Nature Search

Frequency of Prader–Willi syndrome in births conceived via assisted reproductive technology

June-Anne Gold
Chelsey Ruth
Virginia E. Kimonis
Research08 Aug 2013
Genetics in Medicine

Volume: 16, P: 164-169
Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

Eric Bieth
Sanaa Eddiry
Maïthé Tauber
Research11 Jun 2014
European Journal of Human Genetics

Volume: 23, P: 252-255
Diagnosis and management of Silver–Russell syndrome: first international consensus statement

Silver–Russell syndrome (SRS) is an imprinting disorder that causes prenatal and postnatal growth retardation. This Consensus Statement summarizes recommendations for clinical diagnosis, investigation and management of patients with SRS, including the use of growth hormone and gonadotropin-releasing hormone analogues.

Emma L. Wakeling
Frédéric Brioude
Irène Netchine
ReviewsOpen Access02 Sept 2016
Nature Reviews Endocrinology

Volume: 13, P: 105-124
Long-term metabolic risk among children born premature or small for gestational age

Mericq and colleagues review human data supporting an increased risk of metabolic diseases among children born premature or small for gestational age. The adrenal and pubertal modifications that contribute to this risk and the metabolic changes that occur during adolescence and adulthood are discussed.

Veronica Mericq
Alejandro Martinez-Aguayo
Anita Hokken-Koelega
Reviews19 Aug 2016
Nature Reviews Endocrinology

Volume: 13, P: 50-62
T-cell receptor δ gene rearrangements in early thymocytes

Yueh-hsiu Chiei
Makio Iwashima
Mark M. Davis
Research31 Dec 1987
Nature

Volume: 330, P: 722-727
Pregnancy-acquired memory CD4⁺ regulatory T cells improve pregnancy outcome in mice

Obstetric complications are less frequent in subsequent than in first pregnancies, and one potential difference is immunological adaptation of the mothers. Here authors compare the immunological landscape of the uterine microenvironment in mice during first and subsequent pregnancies to find that tolerogenic regulatory T cells recognising foetal antigens accumulate in subsequent pregnancies to enable better foetal development and overall pregnancy outcome.

Kristin Thiele
Christopher Urbschat
Petra Clara Arck
ResearchOpen Access15 Jul 2025
Nature Communications

Volume: 16, P: 1-16
Vertically transferred maternal immune cells promote neonatal immunity against early life infections

Maternal immune cells seed into the foetus during mammalian pregnancy, yet the functional role of these cells is unclear. Here the authors show that maternal immune cells in foetal bone marrow stimulate immune development, subsequently reducing the risk or severity of infections in newborns.

Ina Annelies Stelzer
Christopher Urbschat
Petra Clara Arck
ResearchOpen Access04 Aug 2021
Nature Communications

Volume: 12, P: 1-14
Limited receptor repertoire in a mycobacteria-reactive subset of γδ T lymphocytes

Mary Pat Happ
Ralph T. Kubo
Rebecca L. O'Brien
Research07 Dec 1989
Nature

Volume: 342, P: 696-698
Negative regulation of airway responsiveness that is dependent on γδ T cells and independent of αβ T cells

Michael Lahn
Arihiko Kanehiro
Willi Born
Research01 Oct 1999
Nature Medicine

Volume: 5, P: 1150-1156
Peptide sequences of T-cell receptor δ and γ chains are identical to predicted X and γ proteins

Willi Born
Craig Miles
Ralph T. Kubo
Research10 Dec 1987
Nature

Volume: 330, P: 572-574
Cytosine base editor 4 but not adenine base editor generates off-target mutations in mouse embryos

Hye Kyung Lee, Harold E. Smith et al. examined the fidelity of cytosine base editor 4 (BE4) and adenine base editors (ABEs) in mouse embryos using whole-genome sequencing of a family-based trio cohort. They show that BE4-edited mice carry more single-nucleotide variants and deletions than ABE-edited mice.

