Published in Biochem J on January 01, 1975
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Effects of autoantibodies to the insulin receptor on isolated adipocytes. Studies of insulin binding and insulin action. J Clin Invest (1977) 1.85
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On the immunological nature of the long acting thyroid stimulator. J Clin Endocrinol Metab (1966) 1.06
Experience with the bio-assay of the long-acting thyroid stimulator. J Clin Endocrinol Metab (1966) 0.99
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Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness. Nat Genet (2001) 2.06
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Rationing of growth hormone: who reviews the experts? Lancet (1997) 2.03
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Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin. Hum Genet (1999) 1.54
Identification and characterisation of novel human Y-chromosomal microsatellites from sequence database information. Nucleic Acids Res (2000) 1.53
A simple and rapid method for the preparation of plasma membranes. Biochim Biophys Acta (1983) 1.53
Evidence of RPGRIP1 gene mutations associated with recessive cone-rod dystrophy. J Med Genet (2003) 1.44
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Y-chromosomal STR haplotypes in Pakistani populations. Forensic Sci Int (2001) 1.31
Recovery of adrenocortical function following treatment of tuberculous Addison's disease. Postgrad Med J (1992) 1.30
Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan. Hum Mol Genet (1996) 1.25
A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13. Invest Ophthalmol Vis Sci (2000) 1.23
Network analyses of Y-chromosomal types in Europe, northern Africa, and western Asia reveal specific patterns of geographic distribution. Am J Hum Genet (1998) 1.21
Availability of dinitrophenylated lipid haptens for specific antibody binding depends on the physical properties of host bilayer membranes. J Biol Chem (1982) 1.17
A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32. Am J Hum Genet (1998) 1.15
Differential structuring of human populations for homologous X and Y microsatellite loci. Am J Hum Genet (1997) 1.12
A polymorphic L1 retroposon insertion in the centromere of the human Y chromosome. Hum Mol Genet (2000) 1.08
Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases. J Med Genet (2005) 1.08
Plasma concentrations of asymmetric dimethylarginine, a natural inhibitor of nitric oxide synthase, in normal pregnancy and preeclampsia. Am J Obstet Gynecol (1998) 1.08
Polycystic ovaries and associated metabolic abnormalities in Indian subcontinent Asian women. Clin Endocrinol (Oxf) (1998) 1.04
RP1 protein truncating mutations predominate at the RP1 adRP locus. Invest Ophthalmol Vis Sci (2000) 1.04
Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa. J Med Genet (2005) 1.02
Plasma concentrations of endogenous inhibitor of nitric oxide synthesis in normal pregnancy and pre-eclampsia. Lancet (1993) 1.01
Patterns of male-specific inter-population divergence in Europe, West Asia and North Africa. Ann Hum Genet (2000) 1.00
Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin. Am J Hum Genet (1999) 0.99
Allogeneic cytolysis of reconstituted membrane vesicles. Proc Natl Acad Sci U S A (1979) 0.98
Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene. Pharmacogenomics J (2008) 0.96
Sexually dimorphic and radiation dose dependent effect of cranial irradiation on body mass index. Arch Dis Child (1999) 0.95
An RFLP map for 2q33-q37 from multicase mycobacterial and leishmanial disease families: no evidence for an Lsh/Ity/Bcg gene homologue influencing susceptibility to leprosy. Ann Hum Genet (1993) 0.95
Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24. Invest Ophthalmol Vis Sci (2000) 0.95
Identification of novel TYR and TYRP1 mutations in oculocutaneous albinism. Clin Genet (2005) 0.94
Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online. Hum Mutat (1999) 0.93
A rapid method for the detection of antibodies to cell surface antigens: a solid phase radioimmunoassay using cell membranes. J Immunol Methods (1980) 0.91
Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32. Br J Ophthalmol (1999) 0.91
The influence of lipid substitution on thyrotropin-receptor interactions in artificial vesicles. Endocrinology (1977) 0.91
Rapid progression of fibrosing alveolitis and thyrotoxicosis after antithymocyte globulin therapy for aplastic anemia. Ann Hematol (1995) 0.90
Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreous. Invest Ophthalmol Vis Sci (2001) 0.90
Nucleotide sequence and chromosomal assignment of a cDNA encoding the large isoform of human glutamate decarboxylase. Ann Hum Genet (1992) 0.88
Premature coronary artery disease and the Prader-Willi syndrome. Postgrad Med J (1990) 0.87
Brattleboro rat adrenal contains vasopressin. Nature (1984) 0.87
Cell-mediated lysis of lipid vesicles containing eye muscle protein: implications regarding pathogenesis of Graves ophthalmopathy. Proc Natl Acad Sci U S A (1979) 0.87
Expression of intercellular adhesion molecule-1 (ICAM-1) on human thyroid cells lines correlated with their binding of lymphoblasts. Mol Cell Endocrinol (1990) 0.87
Where will this month's medical school intake go? Lancet (1986) 0.87
Vascular and hormonal responses to arginine: provision of substrate for nitric oxide or non-specific effect? Clin Sci (Lond) (1995) 0.85
