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Research | 7 November 1973
Identification of tRNA Precursor Molecules made by Phage T4
- CHRISTINE GUTHRIE
- , J. G. SEIDMAN
- , S. ALTMAN
- , B. G. BARRELL
- , J. D. SMITH
- & W. H. McCLAIN
Nature New Biology 246 , 6–11

Rights & permissionsfor article Identification of tRNA Precursor Molecules made by Phage T4 . Opens in a new window.
Research | 24 September 2020 | Open
Cells of the adult human heart
- Monika Litviňuková
- , Carlos Talavera-López
- , Henrike Maatz
- , Daniel Reichart
- , Catherine L. Worth
- , Eric L. Lindberg
- , Masatoshi Kanda
- , Krzysztof Polanski
- , Matthias Heinig
- , Michael Lee
- , Emily R. Nadelmann
- , Kenny Roberts
- , Liz Tuck
- , Eirini S. Fasouli
- , Daniel M. DeLaughter
- , Barbara McDonough
- , Hiroko Wakimoto
- , Joshua M. Gorham
- , Sara Samari
- , Krishnaa T. Mahbubani
- , Kourosh Saeb-Parsy
- , Giannino Patone
- , Joseph J. Boyle
- , Hongbo Zhang
- , Hao Zhang
- , Anissa Viveiros
- , Gavin Y. Oudit
- , Omer Ali Bayraktar
- , J. G. Seidman
- , Christine E. Seidman
- , Michela Noseda
- , Norbert Hubner
- & Sarah A. Teichmann
Nature 588 , 466–472

Rights & permissionsfor article Cells of the adult human heart . Opens in a new window.
Correspondence | 28 September 2018
Response to Brodehl et al.
- Andre E. Minoche
- , Claire Horvat
- , Renee Johnson
- , Velimir Gayevskiy
- , Sarah U. Morton
- , Alexander P. Drew
- , Kerhan Woo
- , Aaron L. Statham
- , Ben Lundie
- , Richard D. Bagnall
- , Jodie Ingles
- , Christopher Semsarian
- , J. G. Seidman
- , Christine E. Seidman
- , Marcel E. Dinger
- , Mark J. Cowley
- & Diane Fatkin
Genetics in Medicine 21 , 1248–1249

Rights & permissionsfor article Response to Brodehl et al. . Opens in a new window.
Correspondence | 1 February 1999
QTL influencing autoimmune diabetes and encephalomyelitis map to a 0.15-cM region containing Il2
Nature Genetics 21 , 158–160

Rights & permissionsfor article QTL influencing autoimmune diabetes and encephalomyelitis map to a 0.15-cM region containing <i>Il2</i> . Opens in a new window.
Amendments and Corrections | 1 April 1997
Erratum: Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome
- Craig T. Basson
- , David R. Bachinsky
- , Robert C. Lin
- , Tatjana Levi
- , Jacob A. Elkins
- , Johann Soults
- , David Grayzel
- , Elena Kroumpouzou
- , Thomas A. Traill
- , Janine Leblanc-Straceski
- , Beatrice Renault
- , Raju Kucherlapati
- , J.G. Seidman
- & Christine E. Seidman
Nature Genetics 15 , 411–411

Rights & permissionsfor article Erratum: Mutations in human <i>TBX5</i> cause limb and cardiac malformation in Holt-Oram syndrome . Opens in a new window.
Research | 20 May 2020
poly(UG)-tailed RNAs in genome protection and epigenetic inheritance
- Aditi Shukla
- , Jenny Yan
- , Daniel J. Pagano
- , Anne E. Dodson
- , Yuhan Fei
- , Josh Gorham
- , J. G. Seidman
- , Marvin Wickens
- & Scott Kennedy
Nature 582 , 283–288

Rights & permissionsfor article poly(UG)-tailed RNAs in genome protection and epigenetic inheritance . Opens in a new window.
22 January 2015
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity
- Ahmed A. Alfares
- , Melissa A. Kelly
- , Gregory McDermott
- , Birgit H. Funke
- , Matthew S. Lebo
- , Samantha B. Baxter
- , Jun Shen
- , Heather M. McLaughlin
- , Eugene H. Clark
- , Larry J. Babb
- , Stephanie W. Cox
- , Steven R. DePalma
- , Carolyn Y. Ho
- , J. G. Seidman
- , Christine E. Seidman
- & Heidi L. Rehm
Genetics in Medicine 17 , 880–888

