PubRank

K H Grzeschik

Author PubWeight™ 188.17‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor. Nature 1987 17.08
2 Report of the Committee on the Genetic Constitution of Chromosomes 10, 11, and 12. Cytogenet Cell Genet 1985 5.01
3 The skeletal muscle chloride channel in dominant and recessive human myotonia. Science 1992 4.28
4 GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families. Nature 1991 3.25
5 Differential expression of myogenic determination genes in muscle cells: possible autoactivation by the Myf gene products. EMBO J 1989 2.88
6 Report of the committee on the genetic constitution of chromosome 20. Cytogenet Cell Genet 1990 2.67
7 Cytovillin, a microvillar Mr 75,000 protein. cDNA sequence, prokaryotic expression, and chromosomal localization. J Biol Chem 1989 2.61
8 Chromosome localization in normal human cells and neuroblastomas of a gene related to c-myc. Nature 1984 2.32
9 Regional mapping of six cloned DNA sequences on human chromosome 7. Am J Hum Genet 1986 2.26
10 Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus). Proc Natl Acad Sci U S A 1984 2.23
11 Hepatitis B virus DNA integration in a sequence homologous to v-erb-A and steroid receptor genes in a hepatocellular carcinoma. Nature 1986 2.21
12 Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in man. Proc Natl Acad Sci U S A 1980 2.00
13 Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts. Hum Genet 1992 1.94
14 A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes. Am J Hum Genet 1990 1.94
15 Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome. Hum Genet 1986 1.92
16 Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker. Genomics 1989 1.59
17 A human autosomal phosphoglycerate kinase locus maps near the HLA cluster. Proc Natl Acad Sci U S A 1984 1.55
18 Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19. Hum Genet 1985 1.53
19 Nucleotide sequence of the gene for human transition protein 1 and its chromosomal localization on chromosome 2. Genomics 1990 1.49
20 Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome. Am J Med Genet 2000 1.48
21 The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations. Am J Hum Genet 1999 1.44
22 Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers). Proc Natl Acad Sci U S A 1972 1.42
23 Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome. Hum Mol Genet 1999 1.40
24 Mutation in GLI3 in postaxial polydactyly type A. Nat Genet 1997 1.38
25 Expression pattern in brain of TASK-1, TASK-3, and a tandem pore domain K(+) channel subunit, TASK-5, associated with the central auditory nervous system. Mol Cell Neurosci 2001 1.37
26 Molecular characterization of human zyxin. J Biol Chem 1996 1.36
27 Dispersed human immunoglobulin kappa light-chain genes. Nature 1986 1.35
28 Point mutations in human GLI3 cause Greig syndrome. Hum Mol Genet 1997 1.29
29 Alkali myosin light chains in man are encoded by a multigene family that includes the adult skeletal muscle, the embryonic or atrial, and nonsarcomeric isoforms. Gene 1988 1.29
30 Different patterns of X chromosome inactivity in lymphocytes and fibroblasts of a human balanced X;autosome translocation. Hum Genet 1982 1.25
31 Assignment of the gene for human glucose dehydrogenase (E.C. 1.1.1.47) to chromosome 1 using somatic cell hybrids. Cytogenet Cell Genet 1978 1.22
32 THIK-1 and THIK-2, a novel subfamily of tandem pore domain K+ channels. J Biol Chem 2000 1.20
33 Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome. Cytogenet Cell Genet 2001 1.19
34 Regional localization of 725 human chromosome 7-specific yeast artificial chromosome clones. Genomics 1994 1.18
35 Cloning of cDNA encoding steroid 11 beta-hydroxylase (P450c11). Proc Natl Acad Sci U S A 1987 1.17
