1 n this study the madC gene was identified by
positional cloning.
2 iate gene targets for saturation mapping and
positional cloning.
3 een identified by candidate gene analysis or
positional cloning.
4 problematic for subsequent fine mapping and
positional cloning.
5 ion, such as identification of new genes and
positional cloning.
6 nown genes, and facilitates fine mapping and
positional cloning.
7 all NFkB interacting protein1 (Nkip1), using
positional cloning.
8 athogen through forward genetic analysis and
positional cloning.
9 fn in repeated epilation (Er) mutant mice by
positional cloning.
10 nterval sufficiently to identify the gene by
positional cloning.
11 : genome-wide scan, fine mapping, and, last,
positional cloning.
12 ) identified through a genomewide screen and
positional cloning.
13 We identified the npo gene by
positional cloning.
14 cost, time and labor investment required for
positional cloning.
15 .4 cM interval will be useful for initiating
positional cloning.
16 Positional cloning,
analysis of independent alleles, and
17 This genetic map provides a framework for
positional cloning and a scaffold for integration of the
18 Positional cloning and a transposon-derived allele demon
19 Positional cloning and analysis of additional alleles sh
20 esponse regulator protein 37 (PRR37) through
positional cloning and analysis of SbPRR37 alleles that
21 ins, however, is required to enable powerful
positional cloning and association techniques.
22 iscovery has provided proof of principle for
positional cloning and candidate gene approaches to iden
23 mong the first characterized mutants through
positional cloning and candidate gene strategies.
24 ionally characterized; here, we describe the
positional cloning and characterization of a maize (Zea
25 Here, we report the generation,
positional cloning and characterization of Nell1(6R), a
26 Here, we report the
positional cloning and characterization of the vanishing
27 Here, we have identified the radish gene by
positional cloning and comparative sequencing, finding a
28 Through
positional cloning and degenerate PCR, we sequenced both
29 STR was identified by
positional cloning and encodes a half-size ATP binding c
30 We isolated the gt1 gene using
positional cloning and found that it encodes a class I h
31 We cloned bde by
positional cloning and found that it encodes zea agamous
32 We have isolated the LUT1 gene by
positional cloning and found that, in contrast to all kn
33 The CNA gene was isolated by
positional cloning and found to encode a class III homeo
34 The EDR3 gene was isolated by
positional cloning and found to encode Arabidopsis dynam
35 Positional cloning and functional analysis revealed that
36 Positional cloning and functional assays showed that pol
37 Positional cloning and genetic analysis show that, unlik
38 Positional cloning and genetic complementation reveal th
39 a strong genetic component, and so far, only
positional cloning and genomewide association studies ha
40 plified region using molecular cytogenetics,
positional cloning and genomic sequencing culminated in
41 oci will aid in assessing the feasibility of
positional cloning and help formulate strategies require
42 We present the
positional cloning and initial phenotypic characterizati
43 g integrated with classical linkage maps for
positional cloning and marker-assisted selection.
44 sequence in many species, linkage analysis,
positional cloning and microarray are gradually becoming
45 Here we describe the
positional cloning and molecular characterization of the
46 Positional cloning and morpholino phenocopy revealed tha
47 PHP-like phenotype in humans and mice, using
positional cloning and mouse transgenics, respectively.
48 This article reports the
positional cloning and mutation analysis of the rat PKD
49 Positional cloning and mutational analyses of candidate
50 Positional cloning and mutational analyses revealed that
51 variability in diabetes-related traits via a
positional cloning and positional candidate gene approac
52 Here we isolate alr1 by
positional cloning and report it to encode a transmembra
53 t wab1 encodes a TCP transcription factor by
positional cloning and revertant analysis.
54 Positional cloning and sequencing revealed that flk is a
55 We isolated the Cul4 gene by
positional cloning and showed that it encodes a BROAD-CO
56 AtNUP160 was isolated through
positional cloning and shown to encode a putative homolo
57 all, our report represents a high resolution
positional cloning and translational study for Adamts16
58 Using
positional cloning and virus-induced gene silencing, her
59 uable tool for DNA marker-assisted breeding,
positional cloning,
and a wide range of evolutionary stu
60 Genetic mapping,
positional cloning,
and complementation studies with a d
61 e taste classes are now targets for linkage,
positional cloning,
and genetic association strategies.
