
Homology of a domain of the growth hormone/prolactin receptor family with type III modules of fibronectin. Cell (1990) 1.90
Transport of Ca2+ from sarcoplasmic reticulum to mitochondria in rat ventricular myocytes. J Bioenerg Biomembr (2000) 1.87
Reversible immunocontraception in male monkeys immunized with eppin. Science (2004) 1.84
NHE-RF, a regulatory cofactor for Na(+)-H+ exchange, is a common interactor for merlin and ERM (MERM) proteins. J Biol Chem (1998) 1.75
Kringle 5 of plasminogen is a novel inhibitor of endothelial cell growth. J Biol Chem (1997) 1.68
The Nf2 tumor suppressor gene product is essential for extraembryonic development immediately prior to gastrulation. Genes Dev (1997) 1.67
Intron-dependent evolution: preferred types of exons and introns. FEBS Lett (1987) 1.65
Kringle domains of human angiostatin. Characterization of the anti-proliferative activity on endothelial cells. J Biol Chem (1996) 1.63
Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types. Nat Genet (1994) 1.63
The NTR module: domains of netrins, secreted frizzled related proteins, and type I procollagen C-proteinase enhancer protein are homologous with tissue inhibitors of metalloproteases. Protein Sci (1999) 1.63
Exon scanning for mutation of the NF2 gene in schwannomas. Hum Mol Genet (1994) 1.62
Siderochromes from Pseudomonas fluorescens. I. Isolation and characterization. J Biol Chem (1982) 1.59
Prevalence & risk factors of pre-hypertension & hypertension in an affluent north Indian population. Indian J Med Res (2008) 1.58
A region of deletion on chromosome 22q13 is common to human breast and colorectal cancers. Cancer Res (2000) 1.58
Analysis of both TSC1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosis. Hum Mutat (1999) 1.57
Common evolutionary origin of the fibrin-binding structures of fibronectin and tissue-type plasminogen activator. FEBS Lett (1983) 1.56
Comparative ultrastructure of Ca2+ release units in skeletal and cardiac muscle. Ann N Y Acad Sci (1998) 1.54
Quantification of parasite load in clinical samples of leishmaniasis patients: IL-10 level correlates with parasite load in visceral leishmaniasis. PLoS One (2010) 1.54
The ligand-binding domain of the cell surface receptor for urokinase-type plasminogen activator. J Biol Chem (1991) 1.52
A deletion in the myostatin gene causes the compact (Cmpt) hypermuscular mutation in mice. Mamm Genome (1998) 1.52
Tissue grafts in vitiligo surgery - past, present, and future. Indian J Dermatol (2009) 1.51
Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferase. DNA (1986) 1.50
NHE-RF, a merlin-interacting protein, is primarily expressed in luminal epithelia, proliferative endometrium, and estrogen receptor-positive breast carcinomas. Am J Pathol (2001) 1.47
Association of mammalian trp4 and phospholipase C isozymes with a PDZ domain-containing protein, NHERF. J Biol Chem (2000) 1.46
catena-Poly[ammonium (cadmium-tri-μ-thio-cyanato-κS:N;κN:S)-1,4,10,13,16-hexa-oxa-cyclo-octa-decane (1/1)]. Acta Crystallogr Sect E Struct Rep Online (2012) 1.45
Structural analysis of BAG1 cochaperone and its interactions with Hsc70 heat shock protein. Nat Struct Biol (2001) 1.43
How useful is the Mantoux test in the diagnosis of doubtful cases of cutaneous tuberculosis? Int J Dermatol (2011) 1.42
Cutaneous leishmaniasis in Nepal: Leishmania major as a cause. Trans R Soc Trop Med Hyg (2008) 1.41
Eponyms in dermatology. Skinmed (2004) 1.41
Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomas suggests different genetic mechanisms for pathogenesis of TSC lesions. Am J Hum Genet (2001) 1.39
The B1 subunit of the H+ATPase is a PDZ domain-binding protein. Colocalization with NHE-RF in renal B-intercalated cells. J Biol Chem (2000) 1.39
Localized lepromatous leprosy and its response to chemo-immunotherapy. Int J Dermatol (1994) 1.39
The intricacies of research work. Indian J Dent Res (2010) 1.38
Letter to the editors. Secondary or reinfection cutaneous tuberculosis. Trop Med Int Health (2007) 1.38
Picrorhiza kurroa (Kutaki) Royle ex Benth as a hepatoprotective agent--experimental & clinical studies. J Postgrad Med (1998) 1.37
Kringles: modules specialized for protein binding. Homology of the gelatin-binding region of fibronectin with the kringle structures of proteases. FEBS Lett (1984) 1.36
Frequency and distribution of NF2 mutations in schwannomas. Genes Chromosomes Cancer (1996) 1.34
Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuria. Hum Mol Genet (1993) 1.34