36 The human lysozyme gene. Sequence organization and chromosomal localization. Eur J Biochem 1989 1.13
37 X-linkage of human phosphoglycerate kinase confirmed in man-mouse and man-Chinese hamster somatic cell hybrids. Am J Hum Genet 1971 1.13
38 Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndrome. Hum Mol Genet 1997 1.12
39 The human lactase-phlorizin hydrolase gene is located on chromosome 2. FEBS Lett 1988 1.10
40 Assignment of a structural gene for beta-glucuronidase to human chromosome C7. Somatic Cell Genet 1976 1.10
41 Identification of human RNA transcripts among heterogeneous nuclear RNA from man-mouse somatic cell hybrids. Proc Natl Acad Sci U S A 1975 1.09
42 Further evidence for the dispersion of the human fibrillar collagen genes. Am J Hum Genet 1986 1.09
43 Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt). Mamm Genome 1992 1.08
44 Cloning of a cDNA encoding the human cation-dependent mannose 6-phosphate-specific receptor. Proc Natl Acad Sci U S A 1987 1.07
45 Two nonallelic tRNAiMet genes are located in the p23 leads to q12 region of human chromosome 6. Proc Natl Acad Sci U S A 1983 1.07
46 Partial reactivation of a human inactive X chromosome in human-mouse somatic cell hybrids. Cytogenet Cell Genet 1978 1.06
47 Report of the Committee on the Genetic Constitution of Chromosomes 10, 11, and 12. Cytogenet Cell Genet 1984 1.06
48 Identification of optimized target sequences for the GLI3 zinc finger protein. DNA Cell Biol 1995 1.05
49 Late replicating bands of human chromosomes demonstrated by fluorochrome and Giemsa staining. Humangenetik 1975 1.03
50 PCR mediated detection of a new human receptor-tyrosine-kinase, HEK 2. Oncogene 1993 1.02
51 Assignment of two human cell cycle genes, CDC25C and CCNB1, to 5q31 and 5q12, respectively. Genomics 1992 1.01
52 Localization of the human beta-catenin gene (CTNNB1) to 3p21: a region implicated in tumor development. Genomics 1994 1.01
53 Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome 7. Am J Hum Genet 1987 1.00
54 Chromosome assignment of genes encoding the alpha and beta subunits of glycoprotein hormones in man and mouse. Somatic Cell Genet 1983 0.99
55 Localization of MPI, PKM2, IDHM, and the alpha subunit of hexosaminidase (HEXA) to the q21 leads to qter region of human chromosome 15. Cytogenet Cell Genet 1978 0.99
56 Isolation and characterization of human random cDNA clones homologous to DNA from the X chromosome. Somat Cell Mol Genet 1984 0.99
57 Human ornithine decarboxylase sequences map to chromosome regions 2pter----p23 and 7cen----qter but are not coamplified with the NMYC oncogene. Cytogenet Cell Genet 1986 0.98
58 A human single-copy DNA probe (DR 47) detects a Taq I RFLP on chromosome 9 (D9S5). Nucleic Acids Res 1987 0.97
59 Isolation and subregional mapping of a human cDNA clone detecting a common RFLP on chromosome 12. Hum Genet 1984 0.97
60 Rearrangement of a common cellular DNA domain on chromosome 4 in human primary liver tumors. J Virol 1988 0.97
61 X-linkage of human -galactosidase. Nat New Biol 1972 0.97
62 The gene for SP-40,40, human homolog of rat sulfated glycoprotein 2, rat clusterin, and rat testosterone-repressed prostate message 2, maps to chromosome 8. Genomics 1991 0.97
63 The human transmembrane secretory component (poly-Ig receptor): molecular cloning, restriction fragment length polymorphism and chromosomal sublocalization. Hum Genet 1991 0.96
64 All known human H1 histone genes except the H1(0) gene are clustered on chromosome 6. Genomics 1993 0.95
65 Electrophoretic characterization and genetics of human biliverdin reductase (BLVR; EC 1.3.1.24); assignment of BLVR to the p14 leads to cen region of human chromosome 7 in mouse-human somatic cell hybrids. Biochem Genet 1983 0.94
