CiteULike: dchughes's Brunner:HG [3 articles]

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	Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes. [My Copy] The Journal of clinical investigation, Vol. 97, No. 4. (15 February 1996), pp. 1010-1019. by J. W. Lenders, G. Eisenhofer, N. G. Abeling, et al.W. Berger, D. L. Murphy, C. H. Konings, L. M. Wagemakers, I. J. Kopin, F. Karoum, A. H. van Gennip, H. G. Brunner posted to maob mir by dchughes on 2008-12-16 11:35:35 as
	<I>MYO15A</I> (<I>DFNB3</I>) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation [My Copy] American Journal of Medical Genetics Part A, Vol. 143A, No. 20. (2007), pp. 2382-2389. by Ersan Kalay, Abdullah Uzumcu, Elmar Krieger, et al.Refik Çaylan, Oya Uyguner, Melike Ulubil-Emiroglu, Hidayet Erdol, Hülya Kayserili, Gunter Hafiz, Nermin Ba&scedil;erer, Angelien J. G. M. Heister, Hans C. Hennies, Peter Nürnberg, Seher Ba&scedil;aran, Han G. Brunner, Cor W. R. J. Cremers, Ahmet Karaguzel, Bernd Wollnik, Hannie Kremer posted to deafness mir myo15a myosin by dchughes on 2007-09-27 11:10:17 as along with 1 person shirleym
	Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome. [My Copy] Am J Hum Genet, Vol. 79, No. 2. (August 2006), pp. 370-377. by T. Kleefstra, H. G. Brunner, J. Amiel, et al.A. R. Oudakker, W. M. Nillesen, A. Magee, D. Geneviève, V. Cormier-Daire, H. van Esch, J. P. Fryns, B. C. Hamel, E. A. Sistermans, B. B. de Vries, H. van Bokhoven posted to 9q43 ehmt1 jouberts-syndrome mir by dchughes on 2006-11-29 10:38:44 as along with 2 groups G4ID Genetics-of-Gambling

forensic	589
mir	286
chromatin	169
retrotransposition	166
sperm	150
zona-pellucida	145
mirna	112
mitochondria	98
fraud	97
str	84
genome	78
rnai	78
ancient-dna	76
fertility	74
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retrotransposon	67
art	66
neuroscience	64
avian	57
molecular-phylogenetics	57
evolution	56
sperm-egg-recognition	55
mt-pcr	55
synaptic-plasticity	54
human-variation	54
y-chromosome	53
histone	48
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sine	47
human-genetics	46
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sports-genetics	45
infertility	44
zp3	43
comparative-analysis	42
bioinformatics	41
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fish	39
sex-determination	39
human-identification	38
embryo	38
genetics	36
transcriptional-regulation	36
transcription	34
ethnicity	34
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dog	33
oocyte	32
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human-genome	32
mass-disaster	32
snps	31
genome-duplication	31
forensic-animal	30
ovary	30
epigenetics	29
fertilisation	29
pgd	29
fish-egg-envelope	29
ivf	29
mass-fatalities	29
neuron	28
expression-profiling	28
mammal	28
adaptive-evolution	27
alu	27
disc1	26
splicing	26
oogenesis	26
dna-extraction	26
gene-duplication	25
deafness	25
human-evolution	25
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historical	25
retrovirus	24
chicken-zp	24
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bdnf	24
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cancer	21
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x-inactivation	20
arc	20
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mouse	16
l1	16
species	16
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y-str	15
arf6	15
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rolling-circle-amplification	14
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src	14
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neanderthal	13
fta	13
maob	13
dna-database	13
dendrin	13
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capacitation	12
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aims	12
rapd	12
molecular-biology	12
camkii	12
ubiquitin	12
ethics	12
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cloning	11
stem-cell	11
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axon	11
schizophrenia	11
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hippo	11
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p53	10
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mtpcr	10
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hox	10
pcr	10
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azf	10
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erv	9
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protein	9
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actn3	8
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axonal-transport	8
chicken-genomics	8
ovarian-failure	8
translational-regulation	8
secondary-dna-transfer	8
dna	8
gene	8
fluorescent-protein	8
zona-pellucida-carbohydrate	8
beta-arrestin	8
methylation	8
molecular-clock	8
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rho	8
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ciita	7
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herv	7
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trkc	7
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mao	7
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smc	7
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nuclear-architecture	7
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ahi1	5
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fig-alpha	5
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cep290	4
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acetylcholine-receptor	4
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bmpr2	4
myosin	4
translation	4
atm	4
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es-cells	4
sry	4
transcription-factories	4
kidney	4
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protein-folding	4
paternity-testing	4
protamine	4
encode	4
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ancient-proteomics	4
irs-pcr	4
exonic-splicing-enhancer-elements	4
alzheimers	4
education	4
foxp2	4
fmrp	4
sperm-oocyte-fusion	4
mental-retardation	4
ak2	4
speciation-genetics	4
cold-case	4
sperm-morphology	4
reproduction	4
zpc	4
xist	3
cilia	3
whi2	3
hair-texture	3
svp3	3
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ck2	3
splice-site	3
spleen	3
molecular-sexing	3
crb1	3
long-range-effects	3
vector	3
syntaphilin	3
molecular-biology-education	3
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knockout-mice	3
vectors	3
igf1	3
fto	3
genomics	3
gametes	3
review	3
height-human	3
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basque	3
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autism	3
mouse-ko	3
genetic-technology	3
leptin	3
quantum-dot	3
emulsion-pcr	3
plant	3
dm1	3
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ty3gypsy	3
membranes	3
genotyping	3
genome-annotation	3
htr3e	3
cat	3
vesicles	3
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baculovirus	3
insulin	3
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creld1	3
reproductive-proteins	3
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dna-transposon	3
oncogene	3
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crb2	3
dna-collection	3
fundamental-concepts-in-genetics	3
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arhgef6	3
argonaute	3
orthologs	3
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jak3	3
usp9y	3
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synaptogyrin	3
sex	3
ests	3
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amida	3
protein-protein-interaction	3
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glutamate-receptor	3
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fluorescence-resonance-energy-transfer	3
gene-expression	3
egg-sperm-interactions	3
chip	3
non-coding-dna	3
infant-gut-flora	3
parkinsons	3
mecp2	3
psd	3
adcy1	3
aging	3
oocyte-transcriptome	3
bac	3
fluorescence-complementation	2
epistasis	2
scientific-process	2
psd4	2
blogging	2
hnf4a	2
bmp	2
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avpr2	2
actin-reorganisation	2
prostasomes	2
dmwd	2
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mirtrons	2
monogenic-disorders	2
gene-ontology	2
arhgef17	2
insertional-mutagenesis	2
gap	2
female-reproductive-function	2
sequence	2
progesterone	2
cdh22	2
fusion-genes	2
prion	2
lymphangiogenesis	2
pharmacogenetics	2
il1rap1	2
qprt	2
boston-strangler	2
cumulus-oocyte-complex	2
hypoxia	2
5-ht	2
aneuploidy	2
arhge6	2

dchughes's Brunner:HG [3 articles] Export

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