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1 e electronic publication of classic books in mouse genetics.
2 remains one of the longstanding mysteries of mouse genetics.
3 n vivo roles established by cell biology and mouse genetics.
4 ow-level transcription in this process using mouse genetics.
5  for this apparent noncanonical signal using mouse genetics.
6 e xenografts, patient-derived xenografts and mouse genetics.
7 g molecular and chemical expression aided by mouse genetics.
8  this apparent discrepancy between human and mouse genetics.
9 iques and how they are changing the field of mouse genetics.
10 bral cortex using loss- and gain-of-function mouse genetics.
11 nship between Zic2 and the Shh pathway using mouse genetics.
12 nimals including lesion studies, imaging and mouse genetics.
13 mline capacity of ES cells, and the power of mouse genetics.
14 red mouse strains provide the foundation for mouse genetics.
15                               Here we employ mouse genetics, 2-photon microscopy, electrophysiology a
16                In this study, we incorporate mouse genetics, anatomy, electrophysiology, and single-c
17                                        Using mouse genetics and a BCR-ABL model of CML, we observed c
18 ue of Neuron, Cho et al. (2017) use advanced mouse genetics and biochemical experiments to unravel th
19                           Here, by combining mouse genetics and biochemistry with clinical tissue ana
20                        Perhaps, the power of mouse genetics and biology can be harnessed to identify
21                       Here, we use human and mouse genetics and cell biological and biochemical appro
22 hich have taken advantage of improvements to mouse genetics and circuit-mapping tools.
23              Integrating rat physiology with mouse genetics and clinical results from human by using
24                            Here, we combined mouse genetics and cryo-electron tomography to determine
25                                 We have used mouse genetics and genome-wide analyses to determine how
26  aims to fill this gap by employing advanced mouse genetics and genomics techniques to dissect the im
27                                              Mouse genetics and genomics will help to identify all th
28 cladistic analysis, which is well suited for mouse genetics and has increased flexibility over existi
29                In addition, a combination of mouse genetics and hPSC differentiation approaches have
30 scaffolding protein families and explore how mouse genetics and human genetics have intersected to ad
31                                     By using mouse genetics and in utero electroporation, we provide
32                                    Combining mouse genetics and in vivo ribosome profiling, we observ
33                           Using the tools of mouse genetics and multielectrode recording, we demonstr
34 in contributes to AML using a combination of mouse genetics and primary patient samples.
35 ns of SL and SP cells using a combination of mouse genetics and retrograde labeling.
36                                 Here, we use mouse genetics and scRNA-seq to identify regulators of e
37 how Fgfr2 regulates AF closure by leveraging mouse genetics and single-cell transcriptomics.
38                                 Here, we use mouse genetics and structure function analysis to invest
39 n of single-cell RNA sequencing (scRNA-seq), mouse genetics and tissue injury approaches, we uncover
40               In this study, we used complex mouse genetics and transcriptomic analyses to determine
41                                  We combined mouse genetics and viral strategies to determine how the
42  Inbred strains are a distinctive feature of mouse genetics and we discuss their history, advantages
43  Using primary and engineered human tissues, mouse genetics, and a multi-omics approach, we demonstra
44      Here, we address this controversy using mouse genetics, and demonstrate that brainstem C boutons
45 ree complementary disciplines: cell biology, mouse genetics, and dermatology.
46 on of high-throughput sequencing approaches, mouse genetics, and murine and human organoids and ident
47 vivo spinal cord two-photon calcium imaging, mouse genetics, and persistent pain models to study how
48 hree-dimensional imaging, cell type-specific mouse genetics, and surgical approaches to investigate s
49  Using an in vivo reporter of Shh signaling, mouse genetics, and systems modeling, we show that a spa
50                   To test this, we devised a mouse genetics approach to silence glutamatergic signall
51                                            A mouse genetics approach was used to separate the matted
52                                     With the mouse genetics approach, we show that ablation of ACF7 i
53                      With genome-editing and mouse genetics approach, we show that loss of function o
54 ew focuses on the last year's progress using mouse genetics as a tool to study intrinsic mechanisms o
55 ic combination of bioinformatic analysis and mouse genetics as well as embryo and explant culture exp
56 cluded in this account are the beginnings of mouse genetics at the Bussey Institute, Columbia Univers
57                           Recent advances in mouse genetics combined with neuroanatomical and electro
58                                              Mouse genetics combined with pharmacological probing in
59 s work will become a useful resource for the mouse genetics community to understand gene functions.
