PubMed Health⌕ Search

Biomedical subjects

N M Blake

Publications and source records attributed to N M Blake.

At least 19 recordsLinked to original sources

Postnatal growth of intrinsic connections in mouse barrel cortex.

Surprisingly little is known about the development of connections within a functional area of the cerebral cortex. We examined the postnatal growth of connections in mouse barrel cortex during the second and third weeks after birth, coinciding with the period of rapid synaptogenesis that occurs just after the barrels first form. A barrel is a group of neurons in layer 4 of somatosensory cortex that is part of a cortical column. Each whisker/barrel column is linked anatomically and functionally to a homotopic whisker on the contralateral face. Radial groups of cortical neurons were labeled with the neuronal tracer biotinylated dextran amine in mice ranging in age from postnatal day 8 (P8; P0 is the date of birth) to adulthood. The spatial distributions of retrogradely labeled neurons in different laminae were analyzed. The barrel map in layer 4 was used as a template to compare quantitative data from different animals and to account for substantial changes in barrel and barrel field size during development. Intrinsic projections 1) innervate increasingly more distant targets within barrel cortex up to 3 weeks of age; 2) continue to form in targets after 3 weeks, effectively strengthening existing connections; 3) follow a timetable for growth that is layer-specific; 4) link more distant barrel columns in layer 4 from neurons that are found preferentially in the barrel side and the septa between barrels; and 5) form over the shortest distances between the barrel columns. These data indicate that intrinsic connections in mouse barrel cortex develop by the progressive addition of neuronal connections rather than by sculpting preliminary connections. We describe statistically significant changes in connectivity during development that may be applied to model and assess the development of connections after a variety of experimental perturbations, such as to the environment and/or the genome.

Aging↗

Red cell enzyme and serum protein gene markers in Fijians.

A total of 332 persons from three localities in the Fiji Islands have been tested for genetic variation in 24 red cell enzyme systems and 4 serum protein systems. Polymorphic variation was present at 7 red cell enzyme loci and 1 serum protein locus. The remaining systems were invariant except for a single individual with a slow variant at the GOT1 locus and another individual with a D variant at the TF locus. The series from Nandi differed significantly from the Lau Islands for gene frequencies in GPT, ACP and ESD, Koro Island differed from the other localities at the PGD locus and from Nandi for ESD. Genetic distance analysis reveals that Lau Islands cluster with Western Samoa, Koro Island with New Caledonia (Vanuatu), with Nandi being separate.

Blood Proteins↗

Population genetic studies in the Kimberley of Western Australia.

More than 800 blood samples from members of 13 tribal groups in the northwest of Australia have been tested for 18 enzyme systems controlled by 21 loci and for haemoglobin. Two novel alleles, PGM2(11) and ACP1F, are each restricted to a single tribal population, suggesting relatively recent mutations. Other alleles conform very broadly with their distributions in other Australian Aboriginal populations. In particular, PGM2(3) maintains its inland distribution whilst PGDE and PEP B6 continue to be restricted to the north of the continent. Comparisons between tribes show the Baada to be distinctive, with high values of PGM1(2), GPT2, CA2(4) and ESD2 as well as having the novel allele ACP1F.

Acid Phosphatase↗

Placental enzymes: a population genetic study.

A total of more than 800 placentae from six different population groups have been examined for electrophoretic variation in 13 enzyme systems. Whilst, in many instances, the phenotype designation is presumptive, having been arrived at after critical visual comparison with illustrations in the literature, a number of new alleles have been reported here and further population genetic data have been presented. Two new alleles, MPI3 and MPI4 are described in the mannose phosphate isomerase system the former in both the Port Moresby sample and in the Chinese, whilst the latter was restricted to the Chinese samples. Also, the New Guinea MDHs 3-1 phenotype has been detected for the first time in placentae. In addition, a new allele in the aconitase system, ACONs8 has been described in the Chinese samples.

Aconitate Hydratase↗

Search for a red cell enzyme or serum protein marker in amyotrophic lateral sclerosis and parkinsonism-dementia of Guam.

Frequency distributions were determined for 24 red cell enzyme and four serum protein systems, in an attempt to identify a genetic marker associated with either amyotrophic lateral sclerosis (ALS) or parkinsonism-dementia (PD), two progressive and fatal neurological disorders of unknown cause found with unusually high incidence among the Chamorros of Guam and the Northern Mariana Islands. No striking associations were identified between either disorder and any of the gene markers tested. Thus, no genetic cause is known for either disease; local environmental factors are most likely involved in pathogenesis.

Amyotrophic Lateral Sclerosis↗

A population genetic study of the Banks and Torres Islands (Vanuatu) and of the Santa Cruz Islands and Polynesian Outliers (Solomon Islands).

