S Pang

Author PubWeight™ 83.35‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Clearance of HIV infection in a perinatally infected infant. N Engl J Med 1995 3.76
2 Translocation of the glucose transporter (GLUT4) to the cell surface in permeabilized 3T3-L1 adipocytes: effects of ATP insulin, and GTP gamma S and localization of GLUT4 to clathrin lattices. J Cell Biol 1992 2.71
3 The natriuretic peptide clearance receptor locally modulates the physiological effects of the natriuretic peptide system. Proc Natl Acad Sci U S A 1999 2.48
4 Quantitative polymerase chain reaction does not improve preoperative prostate cancer staging: a clinicopathological molecular analysis of 121 patients. J Urol 1996 2.25
5 Human immunodeficiency virus type 1 T-cell tropism is determined by events prior to provirus formation. J Virol 1990 2.11
6 Molecular cloning and tissue distribution of PHAS-I, an intracellular target for insulin and growth factors. Proc Natl Acad Sci U S A 1994 2.02
7 Swelling-induced release of glutamate, aspartate, and taurine from astrocyte cultures. J Neurosci 1990 1.98
8 Genotyping steroid 21-hydroxylase deficiency: hormonal reference data. J Clin Endocrinol Metab 1983 1.77
9 Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia. J Clin Endocrinol Metab 1977 1.69
10 Scatter factor and hepatocyte growth factor: activities, properties, and mechanism. Cell Growth Differ 1992 1.56
11 GLUT-4 NH2 terminus contains a phenylalanine-based targeting motif that regulates intracellular sequestration. J Cell Biol 1993 1.35
12 HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency. Am J Hum Genet 1981 1.35
13 Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita. J Clin Endocrinol Metab 1999 1.31
14 Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing. Lancet 1979 1.30
15 In vivo pathogenic properties of two clonal human immunodeficiency virus type 1 isolates. J Virol 1995 1.24
16 Etoposide metabolites enhance DNA topoisomerase II cleavage near leukemia-associated MLL translocation breakpoints. Biochemistry 2001 1.16
17 A pilot newborn screening for congenital adrenal hyperplasia in Alaska. J Clin Endocrinol Metab 1982 1.10
18 Low plasma androgens in women with systemic lupus erythematosus. Arthritis Rheum 1987 1.08
19 "Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia. J Clin Endocrinol Metab 1979 1.05
20 Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repression. J Clin Endocrinol Metab 2001 1.04
21 Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia. J Clin Endocrinol Metab 1982 1.02
22 Electromyogram-triggered neuromuscular stimulation for improving the arm function of acute stroke survivors: a randomized pilot study. Arch Phys Med Rehabil 1998 1.02
23 Human health and chemical mixtures: an overview. Environ Health Perspect 1998 1.01
24 The relationship between luteinizing hormone and estradiol secretion in female precocious puberty: evaluation by sensitive gonadotropin assays and the leuprolide stimulation test. J Clin Endocrinol Metab 1993 1.01
25 Prostate-specific targeting using PSA promoter-based lentiviral vectors. Cancer Gene Ther 2001 1.00
26 Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia. J Clin Endocrinol Metab 1980 1.00
27 Serum androgen concentrations in neonates and young infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clin Endocrinol (Oxf) 1979 0.99
28 Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus. Hum Immunol 1980 0.98
29 Amniotic fluid concentrations of delta 5 and delta 4 steroids in fetuses with congenital adrenal hyperplasia due to 21 hydroxylase deficiency and in anencephalic fetuses. J Clin Endocrinol Metab 1980 0.98
30 Highly efficient and consistent gene transfer into dendritic cells utilizing a combination of ultraviolet-irradiated adenovirus and poly(L-lysine) conjugates. Cancer Res 1998 0.96
31 Regulation of the expression of the prostate-specific antigen by claudin-7. J Membr Biol 2003 0.96
32 Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency. J Clin Endocrinol Metab 1981 0.94
33 Adrenocortical tumor in a patient with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Pediatrics 1981 0.92
34 Excitatory amino acid-stimulated uptake of 22Na+ in primary astrocyte cultures. J Neurosci 1989 0.91
35 The 21-hydroxylase activity in the glomerulosa and fasciculata of the adrenal cortex in congenital adrenal hyperplasia. J Clin Endocrinol Metab 1981 0.91
36 Inherited congenital adrenal hyperplasia in the rabbit is caused by a deletion in the gene encoding cytochrome P450 cholesterol side-chain cleavage enzyme. Endocrinology 1993 0.89
37 SULT1A1 catalyzes 2-methoxyestradiol sulfonation in MCF-7 breast cancer cells. Carcinogenesis 2000 0.89
