26 research outputs found
Selective Breeding for a Behavioral Trait Changes Digit Ratio
- Author
- A Ăkten
- AA Bailey
- AA Bailey
- D Rubolini
- DA Putz
- EL Rezende
- Erik I. Svensson
- F Baker
- GD Wilson
- HW Kloepfer
- J Hönekopp
- JC Loehlin
- Jessica L. Malisch
- JG Swallow
- JL Chang
- JL Malsich
- JL CW Malisch
- JT Manning
- JT Manning
- JT Manning
- JT Manning
- JT Manning
- JT Manning
- JT Manning
- KL Gobrogge
- L Pokrywka
- M Romano
- M Voracek
- MH McIntyre
- MH McIntyre
- MP Lombardo
- N Saino
- NT Burley
- Peter L. Hurd
- PL Hurd
- PL Hurd
- R George
- R Gitau
- Reginia H. Y. Yan
- Robert M. Hannon
- RR Sokal
- S Lutchmaya
- SC Gammie
- SM van Anders
- SN Paul
- SN Paul
- Theodore Garland
- VR Phelps
- W Forstmeier
- WM Brown
- WM Brown
- Z Benderlioglu
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2008
- Field of study
The ratio of the length of the second digit (index finger) divided by the fourth digit (ring finger) tends to be lower in men than in women. This 2Dâ¶4D digit ratio is often used as a proxy for prenatal androgen exposure in studies of human health and behavior. For example, 2Dâ¶4D ratio is lower (i.e. more âmasculinizedâ) in both men and women of greater physical fitness and/or sporting ability. Lab mice have also shown variation in 2Dâ¶4D as a function of uterine environment, and mouse digit ratios seem also to correlate with behavioral traits, including daily activity levels. Selective breeding for increased rates of voluntary exercise (wheel running) in four lines of mice has caused correlated increases in aerobic exercise capacity, circulating corticosterone level, and predatory aggression. Here, we show that this selection regime has also increased 2Dâ¶4D. This apparent âfeminizationâ in mice is opposite to the relationship seen between 2Dâ¶4D and physical fitness in human beings. The present results are difficult to reconcile with the notion that 2Dâ¶4D is an effective proxy for prenatal androgen exposure; instead, it may more accurately reflect effects of glucocorticoids, or other factors that regulate any of many genes
Molecular genetics of human primary microcephaly: an overview
- Author
- A Genin
- A Gul
- A Gul
- A Gul
- A Kumar
- A Petrovic
- A Saadi
- Adeel G Chaudhary
- AK Nicholas
- AM Kaindl
- AP Jackson
- Asad Muhammad Ilyas
- AT Pagnamenta
- BD McCreary
- BL Finlay
- C Ponting
- CA Tan
- CG Woods
- CP Ponting
- DL Guernsey
- E Kalay
- E Papari
- E Roberts
- EP Lucas
- F Muhammad
- Farid Ahmed
- GH Mochida
- GK Thornton
- H Darvish
- Hasan Saleh Jamal
- HG Farag
- HT Kim
- Hussain A Algahtani
- HW Kloepfer
- IM Cheeseman
- J Bond
- J Bond
- J Bond
- J Chen
- J Cox
- J Desir
- J Hoyer
- J Van Den Bosch
- JH Cho
- JL Rickmyre
- JN Pulvers
- JS Andersen
- K Bilguvar
- K Brunk
- K Kim
- K Matsuura
- KL Pfaff
- KW Fong
- L Issa
- L Luo
- LY Hung
- LY Hung
- M do Carmo Avides
- M Garshasbi
- M Ghani-Kakhki
- M Kirkham
- M Koyanagi
- M Paramasivam
- M Sajid Hussain
- M Trimborn
- M Trimborn
- M Trimborn
- Mahmood Rasool
- MG Riparbelli
- MJ Grossel
- MJ Grossel
- MJ Hassan
- Mohammad H Al-Qahtani
- MS Al-Dosari
- MS Hussain
- MS Hussain
- Muhammad Faheem
- Muhammad Imran Naseer
- N Kouprina
- N Kraemer
- N Tommerup
- NR Stevens
- P Rakic
- Peter Natesan Pushparaj
- R Basto
- R Craig
- R Gruber
- RD Saunders
- S Awad
- S Campaner
- S Izraeli
- S Passemard
- SA Fietz
- T Kiyomitsu
- T Komai
- T Ohta
- Taha A Kumosani
- TJ McGarry
- TL Megraw
- TW Yu
- X Xu
- X Zhang
- Y Uetake
- YJ Yang
- ZW Zhou
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
International Consensus Statement on Rhinology and Allergy: Rhinosinusitis
- Author
- Aanaes K
- Abadie WM
- Abi Najm S
- Abigail P
- Abrahams JJ
- Abrass LJ
- Abreu CB
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- Abuzeid WM
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- Adappa ND
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- Adriaensen G
- Agache I
- Aghamohammadi A
- Agius AM
- Agyeman AA
- Ahn CN
- Ahn HJ
- Ahn JC
- Ahn SH
- AhovuoâSaloranta A
- Aitken M
- Ajaiyeoba A
- Akbari E
- Akdis CA
- Akira S
- Akiyama K
- Akiyama K
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- American Academy of Pediatrics Steering Committee on Quality Improvement and Management (AAP SCQIM)
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- Zuskin E
- Äulig J
- Publication venue
- 'Wiley'
- Publication date
- 01/01/2021
- Field of study
Background: The 5 years since the publication of the first International Consensus Statement on Allergy and Rhinology: Rhinosinusitis (ICARâRS) has witnessed foundational progress in our understanding and treatment of rhinologic disease. These advances are reflected within the more than 40 new topics covered within the ICARâRSâ2021 as well as updates to the original 140 topics. This executive summary consolidates the evidenceâbased findings of the document. Methods: ICARâRS presents over 180 topics in the forms of evidenceâbased reviews with recommendations (EBRRs), evidenceâbased reviews, and literature reviews. The highest grade structured recommendations of the EBRR sections are summarized in this executive summary. Results: ICARâRSâ2021 covers 22 topics regarding the medical management of RS, which are grade A/B and are presented in the executive summary. Additionally, 4 topics regarding the surgical management of RS are grade A/B and are presented in the executive summary. Finally, a comprehensive evidenceâbased management algorithm is provided. Conclusion: This ICARâRSâ2021 executive summary provides a compilation of the evidenceâbased recommendations for medical and surgical treatment of the most common forms of RS
Skin rash, a kidney mass and a family mystery dating back to World War II
- Author
- Publication venue
- 'AMPCo'
- Publication date
- Field of study
Familial cutaneous leiomyomatosis in multiple generations with varied morphological presentations
- Publication venue
- 'Wiley'
- Publication date
- Field of study
Familial occurrence of mitral valve prolapse in X-linked muscular dystrophy.
- Publication venue
- 'Ovid Technologies (Wolters Kluwer Health)'
- Publication date
- Field of study
Duchenne Muscular Dystrophy in a 46 XY Female
- Publication venue
- 'SAGE Publications'
- Publication date
- Field of study
Gastric Leiomyoma and Hyperplastic Polyposis Coli in a Patient with Multiple Cutaneous and Uterine Leiomyomatosis
- Author
- Publication venue
- 'SAGE Publications'
- Publication date
- Field of study
Adhalin deficiency : An unusual cause of muscular dystrophy
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Weill-Marchesani syndrome in three generations
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/12/1999
- Field of study
Background Weill-Marchesani syndrome is a rare systemic connective tissue disorder consisting of brachymorphy, brachydactyly, ectopia lentis, spherophakia and glaucoma