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Results: 1-25 | 26-42
Results: 1-25/42
STUDIES OF ATYPICAL JNCL SUGGEST OVERLAPPING WITH OTHER NCL FORMS
Authors: WISNIEWSKI KE ZHONG N KACZMARSKI W KACZMARSKI A SKLOWERBROOKS S BROWN WT
Citation: Ke. Wisniewski et al., STUDIES OF ATYPICAL JNCL SUGGEST OVERLAPPING WITH OTHER NCL FORMS, Pediatric neurology, 18(1), 1998, pp. 36-40
COMPOUND HETEROZYGOUS GENOTYPE IS ASSOCIATED WITH PROTRACTED JUVENILENEURONAL CEROID-LIPOFUSCINOSIS
Authors: WISNIEWSKI KE ZHONG N KACZMARSKI W KACZMARSKI A KIDA E BROWN WT SCHWARZ KO LAZZARINI AM RUBIN AJ STENROOS ES JOHNSON WG WISNIEWSKI TM
Citation: Ke. Wisniewski et al., COMPOUND HETEROZYGOUS GENOTYPE IS ASSOCIATED WITH PROTRACTED JUVENILENEURONAL CEROID-LIPOFUSCINOSIS, Annals of neurology, 43(1), 1998, pp. 106-110
MOLECULAR SCREENING OF BATTEN-DISEASE - IDENTIFICATION OF A MISSENSE MUTATION (E295K) IN THE CLN3 GENE
Authors: ZHONG N WISNIEWSKI KE KACZMARSKI AL JU W XU WM XU WW MCLENDON L LIU B KACZMARSKI W BROOKS SS BROWN WT
Citation: N. Zhong et al., MOLECULAR SCREENING OF BATTEN-DISEASE - IDENTIFICATION OF A MISSENSE MUTATION (E295K) IN THE CLN3 GENE, Human genetics, 102(1), 1998, pp. 57-62
RECURSIVELY-ENUMERABLE SUBSETS OF R-Q IN 2 COMPUTING MODELS BLUM-SHUB-SMALE MACHINE AND TURING MACHINE
Authors: ZHONG N
Citation: N. Zhong, RECURSIVELY-ENUMERABLE SUBSETS OF R-Q IN 2 COMPUTING MODELS BLUM-SHUB-SMALE MACHINE AND TURING MACHINE, Theoretical computer science, 197(1-2), 1998, pp. 79-94
AN IMPROVED SYNTHESIS OF 6-O-MONOTOSYL-6-DEOXY-BETA-CYCLODEXTRIN
Authors: ZHONG N BYUN HS BITTMAN R
Citation: N. Zhong et al., AN IMPROVED SYNTHESIS OF 6-O-MONOTOSYL-6-DEOXY-BETA-CYCLODEXTRIN, Tetrahedron letters, 39(19), 1998, pp. 2919-2920
2 COMMON MUTATIONS IN THE CLN2 GENE UNDERLIE LATE INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS
Authors: ZHONG N WISNIEWSKI KE HARTIKAINEN J JU W MOROZIEWICZ DN MCLENDON L BROOKS SS BROWN WT
Citation: N. Zhong et al., 2 COMMON MUTATIONS IN THE CLN2 GENE UNDERLIE LATE INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS, Clinical genetics, 54(3), 1998, pp. 234-238
MOLECULAR ANALYSIS OF CLN3 TO CLARIFY AN ATYPICAL, PROTRACTED JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS
Authors: WISNIEWSKI KE ZHONG N KIDA E KACZMARSKI W KACZMARSKI A BROWN WT SCHWARTZ KO STENROOS S LAZZARINI A RUBIN AJ JOHNSON WG
Citation: Ke. Wisniewski et al., MOLECULAR ANALYSIS OF CLN3 TO CLARIFY AN ATYPICAL, PROTRACTED JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS, Annals of neurology, 42(3), 1997, pp. 49-49
EXPRESSION STUDIES OF CLN3 PROTEIN
Authors: KACZMARSKI W KIDA E LACH A RUBENSTEIN R ZHONG N WISNIEWSKI KE
Citation: W. Kaczmarski et al., EXPRESSION STUDIES OF CLN3 PROTEIN, Neuropediatrics, 28(1), 1997, pp. 33-36