38 Studies of the C-21 and C-19 steroids and HLA genotyping in siblings and parents of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Endocrinol Metab 1980 0.89
39 New studies of the 11 beta-hydroxylase and 18-hydroxylase enzymes in the hypertensive form of congenital adrenal hyperplasia. J Clin Endocrinol Metab 1980 0.88
40 Dihydrotestosterone and its relationship to testosterone in infancy and childhood. J Clin Endocrinol Metab 1979 0.88
41 Selegiline as an adjunct to conventional levodopa therapy in Parkinson's disease. Experience with this type B monoamine oxidase inhibitor in 200 patients. Arch Neurol 1989 0.88
42 The variable bone scan appearances of nonosteogenic fibroma of bone. Clin Nucl Med 1981 0.87
43 The effect of technology on the caring attributes of an international sample of nurses. Int J Nurs Stud 2001 0.87
44 Developmental expression of insulin-regulatable glucose transporter GLUT-4. Am J Physiol 1992 0.86
45 An update of congenital adrenal hyperplasia. Recent Prog Horm Res 1981 0.85
46 In vitro modulation of tumor progression-associated properties of hormone refractory prostate carcinoma cell lines by cytokines. Cancer 1996 0.85
47 HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency. Hum Genet 1981 0.84
48 Hypothalamic-pituitary-adrenal function following cranial irradiation. Horm Res 1997 0.84
49 Congenital adrenal hypoplasia: two new cases. J Endocrinol Invest 1983 0.82
50 Dog safety in rural China: children's sources of safety information and effect on knowledge, attitudes, and practices. Accid Anal Prev 2013 0.81
51 Hormonal phenotype and HLA-genotype in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency). Pediatr Res 1979 0.81
52 Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia. Ann N Y Acad Sci 1985 0.81
53 Induction of cytochrome P450 1B1 in MDA-MB-231 human breast cancer cells by non-ortho-substituted polychlorinated biphenyls. Toxicol In Vitro 2002 0.81
54 Antepartum diagnosis of goitrous hypothyroidism by fetal ultrasonography and amniotic fluid thyrotropin concentration. J Clin Endocrinol Metab 1984 0.81
55 [Changes in TGF-beta 1 and type I, III procollagen gene expression in keloid and hypertrophic scar]. Zhonghua Zheng Xing Shao Shang Wai Ke Za Zhi 1999 0.81
56 The hypothalamic-pituitary-adrenal axis in partial (late-onset) 21-hydroxylase deficiency. J Clin Endocrinol Metab 1988 0.80
57 Caring attributes, professional self concept and technological influences in a sample of Registered Nurses in eleven countries. Int J Nurs Stud 1999 0.80
58 In vivo cancer gene therapy with a recombinant interleukin-2 adenovirus vector. Cancer Gene Ther 1996 0.79
59 Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab 1985 0.79
60 Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa function. J Clin Endocrinol Metab 1983 0.79
61 Mutations in the type II 3 beta-hydroxysteroid dehydrogenase gene in a patient with classic salt-wasting 3 beta-hydroxysteroid dehydrogenase deficiency congenital adrenal hyperplasia. Pediatr Res 1993 0.79
62 Selegiline use to prevent progression of Parkinson's disease. Experience in 22 de novo patients. Arch Neurol 1989 0.79
63 Cobalt chromium-based biodegradable polymer sirolimus-eluting stent: rationale, evidence and clinical experience. Minerva Cardioangiol 2015 0.79
64 Efficacy of intracytoplasmic sperm injection using intentionally cryopreserved epididymal spermatozoa. Hum Reprod 1996 0.78
65 Feasibility of a novel abluminal groove-filled biodegradable polymer sirolimus-eluting stent in patients with complex anatomical and clinical scenarios. Minerva Cardioangiol 2015 0.78
66 Natural immune reactivity-associated therapeutic response in patients with metastatic renal cell carcinoma receiving tumor-infiltrating lymphocytes and interleukin-2-based therapy. J Immunother Emphasis Tumor Immunol 1996 0.77
67 In vitro modulation of the invasive and metastatic potentials of human renal cell carcinoma by interleukin-2 and/or interferon-alpha gene transfer. Cancer 1994 0.77
68 Combined bromocriptine and growth hormone (GH) treatment in GH-deficient children with macroprolactinoma in situ. J Clin Endocrinol Metab 1992 0.76
69 A child found to be HIV positive shortly after birth appears now to be clear of the infection. Nurs Times 1995 0.76
70 Characterization of two novel homozygous missense mutations involving codon 6 and 259 of type II 3beta-hydroxysteroid dehydrogenase (3betaHSD) gene causing, respectively, nonsalt-wasting and salt-wasting 3betaHSD deficiency disorder. J Clin Endocrinol Metab 2000 0.76
71 Insulin stimulates the release of a subset of GPI-anchored proteins in a G-protein independent manner. Mol Membr Biol 2000 0.76
72 Molecular basis of congenital adrenal hyperplasia in two siblings with classical nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency. J Clin Endocrinol Metab 1994 0.76