Rights & permissionsfor article Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity . Opens in a new window.
Research | 1 July 1997
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
- Michael Bamshad
- , Robert C. Lin
- , David J. Law
- , W. Scott Watkins
- , Patrycja A. Krakowiak
- , Mary E. Moore
- , Piergiorgio Franceschini
- , Roberto Lala
- , Lewis B. Holmes
- , Tom C. Gebuhr
- , Benoit G. Bruneau
- , Albert Schinzel
- , J. G. Seidman
- , Christine E. Seidman
- & Lynn B. Jorde
Nature Genetics 16 , 311–315

Rights & permissionsfor article Mutations in human <i>TBX3</i> alter limb, apocrine and genital development in ulnar-mammary syndrome . Opens in a new window.
Research | 1 February 1994
A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3
- Claire L. Shovlin
- , J.M.B. Hughes
- , E.G.D. Tuddenham
- , I. Temperley
- , Y.F.N. Perembelon
- , J. Scott
- , Christine E. Seidman
- & J.G. Seidman
Nature Genetics 6 , 205–209

Rights & permissionsfor article A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3 . Opens in a new window.
Research | 1 August 1985
Human γ-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7
Nature 316 , 549–552

Rights & permissionsfor article Human γ-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7 . Opens in a new window.
Research | 1 April 1993
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3
- Hugh Watkins
- , Calum MacRae
- , Ludwig Thierfelder
- , Yah-Huei Chou
- , Michael Frenneaux
- , William McKenna
- , J.G. Seidman
- & Christine E. Seidman
Nature Genetics 3 , 333–337

Rights & permissionsfor article A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3 . Opens in a new window.
Research | 10 July 1986
Human T-cell γ genes contain N segments and have marked junctional variability
Nature 322 , 184–187

Rights & permissionsfor article Human T-cell <i>γ</i> genes contain <i>N</i> segments and have marked junctional variability . Opens in a new window.
Research | 11 September 2011
Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1
- Scott A LeMaire
- , Merry-Lynn N McDonald
- , Dong-chuan Guo
- , Ludivine Russell
- , Charles C Miller III
- , Ralph J Johnson
- , Mir Reza Bekheirnia
- , Luis M Franco
- , Mary Nguyen
- , Reed E Pyeritz
- , Joseph E Bavaria
- , Richard Devereux
- , Cheryl Maslen
- , Kathryn W Holmes
- , Kim Eagle
- , Simon C Body
- , Christine Seidman
- , J G Seidman
- , Eric M Isselbacher
- , Molly Bray
- , Joseph S Coselli
- , Anthony L Estrera
- , Hazim J Safi
- , John W Belmont
- , Suzanne M Leal
- & Dianna M Milewicz
Nature Genetics 43 , 996–1000

Rights & permissionsfor article Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning <i>FBN1</i> at 15q21.1 . Opens in a new window.
Research | 14 January 2002
Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy
- Brenda Gerull
- , Michael Gramlich
- , John Atherton
- , Mark McNabb
- , Karoly Trombitás
- , Sabine Sasse-Klaassen
- , J.G. Seidman
- , Christine Seidman
- , Henk Granzier
- , Siegfried Labeit
- , Michael Frenneaux
- & Ludwig Thierfelder
Nature Genetics 30 , 201–204

Rights & permissionsfor article Mutations of <i>TTN</i>, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy . Opens in a new window.
Research | 14 January 1982
H–2-like genes in the Tla region of mouse chromosome 17
Nature 295 , 168–170

Rights & permissionsfor article <i>H–2</i>-like genes in the <i>Tla</i> region of mouse chromosome 17 . Opens in a new window.
Research | 1 August 1980
A mutant immunoglobulin light chain is formed by aberrant DNA- and RNA-splicing events
- J. G. Seidman
- & Philip Leder
Nature 286 , 779–783

Rights & permissionsfor article A mutant immunoglobulin light chain is formed by aberrant DNA- and RNA-splicing events . Opens in a new window.
Research | 24 August 2011
Brazilian urban population genetic structure reveals a high degree of admixture
European Journal of Human Genetics 20 , 111–116

Rights & permissionsfor article Brazilian urban population genetic structure reveals a high degree of admixture . Opens in a new window.
Research | 1 March 1999
The pathogenesis of familial hypertrophic cardiomyopathy: Early and evolving effects from an α-cardiac myosin heavy chain missense mutation
Nature Medicine 5 , 327–330

Rights & permissionsfor article The pathogenesis of familial hypertrophic cardiomyopathy: Early and evolving effects from an α-cardiac myosin heavy chain missense mutation . Opens in a new window.
Research | 1 November 1994
Autosomal dominant hypocalcaemia caused by a Ca²⁺-sensing receptor gene mutation
- Martin R. Pollak
- , Edward M. Brown
- , Herschel L. Estep
- , Peter N. McLaine
- , Olga Kifor
- , Ji Park
- , Steven C. Hebert
- , Christine E. Seidman
- & J. G. Seidman
Nature Genetics 8 , 303–307