POLYMORPHISM OF FXR1 SHOWING LACK OF ASSOCIATION WITH AUTISM
Authors: LIMPRASERT P ZHONG N DOBKIN C BROWN WT
Citation: P. Limprasert et al., POLYMORPHISM OF FXR1 SHOWING LACK OF ASSOCIATION WITH AUTISM, American journal of medical genetics, 74(4), 1997, pp. 453-454
MOLECULAR PATHOGENETIC STUDIES OF THE FRAGILE-X-SYNDROME - DOUBLE KNOCKOUTS OF FMR1 AND FXR1 AFFECT EARLY DEVELOPMENT OF XENOPUS OOCYTES
Authors: JU W XU WM HWANG YW BROWN WT ZHONG N
Citation: W. Ju et al., MOLECULAR PATHOGENETIC STUDIES OF THE FRAGILE-X-SYNDROME - DOUBLE KNOCKOUTS OF FMR1 AND FXR1 AFFECT EARLY DEVELOPMENT OF XENOPUS OOCYTES, American journal of human genetics, 61(4), 1997, pp. 171-171
MOLECULAR PATHOGENETIC STUDIES OF THE FRAGILE-X-SYNDROME - A CANDIDATE TRANSCRIPT TARGETED BY THE FRAGILE-X PROTEIN FMRP
Authors: ZHONG N JU W XU WM LIU B DOBKIN C BROWN WT
Citation: N. Zhong et al., MOLECULAR PATHOGENETIC STUDIES OF THE FRAGILE-X-SYNDROME - A CANDIDATE TRANSCRIPT TARGETED BY THE FRAGILE-X PROTEIN FMRP, American journal of human genetics, 61(4), 1997, pp. 1898-1898
DISTRIBUTION OF APOLIPOPROTEIN-E GENOTYPES IN THE FRAGILE-X-SYNDROME,BATTEN-DISEASE, AND DOWN-SYNDROME POPULATIONS
Authors: YE LL JU W XU WM SCHUPF N JENKINS EC BROWN WT ZHONG N
Citation: Ll. Ye et al., DISTRIBUTION OF APOLIPOPROTEIN-E GENOTYPES IN THE FRAGILE-X-SYNDROME,BATTEN-DISEASE, AND DOWN-SYNDROME POPULATIONS, American journal of human genetics, 61(4), 1997, pp. 2275-2275
SYSTEM FOR MANAGING AND REFINING STRUCTURAL CHARACTERISTICS DISCOVERED FROM DATABASES
Authors: ZHONG N OHSUGA S
Citation: N. Zhong et S. Ohsuga, SYSTEM FOR MANAGING AND REFINING STRUCTURAL CHARACTERISTICS DISCOVERED FROM DATABASES, Knowledge-based systems, 9(4), 1996, pp. 267-279
MOLECULAR ANALYSIS OF GENE MUTATION IN BATTEN-DISEASE
Authors: ZHONG N WISNIEWSKY KE LACH A SKLOWERBROOKS S BROWN WT
Citation: N. Zhong et al., MOLECULAR ANALYSIS OF GENE MUTATION IN BATTEN-DISEASE, Annals of neurology, 40(2), 1996, pp. 49-49
CLINICOPATHOLOGICAL AND MOLECULAR CHARACTERISTICS OF ATYPICAL CLN3 CASES
Authors: WISNIEWSKI KE KIDA E ZHONG N KACZMARSKI W LACH A CONNELL F BROOKS SS BROWN WT
Citation: Ke. Wisniewski et al., CLINICOPATHOLOGICAL AND MOLECULAR CHARACTERISTICS OF ATYPICAL CLN3 CASES, Annals of neurology, 40(2), 1996, pp. 170-170
A HIERARCHICAL MODEL LEARNING APPROACH FOR REFINING AND MANAGING CONCEPT CLUSTERS DISCOVERED FROM DATABASES
Authors: ZHONG N OHSUGA S
Citation: N. Zhong et S. Ohsuga, A HIERARCHICAL MODEL LEARNING APPROACH FOR REFINING AND MANAGING CONCEPT CLUSTERS DISCOVERED FROM DATABASES, Data & knowledge engineering, 20(2), 1996, pp. 227-252
FRAGILE-X GRAY ZONE ALLELES - AGG PATTERNS, EXPANSION RISKS, AND ASSOCIATED HAPLOTYPES