As part of a multidisciplinary survey of populations in the Banks and Torres Islands of Vanuatu and the Southern and Central Districts of the Solomon Islands, nearly 2,400 persons have been tested for ABO blood groups and a number of serum protein and red cell enzyme genetic marker systems. For the ABO system, the populations are characterized in general by high gene O and low gene B frequencies except in two of the Polynesian Outlier Islands, Rennell and Bellona, which have high frequencies of B. Among the serum proteins, several alleles have distributions indicating significant movement of people between islands. These include Albumin New Guinea and the transferrin alleles TfD1, and TfBLae, and TfB2. Similar specific alleles for red cell enzymes also show distributions reflecting interisland population movement as well as contact with persons from outside the southern Pacific region. Examples are ACPR1 in the acid phosphatase system, PGM31 and PGM71, PGM92, and PGM102, PGK4 and also HbJTongariki. The data available for 11 polymorphic systems were used to generate genetic distances. Of the four Polynesian Outlier Islands, Anuta is most remote genetically, with Rennell and Bellona also relatively isolated. The fourth Polynesian Outlier, Tikopia, occupies a position genetically close to the Melanesian populations of the Banks and Torres Islands and the southern Solomons. The history of early European contact and voyaging in the Pacific, as well as archaeological and linguistic evidence and local legends, indicate that significant movements of people occurred between islands and provided opportunities for genes to be introduced from Europeans, Africans, and Asians. The genetic marker studies give evidence for genes from all these sources, though at a low level. Despite this admixture, the Polynesian Outlier and Melanesian populations have preserved their own distinctive genetic patterns.

ABO Blood-Group System↗

The genetic demography of the Gainj of Papua New Guinea. I. Local differentiation of blood group, red cell enzyme, and serum protein allele frequencies.

Allele frequencies are reported for 19 blood group, red cell enzyme, and serum protein loci (ABO, Rh, MN, Hb-A, LDH-A, LDH-B, SOD, PGM-1, PGM-2, 6PGD, GPT, ESD, ADA, ACP, PGK, MDH, Alb, Hp, and Tf) determined from 310 blood samples collected among the Gainj, a small population of tribal horticulturalists from highland Papua New Guniea. Fourteen of these loci display genetic variants, and ten of them are sufficiently polymorphic to permit a preliminary analysis of Gainj population structure. Patterns of variation among subdivisions of the population are analyzed using an approach analogous to a multivariate analysis of variance with unbalanced design, and weighted genetic distances are extracted from the results. The distance analysis indicates that patterns of genetic variation within this population reflect the geographical distribution of subdivisions, as well as subdivision size and movement among subdivisions. A parallel analysis of the Gainj and two other tribal groups from highland New Guinea, the Murapin Enga and the Simbai Valley Maring, suggests that the Gainj are both genetically divergent from neighboring populations and internally highly differentiated.

Adult↗

Red cell enzyme polymorphism: gene differentiation in three populations of Maharashtra, India.

Blood samples of 1,266 individuals were collected from three caste populations; Nava Budha (Mahar), Maratha, and a mixed group of Scheduled castes from each of three districts of Maharashtra, Nagpur, Akola, and Thane. The samples were tested for 12 enzyme systems, viz., AcPh, AK, CA-I, CA-II, Est-D, LDH, MDH, Oxidase, PGM-1, PGM-2, 6-PGD, and PHI. The gene frequencies of these loci are within the ranges observed among the Indian populations so far studied. The total differences in gene frequencies for each polymorphic locus was partitioned into three components, i.e., the differences between caste populations, the differences between regions, and the differences due to interaction between caste populations and regions. The results show that besides caste variation for two loci, Est-D and PGM-1, the gene frequencies for AK, Est-D, and G-6PD loci have different geographical distributions.

Erythrocytes↗

HLA antigens in Bali (Indonesia) with a special reference to an isolated community.

One hundred eighty-two Balinese were typed for HLA-A and -B locus antigens. From these, 103 were also typed for HLA-C, 51 for HLA-DR, 172 for Bf and 173 for GLO. These results and the significant phenotypic associations are situated with respect to other South-East Asian populations. In addition to this first study, 175 individuals from an isolated Balinese village typed for HLA-A, -B, -DR, Bf and GLO are presented. The effect of isolation on haplotype (HLA-A/-B/Bf/-DR) variability is discussed.

Asia, Southeastern↗

Genetic survey of an isolated community in Bali, Indonesia. I. Blood groups, serum proteins and hepatitis B serology.

320 adults and children of an isolated community of Bali, Indonesia, have been tested for blood groups ABO, Rh, MNS, P, Lewis, Duffy, Kell, for haptoglobin and transferrin and for hepatitis B surface antigen and antibodies. Phenotype distribution and gene frequencies are given for the total population tested and for two subgroups representative of the inbred population of the isolate and of the non-inbred part of the population. Significant differences between the two subgroups show a clear genetic drift in the inbred population. The study brings biological support to the ethnological hypothesis of population migrations in this area. Tests for hepatitis B surface antigen reveal a lower prevalence of the disease than in most other south-east Asian populations.

Adolescent↗

Blood group, red cell enzyme and serum protein types in the Buka Islanders, Papua New Guinea.

