Jeremy Nathans

Q: What Schools Are Affiliated With Jeremy Nathans

Jeremy Nathans is affiliated with the following schools: University of California, Santa Barbara, MD Anderson Cancer Center, University of Chicago, Stanford University, Massachusetts Institute of Technology, Johns Hopkins University, Harvard University

Jeremy Nathans's AcademicInfluence.com Rankings

Jeremy Nathans

Biology

#2527

World Rank

#3994

Historical Rank

#1128

USA Rank

Genetics

#418

World Rank

#484

Historical Rank

#182

USA Rank

biology Degrees

Download Badge

Biology

Jeremy Nathans's Degrees

Masters Medicine Harvard University

Why Is Jeremy Nathans Influential?

(Suggest an Edit or Addition)

According to Wikipedia, Jeremy Nathans is a professor of molecular biology and genetics at Johns Hopkins University. He is also a member of the National Academy of Sciences and an investigator of the Howard Hughes Medical Institute.

(See a Problem?)

Jeremy Nathans's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

A new member of the frizzled family from Drosophila functions as a Wingless receptor (1996) (1560)
Molecular genetics of human color vision: the genes encoding blue, green, and red pigments. (1986) (1546)
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy (1997) (1331)
Vascular Development in the Retina and Inner Ear Control by Norrin and Frizzled-4, a High-Affinity Ligand-Receptor Pair (2004) (797)
A new secreted protein that binds to Wnt proteins and inhibits their activites (1999) (739)
Molecular genetics of inherited variation in human color vision. (1986) (718)
Apoptotic photoreceptor cell death in mouse models of retinitis pigmentosa. (1994) (661)
Isolation, sequence analysis, and intron-exon arrangement of the gene encoding bovine rhodopsin (1983) (595)
Anterior-Posterior Guidance of Commissural Axons by Wnt-Frizzled Signaling (2003) (590)
A family of secreted proteins contains homology to the cysteine-rich ligand-binding domain of frizzled receptors. (1997) (584)
Epigenomic Signatures of Neuronal Diversity in the Mammalian Brain (2015) (541)
The Role of Frizzled3 and Frizzled6 in Neural Tube Closure and in the Planar Polarity of Inner-Ear Sensory Hair Cells (2006) (514)
A Member of the Frizzled Protein Family Mediating Axis Induction by Wnt-5A (1997) (514)
Rhodopsin mutations in autosomal dominant retinitis pigmentosa. (1991) (482)
Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa. (1991) (480)
The vitelliform macular dystrophy protein defines a new family of chloride channels (2002) (480)
Insights into Wnt binding and signalling from the structures of two Frizzled cysteine-rich domains (2001) (472)
Tissue/planar cell polarity in vertebrates: new insights and new questions (2007) (463)
Isolation and nucleotide sequence of the gene encoding human rhodopsin. (1984) (454)
The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons (1995) (428)
A Large Family of Putative Transmembrane Receptors Homologous to the Product of the Drosophila Tissue Polarity Gene frizzled(*) (1996) (402)
A locus control region adjacent to the human red and green visual pigment genes (1992) (395)
Norrin, Frizzled-4, and Lrp5 Signaling in Endothelial Cells Controls a Genetic Program for Retinal Vascularization (2009) (371)
Retinal Stimulates ATP Hydrolysis by Purified and Reconstituted ABCR, the Photoreceptor-specific ATP-binding Cassette Transporter Responsible for Stargardt Disease* (1999) (366)
Fibroblast growth factor (FGF) homologous factors: new members of the FGF family implicated in nervous system development. (1996) (365)
Biochemical characterization of Wnt-frizzled interactions using a soluble, biologically active vertebrate Wnt protein. (1999) (346)
POU domain factor Brn-3b is required for the development of a large set of retinal ganglion cells. (1996) (334)
A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment (1994) (334)
Absorption spectra of human cone pigments (1992) (333)
Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chain. (1993) (330)
The Evolution and Physiology of Human Color Vision Insights from Molecular Genetic Studies of Visual Pigments (1999) (313)
Frizzled6 controls hair patterning in mice. (2004) (310)
Essential role of POU-domain factor Brn-3c in auditory and vestibular hair cell development. (1997) (308)
