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Characterization of genomic rearrangements of the alpha1-acid glycoprotein/orosomucoid gene in Ghanaians.

• Authors : Yuasa I; Department of Legal Medicine, Faculty of Medicine, Tottori University, Yonago, Japan. ; Nakamura H

Subjects: Orosomucoid/Orosomucoid/Orosomucoid/*genetics; Alleles ; Exons

• Source: Journal of human genetics [J Hum Genet] 2001; Vol. 46 (10), pp. 572-8.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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Genetic polymorphism of orosomucoid (ORM) in populations of the United Kingdom, Indian subcontinent, and Cambodia

• Authors : Mastana, S S; Jayasekara, R; Fisher, P

• Source: Journal of Human Genetics; September 1993, Vol. 38 Issue: 3 p289-296, 8p

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Genetic polymorphisms of orosomucoid and alpha-2-HS-glycoprotein in Thai, Sri Lankan and Paraguayan populations

• Authors : Umetsu, Kazuo; Yuasa, Isao; Yamashita, Takao

• Source: Journal of Human Genetics; September 1989, Vol. 34 Issue: 3 p195-202, 8p

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Genetic polymorphisms of orosomucoid ORM1 and ORM2 in libyans: Occurrence of ORM1*2.1 and three new ORM2 alleles

• Authors : Sebetan, Ismail M; Sagisaka, Kaoru

• Source: Journal of Human Genetics; December 1988, Vol. 33 Issue: 4 p439-443, 5p

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Characterization of genomic rearrangements of the α[sub 1] -acid glycoprotein/orosomucoid gene in Ghanaians.

• Authors : Yuasa, I.; Nakamura, H.; Henke, L.

Subjects: GLYCOPROTEINS; GENETICS; ISOELECTRIC focusing

• Source: Journal of Human Genetics; 2001, Vol. 46 Issue 10, p572, 7p

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Isoelectric focusing studies in Brazilian Indians —uncovering variation of ORM, AHSG and IF—

• Authors : Salzano, Francisco M; Umetsu, Kazuo; Yuasa, Isao

• Source: Journal of Human Genetics; December 1990, Vol. 35 Issue: 4 p283-290, 8p

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A new association between polymorphisms of the SLC6A7 gene in the chromosome 5q31–32 region and asthma.

• Authors : Jeong-Hyun Kim; Hyun Sub Cheong; Byung-Lae Park

Subjects: GENETIC polymorphisms; BRONCHODILATOR agents; ASTHMA

• Source: Journal of Human Genetics. Jun2010, Vol. 55 Issue 6, p358-365. 8p. 2 Diagrams, 4 Charts.

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Fibrillin gene (FBN1) mutations in Japanese patients with Marfan syndrome.

• Authors : Chikumi, H.; Yamamoto, T.; Ohta, Y.

Subjects: MARFAN syndrome; CONNECTIVE tissue diseases; GENETIC mutation

• Source: Journal of Human Genetics; 2000, Vol. 45 Issue 2, p115, 4p

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Language isolates and their genetic identity: a commentary on mitochondrial DNA history of Sri Lankan ethnic people: their relations within the island and with the Indian subcontinental populations.

• Authors : Chaubey, Gyaneshwer

Subjects: MITOCHONDRIAL DNA; ETHNICITY; SRI LankansSRI Lanka

• Source: Journal of Human Genetics. Feb2014, Vol. 59 Issue 2, p61-63. 3p.

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Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex.

• Authors : Zhang, H.; Nanba, E.; Yamamoto, T.

Subjects: GENETIC mutation; TUBEROUS sclerosis; GENETIC polymorphisms

• Source: Journal of Human Genetics; 1999, Vol. 44 Issue 6, p391, 6p

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