62 the rc phenotype development, we carried out
positional cloning,
and mapped the rc locus to a 246-kb
63 ls of drug physiological dependence in mice,
positional cloning,
and sequence and expression analyses
64 n studies and against complete reliance on a
positional cloning approach based on a map of anonymous
65 A
positional cloning approach has become possible after th
66 In the present study, using a
positional cloning approach in a mouse model of interspe
67 A
positional cloning approach indicates that the mutation
68 Using a
positional cloning approach supported by comparative gen
69 We have been using a
positional cloning approach to identify the major genes
70 A
positional cloning approach was used to identify cie1, w
71 A
positional cloning approach was used to identify genes c
72 We have used a
positional cloning approach with one line of ashen mutan
73 Here we show, using a
positional cloning approach, that an F382L amino acid su
74 Taking the
positional cloning approach, the Chr.9_ClpP5 gene, one o
75 Using a
positional cloning approach, we have identified a point
76 Using a
positional cloning approach, we identified the svs mutan
77 Using a
positional cloning approach, we identify that the mutant
78 ries promote the use of a microsynteny-based
positional-cloning approach using the rice genome as a t
79 A
positional-cloning approach, together with the use of bi
80 Positional cloning approaches based on genetic linkage h
81 ng disease-linked mutations with traditional
positional cloning approaches; however, because of the r
82 We identified one of the mutations by
positional cloning as a single base pair change in a gen
83 ATM was originally identified by
positional cloning as the gene that underlies the autoso
84 rst asthma susceptibility gene identified by
positional cloning)
as an asthma gene was presented, alt
85 Positional cloning based on genome-wide linkage analysis
86 s and a benchmark against which the power of
positional cloning by haplotype-based alternatives may b
87 re we present a multiple pairwise method for
positional cloning by LD within a composite likelihood f
88 These results provide a guide to efficient
positional cloning by SNPs and a benchmark against which
89 We used a
positional cloning-
candidate gene approach to identify m
90 ular background of this disease based on the
positional cloning/
candidate approach of the defective g
91 Through
positional cloning,
complementation, and sequencing, we
92 Positional cloning demonstrated that HST is the Arabidop
93 Positional cloning disclosed that the mutant gene encode
94 or which the culpable gene was identified by
positional cloning,
Duchenne muscular dystrophy has serv
95 Positional cloning efforts identified a mutation in a no
96 To expedite linkage studies and
positional cloning efforts in the dog, Minimal Screening
97 PN10 genes influence T2D-susceptibility, and
positional cloning efforts within replicated regions of
98 s centers, implies significance criteria for
positional cloning efforts, and provides working estimat
99 Positional cloning flr identified a tetratricopeptide re
100 Positional cloning followed by functional tests show tha
101 ion factor 1 is the first gene identified by
positional cloning for familial combined hyperlipidemia.
102 Positional cloning for genes causing SRNS has opened the
103 and highlight the power (and limitations) of
positional cloning for the identification of asthma gene
104 The use of
positional cloning for the identification of complex tra
105 , we tested whether we could avoid laborious
positional cloning for the isolation of TALE-induced R g
106 in depth by random germline mutagenesis and
positional cloning (
forward genetics).