The LCCL module. Eur J Biochem (2000) 1.34
Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma. Am J Pathol (1995) 1.32
Siderochromes from Pseudomonas fluorescens. II. Structural homology as revealed by NMR spectroscopy. J Biol Chem (1982) 1.30
Solution conformation of ferrichrome, a microbial iron transport cyclohexapeptide, as deduced by high resolution proton magnetic resonance. J Mol Biol (1970) 1.29
Smac mimetics increase cancer cell response to chemotherapeutics in a TNF-α-dependent manner. Cell Death Differ (2010) 1.29
Skin tuberculosis in children: learning from India. Dermatol Clin (2008) 1.28
Identification of functional arginine residues in ribonuclease A and lysozyme. J Biol Chem (1975) 1.27
Drug susceptibility in Leishmania isolates following miltefosine treatment in cases of visceral leishmaniasis and post kala-azar dermal leishmaniasis. PLoS Negl Trop Dis (2012) 1.27
Monitoring antimicrobial resistance in Neisseria gonorrhoeae in selected countries of the WHO South-East Asia Region between 2009 and 2012: a retrospective analysis. Sex Transm Infect (2013) 1.26
Tethering of the vertebral artery in the congenital arcuate foramen of the atlas vertebra: a possible cause of vertebral artery dissection in children. Dev Med Child Neurol (2001) 1.23
The merlin tumor suppressor localizes preferentially in membrane ruffles. Oncogene (1996) 1.22
Superiority of denaturing high performance liquid chromatography over single-stranded conformation and conformation-sensitive gel electrophoresis for mutation detection in TSC2. Ann Hum Genet (1999) 1.21
Constancy of central conduction delays during development in man: investigation of motor and somatosensory pathways. J Physiol (1991) 1.21
Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas. Cancer Res (1994) 1.20
The SEA module: a new extracellular domain associated with O-glycosylation. Protein Sci (1995) 1.20
Evaluation of the usefulness of Treponema pallidum hemagglutination test in the diagnosis of syphilis in weak reactive Venereal Disease Research Laboratory sera. Indian J Sex Transm Dis (2012) 1.20
Structural alterations in cardiac calcium release units resulting from overexpression of junctin. J Mol Cell Cardiol (2001) 1.18
Dyschromatosis universalis hereditaria: report of a case and review of the literature. Pediatr Dermatol (2002) 1.18
Mutational analysis of patients with neurofibromatosis 2. Am J Hum Genet (1994) 1.17
How soon does cutaneous tuberculosis respond to treatment? Implications for a therapeutic test of diagnosis. Int J Dermatol (2005) 1.16
An anti-Ras function of neurofibromatosis type 2 gene product (NF2/Merlin). J Biol Chem (1994) 1.16
Alternative splicing of the tuberous sclerosis 2 (TSC2) gene in human and mouse tissues. Genomics (1995) 1.16
The neurofibromatosis 2 protein product merlin selectively binds F-actin but not G-actin, and stabilizes the filaments through a lateral association. Biochem J (2001) 1.15
Leiomyoma cutis: a clinicopathological series of 37 cases. Indian J Dermatol (2010) 1.15
Molecular analysis and prenatal diagnosis of human fumarase deficiency. Mol Genet Metab (1998) 1.14
Deletions in the ligand for CD40 in X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1). Int Immunol (1993) 1.13
Microdialysis perfusion of orexin-A in the basal forebrain increases wakefulness in freely behaving rats. Arch Ital Biol (2001) 1.12
Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors. Brain Pathol (1995) 1.12
Morphologic and cytomorphometric analysis of exfoliated buccal mucosal cells in diabetes patients. J Cytol (2010) 1.11
NMR structure of the LCCL domain and implications for DFNA9 deafness disorder. EMBO J (2001) 1.11
Parasite detection in patients with post kala-azar dermal leishmaniasis in India: a comparison between molecular and immunological methods. J Clin Pathol (2003) 1.11
Effect of vitamin D supplementation during pregnancy on neonatal mineral homeostasis and anthropometry of the newborn and infant. Br J Nutr (2012) 1.10
Proton magnetic resonance study of crambin, a hyperstable hydrophobic protein, at 250 and 600 MHz. Biochemistry (1980) 1.10
ABACUS, a direct method for protein NMR structure computation via assembly of fragments. Proteins (2005) 1.10
Exon scanning of the entire TSC2 gene for germline mutations in 40 unrelated patients with tuberous sclerosis. Hum Mutat (1998) 1.09
Novel mutations detected in the TSC2 gene from both sporadic and familial TSC patients. Hum Mol Genet (1996) 1.09