首页
学术期刊
论文检测
AIGC检测
热点
更多
数据
Carbohydrate-deficient glycoprotein syndrome type I: Determination of the oligosaccharide structure of newly synthesized glycoproteins by analysis of calnexin binding
被引:3
|
作者
:
Marquardt, T
论文数:
0
引用数:
0
h-index:
0
Marquardt, T
Ullrich, K
论文数:
0
引用数:
0
h-index:
0
Ullrich, K
Niehues, R
论文数:
0
引用数:
0
h-index:
0
Niehues, R
Koch, HG
论文数:
0
引用数:
0
h-index:
0
Koch, HG
Harms, E
论文数:
0
引用数:
0
h-index:
0
Harms, E
机构
:
来源
:
JOURNAL OF INHERITED METABOLIC DISEASE
|
1996年
/ 19卷
/ 02期
关键词
:
D O I
:
10.1007/BF01799441
中图分类号
:
R5 [内科学];
学科分类号
:
1002 ;
100201 ;
摘要
:
引用
收藏
页码:246 / 250
页数:5
相关论文
共 50 条
[41]
The ABC of carbohydrate deficient glycoprotein syndrome type I
Matthijs, G
论文数:
0
引用数:
0
h-index:
0
机构:
Catholic Univ Louvain, Ctr Human Genet, B-3000 Louvain, Belgium
Catholic Univ Louvain, Ctr Human Genet, B-3000 Louvain, Belgium
Matthijs, G
GLYCOBIOLOGY,
1999,
9
(10)
: 1108
-
1108
[42]
Genotypes and phenotypes of patients in the UK with carbohydrate-deficient glycoprotein syndrome type 1
Imtiaz, F
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1N 1EH, England
Imtiaz, F
Worthington, V
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1N 1EH, England
Worthington, V
Champion, M
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1N 1EH, England
Champion, M
Beesley, C
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1N 1EH, England
Beesley, C
Charlwood, J
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1N 1EH, England
Charlwood, J
Clayton, P
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1N 1EH, England
Clayton, P
Keir, G
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1N 1EH, England
Keir, G
Mian, N
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1N 1EH, England
Mian, N
Winchester, B
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1N 1EH, England
Winchester, B
JOURNAL OF INHERITED METABOLIC DISEASE,
2000,
23
(02)
: 162
-
174
[43]
MANIFESTATION OF CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-1 IN EARLY INFANCY
SCHLUTER, B
论文数:
0
引用数:
0
h-index:
0
SCHLUTER, B
BURK, G
论文数:
0
引用数:
0
h-index:
0
BURK, G
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
JAEKEN, J
ANDLER, W
论文数:
0
引用数:
0
h-index:
0
ANDLER, W
MONATSSCHRIFT KINDERHEILKUNDE,
1995,
143
(01)
: 31
-
35
[44]
Early ocular manifestations in an infant with carbohydrate-deficient glycoprotein syndrome type Ia
Laplace, O
论文数:
0
引用数:
0
h-index:
0
机构:
Ctr Hosp Natl Ophtalmol Qunize Vingts, F-75012 Paris, France
Ctr Hosp Natl Ophtalmol Qunize Vingts, F-75012 Paris, France
Laplace, O
Voegtle, R
论文数:
0
引用数:
0
h-index:
0
机构:
Ctr Hosp Natl Ophtalmol Qunize Vingts, F-75012 Paris, France
Ctr Hosp Natl Ophtalmol Qunize Vingts, F-75012 Paris, France
Voegtle, R
Rigolet, MH
论文数:
0
引用数:
0
h-index:
0
机构:
Ctr Hosp Natl Ophtalmol Qunize Vingts, F-75012 Paris, France
Ctr Hosp Natl Ophtalmol Qunize Vingts, F-75012 Paris, France
Rigolet, MH
Bourcier, T
论文数:
0
引用数:
0
h-index:
0
机构:
Ctr Hosp Natl Ophtalmol Qunize Vingts, F-75012 Paris, France
Ctr Hosp Natl Ophtalmol Qunize Vingts, F-75012 Paris, France
Bourcier, T
Nordmann, JP
论文数:
0
引用数:
0
h-index:
0
机构:
Ctr Hosp Natl Ophtalmol Qunize Vingts, F-75012 Paris, France
Ctr Hosp Natl Ophtalmol Qunize Vingts, F-75012 Paris, France
Nordmann, JP
JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS,
2003,
40
(03)
: 179
-
181
[45]
Carbohydrate deficient glycoprotein (CDG) syndrome type I
Jaeken, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP GASTHUISBERG,DEPT PAEDIAT,B-3000 LOUVAIN,BELGIUM
Jaeken, J
Matthijs, G
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP GASTHUISBERG,DEPT PAEDIAT,B-3000 LOUVAIN,BELGIUM
Matthijs, G
Barone, R
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP GASTHUISBERG,DEPT PAEDIAT,B-3000 LOUVAIN,BELGIUM
Barone, R
Carchon, H
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP GASTHUISBERG,DEPT PAEDIAT,B-3000 LOUVAIN,BELGIUM
Carchon, H
JOURNAL OF MEDICAL GENETICS,
1997,
34
(01)
: 73
-
76
[46]
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME - NOT AN N-LINKED OLIGOSACCHARIDE PROCESSING DEFECT, BUT AN ABNORMALITY IN LIPID-LINKED OLIGOSACCHARIDE BIOSYNTHESIS
POWELL, LD
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CALIF SAN DIEGO,SCH MED,CTR CANC,GLYCOBIOL PROGRAM,LA JOLLA,CA 92093
POWELL, LD
PANEERSELVAM, K