Determinants of visual pigment absorbance: identification of the retinylidene Schiff's base counterion in bovine rhodopsin. (1990) (290)
Norrin/Frizzled4 Signaling in Retinal Vascular Development and Blood Brain Barrier Plasticity (2012) (287)
Frizzled-3 Is Required for the Development of Major Fiber Tracts in the Rostral CNS (2002) (281)
Molecular genetics of human blue cone monochromacy. (1989) (279)
A Novel Signaling Pathway from Rod Photoreceptors to Ganglion Cells in Mammalian Retina (1998) (278)
The Rod Photoreceptor-Specific Nuclear Receptor Nr2e3 Represses Transcription of Multiple Cone-Specific Genes (2005) (260)
A Noninvasive Genetic/Pharmacologic Strategy for Visualizing Cell Morphology and Clonal Relationships in the Mouse (2003) (258)
Stargardt's ABCR is localized to the disc membrane of retinal rod outer segments (1997) (251)
Targeted deletion of the mouse POU domain gene Brn-3a causes selective loss of neurons in the brainstem and trigeminal ganglion, uncoordinated limb movement, and impaired suckling. (1996) (242)
Quantitative analysis of neuronal morphologies in the mouse retina visualized by using a genetically directed reporter (2004) (241)
Canonical WNT signaling components in vascular development and barrier formation. (2014) (234)
Molecular genetics of human retinal disease. (1999) (232)
Distinct Roles of Transcription Factors Brn3a and Brn3b in Controlling the Development, Morphology, and Function of Retinal Ganglion Cells (2009) (231)
Structure-Function Analysis of the Bestrophin Family of Anion Channels* (2003) (228)
Macular degeneration: recent advances and therapeutic opportunities (2006) (218)
Determinants of visual pigment absorbance: role of charged amino acids in the putative transmembrane segments. (1990) (215)
Brn-3b: a POU domain gene expressed in a subset of retinal ganglion cells (1993) (212)
Biochemical defects in ABCR protein variants associated with human retinopathies (2000) (204)
Rhodopsin: structure, function, and genetics. (1992) (199)
Gpr124 controls CNS angiogenesis and blood-brain barrier integrity by promoting ligand-specific canonical wnt signaling. (2014) (198)
Unusual topography of bovine rhodopsin promoter-IacZ fusion gene expression in transgenic mouse retinas (1991) (197)
Identification and Characterization of All-trans-retinol Dehydrogenase from Photoreceptor Outer Segments, the Visual Cycle Enzyme That Reduces All-trans-retinal to All-trans-retinol* (2000) (195)
Genetic heterogeneity among blue-cone monochromats. (1993) (193)
Molecular biology of visual pigments. (1987) (192)
The Genomic Response to Retinal Disease and Injury: Evidence for Endothelin Signaling from Photoreceptors to Glia (2005) (189)
Tip cell-specific requirement for an atypical Gpr124- and Reck-dependent Wnt/β-catenin pathway during brain angiogenesis (2015) (186)
Mechanisms of spectral tuning in the mouse green cone pigment. (1997) (185)
Absorption spectra of the hybrid pigments responsible for anomalous color vision. (1992) (185)
Emergence of Novel Color Vision in Mice Engineered to Express a Human Cone Photopigment (2007) (180)
Molecular genetics of human visual pigments. (1992) (179)
Cellular Resolution Maps of X Chromosome Inactivation: Implications for Neural Development, Function, and Disease (2014) (171)
Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations. (1991) (167)
Frizzled and Dfrizzled-2 function as redundant receptors for Wingless during Drosophila embryonic development. (1999) (166)
Molecular structure of a double helical DNA fragment intercalator complex between deoxy CpG and a terpyridine platinum compound (1978) (162)
Tandem array of human visual pigment genes at Xq28. (1988) (159)
Cloning and expression of goldfish opsin sequences. (1993) (157)
Human rod photoreceptor cGMP-gated channel: amino acid sequence, gene structure, and functional expression (1992) (155)
Transcriptional and epigenomic landscapes of CNS and non-CNS vascular endothelial cells (2018) (155)
Class 5 Transmembrane Semaphorins Control Selective Mammalian Retinal Lamination and Function (2011) (155)
Progressive Cerebellar, Auditory, and Esophageal Dysfunction Caused by Targeted Disruption of thefrizzled-4 Gene (2001) (152)
