[Gilbert's syndrome].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645056
Okada H, Itoh S, Onishi S
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
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Publications
Page 9894 of 10600
[Neonatal adrenoleukodystrophy].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645067
Shimozawa N
[Infantile Refsum disease].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645068
Shimozawa N
[Rhizomelic chondrodysplasia punctata (RCDP)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645069
Shimozawa N
[X-linked adrenoleukodystrophy (ALD)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645071
Imamura A
[Acatalasemia, Takahara disease].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645075
Suzuki Y
[Primary hyperoxaluria type 1 (PH1)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645077
Ogawa Y, Hatano T
[Lysosomal diseases: an overview].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645079
Suzuki Y
[Gaucher disease].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645082
Ida H
[Niemann-Pick disease [type A and B] (acid sphingomyelinase deficiencies)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645083
Higaki K, Ohno K
[Krabbe disease (globoid cell leukodystrophy)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645086
Inui K
[Metachromatic leukodystrophy].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645087
Eto Y, Hasegawa Y, Kurosawa K
[Tay-Sachs disease (beta-hexosaminidase alpha-chain deficiency)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645090
Okada S, Taniike M
[Sandhoff disease (beta-hexosaminidase alpha-chain deficiency)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645091
Taniike M, Okada S
[beta-Galactosidosis (acid beta-galactosidase deficiency: GM1 gangliosidosis, Morquio B disease)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645093
Nishigaki T, Okada S
[GM2 activator protein deficiency (AB variant form of GM2 gangliosidosis)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645095
Kondoh K, Sano A
[Saposin B deficiency].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645097
Kotani Y, Sano A
[Saposin C deficiency].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645098
Sano A
[Acid lipase deficiency (Wolman disease and cholesteryl ester storage disease: CESD)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645100
Tanaka A
[Mucopolysaccharidosis type I (Hurler syndrome, Scheie syndrome)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645101
Sukegawa K, Tomatsu S, Kondo N and 1 more
[Mucopolysaccharidosis type II (Hunter syndrome)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645102
Sukegawa K, Tomatsu S, Kondo N and 1 more
[Mucopolysaccharidosis type IV (Morquio syndrome, beta-galactosidase deficiency)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645104
Sukegawa K, Tomatsu S, Kondo N and 1 more
[Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645105
Sukegawa K, Tomatsu S, Kondo N and 1 more
[Carbohydrate-deficient glycoprotein (CDG) syndrome (Jaeken syndrome)].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645114
Ohno K
[Mitochondria: an overview].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645115
Nonaka I
[Electron transfer complex I deficiency].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645116
Goto Y
[Electron transfer complex IV (cytochrome c oxidase) deficiency].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645119
Nonaka I
[Introduction to connective tissue].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645121
Ninomiya Y
[Osteogenesis imperfecta].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645122
Yoshitaka T, Yoshioka H
[Chondrodysplasia].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645124
Yoshioka H, Yoshitaka T
[Alport syndrome].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645125
Momota R, Oohashi T
[Epidermolysis bullosa hereditaria].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645126
Hirakawa S, Yoshioka H
[Marfan syndrome].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645127
Minami S
[Marfan-related conditions].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645128
Minami S
[Membrane transport system].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645130
Yabuta K
[Selective congenital glucose, galactose malabsorption in the small intestine].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645131
Bamba T, Fukuda M
[Cystinuria].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645133
Owada M, Watanabe S, Tsuda M
[Familial iminoglycinuria].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645136
Ohura T
[Methionine malabsorption syndrome].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645139
Bamba T, Ihara T
[Oculocerebrorenal syndrome of Lowe].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645142
Owada M, Minowa A, Suhara Y
[Hypophosphatemic vitamin D resistant rickets].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645143
Kinuta K, Seino Y
[Cystic fibrosis].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645146
Yoshimura K, Tada H, Anzai C
[Ataxia-telangiectasia].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645148
Fukao T, Kaneko H, Kondo N
[Carbonic anhydrase II deficiency].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645149
Murakami H, Aramaki S, Yoshino M
[Alpha 1-antitrypsin deficiency].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645152
Miyake K
[Hereditary amyloidosis].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645153
Tashima K, Uyama E, Uchino M and 1 more
[Cholinesterase deficiency].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645156
Hada T
[Dipeptidase deficiency].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645157
Takeda H, Takahashi T
[Alloalbuminemia and analbuminemia].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645158
Mori K, Tsuji A, Matsuda Y
[Hypophosphatasia].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645163
Ozono K, Cai G
[Trimethylaminuria].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645164
Yamaguchi S
[Albinism].
