1 YAC framework map that further confirms the
deletion map.
2 satellite instability and were excluded from
deletion mapping.
3 providing an informative basis for detailed
deletion mapping.
4 domain mediates neurexin binding as shown by
deletion mapping.
5 N-terminus in enzyme binding was defined by
deletion mapping.
6 mutations were located by DNA sequencing and
deletion mapping.
7 Internal
deletions mapped a shorter sequence between residues 251
8 Using traditional and DNA microarray-based
deletion mapping,
a 7-bp deletion was found in an exon o
9 Deletion-mapping analyses, using the extensive series of
10 In a detailed
deletion mapping analysis of 67 normal-tumor DNAs utiliz
11 Deletion mapping analysis revealed that a 78-amino acid
12 Deletion mapping analysis showed lowest ANXA7-promoter a
13 Deletion mapping analysis showed that inhibition by E1A
14 Deletion mapping analysis suggests that formation of an
15 ological subtype were selected for PCR-based
deletion mapping analysis using 15 highly polymorphic mi
16 Deletion mapping analysis with various GST-fused Fas cyt
17 Deletion-mapping analysis identified amino acids 40 to 6
18 Deletion-mapping analysis of the HBV core promoter and i
19 ompensation, we constructed a high-density Y-
deletion map and used deletion mutants to manipulate gen
20 CGTG recognition sequence, we have performed
deletion mapping and amino acid substitutions within the
21 Further
deletion mapping and domain swapping experiments with PA
22 Using
deletion mapping and green fluorescent protein chimeras,
23 s the power of integrating GWAS signals with
deletion mapping and identifies critical regulatory sequ
24 site for Peptide 3 on Mdm2 was determined by
deletion mapping and lies adjacent to the binding site o
25 Deletion mapping and mutagenesis analysis identified spe
26 Deletion mapping and mutagenesis studies unveiled that p
27 The leads gained from the
deletion mapping and physical maps should expedite the i
28 Deletion mapping and point mutagenesis defined a region
29 Conversely,
deletion mapping and point mutation analysis of PIF3 for
30 By
deletion mapping and scanning mutation analyses, we have
31 Deletion mapping and sequence analysis showed that the R
32 We report here that
deletion mapping and site-directed mutagenesis identifie
33 In this report, we use
deletion mapping and site-directed mutagenesis to determ
34 cose sites in Drosophila Notch, we conducted
deletion mapping and site-specific mutagenesis and then
35 However,
deletion mapping and the analysis of variable inactivati
36 nt in the proximal region were identified by
deletion mapping and transcription assays.
37 Using
deletion mapping and transient transfection, we show tha
38 EST
deletion maps and the consensus map of group 1 chromosom
39 mapping, linkage disequilibrium mapping, and
deletion mapping,
and new high-throughput sequencing met
40 but has not been amenable to alignment with
deletion maps because the identity of most RLGS fragment
41 ity of GLRB mutations using splicing assays,
deletion mapping,
cell-surface biotinylation, expression
42 Deletion mapping confirmed that hRap1 is tethered to tel
43 We have previously collated the
deletion mapping data of 24 Jacobsen patients with the p
44 interest, perhaps because of the conflicting
deletion mapping data.
45 Truncation and
deletion mapping defined a 51-amino acid sequence betwee
46 High-resolution
deletion mapping defined a consensus region of deletion
47 Deletion mapping defined two minimum regions of deletion
48 Deletion mapping demonstrated 10q loss in 14 of 67 infor
49 Deletion mapping demonstrated that DISC1 has distinct in
50 Deletion mapping experiments demonstrate that a 118-base
51 also has a discrete <20-nt poly(A) tail, and
deletion mapping experiments identified an element homol
52 ApoAI promoter
deletion mapping experiments indicated that ERalpha plus
53 Deletion mapping experiments indicated that the amino te
54 Through
deletion mapping experiments, we demonstrated that the b
55 Using RNA pull-down and
deletion mapping experiments, we show that HuR physicall
56 Further analysis of the
deletion map for the invasive epithelial ovarian tumors
57 ed methylation analysis with high-resolution
deletion maps from microarray-based comparative genomic
58 A
deletion map has allowed us to delimit a smallest region
59 Deletion mapping has defined a region of common loss fla
60 Deletion mapping has localized the beta-catenin binding
61 Deletion mapping identified a 7-Mb critical region flank
62 Previously,
deletion mapping identified a central, conserved region
63 Saturation mutagenesis and
deletion mapping identified residues 156-202 of SNAP25 a
64 The
deletion mapping identified two critical DMD gene hotspo
65 but not unr or PTB4, bound to hIR mRNA, and
deletion mapping implicated a CCU motif 448 nt upstream
66 In addition,
deletion mapping in combination with loss of heterozygos
67 Deletion mapping in combination with promoter activity a
68 Its minimal functional extent based on
deletion mapping in patients was refined to 358 bp.