Hye Kyung Lee
Harold E. Smith
Lothar Hennighausen
ResearchOpen Access09 Jan 2020
Communications Biology

Volume: 3, P: 1-6
The Physiologic Development of Fetuin-A Serum Concentrations in Children

Martin Häusler
Cora Schäfer
Willi Jahnen-Dechent
Research01 Dec 2009
Pediatric Research

Volume: 66, P: 660-664
Topological classification of cycloadditions occurring on-surface and in the solid-state

Understanding cycloaddition mechanisms is beneficial for the creation of extended carbon nanostructures, yet traditional models often overlook symmetry-based mechanistic effects. Here, the authors employ topological classifiers to identify symmetry-forbidden pathways in polycyclic aromatic azomethine ylide cycloadditions, revealing that topologically-allowed endothermic reactions can guide nanographene engineering.

Juan Li
Amir Mirzanejad
Carlos-Andres Palma
ResearchOpen Access03 Dec 2025
Communications Chemistry

Volume: 8, P: 1-10
GROWTH HORMONE THERAPY IN TRACHEOMALACIA

L L Key
S M Willi
N M Wright
Research01 May 1993
Pediatric Research

Volume: 33, P: S49
Risk of celiac disease autoimmunity is modified by interactions between CD247 and environmental exposures

Anna Eurén
Kristian Lynch
Eric Triplett
ResearchOpen Access26 Oct 2024
Scientific Reports

Volume: 14, P: 1-14
γδ T cell effector functions: a blend of innate programming and acquired plasticity

γδ T cells have innate cell-like attributes that allow them to rapidly produce cytokines and become cytotoxic in response to cell stress and infection. Here, the authors describe how they acquire these effector functions through both developmental programming and polarization in the periphery.

Marc Bonneville
Rebecca L. O'Brien
Willi K. Born
Reviews11 Jun 2010
Nature Reviews Immunology

Volume: 10, P: 467-478
The healing touch of epidermal T cells

After skin wounding, tissue repair requires the division and growth of skin epithelial cells. A new study in mice shows that specialized T lymphocytes found in skin, epidermal γδ T cells, are induced by wounding to secrete growth factors that accelerate wound healing.

Willi K. Born
Rebecca L. O'Brien
News & Views01 Jun 2002
Nature Medicine

Volume: 8, P: 560-561
Whole-Body Protein Parameters in Premature Infants: A Comparison of Different ¹⁵N Tracer Substances and Different Methods

Klaus D Wutzke
Willi Heine
Marlies Uhlemann
Research01 Feb 1992
Pediatric Research

Volume: 31, P: 95-101
A Deletion in the Long Arm of Chromosome 18 in a Child with Serum Carnosinase Deficiency

Steven M Willi
Yizong Zhang
Kenton R Holden
Research01 Feb 1997
Pediatric Research

Volume: 41, P: 210-213
Diversity of γδ T-cell antigens

Willi K Born
M Kemal Aydintug
Rebecca L O'Brien
Reviews22 Oct 2012
Cellular & Molecular Immunology

Volume: 10, P: 13-20

Search

Frequency of Prader–Willi syndrome in births conceived via assisted reproductive technology

Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

Diagnosis and management of Silver–Russell syndrome: first international consensus statement

Long-term metabolic risk among children born premature or small for gestational age

T-cell receptor δ gene rearrangements in early thymocytes

Pregnancy-acquired memory CD4⁺ regulatory T cells improve pregnancy outcome in mice

Vertically transferred maternal immune cells promote neonatal immunity against early life infections

Limited receptor repertoire in a mycobacteria-reactive subset of γδ T lymphocytes

Negative regulation of airway responsiveness that is dependent on γδ T cells and independent of αβ T cells

Peptide sequences of T-cell receptor δ and γ chains are identical to predicted X and γ proteins

Cytosine base editor 4 but not adenine base editor generates off-target mutations in mouse embryos

The Physiologic Development of Fetuin-A Serum Concentrations in Children

Topological classification of cycloadditions occurring on-surface and in the solid-state

GROWTH HORMONE THERAPY IN TRACHEOMALACIA

Risk of celiac disease autoimmunity is modified by interactions between CD247 and environmental exposures

γδ T cell effector functions: a blend of innate programming and acquired plasticity

The healing touch of epidermal T cells

Whole-Body Protein Parameters in Premature Infants: A Comparison of Different ¹⁵N Tracer Substances and Different Methods

A Deletion in the Long Arm of Chromosome 18 in a Child with Serum Carnosinase Deficiency

Diversity of γδ T-cell antigens

Search

Quick links

Search

Filter By:

Search

Quick links