Nature Search

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

May Tassabehji
Andrew P. Read
Tom Strachan
Research01 Jan 1993
Nature Genetics

Volume: 3, P: 26-30
Protein Deficiency and the Growing Rat Lung. I. Nutritional Findings and Related Lung Volumes

Masendu Kalenga
Stefan A Tschanz
Peter H Burri
Research01 Jun 1995
Pediatric Research

Volume: 37, P: 783-788
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

Mayada Tassabehji
Andrew P. Read
Tom Strachan
Research13 Feb 1992
Nature

Volume: 355, P: 635-636
Protein Deficiency and the Growing Rat Lung. II. Morphometric Analysis and Morphology

Masendu Kalenga
Stefan A Tschanz
Peter H Burri
Research01 Jun 1995
Pediatric Research

Volume: 37, P: 789-795
Integrin-mediated signal transduction linked to Ras pathway by GRB2 binding to focal adhesion kinase

David D. Schlaepfer
Steven K. Hanks
Peter van der Geer
Research29 Dec 1994
Nature

Volume: 372, P: 786-791
Ancient DNA from the Green Sahara reveals ancestral North African lineage

Pastoralism spread through cultural diffusion into the Green Sahara, where an isolated, distinct North African ancestry persisted.

Nada Salem
Marieke S. van de Loosdrecht
Johannes Krause
ResearchOpen Access02 Apr 2025
Nature

Volume: 641, P: 144-150
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

Kathryn Lunetta and colleagues report a meta-analysis of 22 genome-wide association studies for age at menopause. They identify 13 loci newly associated with age at natural menopause, including several candidate genes with roles in DNA repair and immune function.

Lisette Stolk
John R B Perry
Kathryn L Lunetta
Research22 Jan 2012
Nature Genetics

Volume: 44, P: 260-268
Antenatal Endotoxin and Glucocorticoid Effects on Lung Morphometry in Preterm Lambs

Karen E Willet
Alan H Jobe
Peter D Sly
Research01 Dec 2000
Pediatric Research

Volume: 48, P: 782-788
Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease

Adult forms of inflammatory bowel disease (IBD) are of a polygenic nature, but paediatric and very early onset (VEO) IBD also occur as monogenic forms. Here, using whole exome sequencing, the authors explore both the monogenic and polygenic contribution to VEO-IBD and characterize a rare somatic mosaic VEO-IBD patient.

Eva Gonçalves Serra
Tobias Schwerd
Carl A. Anderson
ResearchOpen Access21 Feb 2020
Nature Communications

Volume: 11, P: 1-15
CNTF and psychiatric disorders

Markus M. Nöthen
Sven Cichon
Marcella Rietschel
Correspondence01 Jun 1996
Nature Genetics

Volume: 13, P: 142-143
Evolutionary analysis of the female-specific avian W chromosome

The evolution of non-recombining chromosomes is poorly understood. Here, the authors sequence the collared flycatcher female-specific W chromosome and show nonrandom survival of genes during W chromosome degeneration which is due to selection for maintaining gene dose and expression levels of essential genes.

Linnéa Smeds
Vera Warmuth
Hans Ellegren
ResearchOpen Access04 Jun 2015
Nature Communications

Volume: 6, P: 1-10
Bricks and mortar of the epidermal barrier

Zoltan Nemes
Peter M Steinert
ResearchOpen Access01 Mar 1999
Experimental & Molecular Medicine

Volume: 31, P: 5-19
Microbial network disturbances in relapsing refractory Crohn’s disease

A disturbed microbial network characterizes relapsing refractory Crohn’s disease and antedates disease recurrence after surgical removal of the active disease segment.

Bahtiyar Yilmaz
Pascal Juillerat
Andrew J. Macpherson
Research21 Jan 2019
Nature Medicine

Volume: 25, P: 323-336
Effects of Neonatal High-Dose Short-Term Glucocorticoid Treatment on the Lung: A Morphologic and Morphometric Study in the Rat

Stefan A Tschanz
Andrew N Makanya
Peter H Burri
Research01 Jan 2003
Pediatric Research

Volume: 53, P: 72-80
The global atlas of edible insects: analysis of diversity and commonality contributing to food systems and sustainability

Evanson R. Omuse
Henri E. Z. Tonnang
Saliou Niassy
ResearchOpen Access29 Feb 2024
Scientific Reports