Authors: ZHONG N JU WN PIETROFESA J WANG DW DOBKIN C BROWN WT
Citation: N. Zhong et al., FRAGILE-X GRAY ZONE ALLELES - AGG PATTERNS, EXPANSION RISKS, AND ASSOCIATED HAPLOTYPES, American journal of medical genetics, 64(2), 1996, pp. 261-265
REVERSE MUTATIONS IN THE FRAGILE-X SYNDROME
Authors: BROWN WT HOUCK GE DING XH ZHONG N NOLIN S GLICKSMAN A DOBKIN C JENKINS EC
Citation: Wt. Brown et al., REVERSE MUTATIONS IN THE FRAGILE-X SYNDROME, American journal of medical genetics, 64(2), 1996, pp. 287-292
TISSUE DIFFERENCES IN FRAGILE-X MOSAICS - MOSAICISM IN BLOOD-CELLS MAY DIFFER GREATLY FROM SKIN
Authors: DOBKIN CS NOLIN SL COHEN I SUDHALTER V BIALER MG DING XH JENKINS EC ZHONG N BROWN WT
Citation: Cs. Dobkin et al., TISSUE DIFFERENCES IN FRAGILE-X MOSAICS - MOSAICISM IN BLOOD-CELLS MAY DIFFER GREATLY FROM SKIN, American journal of medical genetics, 64(2), 1996, pp. 296-301
A SURVEY OF FRAXE ALLELE SIZES IN 3 POPULATIONS
Authors: ZHONG N JU WN CURLEY D WANG DW PIETROFESA J WU GY SHEN Y PANG C POON P LIU XX GOU S KAJANOJA E RYYNANEN M DOBKIN C BROWN WT
Citation: N. Zhong et al., A SURVEY OF FRAXE ALLELE SIZES IN 3 POPULATIONS, American journal of medical genetics, 64(2), 1996, pp. 415-419
INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF FMR1 PROTEIN IN A MALE-PATIENT WITH A LUNG-TUMOR
Authors: OOSTRA B DEGRAAF E ZHONG N WILLEMSEN R
Citation: B. Oostra et al., INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF FMR1 PROTEIN IN A MALE-PATIENT WITH A LUNG-TUMOR, American journal of medical genetics, 64(1), 1996, pp. 18-18
FRAGILE-X FOUNDER EFFECTS AND NEW MUTATIONS IN FINLAND
Authors: ZHONG N KAJANOJA E SMITS B PIETROFESA J CURLEY D WANG DW JU MN NOLIN S DOBKIN C RYYNANEN M BROWN WT
Citation: N. Zhong et al., FRAGILE-X FOUNDER EFFECTS AND NEW MUTATIONS IN FINLAND, American journal of medical genetics, 64(1), 1996, pp. 226-233
FAMILIAL TRANSMISSION OF THE FMR1 CGG REPEAT
Authors: NOLIN SL LEWIS FA YE LL HOUCK GE GLICKSMAN AE LIMPRASERT P LI SY ZHONG N ASHLEY AE FEINGOLD E SHERMAN SL BROWN WT
Citation: Sl. Nolin et al., FAMILIAL TRANSMISSION OF THE FMR1 CGG REPEAT, American journal of human genetics, 59(6), 1996, pp. 1252-1261
THE MOLECULAR-BASIS OF FRAGILE SITES
Authors: DOBKIN C ZHONG N BROWN WT
Citation: C. Dobkin et al., THE MOLECULAR-BASIS OF FRAGILE SITES, American journal of human genetics, 59(2), 1996, pp. 478-478
POSITIVE FRAGILE-X MICROSATELLITE ASSOCIATIONS POINT TO A COMMON MECHANISM OF DYNAMIC MUTATION EVOLUTION
Authors: BROWN WT ZHONG N DOBKIN C
Citation: Wt. Brown et al., POSITIVE FRAGILE-X MICROSATELLITE ASSOCIATIONS POINT TO A COMMON MECHANISM OF DYNAMIC MUTATION EVOLUTION, American journal of human genetics, 58(3), 1996, pp. 641-643
Risultati: 1-25 | 26-42