Peropsin, a novel visual pigment-like protein located in the apical microvilli of the retinal pigment epithelium. (1997) (148)
The Norrin/Frizzled4 signaling pathway in retinal vascular development and disease. (2010) (144)
Red, Green, and Red-Green Hybrid Pigments in the Human Retina: Correlations between Deduced Protein Sequences and Psychophysically Measured Spectral Sensitivities (1998) (142)
Role of a locus control region in the mutually exclusive expression of human red and green cone pigment genes (2002) (141)
Climate change and the integrity of science. (2010) (137)
Frizzled 1 and frizzled 2 genes function in palate, ventricular septum and neural tube closure: general implications for tissue fusion processes (2010) (136)
Frizzled 2 and frizzled 7 function redundantly in convergent extension and closure of the ventricular septum and palate: evidence for a network of interacting genes (2012) (135)
ROLE OF HYDROXYL‐BEARING AMINO ACIDS IN DIFFERENTIALLY TUNING THE ABSORPTION SPECTRA OF THE HUMAN RED AND GREEN CONE PIGMENTS (1993) (133)
Axonal Growth and Guidance Defects in Frizzled3 Knock-Out Mice: A Comparison of Diffusion Tensor Magnetic Resonance Imaging, Neurofilament Staining, and Genetically Directed Cell Labeling (2006) (129)
An MRI-based atlas and database of the developing mouse brain (2011) (126)
Epigenomic landscapes of retinal rods and cones (2016) (121)
A Photoreceptor-Specific Cadherin Is Essential for the Structural Integrity of the Outer Segment and for Photoreceptor Survival (2001) (119)
Complete morphologies of basal forebrain cholinergic neurons in the mouse (2014) (117)
Reck and Gpr124 Are Essential Receptor Cofactors for Wnt7a/Wnt7b-Specific Signaling in Mammalian CNS Angiogenesis and Blood-Brain Barrier Regulation (2017) (115)
The Optokinetic Reflex as a Tool for Quantitative Analyses of Nervous System Function in Mice: Application to Genetic and Drug-Induced Variation (2008) (111)
Estrogen-related receptor beta/NR3B2 controls epithelial cell fate and endolymph production by the stria vascularis. (2007) (111)
Histidine residues regulate the transition of photoexcited rhodopsin to its active conformation, metarhodopsin II (1992) (111)
Mutational Analysis of Norrin-Frizzled4 Recognition* (2006) (110)
Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa. (1994) (106)
Genetically engineered mice with an additional class of cone photoreceptors: Implications for the evolution of color vision (2003) (99)
Sequence variation in the androgen receptor gene is not a common determinant of male sexual orientation. (1993) (98)
ABCR, the ATP-binding Cassette Transporter Responsible for Stargardt Macular Dystrophy, Is an Efficient Target of All-trans-retinal-mediated Photooxidative Damage in Vitro (2001) (96)
Mutually exclusive expression of human red and green visual pigment-reporter transgenes occurs at high frequency in murine cone photoreceptors. (1999) (93)
Frizzled Receptors in Development and Disease. (2016) (93)
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin. (1992) (92)
Human tritanopia associated with a third amino acid substitution in the blue-sensitive visual pigment. (1992) (90)
Morphologies of mouse retinal ganglion cells expressing transcription factors Brn3a, Brn3b, and Brn3c: Analysis of wild type and mutant cells using genetically-directed sparse labeling (2011) (90)
Isoform Diversity among Fibroblast Growth Factor Homologous Factors Is Generated by Alternative Promoter Usage and Differential Splicing* (2000) (90)
Order from disorder: Self-organization in mammalian hair patterning (2006) (86)
Interplay of the Norrin and Wnt7a/Wnt7b signaling systems in blood–brain barrier and blood–retina barrier development and maintenance (2018) (84)
New Mouse Lines for the Analysis of Neuronal Morphology Using CreER(T)/loxP-Directed Sparse Labeling (2009) (84)
An essential role for frizzled 5 in mammalian ocular development (2008) (83)
Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation. (1992) (82)
Production of bovine rhodopsin by mammalian cell lines expressing cloned cDNA: Spectrophotometry and subcellular localization (1989) (81)
Roles of HIFs and VEGF in angiogenesis in the retina and brain. (2019) (77)
Organization of the ABCR gene: analysis of promoter and splice junction sequences. (1998) (76)