Volume: 14, P: 1-17
Publisher Correction: Microbial network disturbances in relapsing refractory Crohn’s disease

Bahtiyar Yilmaz
Pascal Juillerat
Andrew J. Macpherson
Amendments and Corrections07 Mar 2019
Nature Medicine

Volume: 25, P: 701
Author Correction: Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease

Eva Gonçalves Serra
Tobias Schwerd
Carl A. Anderson
Amendments and CorrectionsOpen Access22 Jun 2022
Nature Communications

Volume: 13, P: 1
Adenovirus-mediated overexpression of p14^ARF induces p53 and Bax-independent apoptosis

Philipp G Hemmati
Bernhard Gillissen
Peter T Daniel
Research07 May 2002
Oncogene

Volume: 21, P: 3149-3161
Gamma-glutamyltransferase, arterial remodeling and prehypertension in a healthy population at low cardiometabolic risk

Michaela Kozakova
Amalia Gastaldelli
Carlo Palombo
Research29 Apr 2020
Journal of Human Hypertension

Volume: 35, P: 334-342
Impairment of Rat Postnatal Lung Alveolar Development by Glucocorticoids: Involvement of the p21^CIP1 and p27^KIP1 Cyclin-Dependent Kinase Inhibitors

Sophie Corroyer
Johannes C Schittny
Annick Clement
Research01 Feb 2002
Pediatric Research

Volume: 51, P: 169-176
Loss of the branched-chain amino acid transporter CD98hc alters the development of colonic macrophages in mice

CD98hc in macrophages attenuates the severity of colitis. This change in the macrophage development is associated with increased expression of apoptotic genes, suggesting that CD98hc maintains the gut homeostasis by ensuring the development of gut macrophages.

Philipp Wuggenig
Berna Kaya
Jan Hendrik Niess
ResearchOpen Access18 Mar 2020
Communications Biology

Volume: 3, P: 1-19
Reference database of total retinal vessel surface area derived from volume-rendered optical coherence tomography angiography

Peter M. Maloca
Silvia Feu-Basilio
Javier Zarranz-Ventura
ResearchOpen Access07 Mar 2022
Scientific Reports

Volume: 12, P: 1-9
Goltz–Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap

May-Britt Harmsen
Silvia Azzarello-Burri
Kerstin Kutsche
Research11 Mar 2009
European Journal of Human Genetics

Volume: 17, P: 1207-1215
Validation of virtual reality orbitometry bridges digital and physical worlds

Peter M. Maloca
Balázs Faludi
Philippe C. Cattin
ResearchOpen Access16 Jul 2020
Scientific Reports

Volume: 10, P: 1-9

Search

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

Protein Deficiency and the Growing Rat Lung. I. Nutritional Findings and Related Lung Volumes

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

Protein Deficiency and the Growing Rat Lung. II. Morphometric Analysis and Morphology

Integrin-mediated signal transduction linked to Ras pathway by GRB2 binding to focal adhesion kinase

Ancient DNA from the Green Sahara reveals ancestral North African lineage

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

Antenatal Endotoxin and Glucocorticoid Effects on Lung Morphometry in Preterm Lambs

Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease

CNTF and psychiatric disorders

Evolutionary analysis of the female-specific avian W chromosome

Bricks and mortar of the epidermal barrier

Microbial network disturbances in relapsing refractory Crohn’s disease

Effects of Neonatal High-Dose Short-Term Glucocorticoid Treatment on the Lung: A Morphologic and Morphometric Study in the Rat

The global atlas of edible insects: analysis of diversity and commonality contributing to food systems and sustainability

Publisher Correction: Microbial network disturbances in relapsing refractory Crohn’s disease

Author Correction: Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease

Adenovirus-mediated overexpression of p14^ARF induces p53 and Bax-independent apoptosis

Gamma-glutamyltransferase, arterial remodeling and prehypertension in a healthy population at low cardiometabolic risk

Impairment of Rat Postnatal Lung Alveolar Development by Glucocorticoids: Involvement of the p21^CIP1 and p27^KIP1 Cyclin-Dependent Kinase Inhibitors

Loss of the branched-chain amino acid transporter CD98hc alters the development of colonic macrophages in mice

Reference database of total retinal vessel surface area derived from volume-rendered optical coherence tomography angiography

Goltz–Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap

Validation of virtual reality orbitometry bridges digital and physical worlds

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