Rights & permissionsfor article Autosomal dominant hypocalcaemia caused by a Ca<sup>2+</sup>-sensing receptor gene mutation . Opens in a new window.
Research | 1 December 1995
A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
- Chrystal Ho
- , David A. Conner
- , Martin R. Pollak
- , Daniel J. Ladd
- , Olga Kifor
- , Henry B. Warren
- , Edward M. Brown
- , J.G. Seidman
- & Christine E. Seidman
Nature Genetics 11 , 389–394

Rights & permissionsfor article A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism . Opens in a new window.
Research | 1 March 1994
A complex bilateral polysyndactyly disease locus maps to chromosome 7q36
- Olga Tsukurov
- , Annemie Boehmer
- , Jack Flynn
- , Jean-Philippe Nicolai
- , Ben C. J. Hamel
- , Saskia Traill
- , David Zaleske
- , Henry J. Mankin
- , Howard Yeon
- , Chrystal Ho
- , Cliff Tabin
- , J. G. Seidman
- & Christine Seidman
Nature Genetics 6 , 282–286

Rights & permissionsfor article A complex bilateral polysyndactyly disease locus maps to chromosome 7q36 . Opens in a new window.
Research | 29 November 1984
Two steroid 21-hydroxylase genes are located in the murine S region
- Perrin C. White
- , David D. Chaplin
- , John H. Weis
- , Bo Dupont
- , Maria I. New
- & J. G. Seidman
Nature 312 , 465–467

Rights & permissionsfor article Two steroid 21-hydroxylase genes are located in the murine <i>S</i> region . Opens in a new window.
Research | 5 April 1984
Nucleotide sequence of mutant I-Aβ^bm12 gene is evidence for genetic exchange between mouse immune response genes
- Katherine R. McIntyre
- & J. G. Seidman
Nature 308 , 551–553

Rights & permissionsfor article Nucleotide sequence of mutant <i>I-Aβ</i><sup>bm12</sup> gene is evidence for genetic exchange between mouse immune response genes . Opens in a new window.
Research | 1 November 1998
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
Nature Genetics 20 , 299–303

Rights & permissionsfor article Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction . Opens in a new window.
Research | 1 March 1987
Characterization of an expressed CDS-associated Ti γ-chain reveals C_γ domain polymorphism
- Dan R. Littman
- , Marianne Newton
- , Deirdre Crommie
- , Siew-Lan Ang
- , J. G. Seidman
- , Sonya N. Gettner
- & Arthur Weiss
Nature 326 , 85–88

Rights & permissionsfor article Characterization of an expressed CDS-associated Ti <i>γ</i>-chain reveals <i>C</i><sub>γ</sub> domain polymorphism . Opens in a new window.
Research | 1 August 1979
A κ-immunoglobulin gene is formed by site-specific recombination without further somatic mutation
Nature 280 , 370–375

Rights & permissionsfor article A <i>κ</i>-immunoglobulin gene is formed by site-specific recombination without further somatic mutation . Opens in a new window.
Research | 22 January 2012
Epigenetic repression of cardiac progenitor gene expression by Ezh2 is required for postnatal cardiac homeostasis
Nature Genetics 44 , 343–347

Rights & permissionsfor article Epigenetic repression of cardiac progenitor gene expression by Ezh2 is required for postnatal cardiac homeostasis . Opens in a new window.
Research | 1 July 1992
The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families
- Yah-Huei Wu Chou
- , Edward M. Brown
- , Tatyana Levi
- , Gail Crowe
- , A. Brew Atkinson
- , Hans J. Arnqvist
- , Goran Toss
- , Ghada El-Hajj Fuleihan
- , J. G. Seidman
- & Christine E. Seidman
Nature Genetics 1 , 295–300

Rights & permissionsfor article The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families . Opens in a new window.
Research | 27 February 2005
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss
- Jost Schönberger
- , Libin Wang
- , Jordan T Shin
- , Sang Do Kim
- , Frederic F S Depreux
- , Hao Zhu
- , Leonard Zon
- , Anne Pizard
- , Jae B Kim
- , Calum A MacRae
- , Andy J Mungall
- , J G Seidman
- & Christine E Seidman
Nature Genetics 37 , 418–422