66 Primary gene structure and expression studies of rodent paracellin-1. J Am Soc Nephrol 2001 0.94
67 Isolation and characterization of a hypervariable region [D4S163] on chromosome 4. Nucleic Acids Res 1990 0.94
68 The gene encoding the human preproacrosin (ACR) maps to the q13-qter region on chromosome 22. Hum Genet 1989 0.91
69 Assignment of adenosine deaminase complexing protein (ADCP) gene(s) to human chromosome 2 in rodent-human somatic cell hybrids. Hum Genet 1981 0.91
70 Report of the second international workshop on human chromosome 7 mapping 1994. Cytogenet Cell Genet 1995 0.90
71 The pro alpha 2(V) collagen gene (COL5A2) maps to 2q14----2q32, syntenic to the pro alpha 1 (III) collagen locus (COL3A1). Hum Genet 1986 0.90
72 Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes. Eur J Cell Biol 1990 0.89
73 Cystic fibrosis: typing 48 German families with linked DNA probes. Hum Genet 1987 0.89
74 Identification of a de novo chromosome rearrangement in a man-mouse hybrid clone and its bearing on the cytological map of the human X chromosome. Cytogenet Cell Genet 1976 0.88
75 Localization, analysis and evolution of transposed human immunoglobulin V kappa genes. Gene 1988 0.87
76 Serotonin transporter gene-linked polymorphic region: allele distributions in relationship to body weight and in anorexia nervosa. Life Sci 1997 0.87
77 A simple method for characterising syndactyly in clinical practice. Genet Couns 2005 0.86
78 Anhidrotic ectodermal dysplasia gene region cloned in yeast artificial chromosomes. Genomics 1993 0.86
79 Assignment of human genes: beta-glucuronidase to chromosome 7, adenylate kinase-1 to 9, a second enzyme with enolase activity to 12, and mitochondrial IDH to 15. Birth Defects Orig Artic Ser 1976 0.86
80 The human hepatocyte nuclear factor 3/fork head gene FKHL13: genomic structure and pattern of expression. Genomics 1997 0.86
81 Genomics and transcription analysis of human TFIID. Oncogene 1998 0.86
82 Actin-like sequences are present on human X and Y chromosomes. EMBO J 1984 0.86
83 Assignment of the gene coding for human catalase to the short arm of chromosome 11. Ann Genet 1980 0.86
84 A method for discriminating murine and human chromosomes in somatic cell hybrids. Exp Cell Res 1974 0.86
85 The cellular homologue of the transforming gene of SKV avian retrovirus maps to human chromosome region 1q22----q24. Cytogenet Cell Genet 1986 0.85
86 Complementation after fusion of Sandhoff- and Tay-Sachs fibroblasts. Humangenetik 1975 0.85
87 Assignment of a structural gene for a fourth human diaphorase (DIA4) to chromosome 16 in man-mouse somatic cell hybrids. Hum Genet 1980 0.85
88 Localization of the catalytic subunit C gamma of the cAMP-dependent protein kinase gene (PRKACG) to human chromosome region 9q13. Cytogenet Cell Genet 1992 0.85
89 The human PGM-2 and its chromosomal localization in man-mouse hybrids. Hum Genet 1977 0.85
90 Human CC10, the homologue of rabbit uteroglobin: genomic cloning, chromosomal localization and expression in endometrial cell lines. Hum Mol Genet 1992 0.84
91 Regional assignment of human protooncogene c-myb to 6q21----qter. Somat Cell Mol Genet 1984 0.84
92 Cloning, structure and assignment to chromosome 19q13 of the human Kir2.4 inwardly rectifying potassium channel gene (KCNJ14). Mamm Genome 2000 0.83
93 Clinical impact of chromosome 1 aberrations in neuroblastoma: a metaphase and interphase cytogenetic study. Genes Chromosomes Cancer 1992 0.83
94 Giemsa staining of the sites replicating DNA early in human lymphocyte chromosomes. Cytogenet Cell Genet 1975 0.83