60                                              Mouse genetics confirmed the importance of canonical Wnt
61                                              Mouse genetics demonstrate that KCNJ2-mediated membrane
62 d using high-resolution approaches combining mouse genetics, designer receptor exclusively activated
63                             Here we combined mouse genetics, electrophysiology, and circuit mapping w
64                                  Here we use mouse genetics, electrophysiology, imaging and optogenet
65     The Cre-Lox system is a powerful tool in mouse genetics, enabling precise spatiotemporal control
66                      Biochemical studies and mouse genetics established that sirtuin 5 (SIRT5) contro
67                Described are biochemical and mouse genetics experiments demonstrating that membrane-a
68                                              Mouse genetics experiments have defined crucial roles fo
69 osin contractility in cell aggregates and by mouse genetics experiments.
70 ve combined cell type-specific and inducible mouse genetics, flow experiments in vitro, single-cell R
71          Transgenesis has been a mainstay of mouse genetics for over 30 yr, providing numerous models
72 xP technology is widely used in the field of mouse genetics for spatial and/or temporal regulation of
73 st anticipated and less heralded outcomes of mouse genetics has been to rediscover whole organism phy
74                         The advent of modern mouse genetics has benefited many fields of diseased-bas
75                                   The use of mouse genetics has changed this approach and has rejuven
76  by genome scans of multi-case families, and mouse genetics has contributed to mapping and identifica
77                                              Mouse genetics has made crucial contributions to the und
78                                              Mouse genetics has revived this holistic view of physiol
79                   Discoveries from human and mouse genetics have identified cytoskeletal and signalin
80                                              Mouse genetics have increased our understanding of how b
81                 Recent progress in human and mouse genetics have led to the identification of novel c
82                                        Using mouse genetics, histology, liver damage assays and trans
83        To study this critical function using mouse genetics, however, new reagents are needed that al
84                           Here, we have used mouse genetics, imaging and cell biology approaches to i
85                                  Advances in mouse genetics, in vivo imaging, and circuit tracing met
86                                        Using mouse genetics including females and males in our experi
87                                              Mouse genetics is a frequently used tool that allows dis
88                                  Critically, mouse genetics is a powerful tool for assessing the func
89 t of these pan-genomic mutational resources, mouse genetics is employing a range of diversity resourc
90 ystem that has been profoundly influenced by mouse genetics is skeletal physiology.
91                                              Mouse genetics, lineage tracing, confocal microscopy, an
92                               Together, with mouse genetics, optogenetics, physiology, morphology and
93                                        Using mouse genetics, our data reveal that in the complete abs
94                                        Using mouse genetics, physiological, anatomical, and behaviora
95 cale phenotyping projects such as the Sanger Mouse Genetics project are ongoing efforts to help ident
96  We describe a program, the Sanger Institute Mouse Genetics Project, that provides a step toward the
97 set from the Wellcome Trust Sanger Institute Mouse Genetics Project, where the treatment is a gene ab
98 se mutants generated by the Sanger Institute Mouse Genetics Project.