Cloning and nucleotide sequence of DNA coding for bovine preproparathyroid hormone. (1979) (76)
The evolution of Primate color vision. (2009) (72)
The genes for color vision. (1989) (70)
Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements. (2006) (70)
Functional Assembly of Accessory Optic System Circuitry Critical for Compensatory Eye Movements (2015) (69)
Combinatorial Expression of Brn3 Transcription Factors in Somatosensory Neurons: Genetic and Morphologic Analysis (2012) (67)
Insertional mutagenesis as a probe of rhodopsin's topography, stability, and activity. (1994) (67)
Rhodopsin activation: effects on the metarhodopsin I-metarhodopsin II equilibrium of neutralization or introduction of charged amino acids within putative transmembrane segments. (1993) (66)
Retina-derived POU-domain factor-1: a complex POU-domain gene implicated in the development of retinal ganglion and amacrine cells (1996) (66)
Sox7, Sox17, and Sox18 Cooperatively Regulate Vascular Development in the Mouse Retina (2015) (65)
Signaling by sensory receptors. (2012) (65)
Genetically-Directed, Cell Type-Specific Sparse Labeling for the Analysis of Neuronal Morphology (2008) (64)
An Essential Role for Frizzled5 in Neuronal Survival in the Parafascicular Nucleus of the Thalamus (2008) (64)
Frizzled3 is required for the development of multiple axon tracts in the mouse central nervous system (2014) (63)
Murine and bovine blue cone pigment genes: cloning and characterization of two new members of the S family of visual pigments. (1994) (62)
A sequence upstream of the mouse blue visual pigment gene directs blue cone-specific transgene expression in mouse retinas (1994) (61)
Beta-catenin signaling regulates barrier-specific gene expression in circumventricular organ and ocular vasculatures (2019) (61)
Mechanistic Studies of ABCR, the ABC Transporter in Photoreceptor Outer Segments Responsible for Autosomal Recessive Stargardt Disease (2001) (60)
Four novel mutations in the RPE65 gene in patients with Leber congenital amaurosis (2001) (58)
Expression of the Norrie disease gene (Ndp) in developing and adult mouse eye, ear, and brain. (2011) (58)
A strabismus susceptibility locus on chromosome 7p (2003) (57)
Ca2+-activated Cl− Current from Human Bestrophin-4 in Excised Membrane Patches (2006) (56)
Reck and Gpr124 Are Essential Receptor Cofactors for Wnt7a/Wnt7b-Specific Signaling in Mammalian CNS Angiogenesis and Blood-Brain Barrier Regulation (2017) (55)
An Outer Segment Localization Signal at the C Terminus of the Photoreceptor-Specific Retinol Dehydrogenase (2004) (53)
Morphologic diversity of cutaneous sensory afferents revealed by genetically directed sparse labeling (2012) (53)
Genetic mosaic analysis reveals a major role for frizzled 4 and frizzled 8 in controlling ureteric growth in the developing kidney (2011) (52)
Role of the Brn-3 family of POU-domain genes in the development of the auditory/vestibular, somatosensory, and visual systems. (1997) (52)
Molecular biology of retinal ganglion cells. (1996) (51)
Blue cones and cone bipolar cells share transcriptional specificity as determined by expression of human blue visual pigment-derived transgenes (1994) (51)
cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeat. (1996) (51)
A visual pigment from chicken that resembles rhodopsin: amino acid sequence, gene structure, and functional expression. (1992) (49)
When whorls collide: the development of hair patterns in frizzled 6 mutant mice (2010) (49)
In the eye of the beholder: Visual pigments and inherited variation in human vision (1994) (48)
The Genomic Response of the Retinal Pigment Epithelium to Light Damage and Retinal Detachment (2008) (47)
Frizzled3 controls axonal development in distinct populations of cranial and spinal motor neurons (2013) (47)
Proteolytic Shedding of the Extracellular Domain of Photoreceptor Cadherin (2004) (46)
Identification and characterization of a conserved family of protein serine/threonine phosphatases homologous to Drosophila retinal degeneration C (rdgC) (1997) (45)
Expression of chicken fibroblast growth factor homologous factor (FHF)-1 and of differentially spliced isoforms of FHF-2 during development and involvement of FHF-2 in chicken limb development. (1999) (44)
