74 AN ASSOCIATION OF THE FBN1 GENE POLYMORPHISM WITH TALL STATURE
スポンサーリンク
概要
著者
-
Nakahata T
Department Of Pediatrics Hirosaki University School Of Medicine
-
Kawai M
Department Of Applied Chemistry Nagoya Institute Of Technology
-
Yorifuji T
Department Of Baioscience And Biotechnology Shinshu University
-
Kurokawa K
Department Of Anatomy Shiga University Of Medical Science
-
Yorifuji T
Department Of Pediatrics Kyoto University School Of Medicine
-
Mamada M
Department of Pediatrics, Kyoto University Hospital
-
Momoi T
Department of Pediatrics. Japanese Red Cross Society Wakayama Medical Center
-
Momoi T
First Department of Pediatrics, Japanese Red Cross Society Wakayama Medical Center
-
Nakahata T
Department Of Pediatrics Kyoto University Hospital
-
Kawai M
Department Of Pediatrics Kyoto University School Of Medicine
-
Kurokawa K
Department Of Pediatrics Kyoto University Hospital
-
Mamada M
Department Of Pediatrics Kyoto University Hospital
-
Yorifuji T
Department of Pediatrics, Kyoto University School of Medicine
関連論文
- Mizoribine Pulse Therapy for a Pediatric Patient with Steroid-Resistant Nephrotic Syndrome
- Effective Therapy of a Child Case of Refractory Nephrotic Syndrome with Tacrolimus
- Combined therapy of enalapril and losartan attenuates histologic progression in immunoglobulin A nephropathy
- Mizoribine oral pulse therapy for a patient with severe lupus nephritis
- End-Stage Kidney at the Onset of Nephrotic Syndrome in a 4-Year-Old Girl
- Acute renal failure due to hypertension : Malignant hypertension in an adolescent
- Disseminated candidiasis following prednisolone therapy in systemic lupus erythematosus
- Tubulointerstitial Nephritis and Uveitis Syndrome in Two Siblings
- Childhood idiopathic membranous glomerulonephritis with isolated antinuclear antibody positivity
- Focal Segmental Glomerulosclerosis : Unremitting Proteinuria of Long Duration as a Possible Etiology?
- Acute Glomerulonephritis Superimposed on Focal Segmental Glomerulosclerosis : A Case Report
- Thrombotic Stroke in a Child with Diarrhea-Associated Hemolytic-Uremic Syndrome with a Good Recovery
- A Diabetic Case with Hemoglobin J-Meerut and Low HbA_ Levels
- 近位, および遠位尿細管の機能障害を伴った両側矮小腎を有する1新生児例
- Expression of RET in follicular cell-derived tumors of the thyroid gland : Prevalence and implication of morphological type
- Inhibitory Effect of Thyrotropic Hormone on Apoptosis Induced by Actinomycin D in a Functioning Rat Thyroid Cell Line
- A mammalian dpy-19 homologue is expressed in GABAergic neurons
- S3-7 MDPY-19 is a new surface marker protein of neural stem cells(THE JOINT MEETING OF THE 44TH ANNUAL MEETING OF THE JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY AND THE 35TH ANNUAL MEETING OF THE CLINICAL ELECTRON MICROSCOPY SOCIETY OF JAPAN)
- Immunohistochemical demonstration of the endothelin-converting enzyme-1 in the rat hypothalamo-pituitary axis
- Nonviral gene transfer into the neurons by microelectroporation
- Synthesis and Properties of 4α- and 4β-Aminoprolyl Residue-Containing Analogs of Gramicidin S
- Secretion of Bax-Like Protein into Systemic Circulation from the Posterior Pituitary in the Rat Hypothalamo-Posterior Pituitary System
- Subsequent Progression to Membranous Glomerulonephritis Following Exacerbation of Urticarial Rash in Systemic Lupus Erythematosus : Report of 2 Cases
- Differential Expression of Prolactin Releasing Peptide and Tyrosine Hydroxylase in Fibers Derived from the Same Neurons in the Rat
- Morphological survey of Prolactin-releasing peptide and its receptor with special reference to their functional roles in the brain
- Hypothermia protects non-typical and typical apoptotic like neuronal degeneration by repetitive ischemic attacks in the gerbils
- Taurocyamine-utilizing Mutant of Pseudomonas aeruginosa with Altered Induction of 3-Guanidinopropionate Amidinohydrolase(Microbiology & Fermentation Industry)
- 24 An evaluation about the physical growth and onset of puberty of the extremely low birth weight infants.
- Gene therapy for renal injury model rat using an adenovirus vector encoding the soluble rat Crry gene
- Trisomy 6 in a childhood acute mixed lineage leukemia
- Successful treatment of Wernicke's encephalopathy in a boy with acute mixed lineage leukemia
- Protection from D-galactosamine-induced liver injury by orally active novel peptide leukotriene receptor antagonist, ONO-1078
- Diaminopropane Aminotransferase, a Novel Enzyme of a Coryneform Bacterium(Biological Chemistry)
- Stable-isotope dilution gas chromatography-mass spectrometric measurement of 3-hydroxyglutaric acid, glutaric acid and related metabolites in body fluids of patients with glutaric aciduria type 1 found in newborn screening
- Mesangial cell-predominant functional gene, megsin
- Succinate-semialdehyde Dehydrogenase for L-Arginine and Putrescine Degradation in Brevibacterium helvolum(Microbiology & Fermentation Industry)
- Specific Measurement of Putrescine with Putrescine Oxidase and Aminobutyraldehyde Dehydrogenase(Biological Chemistry)
- Large spleno-caval shunt not accompanied by cirrhosis or encephalopathy
- Metal Ion-Complex Forming Properties of Diastereomeric Dipeptide Derivatives Possessing Two Picolinoylamide Groups
- 23 A CASE OF FOCAL NESIDIOBLASTOSIS TREATED WITH PARTIAL PANCREATECTOMY
- 74 AN ASSOCIATION OF THE FBN1 GENE POLYMORPHISM WITH TALL STATURE
- 72 A NONSENSE MUTATION IN EXON 3 FO THE GH1 GENE CAUSE FAMIKIAK ISOLATED GROWTH HORMONE DEFICIENCY TYPE II
- 71 A NONSENSE MUTATION IN EXON 3 OF THE GH1 GENE CAUSES FAMILIAL ISOLATED GROWTH HORMONE DEFICIENCY TYPE II
- 114 A CASE OF DOWN SYNDROME WITH IDIOPATHIC HYPERCALCEMIA
- 168 A frameshift mutation and a familial deletion mutation of the DAX1 gene in patients with X-linked adrenal hypoplasia congenita
- 186 TYROID DYSFUNCTION IN VERY-LOW-BIRTH-WEIGHT-INFANTS
- 96 A ONE-MONTH-OLD FEMALE NEONATE CASE OF NONCLASSICAL STEROID 21-HYDROXYLASE DEFICIENCY DIAGNOSED BY MOLECULAR ANALYSIS OF THE CYP21 GENE.
- 127 GENETIC ISOLATED GROWTH HORMONE DEFICIENCY TYPE II DUE TO AN Arg^His GH-1 GENE MUTATION
- 204 A CASE OF CHROMOSOME BREAKAGE SYNDROME WITH SEVERE GROWTH FAILURE AND SYSTEMIC BONE DISEASE