95 Expression of aromatic polycyclic hydrocarbon-induced monooxygenase (aryl hydrocarbon hydroxylase) in man x mouse hybrids is associated with human chromosome 2. Hum Genet 1981 0.83
96 Human Sp4 transcription factor gene (SP4) maps to chromosome 7p15. Genomics 1995 0.83
97 Beta 3-adrenergic-receptor allele distributions in children, adolescents and young adults with obesity, underweight or anorexia nervosa. Int J Obes Relat Metab Disord 1997 0.83
98 Regional submapping of human chromosome 6 by the use of human-mouse somatic cell hybrids. Cytogenet Cell Genet 1978 0.83
99 Human Sp3 transcriptional regulator gene (SP3) maps to chromosome 2q31. Genomics 1996 0.83
100 Further support for linkage of extreme obesity to the obese gene in a study group of obese children and adolescents. Exp Clin Endocrinol Diabetes 1997 0.82
101 The breakpoint on 7p in a patient with t(6;7) and craniosynostosis is spanned by a YAC clone containing the D7S503 locus. Hum Genet 1995 0.82
102 Organization and chromosomal localization of the gene for the human bombesin receptor subtype expressed in pregnant uterus. FEBS Lett 1994 0.82
103 Novel interaction partners of Bardet-Biedl syndrome proteins. Cell Motil Cytoskeleton 2008 0.82
104 Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome. Pediatr Nephrol 1996 0.82
105 Identification and characterization of a hypervariable region [D18S27] on chromosome 18. Nucleic Acids Res 1989 0.81
106 Partial gene structure and assignment to chromosome 2q37 of the human inwardly rectifying K+ channel (Kir7.1) gene (KCNJ13). Genomics 1998 0.81
107 The molecular genetic approach to "Bartter's syndrome". J Mol Med (Berl) 1998 0.81
108 Regional localization of loci on chromosome 14 using somatic cell hybrids. Cytogenet Cell Genet 1994 0.81
109 A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p. Genomics 1991 0.81
110 High-resolution genomic mapping of the three human replication protein A genes (RPA1, RPA2, and RPA3). Genomics 1994 0.80
111 Transmission disequilibrium and sequence variants at the leptin receptor gene in extremely obese German children and adolescents. Hum Genet 1998 0.80
112 Prothymosin alpha gene in humans: organization of its promoter region and localization to chromosome 2. Hum Genet 1993 0.80
113 Regional localization of two human cellular Kirsten ras genes on chromosomes 6 and 12. Mol Cell Biol 1984 0.80
114 The neurobeachin gene (Nbea) identifies a new region of homology between mouse central chromosome 3 and human chromosome 13q13. Mamm Genome 1999 0.80
115 Assignment of a gene for arylsulfatase B to human chromosome 5 using human-mouse somatic cell hybrids. Cytogenet Cell Genet 1978 0.80
116 The isolation of genomic recombinants for the human apolipoprotein B gene and the mapping of three common DNA polymorphisms of the gene--a useful marker for human chromosome 2. Hum Genet 1986 0.80
117 A member of the mouse LRR transcript family with homology to the human Sp100 gene. Hereditas 1995 0.80
118 Behold the CHILD, it's only one: CHILD syndrome is not caused by deficiency of 3 beta-hydroxysteroid-Delta 8, Delta 7-isomerase. Am J Med Genet 2000 0.79
119 The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22. Ann Hum Genet 1987 0.79
120 The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP. Hum Genet 1987 0.79
121 The structural gene for transferrin (TF) maps to 3q21----3qter. Ann Genet 1984 0.79
122 Platelet-derived growth factor A chain: confirmation of localization of PDGFA to chromosome 7p22 and description of an unusual minisatellite. Genomics 1992 0.79
123 Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents. Acta Diabetol 2000 0.78
124 Isolation and characterization of a cosmid contig for the GCPS gene region. Hum Genet 1995 0.78