Ryoikibetsu shokogun shirizu | 1998-01-01 | PMID 9645166
Kitano Y
Protective efficacy of a dengue 2 DNA vaccine in mice and the effect of CpG immuno-stimulatory motifs on antibody responses
1998-04-01 | PMID 9645204
Laurence-Moon-Bardet-Biedl syndrome. Clinical, electrophysiological and genetic aspects.
Acta ophthalmologica Scandinavica. Supplement | 1998-01-01 | PMID 9645236
Riise R
Serotype Identification of Avian Infectious Bronchitis Virus by RT-PCR of the Peplomer (S-1) Gene
1998-04-01 | PMID 9645318
Pen Trial Studies on the Use of Live Vaccines to Displace Virulent Mycoplasma gallisepticum in Chickens
1998-04-01 | PMID 9645321
Identification of a human member of the Ly-49 multigene family
1998-06-01 | PMID 9645365
Genetic rearrangements in the pathogenicity locus of Clostridium difficile strain 8864 – implications for transcription, expression and enzymatic activity of toxins A and B
1998-05-01 | PMID 9645428
Klinefelter Syndrome
1998-06-22 | PMID 9645824
A rod end deletion in the intermediate filament protein nestin alters its subcellular localization in neuroepithelial cells of transgenic mice
1998-07-30 | PMID 9645943
Molecular Variants of the EWS-WT1 Gene Fusion in Desmoplastic Small Round Cell Tumor
1998-02-01 | PMID 9646031
Molecular Diagnosis of Ewing Tumors
1998-02-01 | PMID 9646032
Molecular diagnostics in hepatitis C virus infection: clinical applications. Scientific Committee--"Tecnologie molecolari nella diagnostica delle epatopatie" of the Italian Association for the Study of the Liver-AISF.
Italian journal of gastroenterology and hepatology | 1997-04-01 | PMID 9646205
Nucleotide sequence homology to bovine viral diarrhea virus 2 (BVDV 2) in the 5′ untranslated region of BVDVs from cattle with mucosal disease or persistent infection in Japan
1998-02-28 | PMID 9646457
The frequent detection of a treponeme in bovine digital dermatitis by immunocytochemistry and polymerase chain reaction
1998-02-28 | PMID 9646459
Gender and Neurogenic Variables in Tendon Biology and Repetitive Motion Disorders
1998-06-01 | PMID 9646746
Molecular and cellular events in early thymocyte development.
Advances in immunology | 1998-01-01 | PMID 9646843
Rodewald H R, Fehling H J
Regulation of immunoglobulin light chain isotype expression.
Advances in immunology | 1998-01-01 | PMID 9646844
Gorman J R, Alt F W
INHIBITORS OF HIV-1 PROTEASE: A Major Success of Structure-Assisted Drug Design
1998-06-01 | PMID 9646869
Lack of association between apolipoprotein H polymorphism and plasma lipid levels in Koreans.
Clinical biochemistry | 1998-06-01 | PMID 9646954
Hong S H, Song J, Lee D H and 1 more
Tissue-Specific Up-Regulation of B7-1 Expression and Function During the Course of Murine Relapsing Experimental Autoimmune Encephalomyelitis
1998-07-01 | PMID 9647224
An NFAT-Dependent Enhancer Is Necessary for Anti-IgM-Mediated Induction of Murine CD5 Expression in Primary Splenic B Cells
1998-07-01 | PMID 9647234
T Cell Epitopes in Japanese Cedar ( Cryptomeria japonica ) Pollen Allergens: Choice of Major T Cell Epitopes in Cry j 1 and Cry j 2 Toward Design of the Peptide-Based Immunotherapeutics for the Management of Japanese Cedar Pollinosis
1998-07-01 | PMID 9647255
Prenatal testing for late-onset diseases such as mutations in the breast cancer gene 1 (BRCA1). Just a choice or a step in the wrong direction?