Genetic marker studies on a sample of 80 speakers of the Petats and Tinputs families of languages, all pupils at a single high school, indicate a homogeneity among them which can be extrapolated to their areas of origin. Buka and its offshore islands and the northern part of Bougainville Island in the North Solomons Province of Papua New Guinea. Several markers systems, most notably first-locus phosphoglucomutase and liver acetyltransferase, reinforce the morphological evidence that these peoples are quite distinct from most other Papua New Guinea populations, with whom, however, there has been some gene exchange, probably through East New Britain. Their principal affinities are with the peoples of the Solomon Islands to the south.

Acetyltransferases↗

Genetic studies on the Koya Dora and Konda Kammara tribes of Andhra Pradesh, India.

A total of 209 persons belonging to the Koya Dora and Konda Kammara tribes in the East Godavari District of Andhra Pradesh, have been tested for electrophoretic variation in 9 red cell enzyme systems. The gene frequencies for the systems showing variation are, in general, within the range for other Andhra Pradesh tribal populations. There is 1 example of PHI 2-1 in the Konda Kammara, while 1 case each of PHI 3-1 and 2-1 are reported in the Koya Dora. In PGM1, there is one example of the 6-2 phenotype and one of 4-1 in the Koya Dora. The Koya Dora show a relatively lower frequency of the EsD2 allele compared to the Konda Kammara. The gene frequencies for the GLO system are reported here for the first time among Indian tribals and these are within the Indian range. LDH Calcutta 1 was not detected in either population.

Acid Phosphatase↗

Genetic survey of an isolated community in Bali, Indonesia. II. Haemoglobin types and red cell isozymes.

316 adults and children from an isolated community of Bali, Indonesia, have been tested for 18 red cell enzyme systems controlled by 24 loci, and haemoglobin. 13 loci were invariant. The other 11 loci showed variations similar to those found previously in Southeast Asian populations. Of special interest is the occurrence of lactate dehydrogenase Calcutta-1 variants, indicating Indian gene admixture, and PGM92, indicating a Melanesian genetic component. A few individuals were CA1 1-3Bali and this is possibly the same as other CA1 1-3 types found in the Philippines and Guam. Nearly 10% were glucose-6-phosphate dehydrogenase (G6PD) deficient and 2% carried Hb E. A fast electrophoretic variant of G6PD was detected in 5 persons. Two sub-groups of the population were studied. Gene frequencies in the Isolate supported the view that inbreeding and genetic drift have made this sub-group genetically distinct from the non-inbred part of the population.

Adolescent↗

A population genetic study of Goodenough Island, Papua New Guinea.

A sample of 105 coastal people and 82 mountain dwellers from Goodenough Island, off the eastern tip of Papua New Guinea have been tested for four blood group systems, haemoglobin, 17 enzyme systems and four serum proteins. Transferrins D1 and Blae were found in both populations and the frequency of almost 29% for PGDc in the mountain people is one of the highest for the region. Deficiency of G-6 PD and the presence of PGK4 were detected only in the coastal populations.

Adult↗

Serogenetic studies on the Kamea (Kapau) Anga of the interior of the Gulf Province of Papua.

Though the Anga or Kukukuku of Papua New Guinea have been the subjects of occasional human biological investigations in the past, these have all been directed from the north, and their largest division, the Kamea or Kapau, who occupy the southeastern half of their territory, have been substantially neglected. The present paper describes the results of sero-genetic investigations of a small sample of Kamea, who are shown to resemble their fellow-Anga closely in the distribution of their genetic markers, though there are indications that the Kamea have received some gene flow from the south. On the whole, though, the relative uniformity of gene marker distribution throughout the Anga points strongly to their common origin, and the paucity of signs of immigrant gene flow from their neighbours, the victims of their raids, tends to confirm that they practised cannibalism rather than the genetic incorporation of captives.

Blood Group Antigens↗

Genetic studies on some tribes of the Telangana region, Andhra, Pradesh, India.

Phenotype distributions and gene frequencies of nine red cell enzyme systems and haemoglobin are presented for six tribal populations from the Telangana region of Andhra Pradesh. AEO, MN and Rh blood group data are presented for four of these tribes. The results have been compared with these from other Andhra Pradesh tribal Populations. The Yerukula tribe are notable for the presence of PGM7 1 at polymorphic frequency, the occurrence of a single example of PGM10 2 and the absence of Hbs.

Blood Group Antigens↗

Frequency of private electrophoretic variants and indirect estimates of mutation rate in Papua New Guinea.

Data on rare and private electrophoretic variants have been used to estimate mutation rates for populations belonging to 55 language groups in Papua New Guinea. Three different methods yield values of 1.42 x 10(-6), 1.40 x 10(-6), and 5.58 x 10(-6)/locus per generation. The estimates for three islands populations off the north coast of New Guinea--Manus, Karkar, and Siassi--are much lower. The variability in mutation rates estimated from rare electrophoretic variants as a function of population size is discussed. The mean mutation rate in Papua New Guinea is less than half the estimates obtained for Australian Aborigines and Amerindians.

Enzymes↗