69 transferase) domain identified previously by
deletion mapping in recombinant yeast Gcn5.
70 Deletion mapping in tumors over the past decade has narr
71 Using a combination of
deletion mapping,
in vitro mutagenesis, an analogue-sens
72 Deletion mapping indicates that main chain interaction(s
73 Deletion mapping indicates that the proteins bind within
74 Deletion mapping is the primary method used for fine-sca
75 Such
deletion mapping is usually conducted using polymerase c
76 Deletion mapping localized the dopamine receptor-FLN-A i
77 Deletion mapping localized the major NF-kappaB activatin
78 Deletion mapping localized the site of dopamine receptor
79 Deletion mapping localized the sites of interaction betw
80 o aldolase was characterized by biochemical,
deletion mapping,
mutagenesis, and co-immunoprecipitatio
81 rosatellite loci to create a high resolution
deletion map of 150 squamous cell carcinomas of the lary
82 To construct a highly detailed
deletion map of chromosome 11p, we used 13 polymorphic m
83 ctal carcinoma in situ cases and completed a
deletion map of chromosome 16q by means of paraffin-embe
84 We constructed a highly detailed
deletion map of chromosome 17q21 based on PCR amplificat
85 in 6q, we have constructed a high-resolution
deletion map of this chromosome arm in 46 MMs.
86 Deletion mapping of ACE3 revealed that an evolutionarily
87 Deletion mapping of an ARS element linked to the HO gene
88 f an F(2) durum wheat population and through
deletion mapping of awned bread wheat mutants.
89 Deletion mapping of chromosome 13q was performed in four
90 Detailed
deletion mapping of chromosome 6q has shown that the hig
91 Detailed
deletion mapping of chromosome 6q sequences in invasive
92 Deletion mapping of domain I identified the C-terminal 3
93 Deletion mapping of ERT protein suggests that the transa
94 Deletion mapping of INrf2 revealed the requirement of KE
95 Deletion mapping of IQD1 demonstrated the importance of
96 suppressor gene to a 3 cM region on 17q25 by
deletion mapping of microsatellite markers in breast tum
97 we developed a novel and general method for
deletion mapping of non-recombining regions by solving "
98 Deletion mapping of ori-beta identified two required com
99 ed translocations and supportive comparative
deletion mapping of PSS subjects, we have uncovered evid
100 Deletion mapping of Rpa1 defined three domains.
101 Deletion mapping of the 2468-base COX-2 mRNA 3'-untransl
102 In our studies, detailed 3'
deletion mapping of the 5'-DPRS narrowed down the negati
103 Deletion mapping of the BRCA2 promoter identified three
104 Deletion mapping of the C terminus of the alpha1-subunit
105 Deletion mapping of the Cp 3'-UTR indicated an internal
106 Deletion mapping of the Egr-1 promoter revealed that the
107 Deletion mapping of the human presenilin-1 (PS1) promote
108 omic hybridization (CGH) and high-resolution
deletion mapping of the long arm of chromosome 2 (2q) in
109 Deletion mapping of the NS5A protein found that an 85-aa
110 Deletion mapping of the PC3/hchr7 tumors obtained after
111 Deletion mapping of the Rpa2 subunit identified the doma
112 Deletion mapping of the TNFalpha gene revealed that the
113 Deletion mapping of the X-chromosome implicated 5 Mb of
114 Deletion mapping of two Mad members, Mad1 and Mxi1, demo
115 d (RH) mapping in conjunction with a natural
deletion mapping panel.
