نتائج البحث

The human serotonin transporter gene linked polymorphism (5-HTTLPR) shows ten novel allelic variants.

• Authors : Nakamura M; The Department of Neuropsychiatry, Ehime University School of Medicine, Shitsukawa, Shigenobu, Onsen-gun, Ehime 791-0295, Japan.; Ueno S

Subjects: Membrane Transport Proteins* ; Nerve Tissue Proteins* ; Polymorphism, Restriction Fragment Length*

• Source: Molecular psychiatry [Mol Psychiatry] 2000 Jan; Vol. 5 (1), pp. 32-8.Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Print

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Identification of a novel polymorphism of the human dopamine transporter (DAT1) gene and the significant association with alcoholism.

• Authors : Ueno S; Department of Neuropsychiatry, Ehime University School of Medicine, Shigenobu, Onsen-gun, Ehime 791-0295, Japan. ; Nakamura M

Subjects: Genetic Linkage* ; Membrane Glycoproteins* ; Membrane Transport Proteins*

• Source: Molecular psychiatry [Mol Psychiatry] 1999 Nov; Vol. 4 (6), pp. 552-7.Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Print

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Anxiety traits associated with a polymorphism in the serotonin transporter gene regulatory region in the Japanese.

• Authors : Murakami F; Department of Clinical Laboratory Medicine, Tottori University, Faculty of Medicine, Yonago, Japan.; Shimomura T

Subjects: Membrane Transport Proteins* ; Nerve Tissue Proteins* ; Polymorphism, Genetic*

• Source: Journal of human genetics [J Hum Genet] 1999; Vol. 44 (1), pp. 15-7.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print Cited Medium: Print ISSN: 1434-5161 (Print)

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Serotonin transporter gene polymorphisms: ethnic difference and possible association with bipolar affective disorder.

• Authors : Kunugi H; Department of Psychiatry, Teikyo University School of Medicine, Tokyo, Japan.; Hattori M

Subjects: Membrane Transport Proteins* ; Nerve Tissue Proteins* ; Polymorphism, Genetic*

• Source: Molecular psychiatry [Mol Psychiatry] 1997 Oct-Nov; Vol. 2 (6), pp. 457-62.Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Print

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Correlations between class I glucose transporter expression patterns and clinical outcomes in non‐small cell lung cancer.

• Authors : Nakanishi, Yoko; Iwai, Momoko; Hirotani, Yukari

Subjects: LUNG cancer; INTERLEUKINS; RESEARCHJAPAN

• Source: Thoracic Cancer; Sep2023, Vol. 14 Issue 27, p2761-2769, 9p

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In vitro assessment of the inhibitory effect of goreisan extract and its ingredients on the P-glycoprotein drug transporter and cytochrome P-450 metabolic enzymes.

• Authors : Takiyama, Mikina¹ (AUTHOR); Matsumoto, Takashi¹ (AUTHOR); Kaifuchi, Noriko¹ (AUTHOR)

• Source: Xenobiotica. May2022, Vol. 52 Issue 5, p511-519. 9p.

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Low expression of AcrB in the deoxycholate-sensitive strains of Salmonella enterica subspecies enterica serovar Pullorum.

• Authors : Usui M; National Veterinary Assay Laboratory, Ministry of Agriculture, Forestry and Fisheries, Tokyo, Japan.; Asai T

Subjects: Down-Regulation*; Bacterial Proteins/Bacterial Proteins/Bacterial Proteins/*metabolism ; Deoxycholic Acid/Deoxycholic Acid/Deoxycholic Acid/*pharmacology

• Source: Microbiology and immunology [Microbiol Immunol] 2011 May; Vol. 55 (5), pp. 366-8.Publisher: Wiley-Blackwell Country of Publication: Australia NLM ID: 7703966 Publication Model: Print Cited Medium: Internet ISSN: 1348-0421

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Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis: a common mutation, R179X.

• Authors : Miyamoto T; Department of Inherited Metabolic Disease, National Institute of Neuroscience, Kodaira, Tokyo, Japan.; Kanazawa N

Subjects: Membrane Transport Proteins* ; Point Mutation*; Amino Acid Metabolism, Inborn Errors/Amino Acid Metabolism, Inborn Errors/Amino Acid Metabolism, Inborn Errors/*genetics

• Source: Journal of human genetics [J Hum Genet] 2001; Vol. 46 (5), pp. 260-2.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print Cited Medium: Print ISSN: 1434-5161 (Print)

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Current landscape of Oculocutaneous Albinism in Japan.

• Authors : Okamura K; Department of Dermatology, Faculty of Medicine, Yamagata University, Yamagata, Japan.; Suzuki T

Subjects: Mutation*; Albinism, Oculocutaneous/Albinism, Oculocutaneous/Albinism, Oculocutaneous/*epidemiology ; Albinism, Oculocutaneous/Albinism, Oculocutaneous/Albinism, Oculocutaneous/*pathology

• Source: Pigment cell & melanoma research [Pigment Cell Melanoma Res] 2021 Mar; Vol. 34 (2), pp. 190-203. Date of Electronic Publication: 2020 Oct 07.Publisher: Blackwell Munksgaard Country of Publication: England NLM ID: 101318927 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Telethonin variants found in Brugada syndrome, J‐wave pattern ECG, and ARVC reduce peak Nav1.5 currents in HEK‐293 cells.

• Authors : Turker, Isik; Makiyama, Takeru; Ueyama, Takeshi

Subjects: MUSCLE protein metabolism; ARRHYTHMIA; CARDIAC arrestJAPAN

• Source: Pacing & Clinical Electrophysiology; Aug2020, Vol. 43 Issue 8, p838-846, 9p

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