Zobrazeno 1 - 10
of 107
pro vyhledávání: '"J. P. Muh"'
Publikováno v:
Andrologia. 27:91-97
Summary The effect of human follicular fluid (hFF) on the cholesterol and phospholipid content and the movement characteristics of human spermatozoa were studied. Semen was selected by a discontinuous Percoll gradient and incubated during in vitro ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17a383587aac3fb6c10afeb83872ae0e
https://doi.org/10.1111/j.1439-0272.1995.tb01077.x
https://doi.org/10.1111/j.1439-0272.1995.tb01077.x
Publikováno v:
Developmental Medicine & Child Neurology. 34:593-603
Levels of dopamine (DA) and its derivatives homovanillic acid (HVA), 3-4 dihydroxyphenylacetic acid (DOPAC), 3-methoxytyramine (3MT) and norepinephrine+epinephrine (NE + E), and serotonin (5HT) and its derivative 5-hydroxyindolacetic acid (5HIAA) wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7751f0b5d78e9e09baecbb6bc4f0730
https://doi.org/10.1111/j.1469-8749.1992.tb11490.x
https://doi.org/10.1111/j.1469-8749.1992.tb11490.x
Autor:
Gilbert Lelord, J. P. Muh, Josiane Hérault, D. Sauvage, Laurence Hameury, Joëlle Martineau, Elisabeth Petit, Jacques Mallet, P. Guérin, A. Perrot
Publikováno v:
Developmental Medicine & Child Neurology. 36:688-697
The authors determined levels of dopamine (DA) and its derivatives homovanillic acid (HVA), 3-4 dihydroxyphenylacetic acid (DOPAC), 3 methoxytyramine and norepinephrine + epinephrine (NE + E) in the urine, and DA, E and NE in the whole blood of 50 au
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d55f47736351e4f6b2147dca90fa0905
https://doi.org/10.1111/j.1469-8749.1994.tb11911.x
https://doi.org/10.1111/j.1469-8749.1994.tb11911.x
Autor:
Martine Raynaud, Marie-Pierre Moizard, J. P. Muh, Nathalie Ronce, Sylvain Briault, Chantal Gendrot, Juliette Dourlens, Claude Moraine, Annick Toutain
Publikováno v:
Europe PubMed Central
Gene localization was determined by linkage analysis in a large French family with X-linked mental retardation (MRX). Seven living affected males were clinically studied and the clinical picture was characterized by moderate to severe mental handicap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ab84f2938b7b58855bafc88abccaf31
https://doi.org/10.1111/j.1399-0004.1994.tb04012.x
https://doi.org/10.1111/j.1399-0004.1994.tb04012.x
Autor:
Sylviane Védrine, Patrick Vourc'h, Sabine Dessay, Olivier Mbarek, Christian R. Andres, J. P. Muh
Publikováno v:
Developmental Brain Research. 144:159-168
Oligodendrocyte-myelin glycoprotein (OMgp) is expressed on the surface of oligodendrocytes and neurones and is thought to inhibit axonal regeneration after brain injury in adult, like Nogo and myelin-associated glycoprotein (MAG). We previously obser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::561f2f10d74ae1cb0433119c549177ec
https://doi.org/10.1016/s0165-3806(03)00167-6
https://doi.org/10.1016/s0165-3806(03)00167-6
Autor:
J. P. Muh, Thierry Moreau, Patrick Vourc'h, Sylviane Marouillat-Védrine, Flavie Arbion, Christian R. Andres
Publikováno v:
Journal of Neurochemistry. 85:889-897
The oligodendrocyte myelin glycoprotein (OMgp) inhibits neurite outgrowth and axonal regeneration after brain injury, but its normal function remains unknown. Several observations suggest its implication in cell growth regulation. Here we report an a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::609284c2c6d19a9cb5cbaef906a61791
https://doi.org/10.1046/j.1471-4159.2003.01764.x
https://doi.org/10.1046/j.1471-4159.2003.01764.x
Autor:
Catherine Barthélémy, J. P. Muh, Olivier Mbarek, Sylviane Marouillat, Joëlle Martineau, Christian R. Andres
Publikováno v:
American Journal of Medical Genetics. 88:729-732
Neurofibromatosis type 1 (NF1) is increased about 150-fold in autistic patients. The aim of this study was to test for an association between the NF1 locus and autistic disorder. The allele distributions of three markers of the NF1 gene were studied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4651615a431dbd35e31a99dbc4851604
https://doi.org/10.1002/(sici)1096-8628(19991215)88:6<729::aid-ajmg26>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19991215)88:6<729::aid-ajmg26>3.0.co
Autor:
Veronique Mayeux-Portas, Philippe Corcia, Jawad Khoris, J. P. Muh, William Camu, E. Bieth, Christian R. Andres, B. de Toffol, Alain Autret, Philippe Couratier
Publikováno v:
Scopus-Elsevier
Spinal muscular atrophy (SMA) is caused by SMN1 gene deletions or mutations, and ALS is the most frequent motor neuron condition in adults. The authors describe three families in which ALS and SMA coexist. The authors found that no SOD1 mutation was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d4d9ad161cd48b0867aaefd1ea6c15a
https://doi.org/10.1212/01.wnl.0000032500.73621.c5
https://doi.org/10.1212/01.wnl.0000032500.73621.c5
Autor:
Gilbert Lelord, Catherine Barthélémy, J. P. Muh, J. Jouve, Josiane Hérault, Joëlle Martineau, H. Tournade, Anne Perrot-Beaugerie
Publikováno v:
European Child & Adolescent Psychiatry. 2:211-220
Levels of serotonin (5-HT), dopamine (DA), norepinephrine (NE) and epinephrine (E) were determined in the whole blood and urine of 23 children with autism and compared to those of normal children. Very significant group effects (low whole blood 5-HT,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b15d740d1b408b1378a328836c688be9
https://doi.org/10.1007/bf02098580
https://doi.org/10.1007/bf02098580