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CALIF SAN DIEGO,SCH MED,CTR CANC,GLYCOBIOL PROGRAM,LA JOLLA,CA 92093
PANEERSELVAM, K
VIJ, R
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CALIF SAN DIEGO,SCH MED,CTR CANC,GLYCOBIOL PROGRAM,LA JOLLA,CA 92093
VIJ, R
DIAZ, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CALIF SAN DIEGO,SCH MED,CTR CANC,GLYCOBIOL PROGRAM,LA JOLLA,CA 92093
DIAZ, S
MANZI, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CALIF SAN DIEGO,SCH MED,CTR CANC,GLYCOBIOL PROGRAM,LA JOLLA,CA 92093
MANZI, A
BUIST, N
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CALIF SAN DIEGO,SCH MED,CTR CANC,GLYCOBIOL PROGRAM,LA JOLLA,CA 92093
BUIST, N
FREEZE, H
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CALIF SAN DIEGO,SCH MED,CTR CANC,GLYCOBIOL PROGRAM,LA JOLLA,CA 92093
FREEZE, H
VARKI, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CALIF SAN DIEGO,SCH MED,CTR CANC,GLYCOBIOL PROGRAM,LA JOLLA,CA 92093
VARKI, A
JOURNAL OF CLINICAL INVESTIGATION,
1994,
94
(05)
: 1901
-
1909
[47]
Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I
Mizugishi, K
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokyo, Sch Med, Dept Pediat, Tokyo 113, Japan
Mizugishi, K
Yamanaka, K
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokyo, Sch Med, Dept Pediat, Tokyo 113, Japan
Yamanaka, K
Kuwajima, K
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokyo, Sch Med, Dept Pediat, Tokyo 113, Japan
Kuwajima, K
Yuasa, I
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokyo, Sch Med, Dept Pediat, Tokyo 113, Japan
Yuasa, I
Shigemoto, K
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokyo, Sch Med, Dept Pediat, Tokyo 113, Japan
Shigemoto, K
Kondo, I
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokyo, Sch Med, Dept Pediat, Tokyo 113, Japan
Kondo, I
BRAIN & DEVELOPMENT,
1999,
21
(04)
: 223
-
228
[48]
Molecular basis of carbohydrate-deficient glycoprotein syndromes type I with normal phosphomannomutase activity
Freeze, HH
论文数:
0
引用数:
0
h-index:
0
机构:
Burnham Inst, La Jolla, CA 92037 USA
Freeze, HH
Aebi, M
论文数:
0
引用数:
0
h-index:
0
机构:
Burnham Inst, La Jolla, CA 92037 USA
Aebi, M
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE,
1999,
1455
(2-3):
: 167
-
178
[49]
Magnetic resonance imaging and proton MR spectroscopy of the brain in a patient with carbohydrate-deficient glycoprotein syndrome type I
Takeuchi, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokushima, Sch Med, Dept Radiol, Tokushima 770, Japan
Takeuchi, M
Harada, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokushima, Sch Med, Dept Radiol, Tokushima 770, Japan
Harada, M
Hisaoka, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokushima, Sch Med, Dept Radiol, Tokushima 770, Japan
Hisaoka, S
Nishitani, H
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokushima, Sch Med, Dept Radiol, Tokushima 770, Japan
Nishitani, H
Mori, K
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokushima, Sch Med, Dept Radiol, Tokushima 770, Japan
Mori, K
Sakama, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tokushima, Sch Med, Dept Radiol, Tokushima 770, Japan
Sakama, M
JOURNAL OF MAGNETIC RESONANCE IMAGING,
2003,
17
(06)
: 722
-
725
[50]
Analysis of a phosphomannomutase 2 gene in American patients with type 1 carbohydrate-deficient glycoprotein syndrome (CDGS).
Tayebi, N
论文数:
0
引用数:
0
h-index:
0
机构:
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
Tayebi, N
Reissner, K
论文数:
0
引用数:
0
h-index:
0
机构:
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
Reissner, K
Orvisky, E
论文数:
0
引用数:
0
h-index:
0
机构:
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
Orvisky, E
Ehlert, M
论文数:
0
引用数:
0
h-index:
0
机构:
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
Ehlert, M
Martin, BM
论文数:
0
引用数:
0
h-index:
0
机构:
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
Martin, BM
Sidransky, E
论文数:
0
引用数:
0
h-index:
0
机构:
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
Sidransky, E
Ginns, EI
论文数:
0
引用数:
0
h-index:
0
机构:
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
Ginns, EI
Krasnewich, D
论文数:
0
引用数:
0
h-index:
0
机构:
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
NIMH, Clin Neurosci Branch, IRP, NIH, Bethesda, MD 20892 USA
Krasnewich, D
AMERICAN JOURNAL OF HUMAN GENETICS,
1997,
61
(04)
: A348
-
A348
←
1
2
3
4
5
→