Spectral sensitivities of human cone visual pigments determined in vivo and in vitro. (2000) (44)
What can we learn about age-related macular degeneration from other retinal diseases? (1999) (42)
Rac1 plays an essential role in axon growth and guidance and in neuronal survival in the central and peripheral nervous systems (2015) (40)
Genetic ablation of cone photoreceptors eliminates retinal folds in the retinal degeneration 7 (rd7) mouse. (2007) (39)
Hypoxia tolerance in the Norrin-deficient retina and the chronically hypoxic brain studied at single-cell resolution (2019) (36)
How scientists can reduce their carbon footprint (2016) (35)
Response to Comment on "Emergence of Novel Color Vision in Mice Engineered to Express a Human Cone Photopigment" (2007) (35)
Endothelin-2 signaling in the neural retina promotes the endothelial tip cell state and inhibits angiogenesis (2013) (34)
Responses of hair follicle–associated structures to loss of planar cell polarity signaling (2013) (34)
Erratum: Reck and Gpr124 Are Essential Receptor Cofactors for Wnt7a/Wnt7b-Specific Signaling in Mammalian CNS Angiogenesis and Blood-Brain Barrier Regulation (Neuron (2017) 95 (5)(1056–1073.e5) (S0896627317306797) (10.1016/j.neuron.2017.07.031)) (2017) (33)
Individual variation in size of the human red and green visual pigment gene array. (1997) (33)
The spatio-temporal domains of Frizzled6 action in planar polarity control of hair follicle orientation. (2016) (32)
A genome-wide view of the de-differentiation of central nervous system endothelial cells in culture (2020) (32)
Normal Light Response, Photoreceptor Integrity, and Rhodopsin Dephosphorylation in Mice Lacking Both Protein Phosphatases with EF Hands (PPEF-1 and PPEF-2) (2001) (32)
Proximal and Distal Sequences Control UV Cone Pigment Gene Expression in Transgenic Zebrafish* (2004) (31)
The challenge of macular degeneration. (2001) (30)
Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura. (2017) (29)
The role of the hypoxia response in shaping retinal vascular development in the absence of Norrin/Frizzled4 signaling. (2014) (28)
Partial interchangeability of Fz3 and Fz6 in tissue polarity signaling for epithelial orientation and axon growth and guidance (2014) (27)
Comprehensive analysis of a mouse model of spontaneous uveoretinitis using single-cell RNA sequencing (2019) (27)
ABCR: rod photoreceptor-specific ABC transporter responsible for Stargardt disease. (2000) (26)
Molecular determinants in Frizzled, Reck, and Wnt7a for ligand-specific signaling in neurovascular development (2019) (24)
L, M and L–M hybrid cone photopigments in man: deriving λ max from flicker photometric spectral sensitivities (1999) (24)
Cellular and Subcellular Localization, N-terminal Acylation, and Calcium Binding of Caenorhabditis elegans Protein Phosphatase with EF-hands* (2001) (21)
Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347. (1995) (18)
Identification of Astrotactin2 as a Genetic Modifier That Regulates the Global Orientation of Mammalian Hair Follicles (2015) (17)
Patterning of papillae on the mouse tongue: A system for the quantitative assessment of planar cell polarity signaling. (2016) (17)
Identification and characterization of a conserved family of protein serine/threonine phosphatases homologous to Drosophila retinal degeneration C. (1997) (17)
A mouse model for Kinesin Family Member 11 (Kif11)-associated familial exudative vitreoretinopathy. (2020) (16)
The Norrin / Frizzled 4 signaling pathway in retinal vascular development and disease (2010) (16)
Expression and regulation of chicken fibroblast growth factor homologous factor (FHF)-4 at the base of the developing limbs (2000) (15)
Flat mount imaging of mouse skin and its application to the analysis of hair follicle patterning and sensory axon morphology. (2014) (15)
Similarities and differences among inner retinal neurons revealed by the expression of reporter transgenes controlled by Brn-3a, Brn-3b, and Brn-3c promotor sequences (1996) (15)
PHOTOBLEACHING DIFFERENCE ABSORPTION SPECTRA OF HUMAN CONE PIGMENTS: QUANTITATIVE ANALYSIS AND COMPARISON TO OTHER METHODS (1992) (14)
Expression and regulation of chicken fibroblast growth factor homologous factor (FHF)‐4 during craniofacial morphogenesis (2001) (14)