99                     Strategies using reverse mouse genetics provide excellent methods for validating
100 erve as a valuable practical resource in the mouse genetics research community, and also accelerate t
101     The Collaborative Cross (CC) is a robust mouse genetics resource comprised of a panel of recombin
102 o eliminate integrin binding in vitro, while mouse genetics revealed that FNRGE preserves alphav-clas
103             We validate key predictions with mouse genetics, showing the importance of endoderm-deriv
104                           Here, by combining mouse genetics, single-cell and spatial transcriptomics,
105       In this in vivo study, we used complex mouse genetics, single-cell dye tracing, and behavioral
106 is journey, including in vitro brain slices, mouse genetics, single-cell molecular genetics, pharmaco
107  devise genomics, in situ hybridization, and mouse genetics strategies to uncover diverse allelic eff
108                                We show using mouse genetics that zolpidem only needs to work on speci
109                Combining this technique with mouse genetics, the authors demonstrate that vesicle pri
110                                     Based on mouse genetics, the current model of melanophilin functi
111        In this study, we used intersectional mouse genetics to achieve single-cell type labeling and
112 o not negate the invaluable contributions of mouse genetics to biomedical science, but they do show t
113 , we used metabolomics, isotope tracing, and mouse genetics to define a role for liver mTORC1 signali
114  to mutant phenotypes and unlocks the use of mouse genetics to determine functions of orthologous hum
115                     To address this, we used mouse genetics to disrupt an ultra-conserved PE in the T
116        We establish a precedent for applying mouse genetics to dissect viral entry and validate the r
117                                 Here, we use mouse genetics to exploit mosaicism to study cell segreg
118  a combination of high-content screening and mouse genetics to identify the miR-34/449 family as key
119                         To enable the use of mouse genetics to investigate mechanisms underlying gang
120 e of Blood, Yan et al and Walz et al exploit mouse genetics to investigate the contribution of signal
121                              Here, we employ mouse genetics to investigate the functions of enteric s
122                                      We used mouse genetics to model how polygenic thresholds for the
123  use Vibrio cholerae neuraminidase (VCN) and mouse genetics to probe the molecular composition of the
124 eel, who have exploited the use of human and mouse genetics to revolutionize our understanding of the
125                               Here we employ mouse genetics to show that RA derived from the paraxial
126                                      We used mouse genetics to target Gipr expression within adipocyt
127                                      We used mouse genetics to test the hypothesis that genetic modif
128                          We used conditional mouse genetics to test the hypothesis that Purkinje cell
129 eir epithelial counterparts, we used in vivo mouse genetics tools to characterize four prostate strom
130                      We combined conditional mouse genetics, unbiased transcriptomic and epigenomic a
131                                        Using mouse genetics we demonstrate that female cells lacking
132 ing quantitative proteomics, lipidomics, and mouse genetics, we characterize epidermal barrier mainte
133 lution light-sheet imaging and cell-specific mouse genetics, we demonstrate presence of lymphatic ves
134 munohistochemistry, structural modeling, and mouse genetics, we demonstrate that all but one of the s
135                   By combining bacterial and mouse genetics, we demonstrate that C. difficile uses so
136                               Using compound mouse genetics, we discover CNOT3, a core component of t
137                         Through experimental mouse genetics, we dissect the lactation-specific distal
138 ughput approaches, cell culture, and in vivo mouse genetics, we dissected its roles in tissue regener
139                                        Using mouse genetics, we dissected the influence of IPC-derive
140                                        Using mouse genetics, we find that E47 is required for the reg
141                                        Using mouse genetics, we find that Pten and Tsc2 act synergist
142                                        Using mouse genetics, we found that AF pathophysiology caused
143                                        Using mouse genetics, we found that the balance between T-box
144                       By combining human and mouse genetics, we have uncovered a pathway that protect
145 ing a combination of functional genomics and mouse genetics, we identified a role for the transcripti
146                                        Using mouse genetics, we isolated two populations of dopamine-
147                                        Using mouse genetics, we show increasing Hedgehog signaling vi
148                                        Using mouse genetics, we show that expression of mutant TDP-43
149            Using in vivo calcium imaging and mouse genetics, we show that formalin- and prostaglandin
150                          Here, using in vivo mouse genetics, we show that increasing UBE3A in the nuc
151                Here, using NGS and human and mouse genetics, we show that influenza A virus (IAV) rib
152 ersw, three-dimensional (3D) microscopy, and mouse genetics, we show that LCs are situated at the end
153                                        Using mouse genetics, we show that the pleuroperitoneal folds
154                                        Using mouse genetics, we show that the status of Nkx6.1 expres
155                           Furthermore, using mouse genetics, we showed that CR cell density severely
156 13 issue of the JCI, Cutando et al. combined mouse genetics with classic mouse behavioral analysis to
157                                   We combine mouse genetics with optical imaging to show that the SV
158                                 By combining mouse genetics with quantitative positional analysis, we
159                                 By combining mouse genetics with single-cell and chromatin analyses,
160                                  Integrating mouse genetics with single-cell RNA sequencing and epige
161 n various biological contexts (e.g., cancer, mouse genetics, yeast genetics).
162 in various biological contexts, e.g. cancer, mouse genetics, yeast genetics, and analysis of brain im

 
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