Nature Search

A Medium for the Isolation of Streptococcus faecalis, sensu strictu

G. C. MEAD
Research30 Mar 1963
Nature

Volume: 197, P: 1323-1324
Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

S. Nagafuchi
H. Yanagisawa
M. Yamada
Research01 Jan 1994
Nature Genetics

Volume: 6, P: 14-18
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

Susan E. Andrew
Y. Paul Goldberg
Michael R. Hayden
Research01 Aug 1993
Nature Genetics

Volume: 4, P: 398-403
Meiotic stability and genotype – phenotype correlation of the trinucleotide repeat in X–linked spinal and bulbar muscular atrophy

Albert R. La Spada
Daniel B. Roling
Kenneth H. Fischbeck
Research01 Dec 1992
Nature Genetics

Volume: 2, P: 301-304
3-Hydroxyanthranilic Acid, A Carcinogen Produced by Endogenous Metabolism

E. BOYLAND
G. WATSON
Research05 May 1956
Nature

Volume: 177, P: 837-838
Correlation between Solar Activity and the Brightness of Jupiter's Great Red Spot

E. R. GRAF
C. E. SMITH
F. R. MCDEVITT
Research01 Jun 1968
Nature

Volume: 218, P: 857
Atmospheric waves in the ionosphere due to total solar eclipse

R. N. E. BAULCH
E. C. BUTCHER
Research01 Oct 1977
Nature

Volume: 269, P: 497-498
Positions of galactic X-ray sources Cir X-1, TrA X-1 and 3U1626—67

H. V. BRADT
K. M. V. APPARAO
T. H. MARKERT
Research01 Oct 1977
Nature

Volume: 269, P: 496-497
X-Ray and Optical Observations of the Pulsar NP 0532 in the Crab Nebula

H. BRADT
S. RAPPAPORT
J. KRISTIAN
Research24 May 1969
Nature

Volume: 222, P: 728-730
Evidence for a Galactic Component of the Diffuse X-ray Background

B. A. COOKE
R. E. GRIFFITHS
K. A. POUNDS
Research11 Oct 1969
Nature

Volume: 224, P: 134-137
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

Albert R. La Spada
Elizabeth M Wilson
Kenneth H Fischbeck
Research04 Jul 1991
Nature

Volume: 352, P: 77-79
Immune Persistence After Infant Hepatitis-B Vaccination: A Systematic Review and Meta-Analysis

Sajid Mahmood
Kifayat Ullah Shah
Tahir Mehmood Khan
ResearchOpen Access22 Aug 2018
Scientific Reports

Volume: 8, P: 1-8
Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease

R. S. Kandt
J. L. Haines
M. A. Pericak-Vance
Research01 Sept 1992
Nature Genetics

Volume: 2, P: 37-41
Lower-mantle viscosity constrained by seismicity around deglaciated regions

G. Spada
D. A. Yuen
E. Boschi
Research02 May 1991
Nature

Volume: 351, P: 53-55
Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11

Laura P.W. Ranum
Lawrence J. Schut
Dennis M. Livingston
Research01 Nov 1994
Nature Genetics

Volume: 8, P: 280-284
Positions of galactic X-ray sources: 20° < l^II < 55°

R. E. Doxsey
K. M. V. Apparao
J. G. Jernigan
Research01 Sept 1977
Nature

Volume: 269, P: 112-116
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

Lois M. Mulligan
Charis Eng
Bruce A.J. Ponder
Research01 Jan 1994
Nature Genetics

Volume: 6, P: 70-74
Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy

Catherine Tsilfidis
Alex E. MacKenzie
Robert G. Korneluk
Research01 Jun 1992
Nature Genetics

Volume: 1, P: 192-195
Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p

Launce G. Gouw
Craig D. Kaplan
Louis J. Ptácek
Research01 May 1995
Nature Genetics

Volume: 10, P: 89-93
Cosmic X-rays

H. FRIEDMAN
Research30 Nov 1968
Nature

Volume: 220, P: 862-865
Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH

James R. Burke
Jan J. Enghild
Warren J. Strittmatter
Research01 Mar 1996
Nature Medicine

Volume: 2, P: 347-350
Direct detection of novel expanded trinucleotide repeats in the human genome

Martin Schalling
Thomas J. Hudson
David E. Housman
Research01 Jun 1993
Nature Genetics

Volume: 4, P: 135-139
20 IgE LEVELS IN CHILDREN WITH RECIDIVANT RESPIRATORY INFECTIONS

G Bustos
V Croce
R De Spada
Research01 Feb 1981
Pediatric Research

Volume: 15, P: 186
Music in the first days of life

Daniela Perani
Maria Cristina Saccuman
Stefan Koelsch
ResearchOpen Access29 Jul 2008
Nature Precedings

P: 1
Movement of myosin-coated fluorescent beads on actin cables in vitro

Michael P. Sheetz
James A. Spudich
Research05 May 1983
Nature

Volume: 303, P: 31-35
Transient short time periodicities in the optical enission from Cyg X-1