Human reproduction (Oxford, England) | 1998-05-01 | PMID 9647529
Wagner T M, Ahner R
Genes: BRCA1
A logistic regression model including DNA status and morphology of spermatozoa for prediction of fertilization in vitro
1998-05-01 | PMID 9647553
The effects of antioxidant supplementation during Percoll preparation on human sperm DNA integrity
1998-05-01 | PMID 9647554
Enhancement of motility and acrosome reaction in human spermatozoa: differential activation by type-specific phosphodiesterase inhibitors
1998-05-01 | PMID 9647555
Continuing the debate on empty follicle syndrome: can it be associated with normal bioavailability of beta-human chorionic gonadotrophin on the day of oocyte recovery?
1998-05-01 | PMID 9647560
DNA strand breaks and phosphatidylserine redistribution in newly ovulated and cultured mouse and human oocytes: occurrence and relationship to apoptosis
1998-05-01 | PMID 9647566
Structural Analysis of Drosophila Merlin Reveals Functional Domains Important for Growth Control and Subcellular Localization
1998-06-29 | PMID 9647651
Abundance in Sewage of Bacteriophages That Infect Escherichia coli O157:H7 and That Carry the Shiga Toxin 2 Gene
1998-07-01 | PMID 9647813
New approaches for detecting thresholds of human nephrotoxicity using cadmium as an example.
1998-05-01 | PMID 9647892
Features of<i>Tri101</i>, the Trichothecene 3-<i>O</i>-Acetyltransferase Gene, Related to the Self-defense Mechanism in<i>Fusarium graminearum</i>
1998-01-01 | PMID 9648241
Assessment of DNA Damage Induced by Broadband and Narrowband UVB in Cultured Lymphoblasts and Keratinocytes Using the Comet Assay
1998-06-01 | PMID 9648530
Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K.
Diabetes | 1998-07-01 | PMID 9648841
Beards F, Frayling T, Bulman M and 6 more
Identification of polymorphisms in the receptor for advanced glycation end products (RAGE) gene: prevalence in type 2 diabetes and ethnic groups.
1998-07-01 | PMID 9648842
CTLA4 gene haplotypes cannot protect from IDDM in the presence of high-risk HLA DQ8 or DQ2 alleles in German families.
Diabetes | 1998-07-01 | PMID 9648843
Donner H, Seidl C, Braun J and 5 more
Genes: CTLA4
Major susceptibility locus for nephropathy in type 1 diabetes on chromosome 3q: results of novel discordant sib-pair analysis.
1998-07-01 | PMID 9648845
Metabolic Dysfunction in Familial, but Not Sporadic, Amyotrophic Lateral Sclerosis
1998-07-01 | PMID 9648876
Diagnosis of celiac sprue
1998-07-01 | PMID 9649477
The language of gene interaction.
Genetics | 1998-07-01 | PMID 9649511
Phillips P C
Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasia.
1998-07-01 | PMID 9649554
In vivo analysis of Fas/FasL interactions in HIV-infected patients.
1998-07-01 | PMID 9649560
Molecular defects in ferrochelatase in patients with protoporphyria requiring liver transplantation.
1998-07-01 | PMID 9649563
Type III hyperlipoproteinemia and spontaneous atherosclerosis in mice resulting from gene replacement of mouse Apoe with human Apoe*2.
1998-07-01 | PMID 9649566
Milk: integrative signalling between mother and offspring.
Biochemical Society transactions | 1998-05-01 | PMID 9649728
Peaker M
Inborn errors of metabolism in the light of metabolic control analysis.
Biochemical Society transactions | 1998-05-01 | PMID 9649736
Mazat J P, Letellier T, Malgat M and 4 more
Herpes simplex virus type I in brain and the type 4 allele of the apolipoprotein E gene are a combined risk factor for Alzheimer's disease.
Biochemical Society transactions | 1998-05-01 | PMID 9649761
Itzhaki R F, Lin W R
Hyperleptinaemia precedes hyperinsulinaemia in Zucker (fa/fa) rats.
Biochemical Society transactions | 1998-05-01 | PMID 9649773
Rayner D V, Atkinson T, Dalgleish G D and 3 more
Angiotensin-converting enzyme (ACE) gene polymorphism and alcoholism.
Biochemical Society transactions | 1998-05-01 | PMID 9649811
Garrib A, Peters T
Genes: ACE