Rights & permissionsfor article Mutation in the transcriptional coactivator <i>EYA4</i> causes dilated cardiomyopathy and sensorineural hearing loss . Opens in a new window.
Research | 1 October 1993
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2
Nature Genetics 5 , 201–204

Rights & permissionsfor article Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2 . Opens in a new window.
Research | 31 March 1983
Multiple mRNA species with distinct 3′ termini are transcribed from the β₂-microglobulin gene
Nature 302 , 449–452

Rights & permissionsfor article Multiple mRNA species with distinct 3′ termini are transcribed from the β<sub>2</sub>-microglobulin gene . Opens in a new window.
Research | 1 February 1978
Immunoglobulin light-chain structural gene sequences cloned in a bacterial plasmid
Nature 271 , 582–585

Rights & permissionsfor article Immunoglobulin light-chain structural gene sequences cloned in a bacterial plasmid . Opens in a new window.
Research | 1 December 1978
The arrangement and rearrangement of antibody genes
- J. G. Seidman
- & Philip Leder
Nature 276 , 790–795

Rights & permissionsfor article The arrangement and rearrangement of antibody genes . Opens in a new window.
Research | 11 September 1975
Genetic perturbations that reveal tertiary conformation of tRNA precursor molecules
- William H. McClain
- & J. G. Seidman
Nature 257 , 106–110

Rights & permissionsfor article Genetic perturbations that reveal tertiary conformation of tRNA precursor molecules . Opens in a new window.
Research | 1 August 1994
A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1
- Susan Kass
- , Calum MacRae
- , Harry L. Graber
- , Elizabeth A. Sparks
- , Dennis McNamara
- , Harisios Boudoulas
- , Craig T. Basson
- , Peter B. Baker III
- , Robert J. Cody
- , Mark C. Fishman
- , Nancy Cox
- , Augustine Kong
- , Charles F. Wooley
- , J.G. Seidman
- & Christine E. Seidman
Nature Genetics 7 , 546–551

Rights & permissionsfor article A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1 . Opens in a new window.
Research | 23 December 1982
Exon shuffling: mapping polymorphic determinants on hybrid mouse transplantation antigens
Nature 300 , 755–757

Rights & permissionsfor article Exon shuffling: mapping polymorphic determinants on hybrid mouse transplantation antigens . Opens in a new window.
Research | 21 June 2009
Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection
- Daniel S Herman
- , G Kees Hovingh
- , Oleg Iartchouk
- , Heidi L Rehm
- , Raju Kucherlapati
- , J G Seidman
- & Christine E Seidman
Nature Methods 6 , 507–510

Rights & permissionsfor article Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection . Opens in a new window.
Research | 1 August 1996
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
Nature Genetics 13 , 417–421

Rights & permissionsfor article A human <i>MSX1</i> homeodomain missense mutation causes selective tooth agenesis . Opens in a new window.
Research | 1 December 1995
Mutations in the cardiac myosin binding protein–C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
- Hugh Watkins
- , David Conner
- , Ludwig Thierfelder
- , John A. Jarcho
- , Calum MacRae
- , William J. McKenna
- , Barry J. Maron
- , J.G. Seidman
- & Christine E. Seidman
Nature Genetics 11 , 434–437

Rights & permissionsfor article Mutations in the cardiac myosin binding protein–C gene on chromosome 11 cause familial hypertrophic cardiomyopathy . Opens in a new window.
Research | 10 July 1986
Identification of a putative second T-cell receptor
- Michael B. Brenner
- , Joanne McLean
- , Deno P. Dialynas
- , Jack L. Strominger
- , John A. Smith
- , Frances L. Owen
- , J. G. Seidman
- , Stephen Ip
- , Fred Rosen
- & Michael S. Krangel
Nature 322 , 145–149

Rights & permissionsfor article Identification of a putative second T-cell receptor . Opens in a new window.
Research | 11 June 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy
- Claire Horvat
- , Renee Johnson
- , Lien Lam
- , Jacob Munro
- , Francesco Mazzarotto
- , Angharad M. Roberts
- , Daniel S. Herman
- , Michael Parfenov
- , Alireza Haghighi
- , Barbara McDonough
- , Steven R. DePalma
- , Anne M. Keogh
- , Peter S. Macdonald
- , Christopher S. Hayward
- , Amy Roberts
- , Paul J. R. Barton
- , Leanne E. Felkin
- , Eleni Giannoulatou
- , Stuart A. Cook
- , J. G. Seidman
- , Christine E. Seidman
- & Diane Fatkin
Genetics in Medicine 21 , 133–143