125 Physical mapping at 6q27 of the locus for the TATA box-binding protein, the DNA-binding subunit of TFIID and a component of SL1 and TFIIIB, strongly suggests that it is single copy in the human genome. Genomics 1994 0.78
126 Characterization and regional mapping of new anonymous chromosome 20-specific DNA markers isolated from a flow-sorted DNA library. Genomics 1991 0.78
127 Assignment of the human RT6 gene to 11q13 by PCR screening of somatic cell hybrids and in situ hybridization. Genomics 1993 0.78
128 An arrayed library enriched in hncDNA corresponding to transcribed sequences of human chromosome 19: preparation and analysis. Genet Anal 1995 0.78
129 The structural gene for the mitochondrial aldehyde dehydrogenase maps to human chromosome 12. Hum Genet 1986 0.78
130 Direct assignment of citrate synthase (CS) gene to human chromosome 12 in man-mouse somatic cell hybrids. Hum Genet 1977 0.78
131 Two mosaic cases with nonfluorescent Y chromosome analysed with Y-specific DNA probes. Am J Med Genet 1988 0.78
132 CHILD syndrome: the NSDHL gene and its role in CHILD syndrome, a rare hereditary disorder. J Eur Acad Dermatol Venereol 2009 0.78
133 Organization and sequence of the gene encoding the human acrosin-trypsin inhibitor (HUSI-II). Gene 1993 0.78
134 The gene for 17 beta-hydroxysteroid dehydrogenase maps to human chromosome 17, bands q12-q21, and shows an RFLP with ScaI. Hum Genet 1990 0.77
135 Evidence for human DNA-mediated transfer of the suppressed phenotype into malignant Chinese hamster cells. Oncogene 1991 0.77
136 Anonymous DNA sequence from chromosome 21 showing a three allele insertion/deletion RFLP (HGM 9 provisional no. D21S82). Nucleic Acids Res 1987 0.77
137 Human interleukin 2 gene is located on chromosome 4. Cancer Invest 1984 0.77
138 Utilization of somatic cell hybrids for genetic studies in man. Humangenetik 1973 0.77
139 Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individual. Am J Med Genet 2000 0.77
140 Regional mapping of human chromosome 10: assignment of the gene for cytoplasmic glutamate-oxaloacetate transaminase to 10q24 leads to qter. Hum Genet 1976 0.77
141 Mapping of transcribed sequences on human chromosome 19. DNA Seq 1995 0.77
142 Definition of selectable cell surface markers for human chromosomes and chromosome segments in rodent-human hybrids. Somat Cell Mol Genet 1988 0.77
143 Genetic characterization of general transcription factors TFIIF and TFIIB of Homo sapiens sapiens. Cytogenet Cell Genet 1995 0.77
144 Genomic localization of the human gene encoding Dr1, a negative modulator of transcription of class II and class III genes. Cytogenet Cell Genet 1996 0.77
145 Human gap junction protein connexin31: molecular cloning and expression analysis. Biochem Biophys Res Commun 1998 0.77
146 Assignment of the genes for human glyoxalase I to chromosome 6 and for human esterase D to chromosome 13. Cytogenet Cell Genet 1976 0.77
147 Syrian hamster-human somatic cell hybrids: isolation and characterization. Humangenetik 1973 0.77
148 Assignment of the gene for human spasmolytic protein (hSP/SML1) to chromosome 21. Hum Genet 1992 0.77
149 European Gene Mapping Project (EUROGEM): breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme Humain. Ann Hum Genet 1996 0.77
150 Genes for human general transcription initiation factors TFIIIB, TFIIIB-associated proteins, TFIIIC2 and PTF/SNAPC: functional and positional candidates for tumour predisposition or inherited genetic diseases? Oncogene 2001 0.77
151 The role of somatic cell genetics in human gene mapping. Experientia 1986 0.77
152 The novel human HNF-3/fork head-like 5 gene: chromosomal localization and expression pattern. DNA Cell Biol 1997 0.77