116 alignment (number of matches, mismatches and
deletions, mapping quality score returned by the alignme
117 Effective and efficient
deletion mapping requires both extensive genomic coverag
118 Deletion mapping revealed a 71-bp-long minimal replicato
119 Deletion mapping revealed a minimal region of overlap be
120 Deletion mapping revealed four potential candidate regio
121 Deletion mapping revealed that heterozygous deletions en
122 Deletion mapping revealed that the minimal PampC extends
123 sis, combined with proteolytic digestion and
deletion mapping,
revealed the organization of L into a
124 To improve the resolution of
deletion mapping,
screens were planned to distribute del
125 These physical and
deletion maps should prove useful for identification of
126 Deletion mapping showed that intact extracellular cadher
127 es upstream of the transcription start site;
deletion mapping showed that Pcdh15 harbors suppressor a
128 Deletion mapping showed that the MLD included a symmetri
129 Deletion mapping showed that the N terminus of YopE was
130 R structural analyses and the combination of
deletion mapping,
site-directed mutagenesis and LDL rele
131 r these deficits in X-monosomy by means of a
deletion mapping strategy.
132 ts into mouse L cells and performing allelic
deletion mapping studies against this mouse background.
133 Recent
deletion mapping studies have broadly implicated a 1.6-M
134 Deletion mapping studies have delineated a 3.5 Mb candid
135 These and other
deletion mapping studies have suggested the existence of
136 Deletion mapping studies have unambiguously identified a
137 Deletion mapping studies indicate that amino acids 1-100
138 Finer
deletion mapping studies localized the smallest regions
139 d cosmid clones has been isolated for use in
deletion mapping studies of patient DNA.
140 Previous functional and
deletion mapping studies on cervical cancer (CC) have im
141 Deletion mapping studies showed that the C-terminal regi
142 Deletion-mapping studies indicate that the carboxy-termi
143 Further
deletion-mapping studies suggest the presence of two int
144 By a combination of microcell-fusion and
deletion-mapping studies, we previously established that
145 A recent
deletion mapping study of chromosome 9p has also identif
146 Deletion mapping suggests that a 37-aa segment present a
147 Deletion mapping suggests that DNA sequence homologies b
148 We show by
deletion mapping that processing of NF-(kappa)B2(p100) t
149 ve of 15 (4.0% of the sample) had a 2.5-3 Mb
deletion mapping to 22q11.2, a rate higher than that rep
150 istance at 6p25 and a second site of 10.3 cM
deletion mapping to 6p21.3.
151 s a receptor region previously identified by
deletion mapping to be important for ligand binding.
152 Here we employed iterative
deletion mapping to elucidate how the NTD of HSPB6 influ
153 for additional VH gene families and utilized
deletion mapping to explore the extent of VH gene family
154 ave used cross-species sequence analysis and
deletion mapping to facilitate the identification of the
155 Genes and a 3-Mb
deletion mapping to human chromosome 22q11.2 have been i
156 action between ICP0 and ND10, we carried out
deletion mapping to identify the domains of ICP0 respons
157 We used
deletion mapping to identify, and then sequence, BAC clo
158 ese loci demonstrated that the 10p region of
deletion maps to 10p11.2.
159 These
deletions mapped to a poly-T-rich tract just 5' to the i
160 tants possessing amino acid substitutions or
deletions mapping to either the repeat or interrepeat re
161 We found that 35 ASD-associated
deletions mapping to the PTCHD1 locus disrupted exons of
162 n breakpoints from two patients with de novo
deletions mapping to these distal LCRs.
163 bladder and upper urinary tract by detailed
deletion mapping using 31 microsatellite markers on 9q.
164 Additional
deletion mapping using microsatellites localized to the
165 ons on chromosome 5, we performed a detailed
deletion mapping utilizing 66 normal-tumor DNAs from mal
166 The SSLP-based
deletion map was confirmed and genetic distances were de
167 Deletion mapping was employed to determine the physical
168 Deletion mapping was used to identify the domain of Bub1
169 dization (CGH) to lesion-induced mutants for
deletion mapping was validated on a midoleate x-ray muta
170 ups into defined intervals of the Tyr-region
deletion map,
which facilitates the identification of ea
171 By coupling nullisomic
deletion mapping with meiotic linkage mapping, loci know
172 explain the high prevalence of focal genomic
deletions mapping within very large genes in human tumor