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MYHMuslim Youth Helpline (United Kingdom)
MYHMyosin Heavy Chain
MYHMonterey California Hyatt (Amtrak station code; Monterey, CA)
MYHMoorhead Youth Hockey (Moorhead, MN)
MYHMissoula Youth Homes (Missoula, MT)
References in periodicals archive ?
Nakabeppu, "Regulation of intracellular localization of human MTH1, OGG1, and MYH proteins for repair of oxidative DNA damage," Progress in Nucleic Acid Research and Molecular Biology, vol.
Myotubes were identified by immunocytochemistry with anti-myosin heavy chain (MYH) antibody (Figure 3D).
She was shifted to the maternity ward at the Maharaja Yeshwantrao Hospital (MYH), where the baby was delivered via C-section.
The baby weighs 3.5 kg," Dr Lakshmi Maru, head of gynaecology department at MYH said.
In some cases, AFAP is associated with biallelic germline mutations in the base-excision repair gene MUTYH [(or MYH) mutt homolog (Escherichia coli)] showing an autosomal recessive pattern (5).
The current study found significant upregulation of embryonic myosin heavy polypeptide (MYH) isoform genes in the paretic leg.
Individuals with copies of the MutY human homologue (MYH) mutation on both alleles are at increased risk of colon and rectal cancers and are significantly more likely than other individuals to be diagnosed with colorectal adenoma before age 50.
It should read: "I adjured you [historical present] by I-am-who-I-am His name, PSGD' is His name, 'PSGD' is His name, TWBH TYH MYH is His name, YH(WH), the living and existing is His name, hekhalotic passage," instead of Levene's "(he omits 'I adjured you by') I-am-that-I-am, His name PSGDA', His Name A'PSGDA', His Name TWBH TYH MYH, His Name living YH QA', His Name"; cf.
The gene, called MYH, was discovered by Cardiff University and NHS researchers.
Incluso en la PAF atenuada, es dificil definir a partir de que numero de polipos habria que sospecharla y proceder a un estudio del gen APC o del MYH.
Among the biological/anatomical traits identified by this approach are bipedalism, cranial capacity, dentition, an opposable thumb, a lowered larynx, a developed Broca's area of the brain, the presence of a frameshift mutation in the MYH 16 (myosin heavy chain type 16) gene, and the structure of the ASPM (abnormal spindle-like microcephaly) associated gene.