73 Hypothalamic-pituitary-gonadal axis function in pubertal male and female siblings with glucocorticoid-treated nonsalt-wasting 3 beta-hydroxysteroid dehydrogenase deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab 1993 0.76
74 Studies of 3 beta-hydroxysteroid dehydrogenase genes in infants and children manifesting premature pubarche and increased adrenocorticotropin-stimulated delta 5-steroid levels. J Clin Endocrinol Metab 1996 0.76
75 A new model of phycobilisome in Spirulina platensis. Sci China C Life Sci 1999 0.76
76 Newborn screening for congenital adrenal hyperplasia with special reference to screening in Alaska. Ann N Y Acad Sci 1985 0.76
77 Fabrication of Boron-Doped CVD Diamond Microelectrodes. Anal Chem 1998 0.76
78 Prenatal diagnosis and treatment of congenital adrenal hyperplasia. J Pediatr Endocrinol 1995 0.76
79 Delayed puberty in males with chronic renal failure. Kidney Int 1980 0.76
80 First Whole-Genome Sequence of a Clinical Isolate of Multidrug-Resistant Mycobacterium bovis BCG. Genome Announc 2014 0.75
81 A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab 1996 0.75
82 [Expression of proliferating cell nuclear antigen and tumor suppressor gene P53 in mucoepidermoid carcinoma of salivary glands]. Zhonghua Kou Qiang Yi Xue Za Zhi 1996 0.75
83 [Alteration of CD44v3 and CD44v6 expression in oral premalignant epithelia]. Zhonghua Kou Qiang Yi Xue Za Zhi 1999 0.75
84 [Proliferating cell nuclear antigen (PCNA) in oral leukoplakia]. Zhonghua Kou Qiang Yi Xue Za Zhi 1995 0.75
85 Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab 1980 0.75
86 Practical advances in cortisol and dehydroepiandrosterone sulfate radioimmunoassay using the microfilter paper method. J Lab Clin Med 1980 0.75
87 Evidence of a steroidogenic enzyme gene dose effect on adrenal gene expression in hereditary rabbit congenital adrenal hyperplasia. Pediatr Res 1994 0.75
88 Recovery of adrenal function after treatment of adrenocortical carcinoma with o,p'-DDD. Clin Endocrinol (Oxf) 1984 0.75
89 [The tensor fascia lata racket shape myocutaneous island flap]. Zhonghua Zheng Xing Wai Ke Za Zhi 2001 0.75
90 HLA typing of amniotic cells: the prenatal diagnosis of congenital adrenal hyperplasia (21-OH-deficiency type). Transplant Proc 1979 0.75
91 Peer reviewed: evaluating impacts of hormonally active agents in the environment. Environ Sci Technol 2000 0.75
92 Cloning, sequencing, and enzymatic activity of an inducible aldo-keto reductase from Chinese hamster ovary cells. Adv Exp Med Biol 1997 0.75
93 Polycystic ovary syndrome and congenital adrenal hyperplasia. Clin Endocrinol (Oxf) 1984 0.75
94 Births averted in Singapore during 1966-1975. Singap Stat Bull 1977 0.75
95 Copper(II) ion induced monolayer formation of p-tert-butylthiacalix[4]arene at the air-water interface. Spectrochim Acta A Mol Biomol Spectrosc 2001 0.75
96 Swelling-induced membrane transport changes in astrocytes. Acta Physiol Scand Suppl 1989 0.75
97 Comparison of adrenocorticotropin and adrenal steroid responses to corticotropin-releasing hormone versus metyrapone testing in patients with hypopituitarism. Pediatr Res 1994 0.75
98 [Investigation on an ancient edition of On Five Viscera unearthed in Dunhuang-Turfan]. Zhonghua Yi Shi Za Zhi 1995 0.75
99 Detection of heterozygote of 21-hydroxylase deficiency. Lancet 1980 0.75
100 Recurrence of Cushing's disease in childhood after radiotherapy-induced remission. Am J Dis Child 1987 0.75
101 Changes of intracellular Na(+) concentration in erythrocytes caused by pulsed electrical field. Sci China C Life Sci 1997 0.75
102 L-deprenyl, a MAO-B inhibitor, as an adjunct to conventional L-dopa therapy in Parkinson's disease: experience in 200 patients. Adv Neurol 1990 0.75
103 Assembly and structure of neurofilaments isolated from bovine spinal cord. Sci China C Life Sci 1999 0.75
104 Quenching of fluorescence in membrane protein by hypocrellin B. Sci China C Life Sci 1997 0.75
105 Evaluation of a pen device for self-administration of recombinant human FSH in clomiphene citrate-resistant anovulatory women undergoing ovulation induction. Reprod Biomed Online 2004 0.75
106 [Basaloid squamous cell carcinoma: clinical pathological and immunohistochemical study]. Zhonghua Kou Qiang Yi Xue Za Zhi 1998 0.75
107 Caring in context: caring practices in a sample of Hong Kong nurses. Contemp Nurse 1998 0.75
108 Adenovirus-mediated interleukin-2 production by tumors induces growth of cytotoxic tumor-infiltrating lymphocytes against human renal cell carcinoma. J Immunother 1998 0.75
109 Empty sella syndrome in childhood. Pediatr Neurol 1989 0.75
110 Gene therapy: principles and potential. Cancer Surv 1995 0.75