107 Conventional linkage and
positional cloning have led to the mapping of six BBS lo
108 lt; however, genome-wide screens followed by
positional cloning have started to identify such genes f
109 Positional cloning identified a C794T substitution in th
110 Positional cloning identified a causative mutation in th
111 Positional cloning identified a point mutation in the At
112 Positional cloning identified both as mutations of the m
113 Positional cloning identified insertion of ETn2beta (ear
114 Positional cloning identified loss of the newly describe
115 Positional cloning identified novel disease-associated p
116 Positional cloning identified Ppd-H1, the major determin
117 Positional cloning identified REME1 unambiguously as the
118 Positional cloning identified specificity protein 8 (sp8
119 Positional cloning identified the candidate virulence ge
120 Positional cloning identified the mutations 705insG and
121 Positional cloning identified zebrafish smooth muscle my
122 Positional cloning identifies chm as a mutation in the C
123 Positional cloning implicated the serine-threonine kinas
124 a QTL is detected, the region is narrowed by
positional cloning in the hope of determining the underl
125 could dramatically improve the efficiency of
positional cloning in zebrafish and other model organism
126 fish genetics, one-by-one gene studies using
positional cloning,
insertional mutagenesis, antisense m
127 Further identification of Bmgr5 genes by
positional cloning may reveal new and effective approach
128 Further identification of Gvh genes by
positional cloning may yield new insight into genetic co
129 Here, we use
positional cloning methods to identify the major chromos
130 lies that were undetectable with linkage and
positional cloning methods, but compared with these meth
131 Positional cloning,
molecular analysis, and electrophysi
132 Here we identify, by
positional cloning,
mutations in an evolutionarily conse
133 ed-in-Schizophrenia-1 (DISC1), identified by
positional cloning of a balanced translocation (1;11) wi
134 Here, we describe the
positional cloning of a blind zebrafish mutant, wait unt
135 erase (COMT), here designated COMT2, through
positional cloning of a chemically induced mutation resp
136 We report the
positional cloning of a hypermorphic, regulatory mutatio
137 However,
positional cloning of a mutant line with compromised neu
138 In the first
positional cloning of a mutation in X. tropicalis, we sh
139 We report here the
positional cloning of a new unc gene, unc-122, which we
140 This study reports the
positional cloning of a novel protein required for Clara
141 The
positional cloning of a spontaneous mutation that caused
142 e combination of alleles at multiple loci in
positional cloning of a target dormancy gene.
143 Positional cloning of acc identified a serca mutation as
144 Positional cloning of additional causative genes of NPHP
145 Positional cloning of blk1-R identified a predicted miss
146 Positional cloning of blowout identified a nonsense muta
147 vide a rapid and cost-effective approach for
positional cloning of C. elegans mutant loci, and are al
148 traits of interest through fine mapping and
positional cloning of candidate genes.
149 cated as powerful tools for fine mapping and
positional cloning of complex disease genes.
150 nel genes are continuing to be discovered by
positional cloning of disease loci.
151 ium (LD) mapping offers much promise for the
positional cloning of disease-causing genes.
152 Here, we report on the
positional cloning of diwanka and show that it encodes L
153 Positional cloning of dozens of unknown genes that cause
154 n esophageal cancer cell lines led us to the
positional cloning of gene amplified in squamous cell ca
155 would streamline the utility of the map for
positional cloning of genes and QTLs, and functional ana
156 horse gene map and consequently, mapping and
positional cloning of genes governing traits significant
157 (reported here) will greatly facilitate the
positional cloning of genes influencing complex traits o
158 nd transduction have been identified through
positional cloning of genes that cause deafness.
159 th moderate to large effects will facilitate
positional cloning of genes underlying sexual isolation.
160 We report here the
positional cloning of Gpc-B1, a wheat quantitative trait
161 Positional cloning of hus2 reveals a gene sequence simil
162 Positional cloning of ig1 was performed based on the gen
163 n the integrated map provides a platform for
positional cloning of important genes and the targeted s
164 ombination also has been a major obstacle to
positional cloning of key genes.
165 We also report the
positional cloning of Mei1, which encodes a product with
166 Positional cloning of mib revealed that it is a gene in
167 Positional cloning of mis, including genetic rescue and
168 Positional cloning of mouse deafness mutations uncovered
169 Positional cloning of nine genes (NPHP1 through 9) and f
170 Positional cloning of nob identified the causative gene
171 The use of the library in
positional cloning of pest and disease resistance genes
172 lts of this study provide impetus for future
positional cloning of QTLs regulating insulin and glucos
173 These results provide impetus for future
positional cloning of quantitative trait loci (QTLs).
174 Positional cloning of quantitative trait loci in rodents
175 Positional cloning of six novel genes (NPHP1 through 6)
176 Positional cloning of SLY1 revealed that it encodes a pu
177 Positional cloning of the brom bones gene reveals that a
178 ss of narrowing down the critical region for
positional cloning of the Cia10 gene.