Peropsin modulates transit of vitamin A from retina to retinal pigment epithelium (2017) (12)
An evolutionary perspective on the photoreceptor damage response. (2006) (12)
Autosomal dominant retinitis pigmentosa in a large family: a clinical and molecular genetic study. (1994) (11)
Visual pigments and inherited variation in human vision. (1992) (11)
Bovine pancreatic trypsin inhibitor-trypsin complex as a detection system for recombinant proteins. (1993) (10)
Preclinical assessment of CNS drug action using eye movements in mice. (2011) (9)
Dlg1 activates beta-catenin signaling to regulate retinal angiogenesis and the blood-retina and blood-brain barriers (2019) (8)
L, M and L-M hybrid cone photopigments in man: deriving lambda max from flicker photometric spectral sensitivities. (1999) (8)
Affinity capture of polyribosomes followed by RNAseq (ACAPseq), a discovery platform for protein-protein interactions (2018) (7)
Protein-chromophore interactions in rhodopsin studied by site-directed mutagenesis. (1990) (7)
Author response: Transcriptional and epigenomic landscapes of CNS and non-CNS vascular endothelial cells (2018) (7)
Effects of L 1 retrotransposon insertion on transcript processing , localization and accumulation : lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L 1 elements (2006) (7)
The Evolution and Physiology of Human Review Color Vision : Insights from Molecular Genetic Studies of Visual Pigments (1999) (6)
Intramembrane Proteolysis of Astrotactins* (2017) (6)
Author response: Beta-catenin signaling regulates barrier-specific gene expression in circumventricular organ and ocular vasculatures (2019) (6)
Structure of the RECK CC domain, an evolutionary anomaly (2020) (5)
THE CELLULAR COMPASS. (2016) (5)
How to draw the line in biomedical research (2013) (5)
Color Vision : How Our Eyes Reflect Primate Evolution Analyses of primate visual pigments show that our color vision evolved in an unusual way and that the brain is more adaptable than generally thought (2009) (4)
Signaling Pathways in Neurovascular Development. (2022) (4)
Author response: Tip cell-specific requirement for an atypical Gpr124- and Reck-dependent Wnt/β-catenin pathway during brain angiogenesis (2015) (4)
A transcriptome atlas of the mouse iris at single cell resolution defines cell types and the genomic response to pupil dilation (2021) (3)
Defining the binding interface of Amyloid Precursor Protein (APP) and Contactin3 (CNTN3) by site-directed mutagenesis (2019) (3)
The Ca 2 + -activated Cl − Current from Human Bestrophin-4 in Excised Membrane Patches (2006) (3)
Analysis of light–mediated damage in mice lacking protein phosphatases with EF–hands (PPEF–1 and PPEF–2) (2004) (3)
Signaling Mechanisms Controlling Cell Fate and Embryonic Patterning Subject Collection Signal Transduction The Hippo Pathway (2012) (3)
Developmental, cellular, and behavioral phenotypes in a mouse model of congenital hypoplasia of the dentate gyrus (2020) (2)
The WNT7A/WNT7B/GPR124/RECK signaling module plays an essential role in mammalian limb development (2022) (1)
The Rod Photoreceptor-specific Phosphatase PPEF-2 Interacts with 14-3-3 zeta in a Phosphorylation-dependent Manner (2002) (1)
China's plan flawed but courageous. (2010) (1)
Author response: Complete morphologies of basal forebrain cholinergic neurons in the mouse (2014) (1)
Norrin, Frizzled-4, and Lrp5 Signaling in Endothelial Cells Controls a Genetic Program for Retinal Vascularization (2010) (1)
Quantitative phenotype characterization of developing mouse brains by diffusion tensor imaging : Application for the Frizzled-4-/-mutant mice (2008) (1)
Erratum: A strabismus susceptibility locus on chromosome 7p (Proceedings of the National Academy of Sciences of the United States of America (October 14, 2003) 100, 21 (12283-12288)) (2004) (1)
What can we learn about AMD from other retinal diseases ? (1999) (1)
A transcriptome atlas of the mouse iris at single-cell resolution defines cell types and the genomic response to pupil dilation (2021) (1)
Author response: Frizzled3 controls axonal development in distinct populations of cranial and spinal motor neurons (2013) (1)
Population growth: Help to make food go further in Egypt (2017) (1)