G. AURIEMMA
D. CARDINI
M. RANIERI
Research01 Jan 1976
Nature

Volume: 259, P: 27-29
Characteristic Variation of Sco X-1

ROBERT E. WILSON
LAURENCE W. TWIGG
Research23 May 1970
Nature

Volume: 226, P: 734-735
High Energy X-ray Study of M–87

J. E. McCLINTOCK
W. H. G. LEWIN
G. W. CLARK
Research12 Jul 1969
Nature

Volume: 223, P: 162-163
Positions of galactic X-ray sources: 0° < l^II < 20°

R. E. DOXSEY
K. M. V. APPARAO
J. G. JERNIGAN
Research15 Dec 1977
Nature

Volume: 270, P: 586-588
Upper Limit on X-rays from a New Supernova

H. BRADT
S. NARANAN
E. BOLDT
Research01 Jun 1968
Nature

Volume: 218, P: 856-857
Reversal of Boric Acid Inhibition of Growth in Certain Soil Micro-organisms

ALAN M. SHEFNER
BETTY J. BURKHARDT
Research30 Nov 1957
Nature

Volume: 180, P: 1207-1208
Identification and characterization of the gene causing type 1 spinocerebellar ataxia

Sandro Banfi
Antonio Servadio
H.Y. Zoghbi
Research01 Aug 1994
Nature Genetics

Volume: 7, P: 513-520
CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

Yoshiya Kawaguchi
Toshihiro Okamoto
Akira Kakizuka
Research01 Nov 1994
Nature Genetics

Volume: 8, P: 221-228
Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration

Loss-of-function variants in thyroid hormone transporter MCT8 cause a neurodevelopmental and metabolic disorder. Here the authors identify genotype-phenotype relationships, advance insights in MCT8 (dys)function and create a pathogenicity-severity variant classifier.

Stefan Groeneweg
Ferdy S. van Geest
W. Edward Visser
ResearchOpen Access12 Mar 2025
Nature Communications

Volume: 16, P: 1-21
Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Using well-calibrated statistical methods the authors jointly analyze Undiagnosed Diseases Network genomes, identifying known and novel disease genes. Software is publicly available to support future cross-cohort rare disease discovery efforts.

Shilpa Nadimpalli Kobren
Mikhail A. Moldovan
Shamil R. Sunyaev
ResearchOpen Access07 Aug 2025
Nature Communications

Volume: 16, P: 1-19
Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world

Annastiina Lund
Bjarne Udd
Marja-Liisa Savontaus
Research02 Jul 2001
European Journal of Human Genetics

Volume: 9, P: 431-436
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1

Harry T. Orr
Ming-yi Chung
Huda Y. Zoghbi
Research01 Jul 1993
Nature Genetics

Volume: 4, P: 221-226
Gametic and somatic tissue–specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1

Samuel S. Chong
Alanna E. McCall
Huda Y. Zoghbi
Research01 Jul 1995
Nature Genetics

Volume: 10, P: 344-350
Characterization of the full fragile X syndrome mutation in fetal gametes

Henry E. Malter
Jane C. Iber
Ben A. Oostra
Research01 Feb 1997
Nature Genetics

Volume: 15, P: 165-169
Positions of galactic X-ray sources: 55° < l^II < 320°

R. G. DOWER
K. M. V. APPARAO
J. KULIK
Research01 Jun 1978
Nature

Volume: 273, P: 364-367
Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice

Peter M. Bingham
Marion O. Scott
Kenneth H. Fischbeck
Research01 Feb 1995
Nature Genetics

Volume: 9, P: 191-196
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG–repeat

Claude T. Ashley
James S. Sutcliffe
Stephen T. Warren
Research01 Jul 1993
Nature Genetics

Volume: 4, P: 244-251
A fusion of new ideas

Jason B. Bock
Richard H. Scheller
News & Views08 May 1997
Nature

Volume: 387, P: 133-134
The structural basis of phage display elucidated by the crystal structure of the N-terminal domains of g3p

Jacek Lubkowski
Frank Hennecke
Alexander Wlodawer
Research01 Feb 1998
Nature Structural Biology

Volume: 5, P: 140-147
Sea level since the Last Glacial Maximum from the Atlantic coast of Africa

Projections of future sea level rely on the understanding of the relationship between sea-level and past climate changes. This study reconstructs 30,000 years of sea level evolution along Atlantic Africa in response to the climatic modifications.

Matteo Vacchi
Timothy A. Shaw
Benjamin P. Horton
ResearchOpen Access10 Feb 2025
Nature Communications

Volume: 16, P: 1-9
Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases

M. Tachikawa
Y. Nagai
T. Toda
Research01 Jun 2002
Journal of Human Genetics

Volume: 47, P: 275-278
Importance of stress in bubble ordering in the helium gas-bubble superlattice in copper

P. B. Johnson
A. L. Malcolm
D. J. Mazey
Research24 Sept 1987
Nature

Volume: 329, P: 316-318
Pituitary hyperplasia and gigantism in mice caused by a cholera toxin transgene

Frank H. Burton
Karl W. Hasel
J. Gregor Sutcliffe
Research07 Mar 1991
Nature

Volume: 350, P: 74-77
The metabolomic profile of psoriatic arthritis patients unveils the unbalance of disease-related molecules and pathways

M. M. Angioni
C. Piras
A. Cauli
ResearchOpen Access30 Dec 2025
Scientific Reports

Volume: 16, P: 1-13
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

Helen G. Harley
J. David Brook
Duncan J. Shaw
Research06 Feb 1992
Nature

Volume: 355, P: 545-546

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