179 Positional cloning of the Dc locus revealed an insertion
180 Positional cloning of the dreher locus demonstrated that
181 As a prelude to
positional cloning of the fertility restorer, Rf1, FISH
182 The
positional cloning of the gene for vernalization require
183 Here, we report
positional cloning of the gene responsible for productio
184 nalysis of hybrid progeny will be useful for
positional cloning of the genes controlling traits such
185 Positional cloning of the genes responsible for the muta
186 Positional cloning of the ITB1 gene showed that it encod
187 Positional cloning of the mutation resulted in identific
188 Recent
positional cloning of the radiation-induced polycythaemi
189 Positional cloning of the REF1 gene revealed that it enc
190 Surprisingly,
positional cloning of the REF2 locus revealed that it en
191 s a platform for high-resolution mapping and
positional cloning of the resistance genes.
192 Positional cloning of the rmn locus reveals a loss-of-fu
193 Positional cloning of the SIS8 gene revealed that it enc
194 Positional cloning of the six known NPHP genes has linke
195 patibility marker-assisted selection and for
positional cloning of the underlying gene, a necessary g
196 In this study, characterization and
positional cloning of the uniform gray-green (ug) locus
197 We report here the
positional cloning of the wheat vernalization gene VRN2,
198 Positional cloning of the woe2 locus identified a 1308 b
199 Positional cloning of the Wpk gene suggested a MKS3 cand
200 Positional cloning of the wrfr mutation revealed a retro
201 Subsequent
positional cloning of this locus showed that ITB2 encode
202 Positional cloning of toh reveals that it encodes a memb
203 Here we describe the
positional cloning of two soybean genes Rj2 and Rfg1 tha
204 quantitative trait loci and to allow for the
positional cloning of valuable genes.
205 Our
positional cloning of vl indicates these phenotypes resu
206 he use of next-generation sequencing for the
positional cloning of zebrafish mutations has increased
207 explosion in the identification, largely by
positional cloning,
of genes associated with mendelian d
208 didate genes is identified using traditional
positional cloning or high-throughput genomics technique
209 Here we use a combination of
positional cloning,
population genomic resequencing, ass
210 During the
positional cloning process of this 3-Mb locus, several m
211 We undertook a
positional cloning project to identify the causative mut
212 ns and polymorphic genetic markers useful in
positional cloning projects.
213 ntional banded karyotype followed by arduous
positional cloning projects.
214 By
positional cloning,
rescue, and morpholino knockdown exp
215 Positional cloning,
retroviral transduction, and a somat
216 Positional cloning revealed a nonsense mutation of tln1
217 Positional cloning revealed an early frameshift mutation
218 Positional cloning revealed that IBR3 encodes a putative
219 Isolation of SMA4 by
positional cloning revealed that it encodes LACS2, a mem
220 Positional cloning revealed that rim1 encodes an allele
221 Positional cloning revealed that rte encodes a membrane-
222 Fine mapping and
positional cloning revealed that stumpy was the zebrafis
223 Positional cloning revealed that the emm phenotype is ca
224 Positional cloning revealed that the genetic defect unde
225 Positional cloning revealed that the recessive mutation
226 Positional cloning revealed that tls1 encodes a protein
227 mapped to the long arm of chromosome 10 and
positional cloning revealed the existence of a premature
228 revented with prenatal dietary folic acid Cd
positional cloning reveals a missense mutation of a high
229 Positional cloning reveals that fan encodes type 5 adeny
230 Positional cloning reveals that iguana encodes the zebra
231 Positional cloning reveals that mot encodes Med12, a com
232 Positional cloning reveals that prt encodes a previously
233 Positional cloning reveals that rgd2 encodes an ARGONAUT
234 Positional cloning reveals that shiri encodes Med12, a r
235 Positional cloning reveals that sidetracked encodes Plex
236 Positional cloning reveals that the frv locus encodes Tm
237 Positional cloning reveals that the ISE2 gene encodes a
238 Positional cloning showed that MAS2 encodes the putative
239 Positional cloning shows that spi1 encodes a flavin mono
240 rafish traditionally involves time-consuming
positional cloning strategies that result in the identif
241 Using
positional cloning strategies, we characterized an evolu
242 Using a
positional cloning strategy and a retrotransposon insert
243 Here, using a
positional cloning strategy we identified variants of PR
244 Using a
positional cloning strategy, we determined that the bel
245 Through a
positional cloning strategy, we discovered that these ho
246 Using a
positional cloning strategy, we have identified mutation
247 Using a
positional cloning strategy, we identified a gene, six-t
248 Using a
positional cloning strategy, we identified a missense mu
249 and that several genes may be tractable to a
positional cloning strategy.