Rights & permissionsfor article A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy . Opens in a new window.
Research | 2 July 2018
Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy
- Andre E. Minoche
- , Claire Horvat
- , Renee Johnson
- , Velimir Gayevskiy
- , Sarah U. Morton
- , Alexander P. Drew
- , Kerhan Woo
- , Aaron L. Statham
- , Ben Lundie
- , Richard D. Bagnall
- , Jodie Ingles
- , Christopher Semsarian
- , J. G. Seidman
- , Christine E. Seidman
- , Marcel E. Dinger
- , Mark J. Cowley
- & Diane Fatkin
Genetics in Medicine 21 , 650–662

Rights & permissionsfor article Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy . Opens in a new window.
Research | 27 September 2016 | Open
Loss of RNA expression and allele-specific expression associated with congenital heart disease
- David M. McKean
- , Jason Homsy
- , Hiroko Wakimoto
- , Neil Patel
- , Joshua Gorham
- , Steven R. DePalma
- , James S. Ware
- , Samir Zaidi
- , Wenji Ma
- , Nihir Patel
- , Richard P. Lifton
- , Wendy K. Chung
- , Richard Kim
- , Yufeng Shen
- , Martina Brueckner
- , Elizabeth Goldmuntz
- , Andrew J. Sharp
- , Christine E. Seidman
- , Bruce D. Gelb
- & J. G. Seidman
Nature Communications 7 , 1–9

Rights & permissionsfor article Loss of RNA expression and allele-specific expression associated with congenital heart disease . Opens in a new window.
Research | 6 October 2013
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes
- Jason Flannick
- , Nicola L Beer
- , Alexander G Bick
- , Vineeta Agarwala
- , Janne Molnes
- , Namrata Gupta
- , Noël P Burtt
- , Jose C Florez
- , James B Meigs
- , Herman Taylor
- , Valeriya Lyssenko
- , Henrik Irgens
- , Ervin Fox
- , Frank Burslem
- , Stefan Johansson
- , M Julia Brosnan
- , Jeff K Trimmer
- , Christopher Newton-Cheh
- , Tiinamaija Tuomi
- , Anders Molven
- , James G Wilson
- , Christopher J O'Donnell
- , Sekar Kathiresan
- , Joel N Hirschhorn
- , Pål R Njølstad
- , Tim Rolph
- , J G Seidman
- , Stacey Gabriel
- , David R Cox
- , Christine E Seidman
- , Leif Groop
- & David Altshuler
Nature Genetics 45 , 1380–1385

Rights & permissionsfor article Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes . Opens in a new window.
Research | 6 March 2015 | Open
NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity
- Ossama K. Abou Hassan
- , Akl C. Fahed
- , Manal Batrawi
- , Mariam Arabi
- , Marwan M. Refaat
- , Steven R. DePalma
- , J. G. Seidman
- , Christine E. Seidman
- , Fadi F. Bitar
- & Georges M. Nemer
Scientific Reports 5 , 1–8

Rights & permissionsfor article <i>NKX2-5</i> Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity . Opens in a new window.
Research | 19 February 1987
A T-cell receptor γ/CD3 complex found on cloned functional lymphocytes
Nature 325 , 683–688

Rights & permissionsfor article A T-cell receptor γ/CD3 complex found on cloned functional lymphocytes . Opens in a new window.
Research | 1 January 1997
Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome
- Craig T. Basson
- , David R. Bachinsky
- , Robert C. Lin
- , Tatjana Levi
- , Jacob A. Elkins
- , Johann Soults
- , David Grayzel
- , Elena Kroumpouzou
- , Thomas A. Traill
- , Janine Leblanc-Straceski
- , Beatrice Renault
- , Raju Kucherlapati
- , Seidman J.G
- & Christine E. Seidman
Nature Genetics 15 , 30–35

Rights & permissionsfor article Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome . Opens in a new window.
Research | 19 February 1987
Two forms of the T-cell receptor γ protein found on peripheral blood cytotoxic T lymphocytes
- Michael B. Brenner
- , Joanne McLean
- , Harriet Scheft
- , Janice Riberdy
- , Siew-Lan Ang
- , J. G. Seidman
- , Peter Devlin
- & Michael S. Krangel
Nature 325 , 689–694

Rights & permissionsfor article Two forms of the T-cell receptor γ protein found on peripheral blood cytotoxic T lymphocytes . Opens in a new window.
Research | 2 February 1984
Construction, expression and recognition of an H—2 molecule lacking its carboxyl terminus
Nature 307 , 432–436

Rights & permissionsfor article Construction, expression and recognition of an H—2 molecule lacking its carboxyl terminus . Opens in a new window.

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