Zobrazeno 1 - 7
of 7
pro vyhledávání: '"H M, Lachman"'
Autor:
H. M. Lachman
Publikováno v:
Current psychiatry reports. 8(2)
Twin, family, and adoption studies show that genetic factors play a significant role in vulnerability to becoming addicted to drugs. Through a combination of genetic approaches, the variant alleles responsible for interindividual differences in susce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06e586cd8d7cd1728bc255321ad777ae
https://pubmed.ncbi.nlm.nih.gov/16539891
https://pubmed.ncbi.nlm.nih.gov/16539891
Publikováno v:
American journal of medical genetics. 96(3)
Histamine is a central nervous system (CNS) neurotransmitter that has been implicated in the pathophysiology of schizophrenia. Histamine N-methyltransferase (HNMT) terminates the neurotransmitter actions of histamine in the mammalian CNS, and levels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a3998532fc781d3b4d377e96b10421e5
https://pubmed.ncbi.nlm.nih.gov/10898922
https://pubmed.ncbi.nlm.nih.gov/10898922
Publikováno v:
American journal of medical genetics. 96(3)
The absence of father-to-son transmission has been observed in a subset of families with bipolar disorder (BPD), suggestive of a susceptibility gene on the sex-linked portion of the X chromosome. This is supported by some genetic linkage studies that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1144cc6ae1bdddeed465ba0630201271
https://pubmed.ncbi.nlm.nih.gov/10898908
https://pubmed.ncbi.nlm.nih.gov/10898908
Publikováno v:
American journal of medical genetics. 88(4)
Evidence for a bipolar disorder (BPD) susceptibility locus on chromosome 22q11 has been provided in several studies. One candidate gene that maps to this region is the G-protein alpha subunit gene Galphaz (GNAZ). We have identified a common silent po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::679b1bed543c7fedf3e60fb55dcd442b
https://pubmed.ncbi.nlm.nih.gov/10402497
https://pubmed.ncbi.nlm.nih.gov/10402497
Publikováno v:
American journal of medical genetics. 74(4)
Allelic variants at the catechol-O-methyltransferase (COMT) locus are candidates to contribute to genetic components of interindividual differences in vulnerability to substance abuse. COMT plays a prominent role in dopaminergic circuits important fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e67cfc0008820e96d7ad1d08dfaf87cc
https://pubmed.ncbi.nlm.nih.gov/9259381
https://pubmed.ncbi.nlm.nih.gov/9259381
Autor:
H M, Lachman, J R, Kelsoe, R A, Remick, A D, Sadovnick, M H, Rapaport, M, Lin, B A, Pazur, A M, Roe, T, Saito, D F, Papolos
Publikováno v:
American journal of medical genetics. 74(2)
Velo-cardio-facial syndrome (VCFS) is a congenital anomaly characterized by multiple dysmorphisms, cleft palate, cardiac anomalies, and learning disabilities, that results from a microdeletion of chromosome 22q11. An increased prevalence of psychiatr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f07e40718c50fdef48517afcf40f3126
https://pubmed.ncbi.nlm.nih.gov/9129709
https://pubmed.ncbi.nlm.nih.gov/9129709
Autor:
H M, Lachman, B, Morrow, R, Shprintzen, S, Veit, S S, Parsia, G, Faedda, R, Goldberg, R, Kucherlapati, D F, Papolos
Publikováno v:
American journal of medical genetics. 67(5)
Velo-cardio-facial-syndrome (VCFS) is a common congenital disorder associated with typical facial appearance, cleft palate, cardiac defects, and learning disabilities. The majority of patients have an interstitial deletion on chromosome 22q11. In add
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1a976bd0d302296d00cad6ae554b1a7e
https://pubmed.ncbi.nlm.nih.gov/8886163
https://pubmed.ncbi.nlm.nih.gov/8886163