Section 2 L , M and L – M hybrid cone photopigments in man : deriving l max from flicker photometric spectral sensitivities (1999) (1)
Correction: Interplay of the Norrin and Wnt7a/Wnt7b signaling systems in blood–brain barrier and blood–retina barrier development and maintenance (Proceedings of the National Academy of Sciences of the United States of America (2018) 115 (E11827–E11836) DOI: 10.1073/pnas.1813217115) (2019) (1)
Rhodopsin Gene Mutations Causing Retinitis Pigmentosa (1995) (1)
Ganglion cell response properties in the coneless retina of a transgenic mouse (1996) (1)
A New Cl Channel Family Defined by Vitelliform Macular Dystrophy (2003) (0)
Defining the Binding Interaction between Contactin3 and Amyloid Precursor Protein (2018) (0)
Genetics Provides a Window on Human Individuality (2018) (0)
An Evaluation of the Inner Ear in Brn-3c Knockout Mutant Mice (1997) (0)
G-Protein Modulation of Vesicular Glutamate Transport (2005) (0)
CRYSTAL STRUCTURE OF THE CYSTEINE-RICH DOMAIN OF MOUSE FRIZZLED 8 (MFZ8) (2001) (0)
Erratum: A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment (Journal of Neuroscience (October 1994) (5818-5833)) (1995) (0)
Author response: Molecular determinants in Frizzled, Reck, and Wnt7a for ligand-specific signaling in neurovascular development (2019) (0)
Rac1 plays an essential role in axon growth and guidance and in neuronal survival in the central and peripheral nervous systems (2015) (0)
The fibroblast growth factor homologous factor-1 (fhf-1) and methods for its use (1996) (0)
Author response: Dlg1 activates beta-catenin signaling to regulate retinal angiogenesis and the blood-retina and blood-brain barriers (2019) (0)
Author response: Morphologic diversity of cutaneous sensory afferents revealed by genetically directed sparse labeling (2012) (0)
MOLECULAR BIOPHYSICS OF SENSORY PHENOMENA (2005) (0)
Sequences d'acides nucleiques pour transporteur a cassette de fixation a l'atp (1998) (0)
Post-receptoral rod and cone abnormalities in retinitis pigmentosa caused by rhodopsin gene mutations (1996) (0)
Author response: A transcriptome atlas of the mouse iris at single-cell resolution defines cell types and the genomic response to pupil dilation (2021) (0)
TO fibroblast growth factor HOMOLOGOUS FACTORS (FHFs) AND METHOD OF ADMINISTRATION (1997) (0)
CRYSTAL STRUCTURE OF THE CYSTEINE-RICH DOMAIN OF SECRETED FRIZZLED-RELATED PROTEIN 3 (SFRP-3;FZB) (2001) (0)
The Evolution of Primate Color Vision Analyses of primate visual pigments show that our color vision evolved in an unusual way and that the brain is more adaptable than generally thought (2009) (0)
Wnt-frizzled Signaling in Retinal Optic Disc Formation and Adult Retina Degeneration (2009) (0)
Title Peropsin modulates transit of vitamin A from retina to retinal pigment epithelium Permalink (2017) (0)
Bacterial meningitis in the early postnatal mouse studied at single-cell resolution (2023) (0)
Structural insights into plasmalemma vesicle-associated protein (PLVAP): Implications for vascular endothelial diaphragms and fenestrae (2023) (0)
Control of a Brain Stem Motor Program Activation of Nucleus Basalis Facilitates Cortical (2015) (0)
Human Cone Photopigment Emergence of Novel Color Vision in Mice Engineered to Express a (2012) (0)
Written in Our Genes? (2005) (0)
Author response: Epigenomic landscapes of retinal rods and cones (2015) (0)
Author response: Affinity capture of polyribosomes followed by RNAseq (ACAPseq), a discovery platform for protein-protein interactions (2018) (0)
Author response: A genome-wide view of the de-differentiation of central nervous system endothelial cells in culture (2019) (0)
Distinct protective cell type-specific responses induced by chronic hypoxia in a mouse model of retinal hypovascularization revealed by single-cell RNAseq and metabolic profiling (2018) (0)
Crystal structure of mRECK(CC4) in fusion with engineered MBP at medium resolution (2020) (0)
High resolution crystal structure of mRECK(CC4) in fusion with engineered MBP (2020) (0)

This paper list is powered by the following services:

Other Resources About Jeremy Nathans

en.wikipedia.org

What Schools Are Affiliated With Jeremy Nathans?

Jeremy Nathans is affiliated with the following schools:

Jeremy Nathans's Academic­Influence.com Rankings