250 From
positional cloning studies and expression studies, we id
251 ive map provides a useful tool to facilitate
positional cloning studies in the feline model.
252 CAPN10, as well as the latest findings from
positional cloning studies on a number of other complex
253 enges of moving from the linkage mapping and
positional cloning studies on which we have been focused
254 genes, hand in hand with genetic linkage and
positional cloning studies, notably on the ability to ta
255 A
positional cloning study of type 2 diabetes in Mexican A
256 re amenable to physical mapping of genes and
positional cloning than the C-value alone might suggest.
257 We show by
positional cloning that the 30-zinc finger transcription
258 We show, by
positional cloning,
that mab-2 encodes RNT-1, the only C
259 Despite multiple efforts using traditional
positional cloning,
the causative genes for unsolved dys
260 Through
positional cloning,
the EPS1 gene was isolated and found
261 these discoveries, which were the fruits of
positional cloning,
the molecular constituents of the si
262 We used
positional cloning to determine that one mutant is defec
263 We previously used
positional cloning to identify a new locus on chromosome
264 We have used
positional cloning to identify a nine base-pair deletion
265 c growth of cells in the myocardium, we used
positional cloning to identify the heart of glass (heg)
266 Here, we used
positional cloning to identify the mutated pob gene.
267 We used
positional cloning to identify the nrc mutation as a pre
268 We recently used
positional cloning to identify the transcription factor
269 We used
positional cloning to narrow the interval containing sca
270 We localized the recessive ru848 mutation by
positional cloning to the zebrafish homolog of the human
271 ic methodology, from candidate genes through
positional cloning,
to genome-wide association, that hav
272 By
positional cloning using a previously characterized rat
273 interval at the S-locus on chromosome 1, but
positional cloning was hampered by low recombination fre
274 Positional cloning was used to identify a mutation in th
275 By
positional cloning we found a heterozygous mutation L95F
276 Using
positional cloning we have identified an inactivating mu
277 bditis elegans genetic suppressor screen and
positional cloning,
we discovered that loss-of-function
278 By
positional cloning,
we found that dco encodes Gja3/Cx46,
279 By
positional cloning,
we have identified a nonsense mutati
280 Using
positional cloning,
we have identified an identical 334-
281 Using
positional cloning,
we here identify mutations in the ge
282 By
positional cloning,
we here identify san as the zebrafis
283 By
positional cloning,
we identified a deletion encompassin
284 Using
positional cloning,
we identified a maximum of 6 coding
285 By
positional cloning,
we identified a nonsense mutation co
286 Using
positional cloning,
we identified mutations in the phosp
287 Through genetic mapping and
positional cloning,
we identified the causative mutation
288 By
positional cloning,
we identified vac as a point mutatio
289 Using methods of
positional cloning,
we identify a critical genetic inter
290 By
positional cloning,
we identify the mutation in this str
291 By
positional cloning,
we isolated seryl-tRNA synthetase (s
292 Using
positional cloning,
we isolated the gene representing Or
293 By means of
positional cloning,
we reveal that the zebrafish mutant
294 Using
positional cloning,
we show here that unplugged encodes
295 Through
positional cloning,
we show that Mvwf5 is a cis-regulato
296 Through
positional cloning,
we show that the gene mutated in the
297 Through
positional cloning,
we show that the ret mutation is in
298 By use of mutation selection and
positional cloning,
we showed that the largest subunit o
299 largely been accomplished through the use of
positional cloning,
which relies on linkage mapping.
300 ure high-resolution mapping and, ultimately,
positional cloning,
will reveal whether these traits do