SGHTL-34, a thyrotrophin-responsive immortalised human thyroid cell line generated by transfection. Mol Cell Endocrinol (1987) 0.84
Cloning of large isoform of human brain glutamic acid decarboxylase. Lancet (1991) 0.83
African and Levantine origins of Pakistani YAP+ Y chromosomes. Hum Biol (1999) 0.83
Distribution of HLA-A alleles in eight ethnic groups from Pakistan. Tissue Antigens (2003) 0.82
Insulin resistance and endothelial dysfunction in the brothers of Indian subcontinent Asian women with polycystic ovaries. Clin Endocrinol (Oxf) (2004) 0.82
Production of antibodies to the human thyrotropin receptor and their use in characterising eukaryotically expressed functional receptor. Mol Cell Endocrinol (1994) 0.81
Chronic hypernatraemia and hypothermia following subarachnoid haemorrhage. Postgrad Med J (1986) 0.81
Production of glutathione-coated microtitre plates for capturing recombinant glutathione S-transferase fusion proteins as antigens in immunoassays. J Immunol Methods (1998) 0.81
Testosterone selectively increases primary follicles in ovarian cortex grafted onto embryonic chick membranes: relevance to polycystic ovaries. Reproduction (2008) 0.81
Ovarian morphology and insulin sensitivity in women with bulimia nervosa. Clin Endocrinol (Oxf) (1995) 0.81
HLA analysis of the Parsi (Zoroastrian) population in Pakistan. Tissue Antigens (2005) 0.81
HLA polymorphism in six ethnic groups from Pakistan. Tissue Antigens (2002) 0.80
Reduced bone mineral density after surgical treatment for obesity. Int J Obes Relat Metab Disord (1999) 0.80
A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family. Invest Ophthalmol Vis Sci (2001) 0.80
The effect of oxytocin infusion on adenohypophyseal function in man. Clin Endocrinol (Oxf) (1990) 0.79
Characterization of the extracellular region of the human thyrotrophin receptor expressed as a recombinant protein. J Mol Endocrinol (1992) 0.79
Freeze-fracture of reconstituted model membranes used as targets for cell-mediated cytotoxicity. Biochim Biophys Acta (1980) 0.79
The role of oxytocin: present concepts. Clin Endocrinol (Oxf) (1991) 0.79
The use of the amplifiable high-expression vector pEE14 to study the interactions of autoantibodies with recombinant human thyrotrophin receptor. Mol Cell Endocrinol (1992) 0.78
Proopiomelanocortin products and human early-onset obesity. J Clin Endocrinol Metab (1999) 0.78
Effects of arginine vasopressin (AVP) infusions on circulating concentrations of platelet AVP, factor VIII: C and von Willebrand factor. Thromb Haemost (1986) 0.78
Human platelet arginine vasopressin. Clin Endocrinol (Oxf) (1986) 0.78
Regulation of macrophage nitric oxide synthesis by endothelial cells: a role for NG,NG-dimethylarginine. Acta Physiol Scand (1999) 0.78
Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan. Clin Genet (1995) 0.78
Growth hormone deficiency during puberty reduces adult bone mineral density. Arch Dis Child (1992) 0.77
The effect of basic fibroblast growth factor on the growth and function of human thyrocytes. J Endocrinol (1993) 0.77
Effect of hyperthermia on murine cell surface histocompatibility antigens. Cancer Res (1984) 0.77
Clinical application of a radioreceptor assay for thyroid stimulators. Horm Metab Res (1975) 0.77
Thyrocyte release of asymmetric dimethylarginine does not account for human thyrocyte inhibition of endothelial cell cyclic GMP. Eur J Endocrinol (2000) 0.76
The responses of arginine vasopressin and adrenocorticotrophin to nausea induced by ipecacuanha. Clin Endocrinol (Oxf) (1990) 0.76
Letter: Nomenclature of thyroid-stimulating antibodies. Lancet (1975) 0.76
Y haplogroups and aggressive behavior in a Pakistani ethnic group. Aggress Behav (2008) 0.76
Use of human somatotrophin in the treatment of a patient with methylmalonic aciduria. Eur J Pediatr (1995) 0.75
A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis. Scientifica (Cairo) (2012) 0.75
Hypothalamic disease in association with dysgenesis of the corpus callosum. Postgrad Med J (1989) 0.75
Direct evidence for limited clonality of antibodies to glutamic acid decarboxylase (GAD) in stiff man syndrome using baculovirus expressed GAD. J Neurol Neurosurg Psychiatry (1994) 0.75
Effect of arginine vasopressin and oxytocin on acetylcholine-stimulation of corticosteroid and catecholamine secretion from the rat adrenal gland perfused in situ. Neuropeptides (1989) 0.75
Hypokalaemic alkalosis. Postgrad Med J (1998) 0.75
Spontaneous haemorrhage into a pituitary tumour after streptokinase therapy. Postgrad Med J (1993) 0.75
The cell adhesion molecule, VCAM-1, is selectively elevated in serum in pre-eclampsia: does this indicate the mechanism of leucocyte activation? Br J Obstet Gynaecol (1995) 0.75
Ovarian carcinoma producing hypoglycaemia. Postgrad Med J (1998) 0.75
Interaction of thyrotropin and thyroid-stimulating antibodies with recombinant extracellular region of human TSH receptor. Lancet (1992) 0.75
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3. Adv Otorhinolaryngol (2000) 0.75
Immune induction of major histocompatibility complex antigens on a human thyroid cell line (SGHTL-34). J Mol Endocrinol (1989) 0.75
Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r) J Med Genet (2000) 0.75
The interaction of arginine vasopressin and oxytocin with bovine adrenal medulla cells. J Endocrinol (1989) 0.75
Medroxyprogesterone acetate induced Cushing's syndrome. Br J Clin Pharmacol (1997) 0.75
HLA polymorphisms in ethnic groups from Pakistan. Transplant Proc (1999) 0.75