Literature DB >> 4245389

The genetic component in child mortality.

D F Roberts, J Chavez, S D Court.   

Abstract

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Mesh：

Year:  1970        PMID： 4245389      PMCID： PMC2020428          DOI： 10.1136/adc.45.239.33

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  64 in total

1.  Post-transcriptional modification of spliceosomal RNAs is normal in SMN-deficient cells.

Authors:  Svetlana Deryusheva; Maria Choleza; Adrien Barbarossa; Joseph G Gall; Rémy Bordonné
Journal:  RNA       Date:  2011-11-28       Impact factor: 4.942

2.  Genetic counselling: a tool for the prevention of some abnormal pregnancies.

Authors:  M Bobrow
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1976

3.  Discovery, synthesis, and biological evaluation of novel SMN protein modulators.

Authors:  Jingbo Xiao; Juan J Marugan; Wei Zheng; Steve Titus; Noel Southall; Jonathan J Cherry; Matthew Evans; Elliot J Androphy; Christopher P Austin
Journal:  J Med Chem       Date:  2011-08-19       Impact factor: 7.446

4.  Lentivector-mediated SMN replacement in a mouse model of spinal muscular atrophy.

Authors:  Mimoun Azzouz; Thanh Le; G Scott Ralph; Lucy Walmsley; Umrao R Monani; Debbie C P Lee; Fraser Wilkes; Kyriacos A Mitrophanous; Susan M Kingsman; Arthur H M Burghes; Nicholas D Mazarakis
Journal:  J Clin Invest       Date:  2004-12       Impact factor: 14.808

5.  Temporal requirement for high SMN expression in SMA mice.

Authors:  Thanh T Le; Vicki L McGovern; Isaac E Alwine; Xueyong Wang; Aurelie Massoni-Laporte; Mark M Rich; Arthur H M Burghes
Journal:  Hum Mol Genet       Date:  2011-06-13       Impact factor: 6.150

6.  Congenital malformations and genetic diseases in Iranian infants.

Authors:  D D Farhud; G R Walizadeh; M S Kamali
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

7.  Inbreeding and the incidence of childhood genetic disorders in Karnataka, South India.

Authors:  A R Devi; N A Rao; A H Bittles
Journal:  J Med Genet       Date:  1987-06       Impact factor: 6.318

8.  Intragenic complementation of amino and carboxy terminal SMN missense mutations can rescue Smn null mice.

Authors:  Vicki L McGovern; Kaitlyn M Kray; W David Arnold; Sandra I Duque; Chitra C Iyer; Aurélie Massoni-Laporte; Eileen Workman; Aalapi Patel; Daniel J Battle; Arthur H M Burghes
Journal:  Hum Mol Genet       Date:  2020-11-01       Impact factor: 6.150

9.  SMA CARNI-VAL trial part I: double-blind, randomized, placebo-controlled trial of L-carnitine and valproic acid in spinal muscular atrophy.

Authors:  Kathryn J Swoboda; Charles B Scott; Thomas O Crawford; Louise R Simard; Sandra P Reyna; Kristin J Krosschell; Gyula Acsadi; Bakri Elsheik; Mary K Schroth; Guy D'Anjou; Bernard LaSalle; Thomas W Prior; Susan L Sorenson; Jo Anne Maczulski; Mark B Bromberg; Gary M Chan; John T Kissel
Journal:  PLoS One       Date:  2010-08-19       Impact factor: 3.240

10.  Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophy.

Authors:  Stefania Corti; Monica Nizzardo; Martina Nardini; Chiara Donadoni; Sabrina Salani; Dario Ronchi; Francesca Saladino; Andreina Bordoni; Francesco Fortunato; Roberto Del Bo; Dimitra Papadimitriou; Federica Locatelli; Giorgia Menozzi; Sandra Strazzer; Nereo Bresolin; Giacomo P Comi
Journal:  J Clin Invest       Date:  2008-10       Impact factor: 14.808
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