153 Assignment of the human aminopeptidase N (peptidase E) gene to chromosome 15q13-qter. FEBS Lett 1988 0.76
154 Clinical variation in X-linked dominant chondrodysplasia punctata (X-linked dominant ichthyosis). Br J Dermatol 2006 0.76
155 Trophoblast glycoprotein recognised by monoclonal antibody 5T4 maps to human chromosome 6q14-q15. Hum Genet 1990 0.76
156 Genetics of human S-adenosylhomocysteine hydrolase. A new polymorphism in man. Hum Genet 1983 0.76
157 Possible assignment of the glyoxalase I (GLO) gene to chromosome 6 using man-mouse somatic cell hybrids. Hum Genet 1976 0.76
158 Chromosomal localization to 3q21----qter and two TaqI RFLPs of the human prostate-specific acid phosphatase gene (ACPP). Cytogenet Cell Genet 1989 0.76
159 Assignment of a gene for human mitochondrial isocitrate dehydrogenase (ICD-M, EC 1.1.1.41) to chromosome 15. Hum Genet 1976 0.75
160 Isolation and characterization of novel CAG repeat containing genes expressed in human brain. DNA Seq 1999 0.75
161 Progress towards cloning the cystic fibrosis gene. Philos Trans R Soc Lond B Biol Sci 1988 0.75
162 The gene for the alpha polypeptide of pyruvate dehydrogenase is X-linked in humans. Am J Hum Genet 1990 0.75
163 Assignment of the genes for human glyoxalase I to chromosome 6 and for human esterase D to chromosome 13. Birth Defects Orig Artic Ser 1976 0.75
164 Human cDNA probe (OL11) detects RFLP on chromosome 12 (D12S10). Nucleic Acids Res 1987 0.75
165 The anonymous probe DR258 (D7S438) identifies a HindIII polymorphism. Nucleic Acids Res 1990 0.75
166 A human single copy DNA probe (ZB6-1) detects multiple polymorphisms on 6q. Nucleic Acids Res 1988 0.75
167 Prenatal diagnosis of cystic fibrosis. J Clin Chem Clin Biochem 1989 0.75
168 Assignment of the gene encoding the catalytic subunit C beta of cAMP-dependent protein kinase to the p36 band on chromosome 1. Hum Genet 1992 0.75
169 Localization of GOTs to the q24 leads to qter region of human chromosome 10. Birth Defects Orig Artic Ser 1976 0.75
170 An anonymous single copy genomic probe (D8S9) (CW1) detects RFLP on chromosome 8. Nucleic Acids Res 1987 0.75
171 Microdissection and microcloning of human chromosome 7q22-32 region. Somat Cell Mol Genet 1990 0.75
172 Human cDNA probe (OL167,D21S109) detects RFLP on chromosome 21. Nucleic Acids Res 1987 0.75
173 The molecular map of the human genome as a basis for the study of ethnic differences in reactions to xenobiotics. Prog Clin Biol Res 1986 0.75
174 Positioning of 72 potentially full size LTRs of human endogenous retroviruses HERV-K on the human chromosome 19 map. Occurrences of the LTRs in human gene sites. Gene 1997 0.75
175 Regional mapping of human chromosomes 1 and 11. Cytogenet Cell Genet 1975 0.75
176 Status and transcriptional activity of a bovine-papillomavirus-I-based expression vector in a recombinant production cell line. Biotechnol Appl Biochem 1996 0.75
177 Six new polymorphic microsatellite markers used for the integration of genetic and physical maps of human chromosome 7. Hum Genet 1996 0.75
178 Mapping of the human spermidine synthase gene (SRM) to 1p36 and a probable pseudogene (SRML2) to region 3p14-->q21. Cytogenet Cell Genet 1993 0.75
179 Genomics of the human genes encoding four TAFII subunits of TFIID, the three subunits of TFIIA, as well as CDK8 and SURB7. Somat Cell Mol Genet 1999 0.75
180 Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly syndrome (GCPS) gene region. Genomics 1994 0.75
181 Evaluation of random cDNA clones as probes for human restriction fragment length polymorphisms. J Clin Chem Clin Biochem 1988 0.75
182 Localization of the human genes encoding the two subunits of general transcription factor TFIIE. Genomics 1994 0.75
