Articles in 1999

Cloning and characterization of the human UDP-N-acetylglucosamine: α-1,3-D-mannoside β-1,4-N-acetylglucosaminyltransferase IV-homologue (hGnT-IV-H) gene

T. Furukawa
E. M. Youssef
A. Horii
Short Communication01 Oct 1999
A polymorphic CA repeat marker at the human 27-kD calbindin (CALB1) locus

Ken-ichi Morishima
Shinya Matsuura
Kenshi Komatsu
Brief Report01 Oct 1999
The human caspase-activated DNase gene (hCAD): genomic structure, exonic single-nucleotide polymorphisms, and a highly polymorphic dinucleotide repeat at the hCAD locus

N. Sugimoto
Y. Fukuda
J. Inazawa
Short Communication01 Oct 1999
CA repeat polymorphism in the promoter region of the COL1A2 gene

Erin Dietzsch
M. Iqbal Parker
Brief Report01 Oct 1999
An Ile/Val polymorphism at codon 1464 of the ATP7A gene

A. Ogawa
S. Yamamoto
Y. Kohno
Brief Report01 Oct 1999
Novel variants in the promoter region of the CREB gene in schizophrenic patients

Y. Kawanishi
S. Harada
H. Shiraishi
Brief Report01 Oct 1999
Mapping of a gene responsible for dermatitis in NOA (Naruto Research Institute Otsuka Atrichia) mice, an animal model of allergic dermatitis

K. Natori
M. Tamari
Y. Nakamura
Original Article01 Oct 1999
A novel LDLR mutation, H190Y, in a Utah kindred with familial Hypercholesterolemia

P. N. Hopkins
L. L. Wu
R.R. Williams (posthumous)
Original Article01 Oct 1999
C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain

Kavita Bhalla
Helen J. Eyre
David F. Callen
Short Communication01 Oct 1999
Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex

H. Zhang
E. Nanba
K. Takeshita
Short Communication01 Oct 1999
Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) gene

T. Nakajima
T. Hamakubo
M. Emi
Short Communication01 Oct 1999
Novel polymorphisms in the upstream region of the human dopamine D4 receptor (DRD4) gene

Hiroshi Mitsuyasu
Hidetoshi Ozawa
Yasuyuki Fukumaki
Brief Report01 Oct 1999
Prader-Willi syndrome in a child with XYY

A. Honma
R. Ishii
K. Hayasaka
Brief Report01 Oct 1999
A common Ile796Val polymorphism of the human SREBP cleavage-activating protein (SCAP) gene

Kikumi Iwaki
Toshiaki Nakajima
Mitsuru Emi
Brief Report01 Oct 1999
Dinucleotide repeat polymorphism in the third intron of the NRAMP2/DMT1 gene

F. Kishi
S. Fujishima
M. Tabuchi
Brief Report01 Oct 1999
Mutation screening of phenylketonuria in the Far East of Russia

H. Sueoka
A. Moshinetsky
S. Chiba
Original Article01 Oct 1999
Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines

Y. Ariyama
T. Mori
J. Inazawa
Original Article01 Oct 1999
Molecular characterization of galactokinase deficiency in Japanese patients

M. Asada
Y. Okano
G. Isshiki
Original Article01 Oct 1999
Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity

B. J. Scrimshaw
J. M. Faed
K. Yun
Short Communication01 Oct 1999
Transitional change in interaction between HIF-1 and HNF-4 in response to hypoxia

W. Zhang
Terumasa Tsuchiya
Y. Yasukochi
Original Article01 Aug 1999

Cloning and characterization of the human UDP-N-acetylglucosamine: α-1,3-D-mannoside β-1,4-N-acetylglucosaminyltransferase IV-homologue (hGnT-IV-H) gene

A polymorphic CA repeat marker at the human 27-kD calbindin (CALB1) locus

The human caspase-activated DNase gene (hCAD): genomic structure, exonic single-nucleotide polymorphisms, and a highly polymorphic dinucleotide repeat at the hCAD locus

CA repeat polymorphism in the promoter region of the COL1A2 gene

An Ile/Val polymorphism at codon 1464 of the ATP7A gene

Novel variants in the promoter region of the CREB gene in schizophrenic patients

Mapping of a gene responsible for dermatitis in NOA (Naruto Research Institute Otsuka Atrichia) mice, an animal model of allergic dermatitis

A novel LDLR mutation, H190Y, in a Utah kindred with familial Hypercholesterolemia

C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain

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

Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) gene

Novel polymorphisms in the upstream region of the human dopamine D4 receptor (DRD4) gene

Prader-Willi syndrome in a child with XYY

A common Ile796Val polymorphism of the human SREBP cleavage-activating protein (SCAP) gene

Dinucleotide repeat polymorphism in the third intron of the NRAMP2/DMT1 gene

Mutation screening of phenylketonuria in the Far East of Russia

Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines

Molecular characterization of galactokinase deficiency in Japanese patients

Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity

Transitional change in interaction between HIF-1 and HNF-4 in response to hypoxia

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