183 Regional localization of the gene encoding pregnancy specific beta-1-glycoprotein 1 (PSBG1) to human chromosome 19q13.1. Cytogenet Cell Genet 1989 0.75
184 The genes for the highly homologous Ca(2+)-binding proteins oncomodulin and parvalbumin are not linked in the human genome. Genomics 1992 0.75
185 Human cDNA probe (cCW147) detects RFLP on chromosome 5 (D5S9). Nucleic Acids Res 1987 0.75
186 Chromosomal localization of the interferon-inducible human gene encoding mRNA 561. J Interferon Res 1987 0.75
187 The anonymous probe DR281 (D1S99) identifies a mspl polymorphism. Nucleic Acids Res 1990 0.75
188 Assignment of human genes: beta-glucuronidase to chromosome 7, adenylate kinase-1 to 9, a second enzyme with enolase activity to 12, and mitochondrial IDH to 15. Cytogenet Cell Genet 1976 0.75
189 Regional assignment of 30 expressed sequence tags on human chromosome 7 using a somatic cell hybrid panel. Genomics 1995 0.75
190 Elimination of mycoplasma contamination from mammalian cell cultures by the bibenzimidazole derivative Hoechst 33258. Cytogenet Cell Genet 1983 0.75
191 Regional mapping of human chromosomes 1 and 11. Birth Defects Orig Artic Ser 1975 0.75
192 Regional mapping of human chromosome 3. Assignment of a glutathione peroxidase-1 gene to 3p13 leads to 3q12. Hum Genet 1981 0.75
193 Assignment of a gene for human quinoid-dihydropteridine reductase (QDPR, EC 1.6.5.1) to chromosome 4. Hum Genet 1979 0.75
194 Microdissection and microcloning of the long arm of human chromosome 7. Mol Biol Rep 1987 0.75
195 PstI RFLP identified by an anonymous single copy genomic clone localized to chromosome 14 (HGM 9 provisional no. D14S14). Nucleic Acids Res 1987 0.75
196 Dissecting (CAC)5/(GTG)5 multilocus fingerprints from man into individual locus-specific, hypervariable components. Genomics 1992 0.75
197 A series of hypervariable minisatellites at the D7S464 locus. Hum Mol Genet 1992 0.75
198 Status and transcriptional activity of a bovine-papillomavirus-I-based expression vector in a recombinant production cell lines. Biotechnol Appl Biochem 1996 0.75
199 Localization of GOTs to the q24 leads to qter region of human chromosome 10. Cytogenet Cell Genet 1976 0.75
200 Identification of paralogous HERV-K LTRs on human chromosomes 3, 4, 7 and 11 in regions containing clusters of olfactory receptor genes. Mol Genet Genomics 2001 0.75
201 The potassium channel gene HK1 maps to human chromosome 11p14.1, close to the FSHB gene. Hum Genet 1992 0.75
202 Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation. Int J Obes Relat Metab Disord 2001 0.75
203 Regional assignment of 41 human DNA fragments on chromosome 7 by means of a somatic cell hybrid panel. Hum Genet 1990 0.75
204 Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13. Hum Genet 1994 0.75
205 A novel human multi-locus DNA family detected by pJU78 (DF31). Hum Genet 1991 0.75
206 Regional assignment of the gene for human beta-glucuronidase by the use of human-mouse cell hybrids. Cytogenet Cell Genet 1978 0.75
207 Evaluation of a Cys23Ser mutation within the human 5-HT2C receptor gene: no evidence for an association of the mutant allele with obesity or underweight in children, adolescents and young adults. Life Sci 1997 0.75
208 Regional localization of human ecto-5' nucleotidase to chromosome 6q14-q21. Hum Genet 1989 0.75
209 Human cDNA probe detects RFLP on chromosome 12, OL 202 (HGM8 designated no. D12S9). Nucleic Acids Res 1986 0.75
210 Assignment of the gene locus for human phosphoglucomutase 3 to chromosome 6q12-qter. Ann Genet 1980 0.75
211 Mild phenotypic expression of CHILD syndrome in two generations. Br J Dermatol 2009 0.75